12286 lines
637 KiB
JSON
12286 lines
637 KiB
JSON
[
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{
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"Publication Type": "J",
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"Authors": "Protesescu, L; Yakunin, S; Bodnarchuk, MI; Krieg, F; Caputo, R; Hendon, CH; Yang, RX; Walsh, A; Kovalenko, MV",
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"Book Authors": null,
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"Book Editors": null,
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"Book Group Authors": null,
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"Author Full Names": "Protesescu, Loredana; Yakunin, Sergii; Bodnarchuk, Maryna I.; Krieg, Franziska; Caputo, Riccarda; Hendon, Christopher H.; Yang, Ruo Xi; Walsh, Aron; Kovalenko, Maksym V.",
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"Book Author Full Names": null,
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"Group Authors": null,
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"Article Title": "nullocrystals of Cesium Lead Halide Perovskites (CsPbX3, X = Cl, Br, and I): Novel Optoelectronic Materials Showing Bright Emission with Wide Color Gamut",
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"Source Title": "nullO LETTERS",
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"Book Series Title": null,
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"Book Series Subtitle": null,
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"Language": null,
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"Document Type": "Article",
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"Conference Title": null,
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"Conference Date": null,
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"Conference Location": null,
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"Conference Sponsor": null,
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"Conference Host": null,
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"Author Keywords": null,
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"Keywords Plus": null,
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"Abstract": "Metal halides perovskites, such as hybrid organic-inorganic CH3NH3PbI3, are newcomer optoelectronic materials that have attracted enormous attention as solution-deposited absorbing layers in solar cells with power conversion efficiencies reaching 20%. Herein we demonstrate a new avenue for halide perovskites by designing highly luminescent perovskite-based colloidal quantum dot materials. We have synthesized monodisperse colloidal nullocubes (4-15 nm edge lengths) of fully inorganic cesium lead halide perovskites (CsPbX3, X = Cl, Br, and I or mixed halide systems Cl/Br and Br/I) using inexpensive commercial precursors. Through compositional modulations and quantum size-effects, the bandgap energies and emission spectra are readily tunable over the entire visible spectral region of 410-700 nm. The photoluminescence of CsPbX3 nullocrystals is characterized by narrow emission line-widths of 12-42 nm, wide color gamut covering up to 140% of the NTSC color standard, high quantum yields of up to 90%, and radiative lifetimes in the range of 1-29 ns. The compelling combination of enhanced optical properties and chemical robustness makes CsPbX3 nullocrystals appealing for optoelectronic applications, particularly for blue and green spectral regions (410-530 nm), where typical metal chalcogenide-based quantum dots suffer from photodegradation.",
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"Addresses": null,
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"Affiliations": null,
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"Reprint Addresses": null,
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"Email Addresses": null,
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"Researcher Ids": null,
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"ORCIDs": null,
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"Funding Orgs": null,
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"Funding Name Preferred": null,
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|
"Funding Text": null,
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|
"Cited References": null,
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"Cited Reference Count": null,
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"Times Cited, WoS Core": 7392,
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|
"Times Cited, All Databases": 7899,
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"180 Day Usage Count": null,
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"Since 2013 Usage Count": null,
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"Publisher": null,
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"Publisher City": null,
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"Publisher Address": null,
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"ISSN": null,
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"eISSN": null,
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"ISBN": null,
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"Journal Abbreviation": null,
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"Journal ISO Abbreviation": null,
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"Publication Date": "JUN",
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"Publication Year": 2015,
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"Volume": 15,
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"Issue": 6,
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"Part Number": null,
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"Supplement": null,
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"Special Issue": null,
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"Meeting Abstract": null,
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"Start Page": 3692,
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"End Page": 3696,
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"Article Number": null,
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"DOI": "10.1021/nl5048779",
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"DOI Link": "http://dx.doi.org/10.1021/nl5048779",
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"Book DOI": null,
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|
"Early Access Date": null,
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|
"Number of Pages": null,
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|
"WoS Categories": null,
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"Web of Science Index": null,
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|
"Research Areas": "Chemistry; Science & Technology - Other Topics; Materials Science; Physics",
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|
"IDS Number": null,
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|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
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|
"UT (Unique WOS ID)": "WOS:000356316900006",
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|
"Web of Science Record": "View Full Record in Web of Science"
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},
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{
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"Publication Type": "J",
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"Authors": "Nedelcu, G; Protesescu, L; Yakunin, S; Bodnarchuk, MI; Grotevent, MJ; Kovalenko, MV",
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"Book Authors": null,
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"Book Editors": null,
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"Book Group Authors": null,
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"Author Full Names": "Nedelcu, Georgian; Protesescu, Loredana; Yakunin, Sergii; Bodnarchuk, Maryna I.; Grotevent, Matthias J.; Kovalenko, Maksym V.",
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"Book Author Full Names": null,
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"Group Authors": null,
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"Article Title": "Fast Anion-Exchange in Highly Luminescent nullocrystals of Cesium Lead Halide Perovskites (CsPbX3, X = Cl, Br, I)",
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"Source Title": "nullO LETTERS",
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"Book Series Title": null,
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"Book Series Subtitle": null,
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"Language": null,
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"Document Type": "Article",
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"Conference Title": null,
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"Conference Date": null,
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"Conference Location": null,
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"Conference Sponsor": null,
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"Conference Host": null,
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"Author Keywords": null,
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"Keywords Plus": null,
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"Abstract": "Postsynthetic chemical transformations of colloidal nullocrystals, such as ion-exchange reactions, provide an avenue to compositional fine-tuning or to otherwise inaccessible materials and morphologies. While cation-exchange is facile and commonplace, anion-exchange reactions have not received substantial deployment. Here we report fast, low-temperature, deliberately partial, or complete anionexchange in highly luminescent semiconductor nullocrystals of cesium lead halide perovskites (CsPbX3, X = Cl, Br, I). By adjusting the halide ratios in the colloidal nullocrystal solution, the bright photoluminescence can be tuned over the entire visible spectral region (410-700 nm) while maintaining high quantum yields of 20 80% and narrow emission line widths of 10-40 nm (from blue to red). Furthermore, fast internullocrystal anion-exchange is demonstrated, leading to uniform CsPb(Cl/Br)(3) or CsPb(Br/I)(3) compositions simply by mixing CsPbCl3, CsPbBr3, and CsPbI3 nullo crystals in appropriate ratios.",
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"Addresses": null,
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"Affiliations": null,
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"Reprint Addresses": null,
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"Email Addresses": null,
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"Researcher Ids": null,
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"ORCIDs": null,
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"Funding Orgs": null,
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|
"Funding Name Preferred": null,
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|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
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|
"Times Cited, WoS Core": 2047,
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|
"Times Cited, All Databases": 2199,
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|
"180 Day Usage Count": null,
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"Since 2013 Usage Count": null,
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|
"Publisher": null,
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"Publisher City": null,
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|
"Publisher Address": null,
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"ISSN": null,
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"eISSN": null,
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"ISBN": null,
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|
"Journal Abbreviation": null,
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"Journal ISO Abbreviation": null,
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"Publication Date": "AUG",
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"Publication Year": 2015,
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"Volume": 15,
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"Issue": 8,
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"Part Number": null,
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"Supplement": null,
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"Special Issue": null,
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"Meeting Abstract": null,
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"Start Page": 5635,
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"End Page": 5640,
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"Article Number": null,
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"DOI": "10.1021/acs.nullolett.5b02404",
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"DOI Link": "http://dx.doi.org/10.1021/acs.nullolett.5b02404",
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"Book DOI": null,
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"Early Access Date": null,
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|
"Number of Pages": null,
|
|
"WoS Categories": null,
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|
"Web of Science Index": null,
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|
"Research Areas": "Chemistry; Science & Technology - Other Topics; Materials Science; Physics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
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|
"Date of Export": "2025-04-23",
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|
"UT (Unique WOS ID)": "WOS:000359613700119",
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|
"Web of Science Record": "View Full Record in Web of Science"
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},
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{
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"Publication Type": "J",
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"Authors": "Drozdov, AP; Eremets, MI; Troyan, IA; Ksenofontov, V; Shylin, SI",
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"Book Authors": null,
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"Book Editors": null,
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"Book Group Authors": null,
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"Author Full Names": "Drozdov, A. P.; Eremets, M. I.; Troyan, I. A.; Ksenofontov, V.; Shylin, S. I.",
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"Book Author Full Names": null,
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"Group Authors": null,
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"Article Title": "Conventional superconductivity at 203 kelvin at high pressures in the sulfur hydride system",
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"Source Title": "NATURE",
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"Book Series Title": null,
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"Book Series Subtitle": null,
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"Language": null,
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"Document Type": "Article",
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"Conference Title": null,
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"Conference Date": null,
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"Conference Location": null,
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"Conference Sponsor": null,
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"Conference Host": null,
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"Author Keywords": null,
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"Keywords Plus": null,
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"Abstract": "A superconductor is a material that can conduct electricity without resistance below a superconducting transition temperature, T-c. The highest T-c that has been achieved to date is in the copper oxide system(1): 133 kelvin at ambient pressure(2) and 164 kelvin at high pressures(3). As the nature of superconductivity in these materials is still not fully understood (they are not conventional superconductors), the prospects for achieving still higher transition temperatures by this route are not clear. In contrast, the Bardeen-Cooper-Schrieffer theory of conventional superconductivity gives a guide for achieving high T-c with no theoretical upper bound-all that is needed is a favourable combination of high-frequency phonons, strong electron-phonon coupling, and a high density of states(4). These conditions can in principle be fulfilled for metallic hydrogen and covalent compounds dominated by hydrogen(5,6), as hydrogen atoms provide the necessary high-frequency phonon modes as well as the strong electron-phonon coupling. Numerous calculations support this idea and have predicted transition temperatures in the range 50-235 kelvin for many hydrides(7), but only a moderate T-c of 17 kelvin has been observed experimentally(8). Here we investigate sulfur hydride(9), where a T-c of 80 kelvin has been predicted(10). We find that this system transforms to a metal at a pressure of approximately 90 gigapascals. On cooling, we see signatures of superconductivity: a sharp drop of the resistivity to zero and a decrease of the transition temperature with magnetic field, with magnetic susceptibility measurements confirming a T-c of 203 kelvin. Moreover, a pronounced isotope shift of T-c in sulfur deuteride is suggestive of an electron-phonon mechanism of superconductivity that is consistent with the Bardeen-Cooper-Schrieffer scenario. We argue that the phase responsible for high-T-c superconductivity in this system is likely to be H3S, formed from H2S by decomposition under pressure. These findings raise hope for the prospects for achieving room-temperature superconductivity in other hydrogen-based materials.",
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"Addresses": null,
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"Affiliations": null,
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"Reprint Addresses": null,
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"Email Addresses": null,
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"Researcher Ids": null,
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"ORCIDs": null,
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"Funding Orgs": null,
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|
"Funding Name Preferred": null,
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|
"Funding Text": null,
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|
"Cited References": null,
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|
"Cited Reference Count": null,
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"Times Cited, WoS Core": 1830,
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|
"Times Cited, All Databases": 1999,
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|
"180 Day Usage Count": null,
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|
"Since 2013 Usage Count": null,
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"Publisher": null,
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"Publisher City": null,
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"Publisher Address": null,
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"ISSN": null,
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"eISSN": null,
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|
"ISBN": null,
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"Journal Abbreviation": null,
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"Journal ISO Abbreviation": null,
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"Publication Date": "SEP 3",
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"Publication Year": 2015,
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"Volume": 525,
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"Issue": 7567,
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"Part Number": null,
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"Supplement": null,
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"Special Issue": null,
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"Meeting Abstract": null,
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"Start Page": 73,
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|
"End Page": "+",
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|
"Article Number": null,
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|
"DOI": "10.1038/nature14964",
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|
"DOI Link": "http://dx.doi.org/10.1038/nature14964",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000360594100027",
|
|
"Web of Science Record": "View Full Record in Web of Science"
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|
},
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|
{
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|
"Publication Type": "J",
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|
"Authors": "Anasori, B; Xie, Y; Beidaghi, M; Lu, J; Hosler, BC; Hultman, L; Kent, PRC; Gogotsi, Y; Barsoum, MW",
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|
"Book Authors": null,
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|
"Book Editors": null,
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|
"Book Group Authors": null,
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|
"Author Full Names": "Anasori, Babak; Xie, Yu; Beidaghi, Majid; Lu, Jun; Hosler, Brian C.; Hultman, Lars; Kent, Paul R. C.; Gogotsi, Yury; Barsoum, Michel W.",
|
|
"Book Author Full Names": null,
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|
"Group Authors": null,
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"Article Title": "Two-Dimensional, Ordered, Double Transition Metals Carbides (MXenes)",
|
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"Source Title": "ACS nullO",
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|
"Book Series Title": null,
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|
"Book Series Subtitle": null,
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"Language": null,
|
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"Document Type": "Article",
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"Conference Title": null,
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"Conference Date": null,
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"Conference Location": null,
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"Conference Sponsor": null,
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"Conference Host": null,
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"Author Keywords": null,
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"Keywords Plus": null,
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"Abstract": "The higher the chemical diversity and structural complexity of two-dimensional (2D) materials, the higher the likelihood they possess unique and useful properties. Herein, density functional theory (DFT) is used to predict the existence of two new families of 2D ordered, carbides (MXenes), M'M-2 '' C-2 and M'M-2 '' C-2(3), where M' and M '' are two different early transition metals. In these solids, M' layers sandwich M carbide layers. By synthesizing Mo2TiC2Tx, Mo2Ti2C3Tx, and Cr2TiC2Tx (where T is a surface termination), we validated the DFT predictions. Since the Mo and Cr atoms are on the outside, they control the 2D flakes' chemical and electrochemical properties. The latter was proven by showing quite different electrochemical behavior of Mo2TiC2Tx and Ti3C2Tx. This work further expands the family of 2D materials, offering additional choices of structures, chemistries, and ultimately useful properties.",
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"Addresses": null,
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"Affiliations": null,
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"Reprint Addresses": null,
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"Email Addresses": null,
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"Researcher Ids": null,
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"ORCIDs": null,
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|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 1476,
|
|
"Times Cited, All Databases": 1593,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
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"Publisher": null,
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|
"Publisher City": null,
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|
"Publisher Address": null,
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|
"ISSN": null,
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|
"eISSN": null,
|
|
"ISBN": null,
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|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
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"Publication Date": "OCT",
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|
"Publication Year": 2015,
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"Volume": 9,
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"Issue": 10,
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|
"Part Number": null,
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|
"Supplement": null,
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|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 9507,
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|
"End Page": 9516,
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|
"Article Number": null,
|
|
"DOI": "10.1021/acsnullo.5b03591",
|
|
"DOI Link": "http://dx.doi.org/10.1021/acsnullo.5b03591",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry; Science & Technology - Other Topics; Materials Science",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000363915300009",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
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|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Vance, ME; Kuiken, T; Vejerano, EP; McGinnis, SP; Hochella, MF; Rejeski, D; Hull, MS",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Vance, Marina E.; Kuiken, Todd; Vejerano, Eric P.; McGinnis, Sean P.; Hochella, Michael F., Jr.; Rejeski, David; Hull, Matthew S.",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "nullotechnology in the real world: Redeveloping the nullomaterial consumer products inventory",
|
|
"Source Title": "BEILSTEIN JOURNAL OF nullOTECHNOLOGY",
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|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
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"Conference Title": null,
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"Conference Date": null,
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"Conference Location": null,
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"Conference Sponsor": null,
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"Conference Host": null,
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"Author Keywords": null,
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"Keywords Plus": null,
|
|
"Abstract": "To document the marketing and distribution of nullo-enabled products into the commercial marketplace, the Woodrow Wilson International Center for Scholars and the Project on Emerging nullotechnologies created the nullotechnology Consumer Products Inventory (CPI) in 2005. The objective of this present work is to redevelop the CPI by leading a research effort to increase the usefulness and reliability of this inventory. We created eight new descriptors for consumer products, including information pertaining to the nullomaterials contained in each product. The project was motivated by the recognition that a diverse group of stakeholders from academia, industry, and state/ federal government had become highly dependent on the inventory as an important resource and bellweather of the pervasiveness of nullotechnology in society. We interviewed 68 nullotechnology experts to assess key information needs. Their answers guided inventory modifications by providing a clear conceptual framework best suited for user expectations. The revised inventory was released in October 2013. It currently lists 1814 consumer products from 622 companies in 32 countries. The Health and Fitness category contains the most products (762, or 42% of the total). Silver is the most frequently used nullomaterial (435 products, or 24%); however, 49% of the products (889) included in the CPI do not provide the composition of the nullomaterial used in them. About 29% of the CPI (528 products) contain nullomaterials suspended in a variety of liquid media and dermal contact is the most likely exposure scenario from their use. The majority (1288 products, or 71%) of the products do not present enough supporting information to corroborate the claim that nullomaterials are used. The modified CPI has enabled crowdsourcing capabilities, which allow users to suggest edits to any entry and permits researchers to upload new findings ranging from human and environmental exposure data to complete life cycle assessments. There are inherent limitations to this type of database, but these modifications to the inventory addressed the majority of criticisms raised in published literature and in surveys of nullotechnology stakeholders and experts. The development of standardized methods and metrics for nullomaterial characterization and labelling in consumer products can lead to greater understanding between the key stakeholders in nullotechnology, especially consumers, researchers, regulators, and industry.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 1345,
|
|
"Times Cited, All Databases": 1533,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "AUG 21",
|
|
"Publication Year": 2015,
|
|
"Volume": 6,
|
|
"Issue": null,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 1769,
|
|
"End Page": 1780,
|
|
"Article Number": null,
|
|
"DOI": "10.3762/bjnullo.6.181",
|
|
"DOI Link": "http://dx.doi.org/10.3762/bjnullo.6.181",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics; Materials Science; Physics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000359834400001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Deng, J; Ren, PJ; Deng, DH; Bao, XH",
|
|
"Book Authors": null,
|
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"Book Editors": null,
|
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"Book Group Authors": null,
|
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"Author Full Names": "Deng, Jiao; Ren, Pengju; Deng, Dehui; Bao, Xinhe",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Enhanced Electron Penetration through an Ultrathin Graphene Layer for Highly Efficient Catalysis of the Hydrogen Evolution Reaction",
|
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"Source Title": "ANGEWANDTE CHEMIE-INTERNATIONAL EDITION",
|
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"Book Series Title": null,
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"Language": null,
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"Abstract": "Major challenges encountered when trying to replace precious-metal-based electrocatalysts of the hydrogen evolution reaction (HER) in acidic media are related to the low efficiency and stability of non-precious-metal compounds. Therefore, new concepts and strategies have to be devised to develop electrocatalysts that are based on earth-abundant materials. Herein, we report a hierarchical architecture that consists of ultrathin graphene shells (only 1-3 layers) that encapsulate a uniform CoNi nulloalloy to enhance its HER performance in acidic media. The optimized catalyst exhibits high stability and activity with an onset overpotential of almost zero versus the reversible hydrogen electrode (RHE) and an overpotential of only 142 mV at 10 mAcm(-2), which is quite close to that of commercial 40% Pt/C catalysts. Density functional theory (DFT) calculations indicate that the ultrathin graphene shells strongly promote electron penetration from the CoNi nulloalloy to the graphene surface. With nitrogen dopants, they synergistically increase the electron density on the graphene surface, which results in superior HER activity on the graphene shells.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
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"Email Addresses": null,
|
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"Researcher Ids": null,
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"ORCIDs": null,
|
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"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
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"Times Cited, WoS Core": 1160,
|
|
"Times Cited, All Databases": 1202,
|
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"180 Day Usage Count": null,
|
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"Since 2013 Usage Count": null,
|
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"Publisher": null,
|
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"Publisher City": null,
|
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"Publisher Address": null,
|
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"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "FEB 9",
|
|
"Publication Year": 2015,
|
|
"Volume": 54,
|
|
"Issue": 7,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 2100,
|
|
"End Page": 2104,
|
|
"Article Number": null,
|
|
"DOI": "10.1002/anie.201409524",
|
|
"DOI Link": "http://dx.doi.org/10.1002/anie.201409524",
|
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"Book DOI": null,
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"Early Access Date": null,
|
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"Number of Pages": null,
|
|
"WoS Categories": null,
|
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"Web of Science Index": null,
|
|
"Research Areas": "Chemistry",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000349391000013",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "De Roo, J; Ibáñez, M; Geiregat, P; Nedelcu, G; Walravens, W; Maes, J; Martins, JC; Van Driessche, I; Koyalenko, MV; Hens, Z",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
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"Book Group Authors": null,
|
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"Author Full Names": "De Roo, Jonathan; Ibanez, Maria; Geiregat, Pieter; Nedelcu, Georgian; Walravens, Willem; Maes, Jorick; Martins, Jose C.; Van Driessche, Isabel; Koyalenko, Maksym V.; Hens, Zeger",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Highly Dynamic Ligand Binding and Light Absorption Coefficient of Cesium Lead Bromide Perovskite nullocrystals",
|
|
"Source Title": "ACS nullO",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
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"Language": null,
|
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"Document Type": "Article",
|
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"Conference Title": null,
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"Conference Date": null,
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"Conference Location": null,
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"Conference Sponsor": null,
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"Conference Host": null,
|
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"Author Keywords": null,
|
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"Keywords Plus": null,
|
|
"Abstract": "Lead halide perovskite materials have attracted significant attention in the context of photovoltaics and other optoelectronic applications, and recently, research efforts have been directed to nullostructured lead halide perovskites. Collodial nullocrystals (NCs) of cesium lead halides (CsPbX3, X = Cl, Br, I) exhibit bright photoluminescence, with emission tunable over the entire visible spectral region. However, previous studies on CsPbX3 NCs did not address key aspects of their chemistry and photophysics such as surface chemistry and quantitative light absorption. Here, we elaborate on the synthesis of CsPbBr3 NCs and their surface chemistry. In addition, the intrinsic absorption coefficient was determined experimentally by combining elemental analysis with accurate optical absorption measurements. H-1 solution nuclear magnetic resonullce spectroscopy was used to characterize sample purity, elucidate the surface chemistry, and evaluate the influence of purification methods on the surface composition. We find that ligand binding to the NC surface is highly dynamic, and therefore, ligands are easily lost during the isolation and purification procedures. However, when a small amount of both oleic acid and oleylamine is added, the NCs can be purified, maintaining optical, colloidal, and material integrity. In addition, we find that a high amine content in the ligand shell increases the quantum yield due to the improved binding of the carboxylic acid.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 1547,
|
|
"Times Cited, All Databases": 1636,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "FEB",
|
|
"Publication Year": 2016,
|
|
"Volume": 10,
|
|
"Issue": 2,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 2071,
|
|
"End Page": 2081,
|
|
"Article Number": null,
|
|
"DOI": "10.1021/acsnullo.5b06295",
|
|
"DOI Link": "http://dx.doi.org/10.1021/acsnullo.5b06295",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry; Science & Technology - Other Topics; Materials Science",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000370987400044",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Ye, GL; Gong, YJ; Lin, JH; Li, B; He, YM; Pantelides, ST; Zhou, W; Vajtai, R; Ajayan, PM",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Ye, Gonglan; Gong, Yongji; Lin, Junhao; Li, Bo; He, Yongmin; Pantelides, Sokrates T.; Zhou, Wu; Vajtai, Robert; Ajayan, Pulickel M.",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Defects Engineered Monolayer MoS2 for Improved Hydrogen Evolution Reaction",
|
|
"Source Title": "nullO LETTERS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "MoS2 is a promising and low-cost material for electrochemical hydrogen production due to its high activity and stability during the reaction. However, the efficiency of hydrogen production is limited by the amount of active sites, for example, edges, in MoS2. Here, we demonstrate that oxygen plasma exposure and hydrogen treatment on pristine monolayer MoS2 could introduce more active sites via the formation of defects within the monolayer, leading to a high density of exposed edges and a significant improvement of the hydrogen evolution activity. These as-fabricated defects are characterized at the scale from macroscopic continuum to discrete atoms. Our work represents a facile method to increase the hydrogen production in electrochemical reaction of MoS2 via defect engineering, and helps to understand the catalytic properties of MoS2.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 1073,
|
|
"Times Cited, All Databases": 1139,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "FEB",
|
|
"Publication Year": 2016,
|
|
"Volume": 16,
|
|
"Issue": 2,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 1097,
|
|
"End Page": 1103,
|
|
"Article Number": null,
|
|
"DOI": "10.1021/acs.nullolett.5b04331",
|
|
"DOI Link": "http://dx.doi.org/10.1021/acs.nullolett.5b04331",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry; Science & Technology - Other Topics; Materials Science; Physics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000370215200042",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "He, C; Ni, X; Ge, H; Sun, XC; Chen, YB; Lu, MH; Liu, XP; Chen, YF",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "He, Cheng; Ni, Xu; Ge, Hao; Sun, Xiao-Chen; Chen, Yan-Bin; Lu, Ming-Hui; Liu, Xiao-Ping; Chen, Yan-Feng",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Acoustic topological insulator and robust one-way sound transport",
|
|
"Source Title": "NATURE PHYSICS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Topological design of materials enables topological symmetries and facilitates unique backscattering-immune wave transport(1-26). In airborne acoustics, however, the intrinsic longitudinal nature of sound polarization makes the use of the conventional spin-orbital interaction mechanism impossible for achieving band inversion. The topological gauge flux is then typically introduced with a moving background in theoretical models(19-22). Its practical implementation is a serious challenge, though, due to inherent dynamic instabilities and noise. Here we realize the inversion of acoustic energy bands at a double Dirac cone(15,27,28) and provide an experimental demonstration of an acoustic topological insulator. By manipulating the hopping interaction of neighbouring 'atoms' in this new topological material, we successfully demonstrate the acoustic quantum spin Hall effect, characterized by robust pseudospin-dependent one-way edge sound transport. Our results are promising for the exploration of new routes for experimentally studying topological phenomena and related applications, for example, sound-noise reduction.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 989,
|
|
"Times Cited, All Databases": 1056,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "DEC",
|
|
"Publication Year": 2016,
|
|
"Volume": 12,
|
|
"Issue": 12,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 1124,
|
|
"End Page": "+",
|
|
"Article Number": null,
|
|
"DOI": "10.1038/NPHYS3867",
|
|
"DOI Link": "http://dx.doi.org/10.1038/NPHYS3867",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Physics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000389133800014",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Rasool, K; Helal, M; Ali, A; Ren, CE; Gogotsi, Y; Mahmoud, KA",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Rasool, Kashif; Helal, Mohamed; Ali, Adnull; Ren, Chang E.; Gogotsi, Yury; Mahmoud, Khaled A.",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Antibacterial Activity of Ti3C2Tx MXene",
|
|
"Source Title": "ACS nullO",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "MXenes are a family of atomically thin, two-dimensional (2D) transition metal carbides and carbonitrides with many attractive properties. Two-dimensional Ti3C2TX (MXene) has been recently explored for applications in water desalination/purification membranes. A. major success indicator for any water treatment membrane is the resistance to biofouling. To validate this and to understand better the health and environmental impacts of the new 2D carbides, we investigated the antibacterial properties of single- and few-Iayer Ti3C2TX MXene flakes in colloidal solution. The antibacterial properties of Ti3C2TX were tested against Escherichia coli (E.,coli) and Bacillus subtilis (B. subtilis) by using bacterial growth curves based on optical densities (OD) and colonies growth on agar nutritive plates. Ti3C2T shows a higher antibacterial efficiency toward both Gram-negative E. coli and Gram-positive. B. subtilis compared with graphene oxide (GO), which has been widely reported as an antibacterial agent. Concentration dependent antibacterial activity was observed and more than 98% bacterial cell viability loss was found at 200 jzg/mL Ti3C2TX for both bacterial cells within 4 h of exposure, as confirmed by colony forming unit (CFU) and regrowth curve. Antibacterial mechanism investigation by scanning electron microscopy (SEM) and transmission electron microscopy (TEM) coupled with lactate dehydrogenase (LDH) release assay indicated the damage to the cell membrane, which resulted in release of cytoplasmic materials from the bacterial cells. Reactive oxygen species (ROS) dependent and independent stress induction by Ti3C2TX was investigated in two separate abiotic assays. MXenes are expected to be resistant to biofouling and offer bactericidal properties.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 1013,
|
|
"Times Cited, All Databases": 1055,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "MAR",
|
|
"Publication Year": 2016,
|
|
"Volume": 10,
|
|
"Issue": 3,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 3674,
|
|
"End Page": 3684,
|
|
"Article Number": null,
|
|
"DOI": "10.1021/acsnullo.6b00181",
|
|
"DOI Link": "http://dx.doi.org/10.1021/acsnullo.6b00181",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry; Science & Technology - Other Topics; Materials Science",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000372855400072",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Zhang, J; Jia, S; Kholmanov, I; Dong, L; Er, DQ; Chen, WB; Guo, H; Jin, ZH; Shenoy, VB; Shi, L; Lou, J",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Zhang, Jing; Jia, Shuai; Kholmanov, Iskandar; Dong, Liang; Er, Dequan; Chen, Weibing; Guo, Hua; Jin, Zehua; Shenoy, Vivek B.; Shi, Li; Lou, Jun",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Janus Monolayer Transition-Metal Dichalcogenides",
|
|
"Source Title": "ACS nullO",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "The crystal configuration of sandwiched S-Mo-Se structure (Janus SMoSe) at the monolayer limit has been synthesized and carefully characterized in this work. By controlled sulfurization of monolayer MoSe2, the top layer of selenium atoms is substituted by sulfur atoms, while the bottom selenium layer remains intact. The structure of this material is systematically investigated by Raman, photoluminescence, transmission electron microscopy, and X-ray photoelectron spectroscopy and confirmed by time-of-flight secondary ion mass spectrometry. Density functional theory (DFT) calculations are performed to better understand the Raman vibration modes and electronic structures of the Janus SMoSe monolayer, which are found to correlate well with corresponding experimental results. Finally, high basal plane hydrogen evolution reaction activity is discovered for the Janus monolayer, and DFT calculation implies that the activity originates from the synergistic effect of the intrinsic defects and structural strain inherent in the Janus structure.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
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"Researcher Ids": null,
|
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"ORCIDs": null,
|
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"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 1206,
|
|
"Times Cited, All Databases": 1260,
|
|
"180 Day Usage Count": null,
|
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"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
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"Publisher Address": null,
|
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"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "AUG",
|
|
"Publication Year": 2017,
|
|
"Volume": 11,
|
|
"Issue": 8,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 8192,
|
|
"End Page": 8198,
|
|
"Article Number": null,
|
|
"DOI": "10.1021/acsnullo.7b03186",
|
|
"DOI Link": "http://dx.doi.org/10.1021/acsnullo.7b03186",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry; Science & Technology - Other Topics; Materials Science",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000408520900069",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Pei, A; Zheng, GY; Shi, FF; Li, YZ; Cui, Y",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Pei, Allen; Zheng, Guangyuan; Shi, Feifei; Li, Yuzhang; Cui, Yi",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "nulloscale Nucleation and Growth of Electrodeposited Lithium Metal",
|
|
"Source Title": "nullO LETTERS",
|
|
"Book Series Title": null,
|
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"Book Series Subtitle": null,
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"Language": null,
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"Document Type": "Article",
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"Conference Title": null,
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"Conference Sponsor": null,
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"Conference Host": null,
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"Author Keywords": null,
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"Keywords Plus": null,
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|
"Abstract": "Lithium metal has re-emerged as an exciting anode for high energy lithium-ion batteries due to its high specific capacity of 3860 mAh g(-1) and lowest electrochemical potential of all known materials. However, lithium has been plagued by the issues of dendrite formation, high chemical reactivity with electrolyte, and infinite relative volume expansion during plating and stripping, which present safety hazards and low cycling efficiency in batteries with lithium metal electrodes. There have been a lot of recent studies on Li metal although little work has focused on the initial nucleation and growth behavior of Li metal, neglecting a critical fundamental scientific foundation of Li plating. Here, we study experimentally the morphology of lithium in the early stages of nucleation and growth on planar copper electrodes in liquid organic electrolyte. We elucidate the dependence of lithium nuclei size, shape, and areal density on current rate, consistent with classical nucleation and growth theory. We found that the nuclei size is proportional to the inverse of overpotential and the number density of nuclei is proportional to the cubic power of overpotential. Based on this understanding, we propose a strategy to increase the uniformity of electrodeposited lithium on the electrode surface.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 1287,
|
|
"Times Cited, All Databases": 1380,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "FEB",
|
|
"Publication Year": 2017,
|
|
"Volume": 17,
|
|
"Issue": 2,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 1132,
|
|
"End Page": 1139,
|
|
"Article Number": null,
|
|
"DOI": "10.1021/acs.nullolett.6b04755",
|
|
"DOI Link": "http://dx.doi.org/10.1021/acs.nullolett.6b04755",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry; Science & Technology - Other Topics; Materials Science; Physics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000393848800075",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Li, RY; Zhang, LB; Shi, L; Wang, P",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Li, Renyuan; Zhang, Lianbin; Shi, Le; Wang, Peng",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "MXene Ti3C2: An Effective 2D Light-to-Heat Conversion Material",
|
|
"Source Title": "ACS nullO",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "MXene, a new series of 2D material, has been steadily advancing its applications to a variety of fields, such as catalysis, supercapacitor, molecular separation, electromagnetic wave interference shielding. This work reports a carefully designed aqueous droplet light heating system along with a thorough mathematical procedure, which combined leads to a precise determination of internal light-to-heat conversion efficiency of a variety of nullomaterials. The internal light-to-heat conversion efficiency of MXene, more specifically Ti3C2, was measured to be 100%, indicating a perfect energy conversion. Furthermore, a self-floating MXene thin membrane was prepared by simple vacuum filtration and the membrane, in the presence of a rationally chosen heat barrier, produced a light-to-water evaporation efficiency of 84% under one sun irradiation, which is among the state of art energy efficiency for similar photothermal evaporation system. The outstanding internal light-to-heat conversion efficiency and great light-to-water evaporation efficiency reported in this work suggest that MXene is a very promising light-to-heat conversion material and thus deserves more research attention toward practical applications.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 1392,
|
|
"Times Cited, All Databases": 1451,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "APR",
|
|
"Publication Year": 2017,
|
|
"Volume": 11,
|
|
"Issue": 4,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 3752,
|
|
"End Page": 3759,
|
|
"Article Number": null,
|
|
"DOI": "10.1021/acsnullo.6b08415",
|
|
"DOI Link": "http://dx.doi.org/10.1021/acsnullo.6b08415",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry; Science & Technology - Other Topics; Materials Science",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000400233200033",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Cao, Y; Fatemi, V; Fang, S; Watanabe, K; Taniguchi, T; Kaxiras, E; Jarillo-Herrero, P",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Cao, Yuan; Fatemi, Valla; Fang, Shiang; Watanabe, Kenji; Taniguchi, Takashi; Kaxiras, Efthimios; Jarillo-Herrero, Pablo",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Unconventional superconductivity in magic-angle graphene superlattices",
|
|
"Source Title": "NATURE",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "The behaviour of strongly correlated materials, and in particular unconventional superconductors, has been studied extensively for decades, but is still not well understood. This lack of theoretical understanding has motivated the development of experimental techniques for studying such behaviour, such as using ultracold atom lattices to simulate quantum materials. Here we report the realization of intrinsic unconventional superconductivity-which cannot be explained by weak electron-phonon interactions-in a two-dimensional superlattice created by stacking two sheets of graphene that are twisted relative to each other by a small angle. For twist angles of about 1.1 degrees-the first 'magic' angle-the electronic band structure of this 'twisted bilayer graphene' exhibits flat bands near zero Fermi energy, resulting in correlated insulating states at half-filling. Upon electrostatic doping of the material away from these correlated insulating states, we observe tunable zero-resistance states with a critical temperature of up to 1.7 kelvin. The temperature-carrier-density phase diagram of twisted bilayer graphene is similar to that of copper oxides (or cuprates), and includes dome-shaped regions that correspond to superconductivity. Moreover, quantum oscillations in the longitudinal resistance of the material indicate the presence of small Fermi surfaces near the correlated insulating states, in analogy with underdoped cuprates. The relatively high superconducting critical temperature of twisted bilayer graphene, given such a small Fermi surface (which corresponds to a carrier density of about 1011 per square centimetre), puts it among the superconductors with the strongest pairing strength between electrons. Twisted bilayer graphene is a precisely tunable, purely carbon-based, two-dimensional superconductor. It is therefore an ideal material for investigations of strongly correlated phenomena, which could lead to insights into the physics of high-critical-temperature superconductors and quantum spin liquids.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 5816,
|
|
"Times Cited, All Databases": 6389,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "APR 5",
|
|
"Publication Year": 2018,
|
|
"Volume": 556,
|
|
"Issue": 7699,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 43,
|
|
"End Page": "+",
|
|
"Article Number": null,
|
|
"DOI": "10.1038/nature26160",
|
|
"DOI Link": "http://dx.doi.org/10.1038/nature26160",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000429103300032",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Deysher, G; Shuck, CE; Hantanasirisakul, K; Frey, NC; Foucher, AC; Maleski, K; Sarycheva, A; Shenoy, VB; Stach, EA; Anasori, B; Gogotsi, Y",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Deysher, Grayson; Shuck, Christopher Eugene; Hantanasirisakul, Kanit; Frey, Nathan C.; Foucher, Alexandre C.; Maleski, Kathleen; Sarycheva, Asia; Shenoy, Vivek B.; Stach, Eric A.; Anasori, Babak; Gogotsi, Yury",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Synthesis of Mo4VAlC4 MAX Phase and Two-Dimensional Mo4VC4 MXene with Five Atomic Layers of Transition Metals",
|
|
"Source Title": "ACS nullO",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "MXenes are a family of two-dimensional (2D) transition metal carbides, nitrides, and carbonitrides with a general formula of Mn+1XnTx, in which two, three, or four atomic layers of a transition metal (M: Ti, Nb, V, Cr, Mo, Ta, etc.) are interleaved with layers of C and/or N (shown as X), and T-x represents surface termination groups such as -OH, =O, and -F. Here, we report the scalable synthesis and characterization of a MXene with five atomic layers of transition metals (Mo4VC4Tx), by synthesizing its Mo4VAlC4 MAX phase precursor that contains no other MAX phase impurities. These phases display twinning at their central M layers which is not present in any other known MAX phases or MXenes. Transmission electron microscopy and X-ray diffraction were used to examine the structure of both phases. Energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, Raman spectroscopy, and high- resolution scanning transmission electron microscopy with energy-dispersive X-ray spectroscopy were used to study the composition of these materials. Density functional theory calculations indicate that other five transition metal-layer MAX phases (M'M-4 '' AlC4) may be possible, where M' and M '' are two different transition metals. The predicted existence of additional Al-containing MAX phases suggests that more M5C4Tx MXenes can be synthesized. Additionally, we characterized the optical, electronic, and thermal properties of Mo4VC4Tx. This study demonstrates the existence of an additional subfamily of M5X4Tx MXenes as well as a twinned structure, allowing for a wider range of 2D structures and compositions for more control over properties, which could lead to many different applications.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 506,
|
|
"Times Cited, All Databases": 532,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JAN",
|
|
"Publication Year": 2020,
|
|
"Volume": 14,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 204,
|
|
"End Page": 217,
|
|
"Article Number": null,
|
|
"DOI": "10.1021/acsnullo.9b07708",
|
|
"DOI Link": "http://dx.doi.org/10.1021/acsnullo.9b07708",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry; Science & Technology - Other Topics; Materials Science",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000510531500015",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Yasuda, K; Wang, XR; Watanabe, K; Taniguchi, T; Jarillo-Herrero, P",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Yasuda, Kenji; Wang, Xirui; Watanabe, Kenji; Taniguchi, Takashi; Jarillo-Herrero, Pablo",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Stacking-engineered ferroelectricity in bilayer boron nitride",
|
|
"Source Title": "SCIENCE",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Two-dimensional (2D) ferroelectrics with robust polarization down to atomic thicknesses provide building blocks for functional heterostructures. Experimental realization remains challenging because of the requirement of a layered polar crystal. Here, we demonstrate a rational design approach to engineering 2D ferroelectrics from a nonferroelectric parent compound by using van der Waals assembly. Parallel-stacked bilayer boron nitride exhibits out-of-plane electric polarization that reverses depending on the stacking order. The polarization switching is probed through the resistance of an adjacently stacked graphene sheet. Twisting the boron nitride sheets by a small angle changes the dynamics of switching because of the formation of moire ferroelectricity with staggered polarization. The ferroelectricity persists to room temperature while keeping the high mobility of graphene, paving the way for potential ultrathin nonvolatile memory applications.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 544,
|
|
"Times Cited, All Databases": 577,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
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|
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|
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"eISSN": null,
|
|
"ISBN": null,
|
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"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JUN 25",
|
|
"Publication Year": 2021,
|
|
"Volume": 372,
|
|
"Issue": 6549,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 1458,
|
|
"End Page": "+",
|
|
"Article Number": null,
|
|
"DOI": "10.1126/science.abd3230",
|
|
"DOI Link": "http://dx.doi.org/10.1126/science.abd3230",
|
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"Book DOI": null,
|
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"Early Access Date": null,
|
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"Number of Pages": null,
|
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"WoS Categories": null,
|
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"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
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"Open Access Designations": null,
|
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"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000665860000051",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Mathis, TS; Maleski, K; Goad, A; Sarycheva, A; Anayee, M; Foucher, AC; Hantanasirisakul, K; Shuck, CE; Stach, EA; Gogotsi, Y",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
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"Author Full Names": "Mathis, Tyler S.; Maleski, Kathleen; Goad, Adam; Sarycheva, Asia; Anayee, Mark; Foucher, Alexandre C.; Hantanasirisakul, Kanit; Shuck, Christopher E.; Stach, Eric A.; Gogotsi, Yury",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
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"Article Title": "Modified MAX Phase Synthesis for Environmentally Stable and Highly Conductive Ti3C2 MXene",
|
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"Source Title": "ACS nullO",
|
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"Book Series Title": null,
|
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"Book Series Subtitle": null,
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"Language": null,
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"Document Type": "Article",
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"Conference Sponsor": null,
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"Author Keywords": null,
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"Keywords Plus": null,
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"Abstract": "One of the primary factors limiting further research and commercial use of the two-dimensional (2D) titanium carbide MXene Ti3C2, as well as MXenes in general, is the rate at which freshly made samples oxidize and degrade when stored as aqueous suspensions. Here, we show that including excess aluminum during synthesis of the Ti3AlC2 MAX phase precursor leads to Ti3AlC2 grains with improved crystallinity and carbon stoichiometry (termed Al-Ti3AlC2). MXene nullosheets (Al-Ti3C2) produced from this precursor are of higher quality, as evidenced by their increased resistance to oxidation and an increase in their electronic conductivity up to 20 000 S/cm. Aqueous suspensions of stoichiometric single-to few-layer Al-Ti3C2 flakes produced from the modified Al-Ti3AlC2 have a shelf life of over ten months, compared to 1 to 2 weeks for previously published Ti3C2, even when stored in ambient conditions. Freestanding films made from Al-Ti3C2 suspensions stored for ten months show minimal decreases in electrical conductivity and negligible oxidation. Furthermore, oxidation of the improved Al-Ti3C2 in air initiates at temperatures that are 100-150 degrees C higher than that of conventional Ti3C2. The observed improvements in both the shelf life and properties of Al-Ti3C2 will facilitate the widespread use of this material.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
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"Researcher Ids": null,
|
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|
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"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 589,
|
|
"Times Cited, All Databases": 624,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
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"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "APR 27",
|
|
"Publication Year": 2021,
|
|
"Volume": 15,
|
|
"Issue": 4,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 6420,
|
|
"End Page": 6429,
|
|
"Article Number": null,
|
|
"DOI": "10.1021/acsnullo.0c08357",
|
|
"DOI Link": "http://dx.doi.org/10.1021/acsnullo.0c08357",
|
|
"Book DOI": null,
|
|
"Early Access Date": "APR 2021",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry; Science & Technology - Other Topics; Materials Science",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000645436800038",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Chen, SS; Dai, XZ; Xu, S; Jiao, HY; Zhao, L; Huang, JS",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Chen, Shangshang; Dai, Xuezeng; Xu, Shuang; Jiao, Haoyang; Zhao, Liang; Huang, Jinsong",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Stabilizing perovskite-substrate interfaces for high-performance perovskite modules",
|
|
"Source Title": "SCIENCE",
|
|
"Book Series Title": null,
|
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"Book Series Subtitle": null,
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"Language": null,
|
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"Document Type": "Article",
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"Conference Title": null,
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|
"Conference Date": null,
|
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"Conference Location": null,
|
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"Conference Sponsor": null,
|
|
"Conference Host": null,
|
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"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "The interfaces of perovskite solar cells (PSCs) are important in determining their efficiency and stability, but the morphology and stability of imbedded perovskite-substrate interfaces have received less attention than have top interfaces. We found that dimethyl sulfoxide (DMSO), which is a liquid additive broadly applied to enhance perovskite film morphology, was trapped during film formation and led to voids at perovskite-substrate interfaces that accelerated the film degradation under illumination. Partial replacement of DMSO with solid-state carbohydrazide reduces interfacial voids. A maximum stabilized power conversion efficiency (PCE) of 23.6% was realized for blade-coated p-type/intrinsic/n-type (p-i-n) structure PSCs with no efficiency loss after 550-hour operational stability tests at 60 degrees C. The perovskite mini-modules showed certified PCEs of 19.3 and 19.2%, with aperture areas of 18.1 and 50.0 square centimeters, respectively.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 597,
|
|
"Times Cited, All Databases": 626,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "AUG 20",
|
|
"Publication Year": 2021,
|
|
"Volume": 373,
|
|
"Issue": 6557,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 902,
|
|
"End Page": "+",
|
|
"Article Number": null,
|
|
"DOI": "10.1126/science.abi6323",
|
|
"DOI Link": "http://dx.doi.org/10.1126/science.abi6323",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000686562400034",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Bu, TL; Li, J; Li, HY; Tian, CC; Su, J; Tong, GQ; Ono, LK; Wang, C; Lin, ZP; Chai, NAY; Zhang, XL; Chang, JJ; Lu, JF; Zhong, J; Huang, WC; Qi, YB; Cheng, YB; Huang, FZ",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Bu, Tongle; Li, Jing; Li, Hengyi; Tian, Congcong; Su, Jie; Tong, Guoqing; Ono, Luis K.; Wang, Chao; Lin, Zhipeng; Chai, Nianyao; Zhang, Xiao-Li; Chang, Jingjing; Lu, Jianfeng; Zhong, Jie; Huang, Wenchao; Qi, Yabing; Cheng, Yi-Bing; Huang, Fuzhi",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Lead halide-templated crystallization of methylamine-free perovskite for efficient photovoltaic modules",
|
|
"Source Title": "SCIENCE",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Upscaling efficient and stable perovskite layers is one of the most challenging issues in the commercialization of perovskite solar cells. Here, a lead halide-templated crystallization strategy is developed for printing formamidinium (FA)-cesium (Cs) lead triiodide perovskite films. High-quality large-area films are achieved through controlled nucleation and growth of a lead halide_N-methyl-2-pyrrolidone adduct that can react in situ with embedded FAI/CsI to directly form alpha-phase perovskite, sidestepping the phase transformation from delta-phase. A nonencapsulated device with 23% efficiency and excellent long-term thermal stability (at 85 degrees C) in ambient air (similar to 80% efficiency retention after 500 hours) is achieved with further addition of potassium hexafluorophosphate. The slot die-printed minimodules achieve champion efficiencies of 20.42% (certified efficiency 19.3%) and 19.54% with an active area of 17.1 and 65.0 square centimeters, respectively.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 487,
|
|
"Times Cited, All Databases": 510,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JUN 18",
|
|
"Publication Year": 2021,
|
|
"Volume": 372,
|
|
"Issue": 6548,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": "SI",
|
|
"Meeting Abstract": null,
|
|
"Start Page": 1327,
|
|
"End Page": "+",
|
|
"Article Number": null,
|
|
"DOI": "10.1126/science.abh1035",
|
|
"DOI Link": "http://dx.doi.org/10.1126/science.abh1035",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000665616000032",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Zhao, ZD; Wang, R; Peng, CX; Chen, WJ; Wu, TQ; Hu, B; Weng, WJ; Yao, Y; Zeng, JX; Chen, ZH; Liu, PY; Liu, YC; Li, GS; Guo, J; Lu, HB; Guo, ZP",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Zhao, Zedong; Wang, Rong; Peng, Chengxin; Chen, Wuji; Wu, Tianqi; Hu, Bo; Weng, Weijun; Yao, Ying; Zeng, Jiaxi; Chen, Zhihong; Liu, Peiying; Liu, Yicheng; Li, Guisheng; Guo, Jia; Lu, Hongbin; Guo, Zaiping",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Horizontally arranged zinc platelet electrodeposits modulated by fluorinated covalent organic framework film for high-rate and durable aqueous zinc ion batteries",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Rechargeable aqueous zinc-ion batteries (RZIBs) provide a promising complementarity to the existing lithium-ion batteries due to their low cost, non-toxicity and intrinsic safety. However, Zn anodes suffer from zinc dendrite growth and electrolyte corrosion, resulting in poor reversibility. Here, we develop an ultrathin, fluorinated two-dimensional porous covalent organic framework (FCOF) film as a protective layer on the Zn surface. The strong interaction between fluorine (F) in FCOF and Zn reduces the surface energy of the Zn (002) crystal plane, enabling the preferred growth of (002) planes during the electrodeposition process. As a result, Zn deposits show horizontally arranged platelet morphology with (002) orientations preferred. Furthermore, F-containing nullochannels facilitate ion transport and prevent electrolyte penetration for improving corrosion resistance. The FCOF@Zn symmetric cells achieve stability for over 750 h at an ultrahigh current density of 40 mA cm(-2). The high-areal-capacity full cells demonstrate hundreds of cycles under high Zn utilization conditions. Rechargeable aqueous zinc-ion batteries are promising but the zinc anode suffers from dendrite growth and electrolyte corrosion. Here, the authors develop a fluorinated covalent organic framework film as a protective layer for aqueous zinc anode battery.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 485,
|
|
"Times Cited, All Databases": 495,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "NOV 16",
|
|
"Publication Year": 2021,
|
|
"Volume": 12,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 6606,
|
|
"DOI": "10.1038/s41467-021-26947-9",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-021-26947-9",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000719546000021",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Mortazavi, B; Javvaji, B; Shojaei, F; Rabczuk, T; Shapeev, A; Zhuang, XY",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Mortazavi, Bohayra; Javvaji, Brahmanulldam; Shojaei, Fazel; Rabczuk, Timon; Shapeev, Alexander, V; Zhuang, Xiaoying",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Exceptional piezoelectricity, high thermal conductivity and stiffness and promising photocatalysis in two-dimensional MoSi2N4 family confirmed by first-principles",
|
|
"Source Title": "nullO ENERGY",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Chemical vapor deposition has been most recently employed to fabricate centimeter-scale high-quality singlelayer MoSi2N4 (Science; 2020;369; 670). Motivated by this exciting experimental advance, herein we conduct extensive first-principles based simulations to explore the stability, mechanical properties, lattice thermal conductivity, piezoelectric and flexoelectric response, and photocatalytic and electronic features of MA(2)Z(4) (M = Cr, Mo, W; A = Si, Ge; Z = N, P) monolayers. The considered nullosheets are found to exhibit dynamical stability and remarkably high mechanical properties. Moreover, they show diverse electronic properties from antiferromagnetic metal to half metal and to semiconductors with band gaps ranging from 0.31 to 2.57 eV. Among the studied nullosheets, the MoSi2N4 and WSi2N4 monolayers yield appropriate band edge positions, high electron and hole mobilities, and strong visible light absorption, highly promising for applications in optoelectronics and photocatalytic water splitting. The MoSi2N4 and WSi2N4 monolayers are also predicted to show outstandingly high lattice thermal conductivity of 440 and 500 W/mK, respectively. For the first time we show that machine learning interatomic potentials trained over small supercells can be employed to examine the flexoelectric and piezoelectric properties of complex structures. As the most exciting finding, WSi2N4, CrSi2N4 and MoSi2N4 are found to exhibit the highest piezoelectric coefficients, outperforming all other-known 2D materials. Our results highlight that MA(2)Z(4) nullosheets not only undoubtedly outperform the transition metal dichalcogenides family but also can compete with graphene for applications in nulloelectronics, optoelectronic, energy storage/conversion and thermal management systems.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 460,
|
|
"Times Cited, All Databases": 467,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "APR",
|
|
"Publication Year": 2021,
|
|
"Volume": 82,
|
|
"Issue": null,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
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"Meeting Abstract": null,
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"Start Page": null,
|
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"End Page": null,
|
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"Article Number": 105716,
|
|
"DOI": "10.1016/j.nulloen.2020.105716",
|
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"DOI Link": "http://dx.doi.org/10.1016/j.nulloen.2020.105716",
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|
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|
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"Research Areas": "Chemistry; Science & Technology - Other Topics; Materials Science; Physics",
|
|
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|
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"Pubmed Id": null,
|
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"Open Access Designations": null,
|
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"Highly Cited Status": "Y",
|
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"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000634235000004",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Pan, QS; Zhang, LX; Feng, R; Lu, QH; An, K; Chuang, AC; Poplawsky, JD; Liaw, PK; Lu, L",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Pan, Qingsong; Zhang, Liangxue; Feng, Rui; Lu, Qiuhong; An, Ke; Chuang, Andrew Chihpin; Poplawsky, Jonathan D.; Liaw, Peter K.; Lu, Lei",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
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"Article Title": "Gradient cell-structured high-entropy alloy with exceptional strength and ductility",
|
|
"Source Title": "SCIENCE",
|
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"Book Series Title": null,
|
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"Book Series Subtitle": null,
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"Language": null,
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"Conference Sponsor": null,
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"Conference Host": null,
|
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"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Similar to conventional materials, most multicomponent high-entropy alloys (HEAs) lose ductility as they gain strength. In this study, we controllably introduced gradient nulloscaled dislocation cell structures in a stable single-phase HEA with face-centered cubic structure, thus resulting in enhanced strength without apparent loss of ductility. Upon application of strain, the sample-level structural gradient induces progressive formation of a high density of tiny stacking faults (SFs) and twins, nucleating from abundant low-angle dislocation cells. Furthermore, the SF-induced plasticity and the resultant refined structures, coupled with intensively accumulated dislocations, contribute to plasticity, increased strength, and work hardening. These findings offer a promising paradigm for tailoring properties with gradient dislocation cells at the nulloscale and advance our fundamental understanding of the intrinsic deformation behavior of HEAs.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
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"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 470,
|
|
"Times Cited, All Databases": 479,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "NOV 19",
|
|
"Publication Year": 2021,
|
|
"Volume": 374,
|
|
"Issue": 6570,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 984,
|
|
"End Page": "+",
|
|
"Article Number": null,
|
|
"DOI": "10.1126/science.abj8114",
|
|
"DOI Link": "http://dx.doi.org/10.1126/science.abj8114",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
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"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000720789200034",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Stern, MV; Waschitz, Y; Cao, W; Nevo, ; Watanabe, K; Taniguchi, T; Sela, E; Urbakh, M; Hod, O; Ben Shalom, M",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Stern, M. Vizner; Waschitz, Y.; Cao, W.; Nevo, I; Watanabe, K.; Taniguchi, T.; Sela, E.; Urbakh, M.; Hod, O.; Ben Shalom, M.",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Interfacial ferroelectricity by van der Waals sliding",
|
|
"Source Title": "SCIENCE",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
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"Language": null,
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|
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"Conference Sponsor": null,
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"Author Keywords": null,
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|
"Keywords Plus": null,
|
|
"Abstract": "Despite their partial ionic nature, many-layered diatomic crystals avoid internal electric polarization by forming a centrosymmetric lattice at their optimal van der Waals stacking. Here, we report a stable ferroelectric order emerging at the interface between two naturally grown flakes of hexagonal boron nitride, which are stacked together in a metastable non-centrosymmetric parallel orientation. We observe alternating domains of inverted normal polarization, caused by a lateral shift of one lattice site between the domains. Reversible polarization switching coupled to lateral sliding is achieved by scanning a biased tip above the surface. Our calculations trace the origin of the phenomenon to a subtle interplay between charge redistribution and ionic displacement and provide intuitive insights to explore the interfacial polarization and its distinctive slidetronics switching mechanism.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 447,
|
|
"Times Cited, All Databases": 459,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JUN 25",
|
|
"Publication Year": 2021,
|
|
"Volume": 372,
|
|
"Issue": 6549,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 1462,
|
|
"End Page": "+",
|
|
"Article Number": null,
|
|
"DOI": "10.1126/science.abe8177",
|
|
"DOI Link": "http://dx.doi.org/10.1126/science.abe8177",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000665860000052",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Tan, DHS; Chen, YT; Yang, HD; Bao, W; Sreenarayanull, B; Doux, JM; Li, WK; Lu, BY; Ham, SY; Sayahpour, B; Scharf, J; Wu, EA; Deysher, G; Han, HE; Hah, HJ; Jeong, H; Lee, JB; Chen, Z; Meng, YS",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Tan, Darren H. S.; Chen, Yu-Ting; Yang, Hedi; Bao, Wurigumula; Sreenarayanull, Bhagath; Doux, Jean-Marie; Li, Weikang; Lu, Bingyu; Ham, So-Yeon; Sayahpour, Baharak; Scharf, Jonathan; Wu, Erik A.; Deysher, Grayson; Han, Hyea Eun; Hah, Hoe Jin; Jeong, Hyeri; Lee, Jeong Beom; Chen, Zheng; Meng, Ying Shirley",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Carbon-free high-loading silicon anodes enabled by sulfide solid electrolytes",
|
|
"Source Title": "SCIENCE",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "The development of silicon anodes for lithium-ion batteries has been largely impeded by poor interfacial stability against liquid electrolytes. Here, we enabled the stable operation of a 99.9 weight % microsilicon anode by using the interface passivating properties of sulfide solid electrolytes. Bulk and surface characterization, and quantification of interfacial components, showed that such an approach eliminates continuous interfacial growth and irreversible lithium losses. Microsilicon full cells were assembled and found to achieve high areal current density, wide operating temperature range, and high areal loadings for the different cells. The promising performance can be attributed to both the desirable interfacial property between microsilicon and sulfide electrolytes and the distinctive chemomechanical behavior of the lithium-silicon alloy.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 592,
|
|
"Times Cited, All Databases": 632,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "SEP 24",
|
|
"Publication Year": 2021,
|
|
"Volume": 373,
|
|
"Issue": 6562,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": "SI",
|
|
"Meeting Abstract": null,
|
|
"Start Page": 1494,
|
|
"End Page": "+",
|
|
"Article Number": null,
|
|
"DOI": "10.1126/science.abg7217",
|
|
"DOI Link": "http://dx.doi.org/10.1126/science.abg7217",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000698977800047",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Chen, H; Yang, HT; Hu, B; Zhao, Z; Yuan, J; Xing, YQ; Qian, GJ; Huang, ZH; Li, G; Ye, YH; Ma, S; Ni, SL; Zhang, H; Yin, QW; Gong, CS; Tu, ZJ; Lei, HC; Tan, HX; Zhou, S; Shen, CM; Dong, XL; Yan, BH; Wang, ZQ; Gao, HJ",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Chen, Hui; Yang, Haitao; Hu, Bin; Zhao, Zhen; Yuan, Jie; Xing, Yuqing; Qian, Guojian; Huang, Zihao; Li, Geng; Ye, Yuhan; Ma, Sheng; Ni, Shunli; Zhang, Hua; Yin, Qiangwei; Gong, Chunsheng; Tu, Zhijun; Lei, Hechang; Tan, Hengxin; Zhou, Sen; Shen, Chengmin; Dong, Xiaoli; Yan, Binghai; Wang, Ziqiang; Gao, Hong-Jun",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Roton pair density wave in a strong-coupling kagome superconductor",
|
|
"Source Title": "NATURE",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "The transition metal kagome lattice materials host frustrated, correlated and topological quantum states of matter(1-9). Recently, a new family of vanadium-based kagome metals, AV(3)Sb(5) (A = K, Rb or Cs), with topological band structures has been discovered(10,11). These layered compounds are nonmagnetic and undergo charge density wave transitions before developing superconductivity at low temperatures(11-19). Here we report the observation of unconventional superconductivity and a pair density wave (PDW) in CsV3Sb5 using scanning tunnelling microscope/spectroscopy and Josephson scanning tunnelling spectroscopy. We find that CsV3Sb5 exhibits a V-shaped pairing gap Delta similar to 0.5 meV and is a strong-coupling superconductor (2 Delta/k(B)T(c) - 5) that coexists with 4a(0) unidirectional and 2a(0) x 2a(0) charge order. Remarkably, we discover a 3Q PDW accompanied by bidirectional 4a(0)/3 spatial modulations of the superconducting gap, coherence peak and gap depth in the tunnelling conductance. We term this novel quantum state a roton PDW associated with an underlying vortex-antivortex lattice that can account for the observed conductance modulations. Probing the electronic states in the vortex halo in an applied magnetic field, in strong field that suppresses superconductivity and in zero field above T-c, reveals that the PDW is a primary state responsible for an emergent pseudogap and intertwined electronic order. Our findings show striking analogies and distinctions to the phenomenology of high-T-c cuprate superconductors, and provide groundwork for understanding the microscopic origin of correlated electronic states and superconductivity in vanadium-based kagome metals.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 404,
|
|
"Times Cited, All Databases": 443,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "NOV 11",
|
|
"Publication Year": 2021,
|
|
"Volume": 599,
|
|
"Issue": 7884,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 222,
|
|
"End Page": 228,
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s41586-021-03983-5",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41586-021-03983-5",
|
|
"Book DOI": null,
|
|
"Early Access Date": "SEP 2021",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000714336200002",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Kim, JS; Heo, JM; Park, GS; Woo, SJ; Cho, C; Yun, HJ; Kim, DH; Park, J; Lee, SC; Park, SH; Yoon, E; Greenham, NC; Lee, TW",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Kim, Joo Sung; Heo, Jung-Min; Park, Gyeong-Su; Woo, Seung-Je; Cho, Changsoon; Yun, Hyung Joong; Kim, Dong-Hyeok; Park, Jinwoo; Lee, Seung-Chul; Park, Sang-Hwan; Yoon, Eojin; Greenham, Neil C.; Lee, Tae-Woo",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Ultra-bright, efficient and stable perovskite light-emitting diodes",
|
|
"Source Title": "NATURE",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Metal halide perovskites are attracting a lot of attention as next-generation lighte-mitting materials owing to their excellent emission properties, with narrow band emission(1-4). However, perovskite light-emitting diodes (PeLEDs), irrespective of their material type (polycrystals or nullocrystals), have not realized high luminullce, high efficiency and long lifetime simultaneously, as they are influenced by intrinsic limitations related to the trade-off of properties between charge transport and confinement in each type of perovskite material(5-8). Here, we report an ultra-bright, efficient and stable PeLED made of core/shell perovskite nullocrystals with a size of approximately 10 nm, obtained using a simple in situ reaction of benzylphosphonic acid (BPA) additive with three-dimensional (3D) polycrystalline perovskite films, without separate synthesis processes. During the reaction, large 3D crystals are split into nullocrystals and the BPA surroundsthe nullocrystals, achieving strong carrier confinement. The BPA shell passivates the undercoordinated lead atoms by forming covalent bonds, and there by greatly reduces the trap density while maintaining good charge-transport properties for the 3D perovskites. We demonstrate simultaneously efficient, bright and stable PeLEDs that have a maximum brightness of approximately 470,000 cd m(-2), maximum external quantum efficiency of 28.9% (average = 25.2 +/- 1.6% over 40 devices), maximum current efficiency of 151 cd A(-1) and half-lifetime of 520 hat 1,000 cd m(-)(2) (estimated half-lifetime >30,000 h at 100 cd m(-2)). Our work sheds light on the possibility that PeLEDs can be commercialized in the future display industry.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 594,
|
|
"Times Cited, All Databases": 622,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "NOV 24",
|
|
"Publication Year": 2022,
|
|
"Volume": 611,
|
|
"Issue": 7937,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 688,
|
|
"End Page": "+",
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s41586-022-05304-w",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41586-022-05304-w",
|
|
"Book DOI": null,
|
|
"Early Access Date": "NOV 2022",
|
|
"Number of Pages": null,
|
|
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|
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|
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"Open Access Designations": null,
|
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"Highly Cited Status": "Y",
|
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"Hot Paper Status": "N",
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"Date of Export": "2025-04-23",
|
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"UT (Unique WOS ID)": "WOS:000880580300011",
|
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"Web of Science Record": "View Full Record in Web of Science"
|
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},
|
|
{
|
|
"Publication Type": "J",
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"Authors": "Tang, KC; Dong, KC; Li, JC; Gordon, MP; Reichertz, FG; Kim, H; Rho, Y; Wang, QJ; Lin, CY; Grigoropoulos, CP; Javey, A; Urban, JJ; Yao, J; Levinson, R; Wu, JQ",
|
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"Book Authors": null,
|
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"Book Editors": null,
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"Book Group Authors": null,
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"Author Full Names": "Tang, Kechao; Dong, Kaichen; Li, Jiachen; Gordon, Madeleine P.; Reichertz, Finnegan G.; Kim, Hyungjin; Rho, Yoonsoo; Wang, Qingjun; Lin, Chang-Yu; Grigoropoulos, Costas P.; Javey, Ali; Urban, Jeffrey J.; Yao, Jie; Levinson, Ronnen; Wu, Junqiao",
|
|
"Book Author Full Names": null,
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"Group Authors": null,
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"Article Title": "Temperature-adaptive radiative coating for all-season household thermal regulation",
|
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"Source Title": "SCIENCE",
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"Abstract": "The sky is a natural heat sink that has been extensively used for passive radiative cooling of households. A lot of focus has been on maximizing the radiative cooling power of roof coating in the hot daytime using static, cooling-optimized material properties. However, the resultant overcooling in cold night or winter times exacerbates the heating cost, especially in climates where heating dominates energy consumption. We approached thermal regulation from an all-season perspective by developing a mechanically flexible coating that adapts its thermal emittance to different ambient temperatures. The fabricated temperature-adaptive radiative coating (TARC) optimally absorbs the solar energy and automatically switches thermal emittance from 0.20 for ambient temperatures lower than 15 degrees C to 0.90 for temperatures above 30 degrees C, driven by a photonically amplified metal-insulator transition. Simulations show that this system outperforms existing roof coatings for energy saving in most climates, especially those with substantial seasonal variations.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
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"Email Addresses": null,
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"Researcher Ids": null,
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"ORCIDs": null,
|
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"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 411,
|
|
"Times Cited, All Databases": 452,
|
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"180 Day Usage Count": null,
|
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"Since 2013 Usage Count": null,
|
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"Publisher": null,
|
|
"Publisher City": null,
|
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"Publisher Address": null,
|
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"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
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"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "DEC 17",
|
|
"Publication Year": 2021,
|
|
"Volume": 374,
|
|
"Issue": 6574,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": "SI",
|
|
"Meeting Abstract": null,
|
|
"Start Page": 1504,
|
|
"End Page": "+",
|
|
"Article Number": null,
|
|
"DOI": "10.1126/science.abf7136",
|
|
"DOI Link": "http://dx.doi.org/10.1126/science.abf7136",
|
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"Book DOI": null,
|
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"Early Access Date": null,
|
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"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000733380100054",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Liu, YJ; Tao, XY; Wang, Y; Jiang, C; Ma, C; Sheng, OW; Lu, GX; Lou, XW",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Liu, Yujing; Tao, Xinyong; Wang, Yao; Jiang, Chi; Ma, Cong; Sheng, Ouwei; Lu, Gongxun; Lou, Xiong Wen (David)",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Self-assembled monolayers direct a LiF-rich interphase toward long-life lithium metal batteries",
|
|
"Source Title": "SCIENCE",
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"Book Series Title": null,
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"Book Series Subtitle": null,
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|
"Abstract": "High-energy density lithium (Li) metal batteries (LMBs) are promising for energy storage applications but suffer from uncontrollable electrolyte degradation and the consequently formed unstable solid-electrolyte interphase (SEI). In this study, we designed self-assembled monolayers (SAMs) with high-density and long-range-ordered polar carboxyl groups linked to an aluminum oxide-coated separator to provide strong dipole moments, thus offering excess electrons to accelerate the degradation dynamics of carbon-fluorine bond cleavage in Li bis(trifluoromethanesulfonyl)imide. Hence, an SEI with enriched lithium fluoride (LiF) nullocrystals is generated, facilitating rapid Li+ transfer and suppressing dendritic Li growth. In particular, the SAMs endow the full cells with substantially enhanced cyclability under high cathode loading, limited Li excess, and lean electrolyte conditions. As such, our work extends the long-established SAMs technology into a platform to control electrolyte degradation and SEI formation toward LMBs with ultralong life spans.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 569,
|
|
"Times Cited, All Databases": 589,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "FEB 18",
|
|
"Publication Year": 2022,
|
|
"Volume": 375,
|
|
"Issue": 6582,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 739,
|
|
"End Page": "+",
|
|
"Article Number": null,
|
|
"DOI": "10.1126/science.abn1818",
|
|
"DOI Link": "http://dx.doi.org/10.1126/science.abn1818",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000758142600041",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Yu, Z; Rudnicki, PE; Zhang, ZW; Huang, ZJ; Celik, H; Oyakhire, ST; Chen, YL; Kong, X; Kim, SC; Xiao, X; Wang, HS; Zheng, Y; Kamat, GA; Kim, MS; Bent, SF; Qin, J; Cui, Y; Bao, ZN",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Yu, Zhiao; Rudnicki, Paul E.; Zhang, Zewen; Huang, Zhuojun; Celik, Hasan; Oyakhire, Solomon T.; Chen, Yuelang; Kong, Xian; Kim, Sang Cheol; Xiao, Xin; Wang, Hansen; Zheng, Yu; Kamat, Gaurav A.; Kim, Mun Sek; Bent, Stacey F.; Qin, Jian; Cui, Yi; Bao, Zhenull",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Rational solvent molecule tuning for high-performance lithium metal battery electrolytes",
|
|
"Source Title": "NATURE ENERGY",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Electrolyte engineering improved cycling of Li metal batteries and anode-free cells at low current densities; however, high-rate capability and tuning of ionic conduction in electrolytes are desirable yet less-studied. Here, we design and synthesize a family of fluorinated-1,2-diethoxyethanes as electrolyte solvents. The position and amount of F atoms functionalized on 1,2-diethoxyethane were found to greatly affect electrolyte performance. Partially fluorinated, locally polar -CHF2 is identified as the optimal group rather than fully fluorinated -CF3 in common designs. Paired with 1.2 M lithium bis(fluorosulfonyl)imide, these developed single-salt-single-solvent electrolytes simultaneously enable high conductivity, low and stable overpotential, >99.5% Li||Cu half-cell efficiency (up to 99.9%, +/- 0.1% fluctuation) and fast activation (Li efficiency >99.3% within two cycles). Combined with high-voltage stability, these electrolytes achieve roughly 270 cycles in 50-mu m-thin Li||high-loading-NMC811 full batteries and >140 cycles in fast-cycling Cu||microparticle-LiFePO4 industrial pouch cells under realistic testing conditions. The correlation of Li+-solvent coordination, solvation environments and battery performance is investigated to understand structure-property relationships. Cycling capability, especially at high rates, is limited for lithium metal batteries. Here the authors report electrolyte solvent design through fine-tuning of molecular structures to address the cyclability issue and unravel the electrolyte structure-property relationship for battery applications.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 539,
|
|
"Times Cited, All Databases": 561,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JAN",
|
|
"Publication Year": 2022,
|
|
"Volume": 7,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 94,
|
|
"End Page": 106,
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s41560-021-00962-y",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41560-021-00962-y",
|
|
"Book DOI": null,
|
|
"Early Access Date": "JAN 2022",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Energy & Fuels; Materials Science",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000742253900001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Ming, FW; Zhu, YP; Huang, G; Emwas, AH; Liang, HF; Cui, Y; Alshareef, HN",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Ming, Fangwang; Zhu, Yunpei; Huang, Gang; Emwas, Abdul-Hamid; Liang, Hanfeng; Cui, Yi; Alshareef, Husam N.",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Co-Solvent Electrolyte Engineering for Stable Anode-Free Zinc Metal Batteries",
|
|
"Source Title": "JOURNAL OF THE AMERICAN CHEMICAL SOCIETY",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
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|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Anode-free metal batteries can in principle offer higher energy density, but this requires them to have extraordinary Coulombic efficiency (>99.7%). Although Zn-based metal batteries are promising for stationary storage, the parasitic side reactions make anode-free batteries difficult to achieve in practice. In this work, a salting-in-effect-induced hybrid electrolyte is proposed as an effective strategy that enables both a highly reversible Zn anode and good stability and compatibility toward various cathodes. The as-prepared electrolyte can also work well under a wide temperature range (i.e., from -20 to 50 degrees C). It is demonstrated that in the presence of propylene carbonate, triflate anions are involved in the Zn2+ solvation sheath structure, even at a low salt concentration (2.14 M). The unique solvation structure results in the reduction of anions, thus forming a hydrophobic solid electrolyte interphase. The waterproof interphase along with the decreased water activity in the hybrid electrolyte effectively prevents side reactions, thus ensuring a stable Zn anode with an unprecedented Coulombic efficiency (99.93% over 500 cycles at 1 mA cm(-2)). More importantly, we design an anode-free Zn metal battery that exhibits excellent cycling stability (80% capacity retention after 275 cycles at 0.5 mA cm(-2)). This work provides a universal strategy to design co-solvent electrolytes for anode-free Zn metal batteries.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 437,
|
|
"Times Cited, All Databases": 444,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "APR 27",
|
|
"Publication Year": 2022,
|
|
"Volume": 144,
|
|
"Issue": 16,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 7160,
|
|
"End Page": 7170,
|
|
"Article Number": null,
|
|
"DOI": "10.1021/jacs.1c12764",
|
|
"DOI Link": "http://dx.doi.org/10.1021/jacs.1c12764",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000799141600018",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Hai, X; Xi, SB; Mitchell, S; Harrath, K; Xu, HM; Akl, DF; Kong, DB; Li, J; Li, ZJ; Sun, T; Yang, HM; Cui, YG; Su, CL; Zhao, XX; Li, J; Pérez-Ramírez, J; Lu, J",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Hai, Xiao; Xi, Shibo; Mitchell, Sharon; Harrath, Karim; Xu, Haomin; Akl, Dario Faust; Kong, Debin; Li, Jing; Li, Zejun; Sun, Tao; Yang, Huimin; Cui, Yige; Su, Chenliang; Zhao, Xiaoxu; Li, Jun; Perez-Ramirez, Javier; Lu, Jiong",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Scalable two-step annealing method for preparing ultra-high-density single-atom catalyst libraries",
|
|
"Source Title": "NATURE nullOTECHNOLOGY",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "A general versatile approach combining wet-chemistry impregnation and two-step annealing is devised for the scalable synthesis of a library of ultra-high-density single-atom catalysts with drastically enhanced reactivity. The stabilization of transition metals as isolated centres with high areal density on suitably tailored carriers is crucial for maximizing the industrial potential of single-atom heterogeneous catalysts. However, achieving single-atom dispersions at metal contents above 2 wt% remains challenging. Here we introduce a versatile approach combining impregnation and two-step annealing to synthesize ultra-high-density single-atom catalysts with metal contents up to 23 wt% for 15 metals on chemically distinct carriers. Translation to a standardized, automated protocol demonstrates the robustness of our method and provides a path to explore virtually unlimited libraries of mono- or multimetallic catalysts. At the molecular level, characterization of the synthesis mechanism through experiments and simulations shows that controlling the bonding of metal precursors with the carrier via stepwise ligand removal prevents their thermally induced aggregation into nulloparticles. The drastically enhanced reactivity with increasing metal content exemplifies the need to optimize the surface metal density for a given application. Moreover, the loading-dependent site-specific activity observed in three distinct catalytic systems reflects the well-known complexity in heterogeneous catalyst design, which now can be tackled with a library of single-atom catalysts with widely tunable metal loadings.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 422,
|
|
"Times Cited, All Databases": 442,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "FEB",
|
|
"Publication Year": 2022,
|
|
"Volume": 17,
|
|
"Issue": 2,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 174,
|
|
"End Page": "+",
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s41565-021-01022-y",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41565-021-01022-y",
|
|
"Book DOI": null,
|
|
"Early Access Date": "NOV 2021",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics; Materials Science",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000722472000001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
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"Authors": "Zhang, YM; Zhao, JH; Wang, H; Xiao, B; Zhang, W; Zhao, XB; Lv, TP; Thangamuthu, M; Zhang, J; Guo, Y; Ma, JN; Lin, LN; Tang, JW; Huang, R; Liu, QJ",
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"Book Authors": null,
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"Author Full Names": "Zhang, Yumin; Zhao, Jianhong; Wang, Hui; Xiao, Bin; Zhang, Wen; Zhao, Xinbo; Lv, Tianping; Thangamuthu, Madasamy; Zhang, Jin; Guo, Yan; Ma, Jiani; Lin, Lina; Tang, Junwang; Huang, Rong; Liu, Qingju",
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"Book Author Full Names": null,
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"Group Authors": null,
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"Article Title": "Single-atom Cu anchored catalysts for photocatalytic renewable H2 production with a quantum efficiency of 56%",
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"Source Title": "NATURE COMMUNICATIONS",
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"Abstract": "Single-atom catalysts anchoring offers a desirable pathway for efficiency maximization and cost-saving for photocatalytic hydrogen evolution. However, the single-atoms loading amount is always within 0.5% in most of the reported due to the agglomeration at higher loading concentrations. In this work, the highly dispersed and large loading amount (>1 wt%) of copper single-atoms were achieved on TiO2, exhibiting the H-2 evolution rate of 101.7 mmol g(-1) h(-1) under simulated solar light irradiation, which is higher than other photocatalysts reported, in addition to the excellent stability as proved after storing 380 days. More importantly, it exhibits an apparent quantum efficiency of 56% at 365 nm, a significant breakthrough in this field. The highly dispersed and large amount of Cu single-atoms incorporation on TiO2 enables the efficient electron transfer via Cu2+-Cu+ process. The present approach paves the way to design advanced materials for remarkable photocatalytic activity and durability. In this work, the highly dispersed and large loading amount (>1 wt%) of copper single-atoms were achieved on TiO2, resulting into an apparent quantum efficiency of 56% at 365 nm, in addition to an excellent thermal stability as proved after storing 380 days.",
|
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"Addresses": null,
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"Affiliations": null,
|
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"Reprint Addresses": null,
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"Funding Orgs": null,
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"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
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"Cited References": null,
|
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"Cited Reference Count": null,
|
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"Times Cited, WoS Core": 417,
|
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"Times Cited, All Databases": 440,
|
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"180 Day Usage Count": null,
|
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"Since 2013 Usage Count": null,
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"Publisher": null,
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|
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|
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"Publication Date": "JAN 10",
|
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"Publication Year": 2022,
|
|
"Volume": 13,
|
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"Issue": 1,
|
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"Part Number": null,
|
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"Supplement": null,
|
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"Special Issue": null,
|
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"Meeting Abstract": null,
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"Start Page": null,
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"End Page": null,
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"Article Number": 58,
|
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"DOI": "10.1038/s41467-021-27698-3",
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"DOI Link": "http://dx.doi.org/10.1038/s41467-021-27698-3",
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|
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"Research Areas": "Science & Technology - Other Topics",
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"IDS Number": null,
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"Pubmed Id": null,
|
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"Open Access Designations": null,
|
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"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000781259400001",
|
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"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
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"Publication Type": "J",
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"Authors": "Zhou, LD; Zuo, TT; Kwok, CY; Kim, SY; Assoud, A; Zhang, Q; Janek, J; Nazar, LF",
|
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"Book Authors": null,
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"Book Editors": null,
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"Book Group Authors": null,
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"Author Full Names": "Zhou, Laidong; Zuo, Tong-Tong; Kwok, Chun Yuen; Kim, Se Young; Assoud, Abdeljalil; Zhang, Qiang; Janek, Juergen; Nazar, Linda F.",
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"Book Author Full Names": null,
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"Group Authors": null,
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"Article Title": "High areal capacity, long cycle life 4 V ceramic all-solid-state Li-ion batteries enabled by chloride solid electrolytes",
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"Source Title": "NATURE ENERGY",
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"Book Series Title": null,
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"Author Keywords": null,
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"Abstract": "All-solid-state Li batteries (ASSBs) employing inorganic solid electrolytes offer improved safety and are exciting candidates for next-generation energy storage. Herein, we report a family of lithium mixed-metal chlorospinels, Li2InxSc0.666-xCl4 (0 <= x <= 0.666), with high ionic conductivity (up to 2.0 mS cm(-1)) owing to a highly disordered Li-ion distribution, and low electronic conductivity (4.7 x 10(-10) S cm(-1)), which are implemented for high-performance ASSBs. Owing to the excellent interfacial stability of the SE against uncoated high-voltage cathode materials, ASSBs utilizing LiCoO2 or LiNi0.85Co0.1Mn0.05O2 exhibit superior rate capability and long-term cycling (up to 4.8 V versus Li+/Li) compared to state-of-the-art ASSBs. In particular, the ASSB with LiNi0.85Co0.1Mn0.05O2 exhibits a long life of >3,000 cycles with 80% capacity retention at room temperature. High cathode loadings are also demonstrated in ASSBs with stable capacity retention of >4 mAh cm(-2) (similar to 190 mAh g(-1)).",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
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"Email Addresses": null,
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"Researcher Ids": null,
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"ORCIDs": null,
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"Funding Orgs": null,
|
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"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
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"Times Cited, WoS Core": 388,
|
|
"Times Cited, All Databases": 412,
|
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"180 Day Usage Count": null,
|
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"Since 2013 Usage Count": null,
|
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"Publisher": null,
|
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"Publisher City": null,
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"Publisher Address": null,
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"ISSN": null,
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"ISBN": null,
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"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JAN",
|
|
"Publication Year": 2022,
|
|
"Volume": 7,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 83,
|
|
"End Page": 93,
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s41560-021-00952-0",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41560-021-00952-0",
|
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"Book DOI": null,
|
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"Early Access Date": "JAN 2022",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Energy & Fuels; Materials Science",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000737783400001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Jiang, YW; Zhang, ZT; Wang, YX; Li, DL; Coen, CT; Hwaun, E; Chen, G; Wu, HC; Zhong, DL; Niu, SM; Wang, WC; Saberi, A; Lai, JC; Wu, YL; Wang, Y; Trotsyuk, AA; Loh, KY; Shih, CC; Xu, WH; Liang, K; Zhang, KL; Bai, YH; Gurusankar, G; Hu, WP; Jia, W; Cheng, Z; Dauskardt, RH; Gurtner, GC; Tok, JBH; Deisseroth, K; Soltesz, I; Bao, ZN",
|
|
"Book Authors": null,
|
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"Book Editors": null,
|
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|
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"Author Full Names": "Jiang, Yuanwen; Zhang, Zhitao; Wang, Yi-Xuan; Li, Deling; Coen, Charles-Theophile; Hwaun, Ernie; Chen, Gan; Wu, Hung-Chin; Zhong, Donglai; Niu, Simiao; Wang, Weichen; Saberi, Aref; Lai, Jian-Cheng; Wu, Yilei; Wang, Yang; Trotsyuk, Artem A.; Loh, Kang Yong; Shih, Chien-Chung; Xu, Wenhui; Liang, Kui; Zhang, Kailiang; Bai, Yihong; Gurusankar, Gurupranav; Hu, Wenping; Jia, Wang; Cheng, Zhen; Dauskardt, Reinhold H.; Gurtner, Geoffrey C.; Tok, Jeffrey B-H; Deisseroth, Karl; Soltesz, Ivan; Bao, Zhenull",
|
|
"Book Author Full Names": null,
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"Group Authors": null,
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"Article Title": "Topological supramolecular network enabled high-conductivity, stretchable organic bioelectronics",
|
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"Source Title": "SCIENCE",
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"Book Series Title": null,
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|
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|
"Abstract": "Intrinsically stretchable bioelectronic devices based on soft and conducting organic materials have been regarded as the ideal interface for seamless and biocompatible integration with the human body. A remaining challenge is to combine high mechanical robustness with good electrical conduction, especially when patterned at small feature sizes. We develop a molecular engineering strategy based on a topological supramolecular network, which allows for the decoupling of competing effects from multiple molecular building blocks to meet complex requirements. We obtained simultaneously high conductivity and crack-onset strain in a physiological environment, with direct photopatternability down to the cellular scale. We further collected stable electromyography signals on soft and malleable octopus and performed localized neuromodulation down to single-nucleus precision for controlling organ-specific activities through the delicate brainstem.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
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"Email Addresses": null,
|
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"Researcher Ids": null,
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"ORCIDs": null,
|
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"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 383,
|
|
"Times Cited, All Databases": 397,
|
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"180 Day Usage Count": null,
|
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"Since 2013 Usage Count": null,
|
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"Publisher": null,
|
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"Publisher City": null,
|
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"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
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"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "MAR 25",
|
|
"Publication Year": 2022,
|
|
"Volume": 375,
|
|
"Issue": 6587,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": "SI",
|
|
"Meeting Abstract": null,
|
|
"Start Page": 1411,
|
|
"End Page": "+",
|
|
"Article Number": null,
|
|
"DOI": "10.1126/science.abj7564",
|
|
"DOI Link": "http://dx.doi.org/10.1126/science.abj7564",
|
|
"Book DOI": null,
|
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"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000778894800044",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Mehmood, A; Gong, MJ; Jaouen, F; Roy, A; Zitolo, A; Khan, A; Sougrati, MT; Primbs, M; Bonastres, AM; Fongalland, D; Drazic, G; Strasser, P; Kucernak, A",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
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|
|
"Author Full Names": "Mehmood, Asad; Gong, Mengjun; Jaouen, Frederic; Roy, Aaron; Zitolo, Andrea; Khan, Anastassiya; Sougrati, Moulay-Tahar; Primbs, Mathias; Bonastres, Alex Martinez; Fongalland, Dash; Drazic, Goran; Strasser, Peter; Kucernak, Anthony",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
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|
"Article Title": "High loading of single atomic iron sites in Fe-NC oxygen reduction catalysts for proton exchange membrane fuel cells",
|
|
"Source Title": "NATURE CATALYSIS",
|
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"Book Series Title": null,
|
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"Language": null,
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"Author Keywords": null,
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"Keywords Plus": null,
|
|
"Abstract": "Non-precious iron-based catalysts (Fe-NCs) require high active site density to meet the performance targets as cathode catalysts in proton exchange membrane fuel cells. Site density is generally limited to that achieved at a 1-3 wt%(Fe) loading due to the undesired formation of iron-containing nulloparticles at higher loadings. Here we show that by preforming a carbon-nitrogen matrix using a sacrificial metal (Zn) in the initial synthesis step and then exchanging iron into this preformed matrix we achieve 7 wt% iron coordinated solely as single-atom Fe-N-4 sites, as identified by Fe-57 cryogenic Mossbauer spectroscopy and X-ray absorption spectroscopy. Site density values measured by in situ nitrite stripping and ex situ CO chemisorption methods are 4.7 x 10(19) and 7.8 x 10(19) sites g(-1), with a turnover frequency of 5.4 electrons sites(-1) s(-1) at 0.80 V in a 0.5 M H2SO4 electrolyte. The catalyst delivers an excellent proton exchange membrane fuel cell performance with current densities of 41.3 mA cm(-2) at 0.90 ViR-free using H-2-O-2 and 145 mA cm(-2) at 0.80 V (199 mA cm(-2) at 0.80 ViR-free) using H-2-air.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 377,
|
|
"Times Cited, All Databases": 386,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "APR",
|
|
"Publication Year": 2022,
|
|
"Volume": 5,
|
|
"Issue": 4,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 311,
|
|
"End Page": 323,
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s41929-022-00772-9",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41929-022-00772-9",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000787831800012",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Fang, JY; Zheng, QZ; Lou, YY; Zhao, KM; Hu, SN; Li, G; Akdim, O; Huang, XY; Sun, SG",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Fang, Jia-Yi; Zheng, Qi-Zheng; Lou, Yao-Yin; Zhao, Kuang-Min; Hu, Sheng-null; Li, Guang; Akdim, Ouardia; Huang, Xiao-Yang; Sun, Shi-Gang",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Ampere-level current density ammonia electrochemical synthesis using CuCo nullosheets simulating nitrite reductase bifunctional nature",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
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"Document Type": "Article",
|
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"Conference Title": null,
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"Conference Location": null,
|
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"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "The development of electrocatalysts capable of efficient reduction of nitrate (NO3-) to ammonia (NH3) is drawing increasing interest for the sake of low carbon emission and environmental protection. Herein, we present a CuCo bimetallic catalyst able to imitate the bifunctional nature of copper-type nitrite reductase, which could easily remove NO2- via the collaboration of two active centers. Indeed, Co acts as an electron/proton donating center, while Cu facilitates NOx- adsorption/association. The bio-inspired CuCo nullosheet electrocatalyst delivers a 1001% Faradaic efficiency at an ampere-level current density of 1035mAcm(-2) at -0.2V vs. Reversible Hydrogen Electrode. The NH3 production rate reaches a high activity of 4.8mmolcm(-2) h(-1) (960mmol g(cat)(-1) h(-1)). A mechanistic study, using electrochemical in situ Fourier transform infrared spectroscopy and shell-isolated nulloparticle enhanced Raman spectroscopy, reveals a strong synergy between Cu and Co, with Co sites promoting the hydrogenation of NO3- to NH3 via adsorbed *H species. The well-modulated coverage of adsorbed *H and *NO3 led simultaneously to high NH3 selectivity and yield.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 387,
|
|
"Times Cited, All Databases": 389,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "DEC 22",
|
|
"Publication Year": 2022,
|
|
"Volume": 13,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 7899,
|
|
"DOI": "10.1038/s41467-022-35533-6",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-022-35533-6",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000972743600016",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Chen, JD; Chen, CH; Qin, MK; Li, B; Lin, BB; Mao, Q; Yang, HB; Liu, B; Wang, Y",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
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"Book Group Authors": null,
|
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"Author Full Names": "Chen, Jiadong; Chen, Chunhong; Qin, Minkai; Li, Ben; Lin, Binbin; Mao, Qing; Yang, Hongbin; Liu, Bin; Wang, Yong",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
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"Article Title": "Reversible hydrogen spillover in Ru-WO3-x enhances hydrogen evolution activity in neutral pH water splitting",
|
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"Source Title": "NATURE COMMUNICATIONS",
|
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"Book Series Title": null,
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"Author Keywords": null,
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"Abstract": "Noble metal electrocatalysts (e.g., Pt, Ru, etc.) suffer from sluggish kinetics of water dissociation for the electrochemical reduction of water to molecular hydrogen in alkaline and neutral pH environments. Herein, we found that an integration of Ru nulloparticles (NPs) on oxygen-deficient WO3-x manifested a 24.0-fold increase in hydrogen evolution reaction (HER) activity compared with commercial Ru/C electrocatalyst in neutral electrolyte. Oxygen-deficient WO3-x is shown to possess large capacity for storing protons, which could be transferred to the Ru NPs under cathodic potential. This significantly increases the hydrogen coverage on the surface of Ru NPs in HER and thus changes the rate-determining step of HER on Ru from water dissociation to hydrogen recombination.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
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"Researcher Ids": null,
|
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"ORCIDs": null,
|
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"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 349,
|
|
"Times Cited, All Databases": 360,
|
|
"180 Day Usage Count": null,
|
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"Since 2013 Usage Count": null,
|
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"Publisher": null,
|
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"Publisher City": null,
|
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"Publisher Address": null,
|
|
"ISSN": null,
|
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"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "SEP 14",
|
|
"Publication Year": 2022,
|
|
"Volume": 13,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 5382,
|
|
"DOI": "10.1038/s41467-022-33007-3",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-022-33007-3",
|
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"Book DOI": null,
|
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"Early Access Date": null,
|
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"Number of Pages": null,
|
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"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000853935100017",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Shi, XW; Dai, C; Wang, X; Hu, JY; Zhang, JY; Zheng, LX; Mao, L; Zheng, HJ; Zhu, MS",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Shi, Xiaowei; Dai, Chao; Wang, Xin; Hu, Jiayue; Zhang, Junying; Zheng, Lingxia; Mao, Liang; Zheng, Huajun; Zhu, Mingshan",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Protruding Pt single-sites on hexagonal ZnIn2S4 to accelerate photocatalytic hydrogen evolution",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
|
"Book Series Title": null,
|
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"Book Series Subtitle": null,
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"Language": null,
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"Document Type": "Article",
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"Conference Host": null,
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"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "An alternative approach to defect-trapped Pt single-sites on a semiconductor is reported. Here, protruding Pt sites inhibit charge recombination and cause a tip effect which enhances H-2 evolution yield rates with minimal co-catalyst loading. Single-site cocatalysts engineered on supports offer a cost-efficient pathway to utilize precious metals, yet improving the performance further with minimal catalyst loading is still highly desirable. Here we have conducted a photochemical reaction to stabilize ultralow Pt co-catalysts (0.26 wt%) onto the basal plane of hexagonal ZnIn2S4 nullosheets (Pt-SS-ZIS) to form a Pt-S-3 protrusion tetrahedron coordination structure. Compared with the traditional defect-trapped Pt single-site counterparts, the protruding Pt single-sites on h-ZIS photocatalyst enhance the H-2 evolution yield rate by a factor of 2.2, which could reach 17.5 mmol g(-1) h(-1) under visible light irradiation. Importantly, through simple drop-casting, a thin Pt-SS-ZIS film is prepared, and large amount of observable H-2 bubbles are generated, providing great potential for practical solar-light-driven H-2 production. The protruding single Pt atoms in Pt-SS-ZIS could inhibit the recombination of electron-hole pairs and cause a tip effect to optimize the adsorption/desorption behavior of H through effective proton mass transfer, which synergistically promote reaction thermodynamics and kinetics.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 356,
|
|
"Times Cited, All Databases": 363,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "MAR 11",
|
|
"Publication Year": 2022,
|
|
"Volume": 13,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 1287,
|
|
"DOI": "10.1038/s41467-022-28995-1",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-022-28995-1",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000767892300022",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Li, SJ; Cai, MJ; Liu, YP; Wang, CC; Lv, KL; Chen, XB",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Li, Shijie; Cai, Mingjie; Liu, Yanping; Wang, Chunchun; Lv, Kangle; Chen, Xiaobo",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "S-Scheme photocatalyst TaON/Bi2WO6 nullofibers with oxygen vacancies for efficient abatement of antibiotics and Cr(VI): Intermediate eco-toxicity analysis and mechanistic insights",
|
|
"Source Title": "CHINESE JOURNAL OF CATALYSIS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
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"Document Type": "Article",
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|
"Conference Title": null,
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|
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|
|
"Conference Sponsor": null,
|
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|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Enlightened by natural photosynthesis, developing efficient S-scheme heterojunction photocatalysts for deleterious pollutant removal is of prime importance to restore environment. Herein, novel TaON/Bi2WO6 S-scheme heterojunction nullofibers were designed and developed by in-situ growing Bi2WO6 nullosheets with oxygen vacancies (OVs) on TaON nullofibers. Thanks to the efficiently spatial charge disassociation and preserved great redox power by the unique S-scheme mechanism and OVs, as well as firmly interfacial contact by the core-shell 1D/2D fibrous hetero-structure via the in-situ growth, the optimized TaON/Bi2WO6 heterojunction unveils exceptional visible-light photocatalytic property for abatement of tetracycline (TC), levofloxacin (LEV), and Cr(VI), respectively by 2.8-fold, 1.0-fold, and 1.9-fold enhancement compared to the bare Bi2WO6, while maintaining satisfactory stability. Furthermore, the systematic photoreaction tests indicate TaON/Bi2WO6 has the high practicality in the elimination of pollutants in aquatic environment. The degradation pathway of tetracycline and intermediate eco-toxicity were determined based on HPLC-MS combined with QSAR calculation, and a possible photocatalytic mechanism was elucidated. This work provides a guideline for designing high-performance TaON-based S-scheme photocatalysts with defects for environment protection. (C) 2022, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 360,
|
|
"Times Cited, All Databases": 378,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "OCT",
|
|
"Publication Year": 2022,
|
|
"Volume": 43,
|
|
"Issue": 10,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 2652,
|
|
"End Page": 2664,
|
|
"Article Number": null,
|
|
"DOI": "10.1016/S1872-2067(22)64106-8",
|
|
"DOI Link": "http://dx.doi.org/10.1016/S1872-2067(22)64106-8",
|
|
"Book DOI": null,
|
|
"Early Access Date": "OCT 2022",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry; Engineering",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000884673500004",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Liu, HM; Lang, XY; Zhu, C; Timoshenko, J; Rüscher, M; Bai, LC; Guijarro, N; Yin, HB; Peng, Y; Li, JH; Liu, Z; Wang, WC; Roldan Cuenya, B; Luo, JS",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Liu, Huimin; Lang, Xiuyao; Zhu, Chao; Timoshenko, Janis; Ruescher, Martina; Bai, Lichen; Guijarro, Nestor; Yin, Haibo; Peng, Yue; Li, Junhua; Liu, Zheng; Wang, Weichao; Roldan Cuenya, Beatriz; Luo, Jingshan",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Efficient Electrochemical Nitrate Reduction to Ammonia with Copper-Supported Rhodium Cluster and Single-Atom Catalysts",
|
|
"Source Title": "ANGEWANDTE CHEMIE-INTERNATIONAL EDITION",
|
|
"Book Series Title": null,
|
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|
|
"Language": null,
|
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|
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|
|
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|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "The electrochemical nitrate reduction reaction (NITRR) provides a promising solution for restoring the imbalance in the global nitrogen cycle while enabling a sustainable and decentralized route to source ammonia. Here, we demonstrate a novel electrocatalyst for NITRR consisting of Rh clusters and single-atoms dispersed onto Cu nullowires (NWs), which delivers a partial current density of 162 mA cm(-2) for NH3 production and a Faradaic efficiency (FE) of 93 % at -0.2 V vs. RHE. The highest ammonia yield rate reached a record value of 1.27 mmol h(-1) cm(-2). Detailed investigations by electron paramagnetic resonullce, in situ infrared spectroscopy, differential electrochemical mass spectrometry and density functional theory modeling suggest that the high activity originates from the synergistic catalytic cooperation between Rh and Cu sites, whereby adsorbed hydrogen on Rh site transfers to vicinal *NO intermediate species adsorbed on Cu promoting the hydrogenation and ammonia formation.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 369,
|
|
"Times Cited, All Databases": 377,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JUN 7",
|
|
"Publication Year": 2022,
|
|
"Volume": 61,
|
|
"Issue": 23,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": "e202202556",
|
|
"DOI": "10.1002/anie.202202556",
|
|
"DOI Link": "http://dx.doi.org/10.1002/anie.202202556",
|
|
"Book DOI": null,
|
|
"Early Access Date": "APR 2022",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000780914100001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Hao, JC; Zhuang, ZC; Cao, KC; Gao, GH; Wang, C; Lai, FL; Lu, SL; Ma, PM; Dong, WF; Liu, TX; Du, ML; Zhu, H",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Hao, Jiace; Zhuang, Zechao; Cao, Kecheng; Gao, Guohua; Wang, Chan; Lai, Feili; Lu, Shuanglong; Ma, Piming; Dong, Weifu; Liu, Tianxi; Du, Mingliang; Zhu, Han",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Unraveling the electronegativity-dominated intermediate adsorption on high-entropy alloy electrocatalysts",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "High-entropy alloy catalysts are an emerging class of materials and identification of catalytically active sites is critical. Here, we provide evidence that metal site electronegativity differences stabilize bound *OH and *H intermediates. High-entropy alloys have received considerable attention in the field of catalysis due to their exceptional properties. However, few studies hitherto focus on the origin of their outstanding performance and the accurate identification of active centers. Herein, we report a conceptual and experimental approach to overcome the limitations of single-element catalysts by designing a FeCoNiXRu (X: Cu, Cr, and Mn) High-entropy alloys system with various active sites that have different adsorption capacities for multiple intermediates. The electronegativity differences between mixed elements in HEA induce significant charge redistribution and create highly active Co and Ru sites with optimized energy barriers for simultaneously stabilizing OH* and H* intermediates, which greatly enhances the efficiency of water dissociation in alkaline conditions. This work provides an in-depth understanding of the interactions between specific active sites and intermediates, which opens up a fascinating direction for breaking scaling relation issues for multistep reactions.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 410,
|
|
"Times Cited, All Databases": 413,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "MAY 13",
|
|
"Publication Year": 2022,
|
|
"Volume": 13,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 2662,
|
|
"DOI": "10.1038/s41467-022-30379-4",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-022-30379-4",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000795204200020",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "He, ZY; Zhang, J; Gong, ZH; Lei, H; Zhou, D; Zhang, NA; Mai, WJ; Zhao, SJ; Chen, Y",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "He, Zuyun; Zhang, Jun; Gong, Zhiheng; Lei, Hang; Zhou, Deng; Zhang, Nian; Mai, Wenjie; Zhao, Shijun; Chen, Yan",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Activating lattice oxygen in NiFe-based (oxy)hydroxide for water electrolysis",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Transition metal oxides or (oxy)hydroxides have been intensively investigated as promising electrocatalysts for energy and environmental applications. Oxygen in the lattice was reported recently to actively participate in surface reactions. Herein, we report a sacrificial template-directed approach to synthesize Mo-doped NiFe (oxy)hydroxide with modulated oxygen activity as an enhanced electrocatalyst towards oxygen evolution reaction (OER). The obtained MoNiFe (oxy)hydroxide displays a high mass activity of 1910 A/g(metal) at the overpotential of 300 mV. The combination of density functional theory calculations and advanced spectroscopy techniques suggests that the Mo dopant upshifts the O 2p band and weakens the metal-oxygen bond of NiFe (oxy)hydroxide, facilitating oxygen vacancy formation and shifting the reaction pathway for OER. Our results provide critical insights into the role of lattice oxygen in determining the activity of (oxy)hydroxides and demonstrate tuning oxygen activity as a promising approach for constructing highly active electrocatalysts. While (oxy)hydroxides are effective oxygen evolution electrocatalysts, the impacts of pre-catalyst properties on catalyst activities are challenging to assess. Here, authors find Mo dopants in Ni-Fe (oxyhydroxides) to promote lattice oxygen participation and to boost oxygen evolution activities.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
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"Researcher Ids": null,
|
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"ORCIDs": null,
|
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"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 366,
|
|
"Times Cited, All Databases": 370,
|
|
"180 Day Usage Count": null,
|
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"Since 2013 Usage Count": null,
|
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"Publisher": null,
|
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"Publisher City": null,
|
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"Publisher Address": null,
|
|
"ISSN": null,
|
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"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "APR 21",
|
|
"Publication Year": 2022,
|
|
"Volume": 13,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 2191,
|
|
"DOI": "10.1038/s41467-022-29875-4",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-022-29875-4",
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"Book DOI": null,
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|
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"Number of Pages": null,
|
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"Web of Science Index": null,
|
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"Research Areas": "Science & Technology - Other Topics",
|
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"IDS Number": null,
|
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"Pubmed Id": null,
|
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"Open Access Designations": null,
|
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"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000785003900005",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Wright, LG; Onodera, T; Stein, MM; Wang, TY; Schachter, DT; Hu, Z; McMahon, PL",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Wright, Logan G.; Onodera, Tatsuhiro; Stein, Martin M.; Wang, Tianyu; Schachter, Darren T.; Hu, Zoey; McMahon, Peter L.",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
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"Article Title": "Deep physical neural networks trained with backpropagation",
|
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"Source Title": "NATURE",
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"Book Series Title": null,
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"Book Series Subtitle": null,
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"Author Keywords": null,
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"Keywords Plus": null,
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|
"Abstract": "Deep-learning models have become pervasive tools in science and engineering. However, their energy requirements now increasingly limit their scalability(1). Deep-learning accelerators(2-9) aim to perform deep learning energy-efficiently, usually targeting the inference phase and often by exploiting physical substrates beyond conventional electronics. Approaches so far(10-22) have been unable to apply the backpropagation algorithm to train unconventional novel hardware in situ. The advantages of backpropagation have made it the de facto training method for large-scale neural networks, so this deficiency constitutes a major impediment. Here we introduce a hybrid in situ-in silico algorithm, called physics-aware training, that applies backpropagation to train controllable physical systems. Just as deep learning realizes computations with deep neural networks made from layers of mathematical functions, our approach allows us to train deep physical neural networks made from layers of controllable physical systems, even when the physical layers lack any mathematical isomorphism to conventional artificial neural network layers. To demonstrate the universality of our approach, we train diverse physical neural networks based on optics, mechanics and electronics to experimentally perform audio and image classification tasks. Physics-aware training combines the scalability of backpropagation with the automatic mitigation of imperfections and noise achievable with in situ algorithms. Physical neural networks have the potential to perform machine learning faster and more energy-efficiently than conventional electronic processors and, more broadly, can endow physical systems with automatically designed physical functionalities, for example, for robotics(23-26), materials(27-29) and smart sensors(30-32).",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 355,
|
|
"Times Cited, All Databases": 386,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JAN 27",
|
|
"Publication Year": 2022,
|
|
"Volume": 601,
|
|
"Issue": 7894,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 549,
|
|
"End Page": "+",
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s41586-021-04223-6",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41586-021-04223-6",
|
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"Book DOI": null,
|
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"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
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"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000749546400022",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Zhang, JC; Dong, PF; Dang, K; Zhang, YN; Yan, QL; Xiang, H; Su, J; Liu, ZH; Si, MW; Gao, JC; Kong, MF; Zhou, H; Hao, Y",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Zhang, Jincheng; Dong, Pengfei; Dang, Kui; Zhang, Yanni; Yan, Qinglong; Xiang, Hu; Su, Jie; Liu, Zhihong; Si, Mengwei; Gao, Jiacheng; Kong, Moufu; Zhou, Hong; Hao, Yue",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Ultra-wide bandgap semiconductor Ga2O3 power diodes",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
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"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
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"Conference Location": null,
|
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"Conference Sponsor": null,
|
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"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Ultra-wide bandgap semiconductor Ga2O3 based electronic devices are expected to perform beyond wide bandgap counterparts GaN and SiC. However, the reported power figure-of-merit hardly can exceed, which is far below the projected Ga2O3 material limit. Major obstacles are high breakdown voltage requires low doping material and PN junction termination, contradicting with low specific on-resistance and simultaneous achieving of n- and p-type doping, respectively. In this work, we demonstrate that Ga2O3 heterojunction PN diodes can overcome above challenges. By implementing the holes injection in the Ga2O3, bipolar transport can induce conductivity modulation and low resistance in a low doping Ga2O3 material. Therefore, breakdown voltage of 8.32 kV, specific on-resistance of 5.24 m Omega.cm(2), power figure-of-merit of 13.2 GW/cm(2), and turn-on voltage of 1.8 V are achieved. The power figure-of-merit value surpasses the 1-D unipolar limit of GaN and SiC. Those Ga2O3 power diodes demonstrate their great potential for next-generation power electronics applications.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 372,
|
|
"Times Cited, All Databases": 381,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JUL 6",
|
|
"Publication Year": 2022,
|
|
"Volume": 13,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 3900,
|
|
"DOI": "10.1038/s41467-022-31664-y",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-022-31664-y",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000821634700017",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Zhu, JG; Wang, YX; Huang, Y; Gopaluni, RB; Cao, YK; Heere, M; Mühlbauer, MJ; Mereacre, L; Dai, HF; Liu, XH; Senyshyn, A; Wei, XZ; Knapp, M; Ehrenberg, H",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Zhu, Jiangong; Wang, Yixiu; Huang, Yuan; Gopaluni, R. Bhushan; Cao, Yankai; Heere, Michael; Muhlbauer, Martin J.; Mereacre, Liuda; Dai, Haifeng; Liu, Xinhua; Senyshyn, Anatoliy; Wei, Xuezhe; Knapp, Michael; Ehrenberg, Helmut",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Data-driven capacity estimation of commercial lithium-ion batteries from voltage relaxation",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Accurate capacity estimation is crucial for lithium-ion batteries' reliable and safe operation. Here, the authors propose an approach exploiting features from the relaxation voltage curve for battery capacity estimation without requiring other previous cycling information. Accurate capacity estimation is crucial for the reliable and safe operation of lithium-ion batteries. In particular, exploiting the relaxation voltage curve features could enable battery capacity estimation without additional cycling information. Here, we report the study of three datasets comprising 130 commercial lithium-ion cells cycled under various conditions to evaluate the capacity estimation approach. One dataset is collected for model building from batteries with LiNi0.86Co0.11Al0.03O2-based positive electrodes. The other two datasets, used for validation, are obtained from batteries with LiNi0.83Co0.11Mn0.07O2-based positive electrodes and batteries with the blend of Li(NiCoMn)O-2 - Li(NiCoAl)O-2 positive electrodes. Base models that use machine learning methods are employed to estimate the battery capacity using features derived from the relaxation voltage profiles. The best model achieves a root-mean-square error of 1.1% for the dataset used for the model building. A transfer learning model is then developed by adding a featured linear transformation to the base model. This extended model achieves a root-mean-square error of less than 1.7% on the datasets used for the model validation, indicating the successful applicability of the capacity estimation approach utilizing cell voltage relaxation.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 342,
|
|
"Times Cited, All Databases": 360,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "APR 27",
|
|
"Publication Year": 2022,
|
|
"Volume": 13,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 2261,
|
|
"DOI": "10.1038/s41467-022-29837-w",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-022-29837-w",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000788592600010",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Wu, F; Tian, H; Shen, Y; Hou, Z; Ren, J; Gou, GY; Sun, YB; Yang, Y; Ren, TL",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Wu, Fan; Tian, He; Shen, Yang; Hou, Zhan; Ren, Jie; Gou, Guangyang; Sun, Yabin; Yang, Yi; Ren, Tian-Ling",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Vertical MoS2 transistors with sub-1-nm gate lengths",
|
|
"Source Title": "NATURE",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Ultra-scaled transistors are of interest in the development of next-generation electronic devices(1-3). Although atomically thin molybdenum disulfide (MoS2) transistors have been reported(4), the fabrication of devices with gate lengths below 1 nm has been challenging(5). Here we demonstrate side-wall MoS2 transistors with an atomically thin channel and a physical gate length of sub-1 nm using the edge of a graphene layer as the gate electrode. The approach uses large-area graphene and MoS2 films grown by chemical vapour deposition for the fabrication of side-wall transistors on a 2-inch wafer. These devices have On/Off ratios up to 1.02 x 10(5) and subthreshold swing values down to 117 mV dec(-1). Simulation results indicate that the MoS2 side-wall effective channel length approaches 0.34 nm in the On state and 4.54 nm in the Off state. This work can promote Moore's law of the scaling down of transistors for next-generation electronics.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 332,
|
|
"Times Cited, All Databases": 358,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "MAR 10",
|
|
"Publication Year": 2022,
|
|
"Volume": 603,
|
|
"Issue": 7900,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 259,
|
|
"End Page": "+",
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s41586-021-04323-3",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41586-021-04323-3",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000918198200001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Smejkal, L; Sinova, J; Jungwirth, T",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Smejkal, Libor; Sinova, Jairo; Jungwirth, Tomas",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Beyond Conventional Ferromagnetism and Antiferromagnetism: A Phase with Nonrelativistic Spin and Crystal Rotation Symmetry",
|
|
"Source Title": "PHYSICAL REVIEW X",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Recent series of theoretical and experimental reports have driven attention to time-reversal symmetry -breaking spintronic and spin-splitting phenomena in materials with collinear-compensated magnetic order incompatible with conventional ferromagnetism or antiferromagnetism. Here we employ an approach based on nonrelativistic spin-symmetry groups that resolves the conflicting notions of unconventional ferromagnetism or antiferromagnetism by delimiting a third basic collinear magnetic phase. We derive that all materials hosting this collinear-compensated magnetic phase are characterized by crystal-rotation symmetries connecting opposite-spin sublattices separated in the real space and opposite-spin electronic states separated in the momentum space. We describe prominent extraordinary characteristics of the phase, including the alternating spin-splitting sign and broken time-reversal symmetry in the nonrelativistic band structure, the planar or bulk d-, g-, or i-wave symmetry of the spin-dependent Fermi surfaces, spin -degenerate nodal lines and surfaces, band anisotropy of individual spin channels, and spin-split general, as well as time-reversal invariant momenta. Guided by the spin-symmetry principles, we discover in ab initio calculations outlier materials with an extraordinary nonrelativistic spin splitting, whose eV-scale and momentum dependence are determined by the crystal potential of the nonmagnetic phase. This spin -splitting mechanism is distinct from conventional relativistic spin-orbit coupling and ferromagnetic exchange, as well as from the previously considered anisotropic exchange mechanism in compensated magnets. Our results, combined with our identification of material candidates for the phase ranging from insulators and metals to a parent crystal of cuprate superconductors, underpin research of novel quantum phenomena and spintronic functionalities in high-temperature magnets with light elements, vanishing net magnetization, and strong spin coherence. In the discussion, we argue that the conflicting notions of unconventional ferromagnetism or antiferromagnetism, on the one hand, and our symmetry-based delimitation of the third phase, on the other hand, favor a distinct term referring to the phase. The alternating spin polarizations in both the real-space crystal structure and the momentum-space band structure characteristic of this unconventional magnetic phase suggest a term altermagnetism. We point out that d-wave altermagnetism represents a realization of the long-sought-after counterpart in magnetism of the unconventional d-wave superconductivity.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 349,
|
|
"Times Cited, All Databases": 356,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "SEP 23",
|
|
"Publication Year": 2022,
|
|
"Volume": 12,
|
|
"Issue": 3,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 31042,
|
|
"DOI": "10.1103/PhysRevX.12.031042",
|
|
"DOI Link": "http://dx.doi.org/10.1103/PhysRevX.12.031042",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Physics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000865310200001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Zhao, HB; Yu, RF; Ma, SC; Xu, KZ; Chen, Y; Jiang, K; Fang, Y; Zhu, CX; Liu, XC; Tang, Y; Wu, LZ; Wu, YQ; Jiang, QK; He, P; Liu, ZP; Tan, L",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Zhao, Huibo; Yu, Ruofan; Ma, Sicong; Xu, Kaizhuang; Chen, Yang; Jiang, Kun; Fang, Yuan; Zhu, Caixia; Liu, Xiaochen; Tang, Yu; Wu, Lizhi; Wu, Yingquan; Jiang, Qike; He, Peng; Liu, Zhipan; Tan, Li",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "The role of Cu1-O3 species in single-atom Cu/ZrO2 catalyst for CO2 hydrogenation",
|
|
"Source Title": "NATURE CATALYSIS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Copper-based catalysts for the hydrogenation of CO2 to methanol have attracted much interest. The complex nature of these catalysts, however, renders the elucidation of their structure-activity properties difficult. Here we report a copper-based catalyst with isolated active copper sites for the hydrogenation of CO2 to methanol. It is revealed that the single-atom Cu-Zr catalyst with Cu-1-O-3 units contributes solely to methanol synthesis around 180 degrees C, while the presence of small copper clusters or nulloparticles with Cu-Cu structural patterns are responsible for forming the CO by-product. Furthermore, the gradual migration of Cu-1-O-3 units with a quasiplanar structure to the catalyst surface is observed during the catalytic process and accelerates CO2 hydrogenation. The highly active, isolated copper sites and the distinguishable structural pattern identified here extend the horizon of single-atom catalysts for applications in thermal catalytic CO2 hydrogenation and could guide the further design of high-performance copper-based catalysts to meet industrial demand.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 342,
|
|
"Times Cited, All Databases": 351,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "SEP",
|
|
"Publication Year": 2022,
|
|
"Volume": 5,
|
|
"Issue": 9,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 818,
|
|
"End Page": 831,
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s41929-022-00840-0",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41929-022-00840-0",
|
|
"Book DOI": null,
|
|
"Early Access Date": "SEP 2022",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000854746500003",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Zhao, RR; Wang, HF; Du, HR; Yang, Y; Gao, ZH; Qie, L; Huang, YH",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Zhao, Ruirui; Wang, Haifeng; Du, Haoran; Yang, Ying; Gao, Zhonghui; Qie, Long; Huang, Yunhui",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Lanthanum nitrate as aqueous electrolyte additive for favourable zinc metal electrodeposition",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Aqueous zinc batteries are appealing devices for cost-effective and environmentally sustainable energy storage. However, the zinc metal deposition at the anode strongly influences the battery cycle life and performance. To circumvent this issue, here we propose the use of lanthanum nitrate (La(NO3)(3)) as supporting salt for aqueous zinc sulfate (ZnSO4) electrolyte solutions. Via physicochemical and electrochemical characterizations, we demonstrate that this peculiar electrolyte formulation weakens the electric double layer repulsive force, thus, favouring dense metallic zinc deposits and regulating the charge distribution at the zinc metal|electrolyte interface. When tested in Zn||VS2 full coin cell configuration (with cathode mass loading of 16 mg cm(-2)), the electrolyte solution containing the lanthanum ions enables almost 1000 cycles at 1 A g(-1) (after 5 activation cycles at 0.05 A g(-1)) with a stable discharge capacity of about 90 mAh g(-1) and an average cell discharge voltage of similar to 0.54 V. Zinc metal is a promising anode material for aqueous secondary batteries. However, the unfavourable morphologies formed on the electrode surface during cycling limit its application. Here, the authors report the tailoring of the surface morphology using a lanthanum nitrate aqueous electrolyte additive.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 339,
|
|
"Times Cited, All Databases": 346,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JUN 6",
|
|
"Publication Year": 2022,
|
|
"Volume": 13,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 3252,
|
|
"DOI": "10.1038/s41467-022-30939-8",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-022-30939-8",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000808000200007",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Song, Y; Ruan, PC; Mao, CW; Chang, YX; Wang, L; Dai, L; Zhou, P; Lu, BA; Zhou, J; He, ZX",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Song, Yang; Ruan, Pengchao; Mao, Caiwang; Chang, Yuxin; Wang, Ling; Dai, Lei; Zhou, Peng; Lu, Bingan; Zhou, Jiang; He, Zhangxing",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Metal-Organic Frameworks Functionalized Separators for Robust Aqueous Zinc-Ion Batteries",
|
|
"Source Title": "nullO-MICRO LETTERS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Aqueous zinc-ion batteries (AZIBs) are one of the promising energy storage systems, which consist of electrode materials, electrolyte, and separator. The first two have been significantly received ample development, while the prominent role of the separators in manipulating the stability of the electrode has not attracted sufficient attention. In this work, a separator (UiO-66-GF) modified by Zr-based metal organic framework for robust AZIBs is proposed. UiO-66-GF effectively enhances the transport ability of charge carriers and demonstrates preferential orientation of (002) crystal plane, which is favorable for corrosion resistance and dendrite-free zinc deposition. Consequently, ZnlUiO-66-GF-2.21Zn cells exhibit highly reversible plating/stripping behavior with long cycle life over 1650 h at 2.0 mA cm(-2) , and Zn1UiO-66-GF-2.21MnO(2) cells show excellent long-term stability with capacity retention of 85% after 1000 cycles. The reasonable design and application of multifunctional metal organic frameworks modified separators provide useful guidance for constructing durable AZIBs.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 339,
|
|
"Times Cited, All Databases": 352,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "DEC",
|
|
"Publication Year": 2022,
|
|
"Volume": 14,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 218,
|
|
"DOI": "10.1007/s40820-022-00960-z",
|
|
"DOI Link": "http://dx.doi.org/10.1007/s40820-022-00960-z",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics; Materials Science; Physics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000885744900003",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Bai, JX; Shen, RC; Jiang, ZM; Zhang, P; Li, YJ; Li, X",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Bai, Junxian; Shen, Rongchen; Jiang, Zhimin; Zhang, Peng; Li, Youji; Li, Xin",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Integration of 2D layered CdS/WO3 S-scheme heterojunctions and metallic Ti3C2 MXene-based Ohmic junctions for effective photocatalytic H2 generation",
|
|
"Source Title": "CHINESE JOURNAL OF CATALYSIS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article; Proceedings Paper",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "The rapid recombination of photo-generated electron-hole pairs, insufficient active sites, and strong photocorrosion have considerably restricted the practical application of CdS in photocatalytic fields. Herein, we designed and constructed a 2D/2D/2D layered heterojunction photocatalyst with cascaded 2D coupling interfaces. Experiments using electron spin resonullce spectroscopy, ultraviolet photoelectron spectroscopy, and in-situ irradiation X-ray photoelectron spectroscopy were conducted to confirm the 2D layered CdS/WO3 step-scheme (S-scheme) heterojunctions and CdS/MX ohmic junctions. Impressively, it was found that the strong interfacial electric fields in the S-scheme heterojunction photocatalysts could effectively promote spatially directional charge separation and transport between CdS and WO3 nullosheets. In addition, 2D Ti3C2 MXene nullosheets with a smaller work function and excellent metal conductivity when used as a co-catalyst could build ohmic junctions with CdS nullosheets, thus providing a greater number of electron transfer pathways and hydrogen evolution sites. Results showed that the highest visible-light hydrogen evolution rate of the optimized MX-CdS/WO3 layered multi-heterostructures could reach as high as 27.5 mmol/g/h, which was 11.0 times higher than that of pure CdS nullosheets. Notably, the apparent quantum efficiency reached 12.0% at 450 nm. It is hoped that this study offers a reliable approach for developing multifunctional photocatalysts by integrating S-scheme and ohmic-junction built-in electric fields and rationally designing a 2D/2D interface for efficient light-to-hydrogen fuel production. (C) 2022, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 324,
|
|
"Times Cited, All Databases": 339,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "FEB",
|
|
"Publication Year": 2022,
|
|
"Volume": 43,
|
|
"Issue": 2,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 359,
|
|
"End Page": 369,
|
|
"Article Number": null,
|
|
"DOI": "10.1016/S1872-2067(21)63883-4",
|
|
"DOI Link": "http://dx.doi.org/10.1016/S1872-2067(21)63883-4",
|
|
"Book DOI": null,
|
|
"Early Access Date": "JAN 2022",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry; Engineering",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000746696100016",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Landi, S Jr; Segundo, IR; Freitas, E; Vasilevskiy, M; Carneiro, J; Tavares, CJ",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Landi, Salmon, Jr.; Segundo, Iran Rocha; Freitas, Elisabete; Vasilevskiy, Mikhail; Carneiro, Joaquim; Tavares, Carlos Jose",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Use and misuse of the Kubelka-Munk function to obtain the band gap energy from diffuse reflectance measurements",
|
|
"Source Title": "SOLID STATE COMMUNICATIONS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "The determination of the optical band gap energy (E-g) is important for optimization of the generation of electron/hole pairs in semiconductor materials under illumination. For this purpose, the classical theory proposed by Kubelka and Munk (K-M) has been largely employed for the study of amorphous and polycrystalline materials. In this paper, the authors demonstrate, step by step, how to use the K-M function and apply it thoroughly to the determination of the E-g of TiO2 semiconductor powder (pressed at different thicknesses) from diffuse reflectance spectroscopy (DRS) measurements. For the sample thicknesses 1-4 mm, E-g values of 3.12-3.14 eV were obtained. With this work it is envisaged a clarification to the procedure of determination of the E-g from the K-M theory and DRS data, since some drawbacks, and misconceptions have been identified in the recent literature. In particular, the widely used practice of determining the E-g of a material directly from the K-M function is found to be inadequate.",
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"Addresses": null,
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"Affiliations": null,
|
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"Reprint Addresses": null,
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"Email Addresses": null,
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"Researcher Ids": null,
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"Funding Orgs": null,
|
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"Funding Name Preferred": null,
|
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"Funding Text": null,
|
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"Cited References": null,
|
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"Cited Reference Count": null,
|
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"Times Cited, WoS Core": 328,
|
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"Times Cited, All Databases": 332,
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"180 Day Usage Count": null,
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"Since 2013 Usage Count": null,
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"ISSN": null,
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"eISSN": null,
|
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"ISBN": null,
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"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JAN",
|
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"Publication Year": 2022,
|
|
"Volume": 341,
|
|
"Issue": null,
|
|
"Part Number": null,
|
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"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
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"Start Page": null,
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"End Page": null,
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"Article Number": 114573,
|
|
"DOI": "10.1016/j.ssc.2021.114573",
|
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"DOI Link": "http://dx.doi.org/10.1016/j.ssc.2021.114573",
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"Book DOI": null,
|
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"Early Access Date": "OCT 2021",
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"Number of Pages": null,
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"WoS Categories": null,
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"Web of Science Index": null,
|
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"Research Areas": "Physics",
|
|
"IDS Number": null,
|
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"Pubmed Id": null,
|
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"Open Access Designations": null,
|
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"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000725057500009",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Sidhik, S; Wang, YF; De Siena, M; Asadpour, R; Torma, AJ; Terlier, T; Ho, K; Li, WB; Puthirath, AB; Shuai, XT; Agrawal, A; Traore, B; Jones, M; Giridharagopal, R; Ajayan, PM; Strzalka, J; Ginger, DS; Katan, C; Alam, MA; Even, J; Kanatzidis, MG; Mohite, AD",
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"Book Authors": null,
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"Book Editors": null,
|
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"Book Group Authors": null,
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"Author Full Names": "Sidhik, Siraj; Wang, Yafei; De Siena, Michael; Asadpour, Reza; Torma, Andrew J.; Terlier, Tanguy; Ho, Kevin; Li, Wenbin; Puthirath, Anulld B.; Shuai, Xinting; Agrawal, Ayush; Traore, Boubacar; Jones, Matthew; Giridharagopal, Rajiv; Ajayan, Pulickel M.; Strzalka, Joseph; Ginger, David S.; Katan, Claudine; Alam, Muhammad Ashraful; Even, Jacky; Kanatzidis, Mercouri G.; Mohite, Aditya D.",
|
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"Book Author Full Names": null,
|
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"Group Authors": null,
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"Article Title": "Deterministic fabrication of 3D/2D perovskite bilayer stacks for durable and efficient solar cells",
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"Source Title": "SCIENCE",
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"Book Series Title": null,
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"Author Keywords": null,
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"Keywords Plus": null,
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"Abstract": "Realizing solution-processed heterostructures is a long-enduring challenge in halide perovskites because of solvent incompatibilities that disrupt the underlying layer. By leveraging the solvent dielectric constant and Gutmann donor number, we could grow phase-pure two-dimensional (2D) halide perovskite stacks of the desired composition, thickness, and bandgap onto 3D perovskites without dissolving the underlying substrate. Characterization reveals a 3D-2D transition region of 20 nullometers mainly determined by the roughness of the bottom 3D layer. Thickness dependence of the 2D perovskite layer reveals the anticipated trends for n-i-p and p-i-n architectures, which is consistent with band alignment and carrier transport limits for 2D perovskites. We measured a photovoltaic efficiency of 24.5%, with exceptional stability of T-99 (time required to preserve 99% of initial photovoltaic efficiency) of >2000 hours, implying that the 3D/2D bilayer inherits the intrinsic durability of 2D perovskite without compromising efficiency.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
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"Email Addresses": null,
|
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"Researcher Ids": null,
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"ORCIDs": null,
|
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"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
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"Times Cited, WoS Core": 319,
|
|
"Times Cited, All Databases": 332,
|
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"180 Day Usage Count": null,
|
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"Since 2013 Usage Count": null,
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"Publisher": null,
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"Publisher City": null,
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"Publisher Address": null,
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"ISSN": null,
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"eISSN": null,
|
|
"ISBN": null,
|
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"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "SEP 23",
|
|
"Publication Year": 2022,
|
|
"Volume": 377,
|
|
"Issue": 6613,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 1425,
|
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"End Page": 1430,
|
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"Article Number": null,
|
|
"DOI": "10.1126/science.abq7652",
|
|
"DOI Link": "http://dx.doi.org/10.1126/science.abq7652",
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"Book DOI": null,
|
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"Early Access Date": null,
|
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"Number of Pages": null,
|
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"WoS Categories": null,
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"Web of Science Index": null,
|
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"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000887934300037",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Liu, W; Zhai, PB; Li, AW; Wei, B; Si, KP; Wei, Y; Wang, XG; Zhu, GD; Chen, Q; Gu, XK; Zhang, RF; Zhou, W; Gong, YJ",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Liu, Wei; Zhai, Pengbo; Li, Aowen; Wei, Bo; Si, Kunpeng; Wei, Yi; Wang, Xingguo; Zhu, Guangda; Chen, Qian; Gu, Xiaokang; Zhang, Ruifeng; Zhou, Wu; Gong, Yongji",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Electrochemical CO2 reduction to ethylene by ultrathin CuO nulloplate arrays",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
|
"Book Series Title": null,
|
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"Book Series Subtitle": null,
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"Language": null,
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"Document Type": "Article",
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"Conference Title": null,
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"Conference Date": null,
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"Conference Sponsor": null,
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"Conference Host": null,
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"Author Keywords": null,
|
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"Keywords Plus": null,
|
|
"Abstract": "Electrochemical reduction of CO2 to multi-carbon fuels and chemical feedstocks is an appealing approach to mitigate excessive CO2 emissions. However, the reported catalysts always show either a low Faradaic efficiency of the C2+ product or poor long-term stability. Herein, we report a facile and scalable anodic corrosion method to synthesize oxygen-rich ultrathin CuO nulloplate arrays, which form Cu/Cu2O heterogeneous interfaces through self-evolution during electrocatalysis. The catalyst exhibits a high C2H4 Faradaic efficiency of 84.5%, stable electrolysis for similar to 55 h in a flow cell using a neutral KCI electrolyte, and a full-cell ethylene energy efficiency of 27.6% at 200 mA cm(-2) in a membrane electrode assembly electrolyzer. Mechanism analyses reveal that the stable nullostructures, stable Cu/Cu2O interfaces, and enhanced adsorption of the *OCCOH intermediate preserve selective and prolonged C2H4 production. The robust and scalable produced catalyst coupled with mild electrolytic conditions facilitates the practical application of electrochemical CO2 reduction.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
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"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 333,
|
|
"Times Cited, All Databases": 349,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "APR 6",
|
|
"Publication Year": 2022,
|
|
"Volume": 13,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 1877,
|
|
"DOI": "10.1038/s41467-022-29428-9",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-022-29428-9",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000779311200034",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Zhang, F; Park, SY; Yao, CL; Lu, HP; Dunfield, SP; Xiao, CX; Ulicná, S; Zhao, XM; Du Hill, L; Chen, XH; Wang, XM; Mundt, LE; Stone, KH; Schelhas, LT; Teeter, G; Parkin, S; Ratcliff, EL; Loo, YL; Berry, JJ; Beard, MC; Yan, YF; Larson, BW; Zhu, K",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Zhang, Fei; Park, So Yeon; Yao, Canglang; Lu, Haipeng; Dunfield, Sean P.; Xiao, Chuanxiao; Ulicna, Sona; Zhao, Xiaoming; Du Hill, Linze; Chen, Xihan; Wang, Xiaoming; Mundt, Laura E.; Stone, Kevin H.; Schelhas, Laura T.; Teeter, Glenn; Parkin, Sean; Ratcliff, Erin L.; Loo, Yueh-Lin; Berry, Joseph J.; Beard, Matthew C.; Yan, Yanfa; Larson, Bryon W.; Zhu, Kai",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Metastable Dion-Jacobson 2D structure enables efficient and stable perovskite solar cells",
|
|
"Source Title": "SCIENCE",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
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"Document Type": "Article",
|
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"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "The performance of three-dimensional (3D) organic-inorganic halide perovskite solar cells (PSCs) can be enhanced through surface treatment with 2D layered perovskites that have efficient charge transport. We maximized hole transport across the layers of a metastable Dion-Jacobson (DJ) 2D perovskite that tuned the orientational arrangements of asymmetric bulky organic molecules. The reduced energy barrier for hole transport increased out-of-plane transport rates by a factor of 4 to 5, and the power conversion efficiency (PCE) for the 2D PSC was 4.9%. With the metastable DJ 2D surface layer, the PCE of three common 3D PSCs was enhanced by approximately 12 to 16% and could reach approximately 24.7%. For a triple-cation-mixed-halide PSC, 90% of the initial PCE was retained after 1000 hours of 1-sun operation at similar to 40 degrees C in nitrogen.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 319,
|
|
"Times Cited, All Databases": 330,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JAN 7",
|
|
"Publication Year": 2022,
|
|
"Volume": 375,
|
|
"Issue": 6576,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 71,
|
|
"End Page": "+",
|
|
"Article Number": "eabj2637",
|
|
"DOI": "10.1126/science.abj2637",
|
|
"DOI Link": "http://dx.doi.org/10.1126/science.abj2637",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000740261400042",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Hu, YX; Miao, JS; Hua, T; Huang, ZY; Qi, YY; Zou, Y; Qiu, YT; Xia, H; Liu, H; Cao, XS; Yang, CL",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Hu, Yu Xuan; Miao, Jingsheng; Hua, Tao; Huang, Zhongyan; Qi, Yanyu; Zou, Yang; Qiu, Yuntao; Xia, Han; Liu, He; Cao, Xiaosong; Yang, Chuluo",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Efficient selenium-integrated TADF OLEDs with reduced roll-off",
|
|
"Source Title": "NATURE PHOTONICS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Organic light emitters based on multiresonullce-induced thermally activated delayed fluorescent materials have great potential for realizing efficient, narrowband organic light-emitting diodes (OLEDs). However, at high brightness operation, efficiency roll-off attributed to the slow reverse intersystem crossing (RISC) process hinders the use of multiresonullce-induced thermally activated delayed fluorescent materials in practical applications. Here we report a heavy-atom incorporating emitter, BNSeSe, which is based on a selenium-integrated boron-nitrogen skeleton and exhibits 100% photoluminescence quantum yield and a high RISC rate (k(RISC)) of 2.0 x 10(6) s(-1). The corresponding green OLEDs exhibit excellent external quantum efficiencies of up to 36.8% and ultra-low roll-off character at high brightnesses (with very small roll-off values of 2.8% and 14.9% at 1,000 cd m(-2) and 10,000 cd m(-2), respectively). Furthermore, the outstanding capability to harvest triplet excitons also enables BNSeSe to be a superior sensitizer for a hyperfluorescence OLED, which shows state-of-the-art performance with a high excellent external quantum efficiency of 40.5%, power efficiency beyond 200 lm W-1, and luminullce close to 20,0000 cd m(-2). Green OLEDs based on BNSeSe offer high operational efficiency and reduced efficiency roll-off.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 319,
|
|
"Times Cited, All Databases": 329,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "NOV",
|
|
"Publication Year": 2022,
|
|
"Volume": 16,
|
|
"Issue": 11,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 803,
|
|
"End Page": "+",
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s41566-022-01083-y",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41566-022-01083-y",
|
|
"Book DOI": null,
|
|
"Early Access Date": "OCT 2022",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Optics; Physics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000867521100001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Liang, JW; Hu, XZ; Wang, C; Liang, C; Chen, C; Xiao, M; Li, JS; Tao, C; Xing, GC; Yu, R; Ke, WJ; Fang, GJ",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Liang, Jiwei; Hu, Xuzhi; Wang, Chen; Liang, Chao; Chen, Cong; Xiao, Meng; Li, Jiashuai; Tao, Chen; Xing, Guichuan; Yu, Rui; Ke, Weijun; Fang, Guojia",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Origins and influences of metallic lead in perovskite solar cells",
|
|
"Source Title": "JOULE",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Metallic lead (Pb-0) impurities in metal-halide perovskites have attracted tremendous research concerns owing to their detrimental effects on perovskite solar cells (PSCs). However, the origins and influences of the Pb-0 behind this issue have yet to bewell understood. Herein, we show that Pb-0 is hardly formed in the growth of halide perovskites but is easily postformed in the perovskite films with excess PbI2. It is found that Pb-0 impurities are decomposition byproducts of residual PbI2 in perovskites under light or X-ray irradiation. Therefore, PSCs obtained using photodegraded PbI2 films show large efficiency and stability losses. By contrast, the perovskite devices without detectable Pb-0 impurities have a much better efficiency and stability. This work reveals the origins and influences of Pb-0 in halide perovskites and provides a strategy for avoiding the formation of detrimental Pb-0 byproducts, which would drive further enhancements in device performance of halide perovskite solar cells, detectors, etc.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 325,
|
|
"Times Cited, All Databases": 330,
|
|
"180 Day Usage Count": null,
|
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"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "APR 20",
|
|
"Publication Year": 2022,
|
|
"Volume": 6,
|
|
"Issue": 4,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 816,
|
|
"End Page": 833,
|
|
"Article Number": null,
|
|
"DOI": "10.1016/j.joule.2022.03.005",
|
|
"DOI Link": "http://dx.doi.org/10.1016/j.joule.2022.03.005",
|
|
"Book DOI": null,
|
|
"Early Access Date": "APR 2022",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry; Energy & Fuels; Materials Science",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000798575600013",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Li, D; Yang, YJ; Yang, J; Fang, MM; Tang, BZ; Li, Z",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Li, Dan; Yang, Yujie; Yang, Jie; Fang, Manman; Tang, Ben Zhong; Li, Zhen",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Completely aqueous processable stimulus responsive organic room temperature phosphorescence materials with tunable afterglow color",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
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"Book Series Title": null,
|
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"Book Series Subtitle": null,
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"Language": null,
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"Document Type": "Article",
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"Conference Title": null,
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"Conference Date": null,
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"Conference Location": null,
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"Conference Sponsor": null,
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"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Stimuli responsive luminescent materials are important in applied research but many of these materials are based on fluorescent stimuli responsive materials. Here, the authors report a stimulus-responsive room temperature phosphorescent materials composed of a phosphorescent chromophore of arylboronic acid and poly(vinylalcohol) with color tunable and water process able properties. Many luminescent stimuli responsive materials are based on fluorescence emission, while stimuli-responsive room temperature phosphorescent materials are less explored. Here, we show a kind of stimulus-responsive room temperature phosphorescence materials by the covalent linkage of phosphorescent chromophore of arylboronic acid and polymer matrix of poly(vinylalcohol). Attributed to the rigid environment offered from hydrogen bond and B-O covalent bond between arylboronic acid and poly(vinylalcohol), the yielded polymer film exhibits ultralong room temperature phosphorescence with lifetime of 2.43 s and phosphorescence quantum yield of 7.51%. Interestingly, the RTP property of this film is sensitive to the water and heat stimuli, because water could destroy the hydrogen bonds between adjacent poly(vinylalcohol) polymers, then changing the rigidity of this system. Furthermore, by introducing another two fluorescent dyes to this system, the color of afterglow with stimulus response effect could be adjusted from blue to green to orange through triplet-to-singlet Forster-resonullce energy-transfer. Finally, due to the water/heat-sensitive, multicolor and completely aqueous processable feature for these three afterglow hybrids, they are successfully applied in multifunctional ink for anti-counterfeit, screen printing and fingerprint record.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 322,
|
|
"Times Cited, All Databases": 329,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JAN 17",
|
|
"Publication Year": 2022,
|
|
"Volume": 13,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 347,
|
|
"DOI": "10.1038/s41467-022-28011-6",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-022-28011-6",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000744540800018",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Mielke, C; Das, D; Yin, JX; Liu, H; Gupta, R; Jiang, YX; Medarde, M; Wu, X; Lei, HC; Chang, J; Dai, PC; Si, Q; Miao, H; Thomale, R; Neupert, T; Shi, Y; Khasanov, R; Hasan, MZ; Luetkens, H; Guguchia, Z",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Mielke, C.; Das, D.; Yin, J-X; Liu, H.; Gupta, R.; Jiang, Y-X; Medarde, M.; Wu, X.; Lei, H. C.; Chang, J.; Dai, Pengcheng; Si, Q.; Miao, H.; Thomale, R.; Neupert, T.; Shi, Y.; Khasanov, R.; Hasan, M. Z.; Luetkens, H.; Guguchia, Z.",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Time-reversal symmetry-breaking charge order in a kagome superconductor",
|
|
"Source Title": "NATURE",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
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"Language": null,
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"Conference Title": null,
|
|
"Conference Date": null,
|
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|
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"Conference Sponsor": null,
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|
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|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "The kagome lattice(1), which is the most prominent structural motif in quantum physics, benefits from inherent non-trivial geometry so that it can host diverse quantum phases, ranging from spin-liquid phases, to topological matter, to intertwined orders(2-8) and, most rarely, to unconventional superconductivity(6,9). Recently, charge sensitive probes have indicated that the kagome superconductors AV(3)Sb(5) (A = K, Rb, Cs)(9-11) exhibit unconventional chiral charge order(12-19), which is analogousto the long-sought-after quantum order in the Haldane model(20) or Varma model(21). However, direct evidence for the time-reversal symmetry breaking of the charge order remains elusive. Here we use muon spin relaxation to probe the kagome charge order and superconductivity in KV3Sb5. We observe a noticeable enhancement of the internal field width sensed by the muon ensemble, which takes place just below the charge orderingtemperature and persists into the superconducting state. Notably, the muon spin relaxation rate below the charge orderingtemperature is substantially enhanced by applying an external magnetic field. We further show the multigap nature of superconductivity in KV3Sb5 and that the T-c/lambda(-2)(ab) ratio (where T-c is the superconducting transition temperature and lambda(ab) is the magnetic penetration depth in the kagome plane) is comparable to those of unconventional high-temperature superconductors. Our results point to time-reversal symmetry-breaking charge order intertwining with unconventional superconductivity in the correlated kagome lattice.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 315,
|
|
"Times Cited, All Databases": 329,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "FEB 10",
|
|
"Publication Year": 2022,
|
|
"Volume": 602,
|
|
"Issue": 7896,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 245,
|
|
"End Page": "+",
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s41586-021-04327-z",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41586-021-04327-z",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000753550800017",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Zhang, WW; Chen, LJ; Dai, S; Zhao, CX; Ma, C; Wei, L; Zhu, MH; Chong, SY; Yang, HF; Liu, LJ; Bai, Y; Yu, MJ; Xu, YJ; Zhu, XW; Zhu, Q; An, SH; Sprick, RS; Little, MA; Wu, XF; Jiang, S; Wu, YZ; Zhang, YB; Tian, H; Zhu, WH; Cooper, A",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Zhang, Weiwei; Chen, Linjiang; Dai, Sheng; Zhao, Chengxi; Ma, Cheng; Wei, Lei; Zhu, Minghui; Chong, Samantha Y.; Yang, Haofan; Liu, Lunjie; Bai, Yang; Yu, Miaojie; Xu, Yongjie; Zhu, Xiao-Wei; Zhu, Qiang; An, Shuhao; Sprick, Reiner Sebastian; Little, Marc A.; Wu, Xiaofeng; Jiang, Shan; Wu, Yongzhen; Zhang, Yue-Biao; Tian, He; Zhu, Wei-Hong; Cooper, Andrew, I",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Reconstructed covalent organic frameworks",
|
|
"Source Title": "NATURE",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Covalent organic frameworks (COFs) are distinguished from other organic polymers by their crystallinity(1-3), but it remains challenging to obtain robust, highly crystalline COFs because the framework-forming reactions are poorly reversible(4,5). More reversible chemistry can improve crystallinity(6-9), but this typically yields COFs with poor physicochemical stability and limited application scope(5). Here we report a general and scalable protocol to prepare robust, highly crystalline imine COFs, based on an unexpected framework reconstruction. In contrast to standard approaches in which monomers are initially randomly aligned, our method involves the pre-organization of monomers using a reversible and removable covalent tether, followed by confined polymerization. This reconstruction route produces reconstructed COFs with greatly enhanced crystallinity and much higher porosity by means of a simple vacuum-free synthetic procedure. The increased crystallinity in the reconstructed COFs improves charge carrier transport, leading to sacrificial photocatalytic hydrogen evolution rates of up to 27.98 mmol h(-1) g(-1). This nulloconfinement-assisted reconstruction strategy is a step towards programming function in organic materials through atomistic structural control.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 318,
|
|
"Times Cited, All Databases": 327,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "APR 7",
|
|
"Publication Year": 2022,
|
|
"Volume": 604,
|
|
"Issue": 7904,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 72,
|
|
"End Page": "+",
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s41586-022-04443-4",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41586-022-04443-4",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000779100400018",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Chen, RT; Ren, ZF; Liang, Y; Zhang, GH; Dittrich, T; Liu, RZ; Liu, Y; Zhao, Y; Pang, S; An, HY; Ni, CW; Zhou, PW; Han, KL; Fan, FT; Li, C",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Chen, Ruotian; Ren, Zefeng; Liang, Yu; Zhang, Guanhua; Dittrich, Thomas; Liu, Runze; Liu, Yang; Zhao, Yue; Pang, Shan; An, Hongyu; Ni, Chenwei; Zhou, Panwang; Han, Keli; Fan, Fengtao; Li, Can",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Spatiotemporal imaging of charge transfer in photocatalyst particles",
|
|
"Source Title": "NATURE",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "The water-splitting reaction using photocatalyst particles is a promising route for solar fuel production(1-4). Photo-induced charge transfer from a photocatalyst to catalytic surface sites is key in ensuring photocatalytic efficiency(5); however, it is challenging to understand this process, which spans a wide spatiotemporal range from nullometres to micrometres and from femtoseconds to seconds(6-8). Although the steady-state charge distribution on single photocatalyst particles has been mapped by microscopic techniques(9-11), and the charge transfer dynamics in photocatalyst aggregations have been revealed by time-resolved spectroscopy(12,13), spatiotemporally evolving charge transfer processes in single photocatalyst particles cannot be tracked, and their exact mechanism is unknown. Here we perform spatiotemporally resolved surface photovoltage measurements on cuprous oxide photocatalyst particles to map holistic charge transfer processes on the femtosecond to second timescale at the single-particle level. We find that photogenerated electrons are transferred to the catalytic surface quasi-ballistically through inter-facet hot electron transfer on a subpicosecond timescale, whereas photogenerated holes are transferred to a spatially separated surface and stabilized through selective trapping on a microsecond timescale. We demonstrate that these ultrafast-hot-electron-transfer and anisotropic-trapping regimes, which challenge the classical perception of a drift-diffusion model, contribute to the efficient charge separation in photocatalysis and improve photocatalytic performance. We anticipate that our findings will be used to illustrate the universality of other photoelectronic devices and facilitate the rational design of photocatalysts.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 312,
|
|
"Times Cited, All Databases": 328,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "OCT 13",
|
|
"Publication Year": 2022,
|
|
"Volume": 610,
|
|
"Issue": 7931,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 296,
|
|
"End Page": "+",
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s41586-022-05183-1",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41586-022-05183-1",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000867324800024",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Chen, L; Deng, SQ; Liu, H; Wu, J; Qi, H; Chen, J",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Chen, Liang; Deng, Shiqing; Liu, Hui; Wu, Jie; Qi, He; Chen, Jun",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Giant energy-storage density with ultrahigh efficiency in lead-free relaxors via high-entropy design",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Next-generation advanced high/pulsed power capacitors rely heavily on dielectric ceramics with high energy storage performance. However, thus far, the huge challenge of realizing ultrahigh recoverable energy storage density (W-rec) accompanied by ultrahigh efficiency (eta) still existed and has become a key bottleneck restricting the development of dielectric materials in cutting-edge energy storage applications. Here, we propose a high-entropy strategy to design local polymorphic distortion including rhombohedral-orthorhombic-tetragonal-cubic multiphase nulloclusters and random oxygen octahedral tilt, resulting inultra small polar nulloregions, an enhanced breakdown electric field, and delayed polarization saturation. A giant W-rec similar to 10.06 J cm(-3) is realized in lead-free relaxor ferroelectrics, especially with an ultrahigh eta similar to 90.8%, showing breakthrough progress in the comprehensive energy storage performance for lead-free bulk ceramics. This work opens up an effective avenue to design dielectric materials with ultrahigh comprehensive energy storage performance to meet the demanding requirements of advanced energy storage applications.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
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"Email Addresses": null,
|
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"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 318,
|
|
"Times Cited, All Databases": 326,
|
|
"180 Day Usage Count": null,
|
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"Since 2013 Usage Count": null,
|
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"Publisher": null,
|
|
"Publisher City": null,
|
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"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JUN 2",
|
|
"Publication Year": 2022,
|
|
"Volume": 13,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 3089,
|
|
"DOI": "10.1038/s41467-022-30821-7",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-022-30821-7",
|
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"Book DOI": null,
|
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"Early Access Date": null,
|
|
"Number of Pages": null,
|
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"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000805202900032",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Pan, D; Yang, G; Abo-Dief, HM; Dong, JW; Su, FM; Liu, CT; Li, YF; Xu, BB; Murugadoss, V; Naik, N; El-Bahy, SM; El-Bahy, ZM; Huang, MA; Guo, ZH",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Pan, Duo; Yang, Gui; Abo-Dief, Hala M.; Dong, Jingwen; Su, Fengmei; Liu, Chuntai; Li, Yifan; Xu, Ben Bin; Murugadoss, Vignesh; Naik, Nithesh; El-Bahy, Salah M.; El-Bahy, Zeinhom M.; Huang, Minull; Guo, Zhanhu",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Vertically Aligned Silicon Carbide nullowires/ Boron Nitride Cellulose Aerogel Networks Enhanced Thermal Conductivity and Electromagnetic Absorbing of Epoxy Composites",
|
|
"Source Title": "nullO-MICRO LETTERS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
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"Language": null,
|
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"Document Type": "Article",
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"Conference Title": null,
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"Conference Date": null,
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"Conference Location": null,
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"Conference Sponsor": null,
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"Conference Host": null,
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"Author Keywords": null,
|
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"Keywords Plus": null,
|
|
"Abstract": "With the innovation of microelectronics technology, the heat dissipation problem inside the device will face a severe test. In this work, cellulose aerogel (CA) with highly enhanced thermal conductivity (TC) in vertical planes was successfully obtained by constructing a vertically aligned silicon carbide nullowires (SiC NWs)/boron nitride (BN) network via the ice template-assisted strategy. The unique network structure of SiC NWs connected to BN ensures that the TC of the composite in the vertical direction reaches 2.21 W m(-1) K-1 at a low hybrid filler loading of 16.69 wt%, which was increased by 890% compared to pure epoxy (EP). In addition, relying on unique porous network structure of CA, EP-based composite also showed higher TC than other comparative samples in the horizontal direction. Meanwhile, the composite exhibits good electrically insulating with a volume electrical resistivity about 2.35 x 1011 Omega cm and displays excellent electromagnetic wave absorption performance with a minimum reflection loss of - 21.5 dB and a wide effective absorption bandwidth (< - 10 dB) from 8.8 to 11.6 GHz. Therefore, this work provides a new strategy for manufacturing polymer-based composites with excellent multifunctional performances in microelectronic packaging applications.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 312,
|
|
"Times Cited, All Databases": 324,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "DEC",
|
|
"Publication Year": 2022,
|
|
"Volume": 14,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 118,
|
|
"DOI": "10.1007/s40820-022-00863-z",
|
|
"DOI Link": "http://dx.doi.org/10.1007/s40820-022-00863-z",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics; Materials Science; Physics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000789072200001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Rong, CL; Shen, XJ; Wang, Y; Thomsen, L; Zhao, TW; Li, YB; Lu, XY; Amal, R; Zhao, C",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Rong, Chengli; Shen, Xiangjian; Wang, Yuan; Thomsen, Lars; Zhao, Tingwen; Li, Yibing; Lu, Xunyu; Amal, Rose; Zhao, Chuan",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Electronic Structure Engineering of Single-Atom Ru Sites via Co-N4 Sites for Bifunctional pH-Universal Water Splitting",
|
|
"Source Title": "ADVANCED MATERIALS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
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"Document Type": "Article",
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|
"Conference Title": null,
|
|
"Conference Date": null,
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"Conference Location": null,
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"Conference Sponsor": null,
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"Conference Host": null,
|
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"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "The development of bifunctional water-splitting electrocatalysts that are efficient and stable over a wide range of pH is of great significance but challenging. Here, an atomically dispersed Ru/Co dual-sites catalyst is reported anchored on N-doped carbon (Ru/Co-N-C) for outstanding oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) in both acidic and alkaline electrolytes. The Ru/Co-N-C catalyst requires the overpotential of only 13 and 23 mV for HER, 232 and 247 mV for OER to deliver a current density of 10 mA cm(geo)(-2) in 0.5 m H2SO4 and 1 m KOH, respectively, outperforming benchmark catalysts Pt/C and RuO2. Theoretical calculations reveal that the introduction of Co-N4 sites into Ru/Co-N-C efficiently modify the electronic structure of Ru by enlarging Ru-O covalency and increasing Ru electron density, which in turn optimize the bonding strength between oxygen/hydrogen intermediate species with Ru sites, thereby enhancing OER and HER performance. Furthermore, the incorporation of Co-N4 sites induces electron redistribution around Ru-N4, thus enhancing corrosion-resistance of Ru/Co-N-C during acid and alkaline electrolysis. The Ru/Co-N-C has been applied in a proton exchange membrane water electrolyzer and steady operation is demonstrated at a high current density of 450 mA cm(geo)(-2) for 330 h.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 307,
|
|
"Times Cited, All Databases": 312,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "MAY",
|
|
"Publication Year": 2022,
|
|
"Volume": 34,
|
|
"Issue": 21,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 2110103,
|
|
"DOI": "10.1002/adma.202110103",
|
|
"DOI Link": "http://dx.doi.org/10.1002/adma.202110103",
|
|
"Book DOI": null,
|
|
"Early Access Date": "APR 2022",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry; Science & Technology - Other Topics; Materials Science; Physics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000786440900001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Wu, Y; Zhao, Y; Zhou, M; Tan, SJ; Peymanfar, R; Aslibeiki, B; Ji, GB",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Wu, Yue; Zhao, Yue; Zhou, Ming; Tan, Shujuan; Peymanfar, Reza; Aslibeiki, Bagher; Ji, Guangbin",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Ultrabroad Microwave Absorption Ability and Infrared Stealth Property of nullo-Micro CuS@rGO Lightweight Aerogels",
|
|
"Source Title": "nullO-MICRO LETTERS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Developing ultrabroad radar-infrared compatible stealth materials has turned into a research hotspot, which is still a problem to be solved. Herein, the copper sulfide wrapped by reduced graphene oxide to obtain three-dimensional (3D) porous network composite aerogels (CuS@rGO) were synthesized via thermal reduction ways (hydrothermal, ascorbic acid reduction) and freeze-drying strategy. It was discovered that the phase components (rGO and CuS phases) and micro/nullo structure (microporous and nullosheet) were well-modified by modulating the additive amounts of CuS and changing the reduction ways, which resulted in the variation of the pore structure, defects, complex permittivity, microwave absorption, radar cross section (RCS) reduction value and infrared (IR) emissivity. Notably, the obtained CuS@rGO aerogels with a single dielectric loss type can achieve an ultrabroad bandwidth of 8.44 GHz at 2.8 mm with the low filler content of 6 wt% by a hydrothermal method. Besides, the composite aerogel via the ascorbic acid reduction realizes the minimum reflection loss (RLmin) of - 60.3 dB with the lower filler content of 2 wt%. The RCS reduction value can reach 53.3 dB m(2), which effectively reduces the probability of the target being detected by the radar detector. Furthermore, the laminated porous architecture and multicomponent endowed composite aerogels with thermal insulation and IR stealth versatility. Thus, this work offers a facile method to design and develop porous rGO-based composite aerogel absorbers with radar-IR compatible stealth.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 310,
|
|
"Times Cited, All Databases": 324,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "DEC",
|
|
"Publication Year": 2022,
|
|
"Volume": 14,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 171,
|
|
"DOI": "10.1007/s40820-022-00906-5",
|
|
"DOI Link": "http://dx.doi.org/10.1007/s40820-022-00906-5",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics; Materials Science; Physics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000842159200002",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Zhao, W; Yan, PY; Li, BY; Bahri, M; Liu, LJ; Zhou, X; Clowes, R; Browning, ND; Wu, Y; Ward, JW; Cooper, A",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Zhao, Wei; Yan, Peiyao; Li, Boyu; Bahri, Mounib; Liu, Lunjie; Zhou, Xiang; Clowes, Rob; Browning, Nigel D.; Wu, Yue; Ward, John W.; Cooper, Andrew, I",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Accelerated Synthesis and Discovery of Covalent Organic Framework Photocatalysts for Hydrogen Peroxide Production",
|
|
"Source Title": "JOURNAL OF THE AMERICAN CHEMICAL SOCIETY",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "A high-throughput sonochemical synthesis and testing strategy was developed to discover covalent organic frameworks (COFs) for photocatalysis. In total, 76 conjugated polymers were synthesized, including 60 crystalline COFs of which 18 were previously unreported. These COFs were then screened for photocatalytic hydrogen peroxide (H2O2) production using water and oxygen. One of these COFs, sonoCOF-F2, was found to be an excellent photocatalyst for photocatalytic H2O2 production even in the absence of sacrificial donors. However, after long-term photocatalytic tests (96 h), the imine sonoCOF-F2 transformed into an amide-linked COF with reduced crystallinity and loss of electronic conjugation, decreasing the photocatalytic activity. When benzyl alcohol was introduced to form a two-phase catalytic system, the photostability of sonoCOF-F2 was greatly enhanced, leading to stable H2O2 production for at least 1 week.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 296,
|
|
"Times Cited, All Databases": 305,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JUN 8",
|
|
"Publication Year": 2022,
|
|
"Volume": 144,
|
|
"Issue": 22,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 9902,
|
|
"End Page": 9909,
|
|
"Article Number": null,
|
|
"DOI": "10.1021/jacs.2c02666",
|
|
"DOI Link": "http://dx.doi.org/10.1021/jacs.2c02666",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000810004300001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Qin, Y; Yu, TT; Deng, SH; Zhou, XY; Lin, DM; Zhang, Q; Jin, ZY; Zhang, DF; He, YB; Qiu, HJ; He, LH; Kang, FY; Li, KK; Zhang, TY",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Qin, Yin; Yu, Tingting; Deng, Sihao; Zhou, Xiao-Ye; Lin, Dongmei; Zhang, Qian; Jin, Zeyu; Zhang, Danfeng; He, Yan-Bing; Qiu, Hua-Jun; He, Lunhua; Kang, Feiyu; Li, Kaikai; Zhang, Tong-Yi",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "RuO2 electronic structure and lattice strain dual engineering for enhanced acidic oxygen evolution reaction performance",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
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"Abstract": "While water splitting in acid offers higher operational performances than in alkaline conditions, there are few high-activity, acid-stable oxygen evolution electrocatalysts. Here, authors examine electrochemical Li intercalation to improve the activity and stability of RuO2 for acidic water oxidation. Developing highly active and durable electrocatalysts for acidic oxygen evolution reaction remains a great challenge due to the sluggish kinetics of the four-electron transfer reaction and severe catalyst dissolution. Here we report an electrochemical lithium intercalation method to improve both the activity and stability of RuO2 for acidic oxygen evolution reaction. The lithium intercalates into the lattice interstices of RuO2, donates electrons and distorts the local structure. Therefore, the Ru valence state is lowered with formation of stable Li-O-Ru local structure, and the Ru-O covalency is weakened, which suppresses the dissolution of Ru, resulting in greatly enhanced durability. Meanwhile, the inherent lattice strain results in the surface structural distortion of LixRuO2 and activates the dangling O atom near the Ru active site as a proton acceptor, which stabilizes the OOH* and dramatically enhances the activity. This work provides an effective strategy to develop highly efficient catalyst towards water splitting.",
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"Addresses": null,
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"Affiliations": null,
|
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"Reprint Addresses": null,
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"Funding Name Preferred": null,
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"Funding Text": null,
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"Cited References": null,
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"Cited Reference Count": null,
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"Times Cited, WoS Core": 317,
|
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"Times Cited, All Databases": 323,
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"Publication Date": "JUL 1",
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"Publication Year": 2022,
|
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"Volume": 13,
|
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"Issue": 1,
|
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"Part Number": null,
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"Supplement": null,
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"Special Issue": null,
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"Start Page": null,
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"End Page": null,
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"Article Number": 3784,
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"DOI": "10.1038/s41467-022-31468-0",
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"DOI Link": "http://dx.doi.org/10.1038/s41467-022-31468-0",
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"Research Areas": "Science & Technology - Other Topics",
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"Open Access Designations": null,
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"Highly Cited Status": "Y",
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"Hot Paper Status": "N",
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"Date of Export": "2025-04-23",
|
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"UT (Unique WOS ID)": "WOS:000819790100020",
|
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"Web of Science Record": "View Full Record in Web of Science"
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},
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{
|
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"Publication Type": "J",
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"Authors": "Rao, ZY; Tung, PY; Xie, RW; Wei, Y; Zhang, HB; Ferrari, A; Klaver, TPC; Körmann, F; Sukumar, PT; da Silva, AK; Chen, Y; Li, ZM; Ponge, D; Neugebauer, J; Gutfleisch, O; Bauer, S; Raabe, D",
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"Book Authors": null,
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"Author Full Names": "Rao, Ziyuan; Tung, Po-Yen; Xie, Ruiwen; Wei, Ye; Zhang, Hongbin; Ferrari, Alberto; Klaver, T. P. C.; Koermann, Fritz; Sukumar, Prithiv Thoudden; da Silva, Alisson Kwiatkowski; Chen, Yao; Li, Zhiming; Ponge, Dirk; Neugebauer, Joerg; Gutfleisch, Oliver; Bauer, Stefan; Raabe, Dierk",
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"Book Author Full Names": null,
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"Article Title": "Machine learning-enabled high-entropy alloy discovery",
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"Source Title": "SCIENCE",
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"Abstract": "High-entropy alloys are solid solutions of multiple principal elements that are capable of reaching composition and property regimes inaccessible for dilute materials. Discovering those with valuable properties, however, too often relies on serendipity, because thermodynamic alloy design rules alone often fail in high-dimensional composition spaces. We propose an active learning strategy to accelerate the design of high-entropy Invar alloys in a practically infinite compositional space based on very sparse data. Our approach works as a closed-loop, integrating machine learning with density-functional theory, thermodynamic calculations, and experiments. After processing and characterizing 17 new alloys out of millions of possible compositions, we identified two high-entropy Invar alloys with extremely low thermal expansion coefficients around 2 x 10-6 per degree kelvin at 300 kelvin. We believe this to be a suitable pathway for the fast and automated discovery of high-entropy alloys with optimal thermal, magnetic, and electrical properties.",
|
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"Addresses": null,
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"Affiliations": null,
|
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"Reprint Addresses": null,
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"Email Addresses": null,
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"Researcher Ids": null,
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"ORCIDs": null,
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"Funding Orgs": null,
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"Funding Name Preferred": null,
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"Funding Text": null,
|
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"Cited References": null,
|
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"Cited Reference Count": null,
|
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"Times Cited, WoS Core": 308,
|
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"Times Cited, All Databases": 322,
|
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"180 Day Usage Count": null,
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"Since 2013 Usage Count": null,
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"Publisher": null,
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"ISBN": null,
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|
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|
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"Publication Date": "OCT 7",
|
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"Publication Year": 2022,
|
|
"Volume": 378,
|
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"Issue": 6615,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
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"Meeting Abstract": null,
|
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"Start Page": 78,
|
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"End Page": 84,
|
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"Article Number": null,
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"DOI": "10.1126/science.abo4940",
|
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"DOI Link": "http://dx.doi.org/10.1126/science.abo4940",
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"Book DOI": null,
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"Early Access Date": null,
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"Number of Pages": null,
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"WoS Categories": null,
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"Web of Science Index": null,
|
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"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
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"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
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"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000909870100058",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Mendes, CR; Dilarri, G; Forsan, CF; Sapata, VDR; Lopes, PRM; de Moraes, PB; Montagnolli, RN; Ferreira, H; Bidoia, ED",
|
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"Book Authors": null,
|
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"Book Editors": null,
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"Book Group Authors": null,
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"Author Full Names": "Mendes, Carolina Rosai; Dilarri, Guilherme; Forsan, Carolina Froes; Ruy Sapata, Vinicius de Moraes; Matos Lopes, Paulo Renato; de Moraes, Peterson Bueno; Montagnolli, Renato Nallin; Ferreira, Henrique; Bidoia, Ederio Dino",
|
|
"Book Author Full Names": null,
|
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"Group Authors": null,
|
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"Article Title": "Antibacterial action and target mechanisms of zinc oxide nulloparticles against bacterial pathogens",
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"Source Title": "SCIENTIFIC REPORTS",
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"Book Series Title": null,
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"Keywords Plus": null,
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"Abstract": "Zinc oxide nulloparticles (ZnO NPs) are one of the most widely used nulloparticulate materials due to their antimicrobial properties, but their main mechanism of action (MOA) has not been fully elucidated. This study characterized ZnO NPs by using X-ray diffraction, FT-IR spectroscopy and scanning electron microscopy. Antimicrobial activity of ZnO NPs against the clinically relevant bacteria Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa, and the Gram-positive model Bacillus subtilis was evaluated by performing resazurin microtiter assay (REMA) after exposure to the ZnO NPs at concentrations ranging from 0.2 to 1.4 mM. Sensitivity was observed at 0.6 mM for the Gram-negative and 1.0 mM for the Gram-positive cells. Fluorescence microscopy was used to examine the interference of ZnO NPs on the membrane and the cell division apparatus of B. subtilis (amy::pspac-ftsZ-gfpmut1) expressing FtsZ-GFP. The results showed that ZnO NPs did not interfere with the assembly of the divisional Z-ring. However, 70% of the cells exhibited damage in the cytoplasmic membrane after 15 min of exposure to the ZnO NPs. Electrostatic forces, production of Zn2+ ions and the generation of reactive oxygen species were described as possible pathways of the bactericidal action of ZnO. Therefore, understanding the bactericidal MOA of ZnO NPs can potentially help in the construction of predictive models to fight bacterial resistance.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
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"Email Addresses": null,
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"Researcher Ids": null,
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|
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|
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"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
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"Times Cited, WoS Core": 307,
|
|
"Times Cited, All Databases": 312,
|
|
"180 Day Usage Count": null,
|
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"Since 2013 Usage Count": null,
|
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"Publisher": null,
|
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|
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"Publisher Address": null,
|
|
"ISSN": null,
|
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|
|
"ISBN": null,
|
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"Journal Abbreviation": null,
|
|
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|
|
"Publication Date": "FEB 16",
|
|
"Publication Year": 2022,
|
|
"Volume": 12,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 2658,
|
|
"DOI": "10.1038/s41598-022-06657-y",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41598-022-06657-y",
|
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"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000757107700007",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Peng, LS; Yang, J; Yang, YQ; Qian, FR; Wang, Q; Sun-Waterhouse, D; Shang, L; Zhang, TR; Waterhouse, GIN",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
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|
|
"Author Full Names": "Peng, Lishan; Yang, Jiao; Yang, Yuqi; Qian, Fangren; Wang, Qing; Sun-Waterhouse, Dongxiao; Shang, Lu; Zhang, Tierui; Waterhouse, Geoffrey I. N.",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Mesopore-Rich Fe-N-C Catalyst with FeN4-O-NC Single-Atom Sites Delivers Remarkable Oxygen Reduction Reaction Performance in Alkaline Media",
|
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"Source Title": "ADVANCED MATERIALS",
|
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"Book Series Title": null,
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"Language": null,
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|
|
"Abstract": "Fe-N-C catalysts offer excellent performance for the oxygen reduction reaction (ORR) in alkaline media. With a view toward boosting the intrinsic ORR activity of Fe single-atom sites in Fe-N-C catalysts, fine-tuning the local coordination of the Fe sites to optimize the binding energies of ORR intermediates is imperative. Herein, a porous FeN4-O-NCR electrocatalyst rich in catalytically accessible FeN4-O sites (wherein the Fe single atoms are coordinated to four in-plane nitrogen atoms and one subsurface axial oxygen atom) supported on N-doped carbon nullorods (NCR) is reported. Fe K-edge X-ray absorption spectroscopy (XAS) verifies the presence of FeN4-O active sites in FeN4-O-NCR, while density functional theory calculations reveal that the FeN4-O coordination offers a lower energy and more selective 4-electron/4-proton ORR pathway compared to traditional FeN4 sites. Electrochemical tests validate the outstanding intrinsic activity of FeN4-O-NCR for alkaline ORR, outperforming Pt/C and almost all other M-N-C catalysts reported to date. A primary zinc-air battery constructed using FeN4-O-NCR delivers a peak power density of 214.2 mW cm(-2) at a current density of 334.1 mA cm(-2), highlighting the benefits of optimizing the local coordination of iron single atoms.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
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|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 311,
|
|
"Times Cited, All Databases": 318,
|
|
"180 Day Usage Count": null,
|
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"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JUL",
|
|
"Publication Year": 2022,
|
|
"Volume": 34,
|
|
"Issue": 29,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 2202544,
|
|
"DOI": "10.1002/adma.202202544",
|
|
"DOI Link": "http://dx.doi.org/10.1002/adma.202202544",
|
|
"Book DOI": null,
|
|
"Early Access Date": "JUN 2022",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry; Science & Technology - Other Topics; Materials Science; Physics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000809631500001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Chen, SY; Luo, T; Li, XQ; Chen, KJ; Fu, JW; Liu, K; Cai, C; Wang, QY; Li, HM; Chen, Y; Ma, C; Zhu, L; Lu, YR; Chan, TS; Zhu, MS; Cortes, E; Liu, M",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Chen, Shanyong; Luo, Tao; Li, Xiaoqing; Chen, Kejun; Fu, Junwei; Liu, Kang; Cai, Chao; Wang, Qiyou; Li, Hongmei; Chen, Yu; Ma, Chao; Zhu, Li; Lu, Ying-Rui; Chan, Ting-Shan; Zhu, Mingshan; Cortes, Emiliano; Liu, Min",
|
|
"Book Author Full Names": null,
|
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"Group Authors": null,
|
|
"Article Title": "Identification of the Highly Active Co-N4 Coordination Motif for Selective Oxygen Reduction to Hydrogen Peroxide",
|
|
"Source Title": "JOURNAL OF THE AMERICAN CHEMICAL SOCIETY",
|
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"Book Series Title": null,
|
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"Language": null,
|
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"Author Keywords": null,
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"Keywords Plus": null,
|
|
"Abstract": "Electrosynthesis of hydrogen peroxide (H2O2) through oxygen reduction reaction (ORR) is an environment-friendly and sustainable route for obtaining a fundamental product in the chemical industry. Co-N4 single-atom catalysts (SAC) have sparkled attention for being highly active in both 2e- ORR, leading to H2O2 and 4e- ORR, in which H2O is the main product. However, there is still a lack of fundamental insights into the structure-function relationship between CoN4 and the ORR mechanism over this family of catalysts. Here, by combining theoretical simulation and experiments, we unveil that pyrrole-type CoN4 (Co-N SACDp) is mainly responsible for the 2e- ORR, while pyridine-type CoN4 catalyzes the 4e- ORR. Indeed, Co-N SACDp exhibits a remarkable H2O2 selectivity of 94% and a superb H2O2 yield of 2032 mg for 90 h in a flow cell, outperforming most reported catalysts in acid media. Theoretical analysis and experimental investigations confirm that Co-N SACDp-with weakening O-2/HOO* interaction-boosts the H2O2 production.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
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"Email Addresses": null,
|
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"Researcher Ids": null,
|
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"ORCIDs": null,
|
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"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 297,
|
|
"Times Cited, All Databases": 307,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "AUG 17",
|
|
"Publication Year": 2022,
|
|
"Volume": 144,
|
|
"Issue": 32,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 14505,
|
|
"End Page": 14516,
|
|
"Article Number": null,
|
|
"DOI": "10.1021/jacs.2c01194",
|
|
"DOI Link": "http://dx.doi.org/10.1021/jacs.2c01194",
|
|
"Book DOI": null,
|
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"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000860150500001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Wang, PT; Yang, H; Tang, C; Wu, Y; Zheng, Y; Cheng, T; Davey, K; Huang, XQ; Qiao, SZ",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Wang, Pengtang; Yang, Hao; Tang, Cheng; Wu, Yu; Zheng, Yao; Cheng, Tao; Davey, Kenneth; Huang, Xiaoqing; Qiao, Shi-Zhang",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Boosting electrocatalytic CO2-to-ethanol production via asymmetric C-C coupling",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
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"Book Series Title": null,
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"Book Series Subtitle": null,
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"Language": null,
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"Document Type": "Article",
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"Author Keywords": null,
|
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"Keywords Plus": null,
|
|
"Abstract": "It is of high interest to convert CO2 into valuable ethanol product. Here the authors demonstrate the asymmetric C-C coupling triggered on Ag-modified oxide-derived Cu sites can accelerate and steer the reaction pathway for ethanol production with high faradaic efficiency and current density. Electroreduction of carbon dioxide (CO2) into multicarbon products provides possibility of large-scale chemicals production and is therefore of significant research and commercial interest. However, the production efficiency for ethanol (EtOH), a significant chemical feedstock, is impractically low because of limited selectivity, especially under high current operation. Here we report a new silver-modified copper-oxide catalyst (dCu(2)O/Ag-2.3%) that exhibits a significant Faradaic efficiency of 40.8% and energy efficiency of 22.3% for boosted EtOH production. Importantly, it achieves CO2-to-ethanol conversion under high current operation with partial current density of 326.4 mA cm(-2) at -0.87 V vs reversible hydrogen electrode to rank highly significantly amongst reported Cu-based catalysts. Based on in situ spectra studies we show that significantly boosted production results from tailored introduction of Ag to optimize the coordinated number and oxide state of surface Cu sites, in which the *CO adsorption is steered as both atop and bridge configuration to trigger asymmetric C-C coupling for stablization of EtOH intermediates.",
|
|
"Addresses": null,
|
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"Affiliations": null,
|
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"Reprint Addresses": null,
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"Email Addresses": null,
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"Researcher Ids": null,
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"ORCIDs": null,
|
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"Funding Orgs": null,
|
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"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 302,
|
|
"Times Cited, All Databases": 310,
|
|
"180 Day Usage Count": null,
|
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"Since 2013 Usage Count": null,
|
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"Publisher": null,
|
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"Publisher City": null,
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"Publisher Address": null,
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"ISSN": null,
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"eISSN": null,
|
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"ISBN": null,
|
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"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JUN 29",
|
|
"Publication Year": 2022,
|
|
"Volume": 13,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
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"Start Page": null,
|
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"End Page": null,
|
|
"Article Number": 3754,
|
|
"DOI": "10.1038/s41467-022-31427-9",
|
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"DOI Link": "http://dx.doi.org/10.1038/s41467-022-31427-9",
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"Book DOI": null,
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"Early Access Date": null,
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"Number of Pages": null,
|
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"WoS Categories": null,
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"Web of Science Index": null,
|
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"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000830675000015",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Li, CL; Hu, H; Yang, MF; Pei, ZY; Zhou, Q; Ren, X; Liu, B; Liu, DW; Zeng, XG; Zhang, GL; Zhang, HB; Liu, JJ; Wang, Q; Deng, XJ; Xiao, CJ; Yao, YG; Xue, DS; Zuo, W; Su, Y; Wen, WB; Ouyang, ZY",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Li, Chunlai; Hu, Hao; Yang, Meng-Fei; Pei, Zhao-Yu; Zhou, Qin; Ren, Xin; Liu, Bin; Liu, Dawei; Zeng, Xingguo; Zhang, Guangliang; Zhang, Hongbo; Liu, Jianjun; Wang, Qiong; Deng, Xiangjin; Xiao, Caijin; Yao, Yonggang; Xue, Dingshuai; Zuo, Wei; Su, Yan; Wen, Weibin; Ouyang, Ziyuan",
|
|
"Book Author Full Names": null,
|
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"Group Authors": null,
|
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"Article Title": "Characteristics of the lunar samples returned by the Chang'E-5 mission",
|
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"Source Title": "NATIONAL SCIENCE REVIEW",
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"Book Series Title": null,
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"Book Series Subtitle": null,
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"Language": null,
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"Document Type": "Article",
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"Conference Date": null,
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"Conference Sponsor": null,
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"Conference Host": null,
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"Author Keywords": null,
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"Keywords Plus": null,
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"Abstract": "The CE-5 sample is consistent with weathered mare basalts in mineralogy and petrochemistry, and is classified as low-Ti/low-Al/low-K type with lower REE (rare earth element) contents than KREEP (potassium, rare earth element, and phosphorus). This new sample characterized by high FeO and low Mg index could represent a new lunar basalt. Forty-five years after the Apollo and Luna missions returned lunar samples, China's Chang'E-5 (CE-5) mission collected new samples from the mid-latitude region in the northeastern Oceanus Procellarum of the Moon. Our study shows that 95% of CE-5 lunar soil sizes are found to be within the range of 1.40-9.35 mu m, while 95% of the soils by mass are within the size range of 4.84-432.27 mu m. The bulk density, true density and specific surface area of CE-5 soils are 1.2387 g/cm(3), 3.1952 g/cm(3) and 0.56 m(2)/g, respectively. Fragments from the CE-5 regolith are classified into igneous clasts (mostly basalt), agglutinate and glass. A few breccias were also found. The minerals and compositions of CE-5 soils are consistent with mare basalts and can be classified as low-Ti/low-Al/low-K type with lower rare-earth-element contents than materials rich in potassium, rare earth element and phosphorus. CE-5 soils have high FeO and low Mg index, which could represent a new class of basalt.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
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"Researcher Ids": null,
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"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 278,
|
|
"Times Cited, All Databases": 308,
|
|
"180 Day Usage Count": null,
|
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"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
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"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
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"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "FEB 3",
|
|
"Publication Year": 2022,
|
|
"Volume": 9,
|
|
"Issue": 2,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": "nwab188",
|
|
"DOI": "10.1093/nsr/nwab188",
|
|
"DOI Link": "http://dx.doi.org/10.1093/nsr/nwab188",
|
|
"Book DOI": null,
|
|
"Early Access Date": "FEB 2022",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000753113800002",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Wan, X; Liu, QT; Liu, JY; Liu, SY; Liu, XF; Zheng, LR; Shang, JX; Yu, RH; Shui, JL",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Wan, Xin; Liu, Qingtao; Liu, Jieyuan; Liu, Shiyuan; Liu, Xiaofang; Zheng, Lirong; Shang, Jiaxiang; Yu, Ronghai; Shui, Jianglan",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Iron atom-cluster interactions increase activity and improve durability in Fe-N-C fuel cells",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
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"Language": null,
|
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"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
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"Conference Sponsor": null,
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|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Simultaneously increasing the activity and stability of the single-atom active sites of M-N-C catalysts is critical but remains a great challenge. Here, we report an Fe-N-C catalyst with nitrogen-coordinated iron clusters and closely surrounding Fe-N-4 active sites for oxygen reduction reaction in acidic fuel cells. A strong electronic interaction is built between iron clusters and satellite Fe-N-4 due to unblocked electron transfer pathways and very short interacting distances. The iron clusters optimize the adsorption strength of oxygen reduction intermediates on Fe-N-4 and also shorten the bond amplitude of Fe-N-4 with incoherent vibrations. As a result, both the activity and stability of Fe-N-4 sites are increased by about 60% in terms of turnover frequency and demetalation resistance. This work shows the great potential of strong electronic interactions between multiphase metal species for improvements of single-atom catalysts. It is challenging to break the activity-stability trade-off in Fe-N-C fuel cell catalysts. Here, the authors show that interactions between iron atoms and clusters accelerate reaction kinetics and suppress demetalation to improve fuel cell stability.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 305,
|
|
"Times Cited, All Databases": 312,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "MAY 26",
|
|
"Publication Year": 2022,
|
|
"Volume": 13,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 2963,
|
|
"DOI": "10.1038/s41467-022-30702-z",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-022-30702-z",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000800650200024",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Hou, YL; Sheng, ZZ; Fu, C; Kong, J; Zhang, XT",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Hou, Yinglai; Sheng, Zhizhi; Fu, Chen; Kong, Jie; Zhang, Xuetong",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Hygroscopic holey graphene aerogel fibers enable highly efficient moisture capture, heat allocation and microwave absorption",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
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|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Aerogel fibers have been recognized as the rising star in the fields of thermal insulation and wearable textiles. Yet, the lack of functionalization in aerogel fibers limits their applications. Herein, we report hygroscopic holey graphene aerogel fibers (LiCl@HGAFs) with integrated functionalities of highly efficient moisture capture, heat allocation, and microwave absorption. LiCl@HGAFs realize the water sorption capacity over 4.15 g g(-1), due to the high surface area and high water uptake kinetics. Moreover, the sorbent can be regenerated through both photo-thermal and electro-thermal approaches. Along with the water sorption and desorption, LiCl@HGAFs experience an efficient heat transfer process, with a heat storage capacity of 6.93 kJ g(-1). The coefficient of performance in the heating and cooling mode can reach 1.72 and 0.70, respectively. Notably, with the entrapped water, LiCl@HGAFs exhibit broad microwave absorption with a bandwidth of 9.69 GHz, good impedance matching, and a high attenuation constant of 585. In light of these findings, the multifunctional LiCl@HGAFs open an avenue for applications in water harvest, heat allocation, and microwave absorption. This strategy also suggests the possibility to functionalize aerogel fibers towards even broader applications. Functionalization of aerogel fibers, characterized by high porosity and low thermal conductivity, to obtain multifunctional materials is highly desirable. Here the authors report hygroscopic holey graphene aerogel fibers hosting LiCl salt, enabling moisture capture, heat allocation, and microwave absorption performance.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 293,
|
|
"Times Cited, All Databases": 302,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "MAR 9",
|
|
"Publication Year": 2022,
|
|
"Volume": 13,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 1227,
|
|
"DOI": "10.1038/s41467-022-28906-4",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-022-28906-4",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000766759300018",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Xiao, FM; Gao, HQ; Lei, YX; Dai, WB; Liu, MC; Zheng, XY; Cai, ZX; Huang, XB; Wu, HY; Ding, D",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Xiao, Fuming; Gao, Heqi; Lei, Yunxiang; Dai, Wenbo; Liu, Miaochang; Zheng, Xiaoyan; Cai, Zhengxu; Huang, Xiaobo; Wu, Huayue; Ding, Dan",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Guest-host doped strategy for constructing ultralong-lifetime near-infrared organic phosphorescence materials for bioimaging",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Organic near-infrared room temperature phosphorescence materials have unparalleled advantages in bioimaging due to their excellent penetrability. However, limited by the energy gap law, the near-infrared phosphorescence materials (>650 nm) are very rare, moreover, the phosphorescence lifetimes of these materials are very short. In this work, we have obtained organic room temperature phosphorescence materials with long wavelengths (600/657-681/732 nm) and long lifetimes (102-324 ms) for the first time through the guest-host doped strategy. The guest molecule has sufficient conjugation to reduce the lowest triplet energy level and the host assists the guest in exciton transfer and inhibits the non-radiative transition of guest excitons. These materials exhibit good tissue penetration in bioimaging. Thanks to the characteristic of long lifetime and long wavelength emissive phosphorescence materials, the tumor imaging in living mice with a signal to background ratio value as high as 43 is successfully realized. This work provides a practical solution for the construction of organic phosphorescence materials with both long wavelengths and long lifetimes.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 288,
|
|
"Times Cited, All Databases": 296,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JAN 10",
|
|
"Publication Year": 2022,
|
|
"Volume": 13,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 186,
|
|
"DOI": "10.1038/s41467-021-27914-0",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-021-27914-0",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000849942600001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Qi, Y; Zhang, JW; Kong, Y; Zhao, Y; Chen, SS; Li, D; Liu, W; Chen, YF; Xie, TF; Cui, JY; Li, C; Domen, K; Zhang, FX",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Qi, Yu; Zhang, Jiangwei; Kong, Yuan; Zhao, Yue; Chen, Shanshan; Li, Deng; Liu, Wei; Chen, Yifan; Xie, Tengfeng; Cui, Junyan; Li, Can; Domen, Kazunari; Zhang, Fuxiang",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Unraveling of cocatalysts photodeposited selectively on facets of BiVO4 to boost solar water splitting",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Artificial photosynthesis offers an integrated means to convert light to fuel, but efficiencies are often low. Here, authors report a Z-scheme system utilizing Ir and FeCoOx co-catalysts to enhance charge separation on BiVO4 facets that achieves high quantum efficiencies for overall water splitting. Bismuth vanadate (BiVO4) has been widely investigated as a photocatalyst or photoanode for solar water splitting, but its activity is hindered by inefficient cocatalysts and limited understanding of the underlying mechanism. Here we demonstrate significantly enhanced water oxidation on the particulate BiVO4 photocatalyst via in situ facet-selective photodeposition of dual-cocatalysts that exist separately as metallic Ir nulloparticles and nullocomposite of FeOOH and CoOOH (denoted as FeCoOx), as revealed by advanced techniques. The mechanism of water oxidation promoted by the dual-cocatalysts is experimentally and theoretically unraveled, and mainly ascribed to the synergistic effect of the spatially separated dual-cocatalysts (Ir, FeCoOx) on both interface charge separation and surface catalysis. Combined with the H-2-evolving photocatalysts, we finally construct a Z-scheme overall water splitting system using [Fe(CN)(6)](3-/4-) as the redox mediator, whose apparent quantum efficiency at 420 nm and solar-to-hydrogen conversion efficiency are optimized to be 12.3% and 0.6%, respectively.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
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"Researcher Ids": null,
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|
"ORCIDs": null,
|
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"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 286,
|
|
"Times Cited, All Databases": 295,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
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"Publisher": null,
|
|
"Publisher City": null,
|
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"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JAN 25",
|
|
"Publication Year": 2022,
|
|
"Volume": 13,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 484,
|
|
"DOI": "10.1038/s41467-022-28146-6",
|
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"DOI Link": "http://dx.doi.org/10.1038/s41467-022-28146-6",
|
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"Book DOI": null,
|
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"Early Access Date": null,
|
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"Number of Pages": null,
|
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"WoS Categories": null,
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"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000747410400003",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Xiao, F; Wang, Q; Xu, GL; Qin, XP; Hwang, IH; Sun, CJ; Liu, M; Hua, W; Wu, HW; Zhu, SQ; Li, JC; Wang, JG; Zhu, YM; Wu, DJ; Wei, ZD; Gu, M; Amine, K; Shao, MH",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Xiao, Fei; Wang, Qi; Xu, Gui-Liang; Qin, Xueping; Hwang, Inhui; Sun, Cheng-Jun; Liu, Min; Hua, Wei; Wu, Hsi-wen; Zhu, Shangqian; Li, Jin-Cheng; Wang, Jian-Gan; Zhu, Yuanmin; Wu, Duojie; Wei, Zidong; Gu, Meng; Amine, Khalil; Shao, Minhua",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Atomically dispersed Pt and Fe sites and Pt-Fe nulloparticles for durable proton exchange membrane fuel cells",
|
|
"Source Title": "NATURE CATALYSIS",
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"Book Series Title": null,
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"Language": null,
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"Document Type": "Article",
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"Conference Location": null,
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"Conference Sponsor": null,
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"Conference Host": null,
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"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Proton exchange membrane fuel cells convert hydrogen and oxygen into electricity without emissions. The high cost and low durability of Pt-based electrocatalysts for the oxygen reduction reaction hinder their wide application, and the development of non-precious metal electrocatalysts is limited by their low performance. Here we design a hybrid electrocatalyst that consists of atomically dispersed Pt and Fe single atoms and Pt-Fe alloy nulloparticles. Its Pt mass activity is 3.7 times higher than that of commercial Pt/C in a fuel cell. More importantly, the fuel cell with a low Pt loading in the cathode (0.015 mg(P)(t) cm(-2)) shows an excellent durability, with a 97% activity retention after 100,000 cycles and no noticeable current drop at 0.6V for over 200 hours. These results highlight the importance of the synergistic effects among active sites in hybrid electrocatalysts and provide an alternative way to design more active and durable low-Pt electrocatalysts for electrochemical devices.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 279,
|
|
"Times Cited, All Databases": 284,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JUN",
|
|
"Publication Year": 2022,
|
|
"Volume": 5,
|
|
"Issue": 6,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 503,
|
|
"End Page": 512,
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s41929-022-00796-1",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41929-022-00796-1",
|
|
"Book DOI": null,
|
|
"Early Access Date": "JUN 2022",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000805042200002",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Song, LM; Zhang, F; Chen, YQ; Guan, L; Zhu, YQ; Chen, M; Wang, HL; Putra, BR; Zhang, R; Fan, BB",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Song, Limeng; Zhang, Fan; Chen, Yongqiang; Guan, Li; Zhu, Yanqiu; Chen, Mao; Wang, Hailong; Putra, Budi Riza; Zhang, Rui; Fan, Bingbing",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Multifunctional SiC@SiO2 nullofiber Aerogel with Ultrabroadband Electromagnetic Wave Absorption",
|
|
"Source Title": "nullO-MICRO LETTERS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
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"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
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"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Traditional ceramic materials are generally brittle and not flexible with high production costs, which seriously hinders their practical applications. Multifunctional nullofiber ceramic aerogels are highly desirable for applications in extreme environments, however, the integration of multiple functions in their preparation is extremely challenging. To tackle these challenges, we fabricated a multifunctional SiC@SiO2 nullofiber aerogel (SiC@SiO2 NFA) with a three-dimensional (3D) porous cross-linked structure through a simple chemical vapor deposition method and subsequent heat-treatment process. The as-prepared SiC@SiO2 NFA exhibits an ultralow density (similar to 11 mg cm(- 3)), ultra-elastic, fatigue-resistant and refractory performance, high temperature thermal stability, thermal insulation properties, and significant strain-dependent piezoresistive sensing behavior. Furthermore, the SiC@SiO2 NFA shows a superior electromagnetic wave absorption performance with a minimum refection loss (RLmin) value of - 50.36 dB and a maximum effective absorption bandwidth (EAB(max)) of 8.6 GHz. The successful preparation of this multifunctional aerogel material provides a promising prospect for the design and fabrication of the cutting-edge ceramic materials.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 282,
|
|
"Times Cited, All Databases": 286,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "DEC",
|
|
"Publication Year": 2022,
|
|
"Volume": 14,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 152,
|
|
"DOI": "10.1007/s40820-022-00905-6",
|
|
"DOI Link": "http://dx.doi.org/10.1007/s40820-022-00905-6",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics; Materials Science; Physics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000832688000001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Zhang, Y; Yang, JL; Hou, XY; Li, G; Wang, L; Bai, NN; Cai, MK; Zhao, LY; Wang, Y; Zhang, JM; Chen, K; Wu, X; Yang, CH; Dai, Y; Zhang, ZY; Guo, CF",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Zhang, Yuan; Yang, Junlong; Hou, Xingyu; Li, Gang; Wang, Liu; Bai, Ningning; Cai, Minkun; Zhao, Lingyu; Wang, Yan; Zhang, Jianming; Chen, Ke; Wu, Xiang; Yang, Canhui; Dai, Yuan; Zhang, Zhengyou; Guo, Chuan Fei",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Highly stable flexible pressure sensors with a quasi-homogeneous composition and interlinked interfaces",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "E-skins often have poor interfaces that lead to unstable performances. Here, authors report e-skins with a quasi-homogeneous composition and bonded micro-structured interfaces, through which both the sensitivity and stability of the devices are improved. Electronic skins (e-skins) are devices that can respond to mechanical stimuli and enable robots to perceive their surroundings. A great challenge for existing e-skins is that they may easily fail under extreme mechanical conditions due to their multilayered architecture with mechanical mismatch and weak adhesion between the interlayers. Here we report a flexible pressure sensor with tough interfaces enabled by two strategies: quasi-homogeneous composition that ensures mechanical match of interlayers, and interlinked microconed interface that results in a high interfacial toughness of 390 J center dot m(-2). The tough interface endows the sensor with exceptional signal stability determined by performing 100,000 cycles of rubbing, and fixing the sensor on a car tread and driving 2.6 km on an asphalt road. The topological interlinks can be further extended to soft robot-sensor integration, enabling a seamless interface between the sensor and robot for highly stable sensing performance during manipulation tasks under complicated mechanical conditions.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 274,
|
|
"Times Cited, All Databases": 282,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "MAR 10",
|
|
"Publication Year": 2022,
|
|
"Volume": 13,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 1317,
|
|
"DOI": "10.1038/s41467-022-29093-y",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-022-29093-y",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000767467900015",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Zhou, X; Ke, MK; Huang, GX; Chen, C; Chen, WX; Liang, K; Qu, YT; Yang, J; Wang, Y; Li, FT; Yu, HQ; Wu, YE",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Zhou, Xiao; Ke, Ming-Kun; Huang, Gui-Xiang; Chen, Cai; Chen, Wenxing; Liang, Kuang; Qu, Yunteng; Yang, Jia; Wang, Ying; Li, Fengting; Yu, Han-Qing; Wu, Yuen",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Identification of Fenton-like active Cu sites by heteroatom modulation of electronic density",
|
|
"Source Title": "PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Developing heterogeneous catalysts with atomically dispersed active sites is vital to boost peroxymonosulfate (PMS) activation for Fenton-like activity, but how to controllably adjust the electronic configuration of metal centers to further improve the activation kinetics still remains a great challenge. Herein, we report a systematic investigation into heteroatom-doped engineering for tuning the electronic structure of Cu-N-4 sites by integrating electron-deficient boron (B) or electron-rich phosphorus (P) heteroatoms into carbon substrate for PMS activation. The electron-depleted Cu-N-4/C-B is found to exhibit the most active oxidation capacity among the prepared Cu-N-4 single-atom catalysts, which is at the top rankings of the Cu-based catalysts and is superior to most of the state-of-the-art heterogeneous Fenton-like catalysts. Conversely, the electron-enriched Cu-N-4/C-P induces a decrease in PMS activation. Both experimental results and theoretical simulations unravel that the long-range interaction with B atoms decreases the electronic density of Cu active sites and down-shifts the d-band center, and thereby optimizes the adsorption energy for PMS activation. This study provides an approach to finely control the electronic structure of Cu-N-4 sites at the atomic level and is expected to guide the design of smart Fenton-like catalysts.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 282,
|
|
"Times Cited, All Databases": 284,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "FEB 22",
|
|
"Publication Year": 2022,
|
|
"Volume": 119,
|
|
"Issue": 8,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": "e2119492119",
|
|
"DOI": "10.1073/pnas.2119492119",
|
|
"DOI Link": "http://dx.doi.org/10.1073/pnas.2119492119",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000766924200016",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Zheng, SS; Sun, Y; Xue, HG; Braunstein, P; Huang, W; Pang, H",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Zheng, Shasha; Sun, Yan; Xue, Huaiguo; Braunstein, Pierre; Huang, Wei; Pang, Huan",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Dual-ligand and hard-soft-acid-base strategies to optimize metal-organic framework nullocrystals for stable electrochemical cycling performance",
|
|
"Source Title": "NATIONAL SCIENCE REVIEW",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Most metal-organic frameworks (MOFs) hardly maintain their physical and chemical properties after exposure to acidic, neutral, or alkaline aqueous solutions, resulting in insufficient stability, therefore limiting their applications. Thus, the design and synthesis of stable size/morphology-controlled MOF nullocrystals is critical but challenging. In this study, dual-ligand and hard-soft-acid-base strategies were used to fabricate a variety of 3D pillared-layer [Ni(thiophene-2,5-dicarboxylate)(4,4'-bipyridine)](n) MOF nullocrystals (1D nullofibers, 2D nullosheets and 3D aggregates) with controllable morphology by varying the concentration of 4,4'-bipyridine and thus controlling the crystal growth direction. Owing to the shorter ion diffusion length, enhanced electron/ion transfer and strong interactions between thiophene-2,5-dicarboxylate and 4,4'-bipyridine, the 2D nullosheets showed much larger specific capacitance than 1D nullofibers and 3D aggregates. A single device with an output voltage as high as 3.0 V and exceptional cycling performance (95% of retention after 5000 cycles at 3 mA cm(-2)) was realized by configuring two aqueous asymmetric supercapacitive devices in series. The excellent cycling property and charge-discharge mechanism are consistent with the hard-soft-acid-base theory.",
|
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"Addresses": null,
|
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"Affiliations": null,
|
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"Reprint Addresses": null,
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"Researcher Ids": null,
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"Funding Name Preferred": null,
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"Funding Text": null,
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"Cited References": null,
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"Cited Reference Count": null,
|
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"Times Cited, WoS Core": 284,
|
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"Times Cited, All Databases": 295,
|
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"180 Day Usage Count": null,
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"Since 2013 Usage Count": null,
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"Publisher": null,
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"Publisher City": null,
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"ISSN": null,
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|
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"ISBN": null,
|
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"Journal Abbreviation": null,
|
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"Journal ISO Abbreviation": null,
|
|
"Publication Date": "AUG 9",
|
|
"Publication Year": 2022,
|
|
"Volume": 9,
|
|
"Issue": 7,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
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"Meeting Abstract": null,
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"Start Page": null,
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"End Page": null,
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"Article Number": "nwab197",
|
|
"DOI": "10.1093/nsr/nwab197",
|
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"DOI Link": "http://dx.doi.org/10.1093/nsr/nwab197",
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"Book DOI": null,
|
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"Early Access Date": "AUG 2022",
|
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"Number of Pages": null,
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"WoS Categories": null,
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"Web of Science Index": null,
|
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"Research Areas": "Science & Technology - Other Topics",
|
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"IDS Number": null,
|
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"Pubmed Id": null,
|
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"Open Access Designations": null,
|
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"Highly Cited Status": "Y",
|
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"Hot Paper Status": "N",
|
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"Date of Export": "2025-04-23",
|
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"UT (Unique WOS ID)": "WOS:000837772000003",
|
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"Web of Science Record": "View Full Record in Web of Science"
|
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},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Fu, JH; Fong, PWK; Liu, H; Huang, CS; Lu, XH; Lu, SR; Abdelsamie, M; Kodalle, T; Sutter-Fella, CM; Yang, Y; Li, G",
|
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"Book Authors": null,
|
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"Book Editors": null,
|
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"Book Group Authors": null,
|
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"Author Full Names": "Fu, Jiehao; Fong, Patrick W. K.; Liu, Heng; Huang, Chieh-Szu; Lu, Xinhui; Lu, Shirong; Abdelsamie, Maged; Kodalle, Tim; Sutter-Fella, Carolin M.; Yang, Yang; Li, Gang",
|
|
"Book Author Full Names": null,
|
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"Group Authors": null,
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"Article Title": "19.31% binary organic solar cell and low non-radiative recombination enabled by non-monotonic intermediate state transition",
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"Source Title": "NATURE COMMUNICATIONS",
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"Book Series Title": null,
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"Author Keywords": null,
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"Keywords Plus": null,
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"Abstract": "Non-radiative recombination loss suppression is critical for boosting performance of organic solar cells. Here, the authors regulate self-organization of bulk-heterojunction in a non-monotonic manner, and achieve device efficiency over 19% with low non-radiative recombination loss down to 0.168 eV. Non-fullerene acceptors based organic solar cells represent the frontier of the field, owing to both the materials and morphology manipulation innovations. Non-radiative recombination loss suppression and performance boosting are in the center of organic solar cell research. Here, we developed a non-monotonic intermediate state manipulation strategy for state-of-the-art organic solar cells by employing 1,3,5-trichlorobenzene as crystallization regulator, which optimizes the film crystallization process, regulates the self-organization of bulk-heterojunction in a non-monotonic manner, i.e., first enhancing and then relaxing the molecular aggregation. As a result, the excessive aggregation of non-fullerene acceptors is avoided and we have achieved efficient organic solar cells with reduced non-radiative recombination loss. In PM6:BTP-eC9 organic solar cell, our strategy successfully offers a record binary organic solar cell efficiency of 19.31% (18.93% certified) with very low non-radiative recombination loss of 0.190 eV. And lower non-radiative recombination loss of 0.168 eV is further achieved in PM1:BTP-eC9 organic solar cell (19.10% efficiency), giving great promise to future organic solar cell research.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
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"Researcher Ids": null,
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|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
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"Times Cited, WoS Core": 399,
|
|
"Times Cited, All Databases": 407,
|
|
"180 Day Usage Count": null,
|
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"Since 2013 Usage Count": null,
|
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"Publisher": null,
|
|
"Publisher City": null,
|
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"Publisher Address": null,
|
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"ISSN": null,
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|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "MAR 30",
|
|
"Publication Year": 2023,
|
|
"Volume": 14,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
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"End Page": null,
|
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"Article Number": null,
|
|
"DOI": "10.1038/s41467-023-37526-5",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-023-37526-5",
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"Book DOI": null,
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"Early Access Date": null,
|
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"Number of Pages": null,
|
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"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000961133600031",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Lin, H; Yang, M; Ru, XN; Wang, GS; Yin, S; Peng, FG; Hong, CJ; Qu, MH; Lu, JX; Fang, L; Han, C; Procel, P; Isabella, O; Gao, PQ; Li, ZG; Xu, XX",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Lin, Hao; Yang, Miao; Ru, Xiaoning; Wang, Genshun; Yin, Shi; Peng, Fuguo; Hong, Chengjian; Qu, Minghao; Lu, Junxiong; Fang, Liang; Han, Can; Procel, Paul; Isabella, Olindo; Gao, Pingqi; Li, Zhenguo; Xu, Xixiang",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Silicon heterojunction solar cells with up to 26.81% efficiency achieved by electrically optimized nullocrystalline-silicon hole contact layers",
|
|
"Source Title": "NATURE ENERGY",
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"Book Series Title": null,
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"Language": null,
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"Conference Sponsor": null,
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"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Improvements in the power conversion efficiency of silicon heterojunction solar cells would consolidate their potential for commercialization. Now, Lin et al. demonstrate 26.81% efficiency devices using a p-doped nullocrystalline silicon and low-sheet-resistance transparent conductive oxide contact layer. Silicon heterojunction (SHJ) solar cells have reached high power conversion efficiency owing to their effective passivating contact structures. Improvements in the optoelectronic properties of these contacts can enable higher device efficiency, thus further consolidating the commercial potential of SHJ technology. Here we increase the efficiency of back junction SHJ solar cells with improved back contacts consisting of p-type doped nullocrystalline silicon and a transparent conductive oxide with a low sheet resistance. The electrical properties of the hole-selective contact are analysed and compared with a p-type doped amorphous silicon contact. We demonstrate improvement in the charge carrier transport and a low contact resistivity (<5 m ohm cm(2)). Eventually, we report a series of certified power conversion efficiencies of up to 26.81% and fill factors up to 86.59% on industry-grade silicon wafers (274 cm(2), M6 size).",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 347,
|
|
"Times Cited, All Databases": 357,
|
|
"180 Day Usage Count": null,
|
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"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "AUG",
|
|
"Publication Year": 2023,
|
|
"Volume": 8,
|
|
"Issue": 8,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 789,
|
|
"End Page": "+",
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s41560-023-01255-2",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41560-023-01255-2",
|
|
"Book DOI": null,
|
|
"Early Access Date": "MAY 2023",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Energy & Fuels; Materials Science",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000984178200002",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Liang, Z; Zhang, Y; Xu, HF; Chen, WJ; Liu, BY; Zhang, JY; Zhang, H; Wang, ZH; Kang, DH; Zeng, JR; Gao, XY; Wang, QS; Hu, HJ; Zhou, HM; Cai, XB; Tian, XY; Reiss, P; Xu, BM; Kirchartz, T; Xiao, ZG; Dai, SY; Park, NG; Ye, JJ; Pan, X",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Liang, Zheng; Zhang, Yong; Xu, Huifen; Chen, Wenjing; Liu, Boyuan; Zhang, Jiyao; Zhang, Hui; Wang, Zihan; Kang, Dong-Ho; Zeng, Jianrong; Gao, Xingyu; Wang, Qisheng; Hu, Huijie; Zhou, Hongmin; Cai, Xiangbin; Tian, Xingyou; Reiss, Peter; Xu, Baomin; Kirchartz, Thomas; Xiao, Zhengguo; Dai, Songyuan; Park, Nam-Gyu; Ye, Jiajiu; Pan, Xu",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Homogenizing out-of-plane cation composition in perovskite solar cells",
|
|
"Source Title": "NATURE",
|
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|
|
"Keywords Plus": null,
|
|
"Abstract": "Perovskite solar cells with the formula FA(1-x)CsxPbI(3), where FA is formamidinium, provide an attractive option for integrating high efficiency, durable stability and compatibility with scaled-up fabrication. Despite the incorporation of Cs cations, which could potentially enable a perfect perovskite lattice(1,2), the compositional inhomogeneity caused by A-site cation segregation is likely to be detrimental to the photovoltaic performance of the solar cells(3,4). Here we visualized the out-of-plane compositional inhomogeneity along the vertical direction across perovskite films and identified the underlying reasons for the inhomogeneity and its potential impact for devices. We devised a strategy using 1-(phenylsulfonyl)pyrrole to homogenize the distribution of cation composition in perovskite films. The resultant p-i-n devices yielded a certified steady-state photon-to-electron conversion efficiency of 25.2% and durable stability.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 415,
|
|
"Times Cited, All Databases": 427,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "DEC 21",
|
|
"Publication Year": 2023,
|
|
"Volume": 624,
|
|
"Issue": 7992,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 557,
|
|
"End Page": "+",
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s41586-023-06784-0",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41586-023-06784-0",
|
|
"Book DOI": null,
|
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"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001169177500001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Chong, LA; Gao, GP; Wen, JG; Li, HX; Xu, HP; Green, Z; Sugar, JD; Kropf, AJ; Xu, WQ; Lin, XM; Xu, H; Wang, LW; Liu, DJ",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Chong, Lina; Gao, Guoping; Wen, Jianguo; Li, Haixia; Xu, Haiping; Green, Zach; Sugar, Joshua D.; Kropf, A. Jeremy; Xu, Wenqian; Lin, Xiao-Min; Xu, Hui; Wang, Lin-Wang; Liu, Di-Jia",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "La- and Mn-doped cobalt spinel oxygen evolution catalyst for proton exchange membrane electrolysis",
|
|
"Source Title": "SCIENCE",
|
|
"Book Series Title": null,
|
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"Book Series Subtitle": null,
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"Language": null,
|
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|
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|
|
"Keywords Plus": null,
|
|
"Abstract": "Discovery of earth-abundant electrocatalysts to replace iridium for the oxygen evolution reaction (OER) in a proton exchange membrane water electrolyzer (PEMWE) represents a critical step in reducing the cost for green hydrogen production. We report a nullofibrous cobalt spinel catalyst codoped with lanthanum (La) and manganese (Mn) prepared from a zeolitic imidazolate framework embedded in electrospun polymer fiber. The catalyst demonstrated a low overpotential of 353 millivolts at 10 milliamperes per square centimeter and a low degradation for OER over 360 hours in acidic electrolyte. A PEMWE containing this catalyst at the anode demonstrated a current density of 2000 milliamperes per square centimeter at 2.47 volts (Nafion 115 membrane) or 4000 milliamperes per square centimeter at 3.00 volts (Nafion 212 membrane) and low degradation in an accelerated stress test.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 332,
|
|
"Times Cited, All Databases": 338,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "MAY 11",
|
|
"Publication Year": 2023,
|
|
"Volume": 380,
|
|
"Issue": 6645,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 609,
|
|
"End Page": 616,
|
|
"Article Number": null,
|
|
"DOI": "10.1126/science.ade1499",
|
|
"DOI Link": "http://dx.doi.org/10.1126/science.ade1499",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000999020900004",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Zhang, ZW; Li, YZ; Xu, R; Zhou, WJ; Li, YB; Oyakhire, ST; Wu, YC; Xu, JW; Wang, HS; Yu, ZA; Boyle, DT; Huang, W; Ye, YS; Chen, H; Wan, JY; Bao, ZN; Chiu, W; Cui, Y",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Zhang, Zewen; Li, Yuzhang; Xu, Rong; Zhou, Weijiang; Li, Yanbin; Oyakhire, Solomon T.; Wu, Yecun; Xu, Jinwei; Wang, Hansen; Yu, Zhiao; Boyle, David T.; Huang, William; Ye, Yusheng; Chen, Hao; Wan, Jiayu; Bao, Zhenull; Chiu, Wah; Cui, Yi",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Capturing the swelling of solid-electrolyte interphase in lithium metal batteries",
|
|
"Source Title": "SCIENCE",
|
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"Book Series Title": null,
|
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"Book Series Subtitle": null,
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"Language": null,
|
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"Document Type": "Article",
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|
|
"Conference Date": null,
|
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"Conference Location": null,
|
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"Conference Sponsor": null,
|
|
"Conference Host": null,
|
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"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Although liquid-solid interfaces are foundational in broad areas of science, characterizing this delicate interface remains inherently difficult because of shortcomings in existing tools to access liquid and solid phases simultaneously at the nulloscale. This leads to substantial gaps in our understanding of the structure and chemistry of key interfaces in battery systems. We adopt and modify a thin film vitrification method to preserve the sensitive yet critical interfaces in batteries at native liquid electrolyte environments to enable cryo-electron microscopy and spectroscopy. We report substantial swelling of the solid-electrolyte interphase (SEI) on lithium metal anode in various electrolytes. The swelling behavior is dependent on electrolyte chemistry and is highly correlated to battery performance. Higher degrees of SEI swelling tend to exhibit poor electrochemical cycling.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
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"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 267,
|
|
"Times Cited, All Databases": 289,
|
|
"180 Day Usage Count": null,
|
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"Since 2013 Usage Count": null,
|
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"Publisher": null,
|
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"Publisher City": null,
|
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"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JAN 7",
|
|
"Publication Year": 2022,
|
|
"Volume": 375,
|
|
"Issue": 6576,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 66,
|
|
"End Page": "+",
|
|
"Article Number": "eabi8703",
|
|
"DOI": "10.1126/science.abi8703",
|
|
"DOI Link": "http://dx.doi.org/10.1126/science.abi8703",
|
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"Book DOI": null,
|
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"Early Access Date": null,
|
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"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000740261400041",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Wang, D; Zhou, CK; Filatov, AS; Cho, WJ; Lagunas, F; Wang, MZ; Vaikuntanathan, S; Liu, C; Klie, RF; Talapin, DV",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Wang, Di; Zhou, Chenkun; Filatov, Alexander S.; Cho, Wooje; Lagunas, Francisco; Wang, Mingzhan; Vaikuntanathan, Suriyanarayanull; Liu, Chong; Klie, Robert F.; Talapin, Dmitri V.",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Direct synthesis and chemical vapor deposition of 2D carbide and nitride MXenes",
|
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"Source Title": "SCIENCE",
|
|
"Book Series Title": null,
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"Book Series Subtitle": null,
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"Language": null,
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"Conference Sponsor": null,
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"Conference Host": null,
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"Author Keywords": null,
|
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"Keywords Plus": null,
|
|
"Abstract": "Two-dimensional transition-metal carbides and nitrides (MXenes) are a large family of materials actively studied for various applications, especially in the field of energy storage. MXenes are commonly synthesized by etching the layered ternary compounds, called MAX phases. We demonstrate a direct synthetic route for scalable and atom-economic synthesis of MXenes, including compounds that have not been synthesized from MAX phases, by the reactions of metals and metal halides with graphite, methane, or nitrogen. The direct synthesis enables chemical vapor deposition growth of MXene carpets and complex spherulite-like morphologies that form through buckling and release of MXene carpet to expose fresh surface for further reaction. The directly synthesized MXenes showed excellent energy storage capacity for lithium-ion intercalation.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
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"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 343,
|
|
"Times Cited, All Databases": 360,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "MAR 24",
|
|
"Publication Year": 2023,
|
|
"Volume": 379,
|
|
"Issue": 6638,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 1242,
|
|
"End Page": 1247,
|
|
"Article Number": null,
|
|
"DOI": "10.1126/science.add9204",
|
|
"DOI Link": "http://dx.doi.org/10.1126/science.add9204",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000994409800005",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Li, CW; Wang, XM; Bi, EB; Jiang, FY; Park, SM; Li, Y; Chen, L; Wang, ZW; Zeng, LW; Chen, H; Liu, YJ; Grice, CR; Abudulimu, A; Chung, JH; Xian, YM; Zhu, T; Lai, HG; Chen, B; Ellingson, RJ; Fu, F; Ginger, DS; Song, ZN; Sargent, EH; Yan, YF",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Li, Chongwen; Wang, Xiaoming; Bi, Enbing; Jiang, Fangyuan; Park, So Min; Li, You; Chen, Lei; Wang, Zaiwei; Zeng, Lewei; Chen, Hao; Liu, Yanjiang; Grice, Corey R.; Abudulimu, Abasi; Chung, Jaehoon; Xian, Yeming; Zhu, Tao; Lai, Huagui; Chen, Bin; Ellingson, Randy J.; Fu, Fan; Ginger, David S.; Song, Zhaoning; Sargent, Edward H.; Yan, Yanfa",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Rational design of Lewis base molecules for stable and efficient inverted perovskite solar cells",
|
|
"Source Title": "SCIENCE",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
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"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
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"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Lewis base molecules that bind undercoordinated lead atoms at interfaces and grain boundaries (GBs) are known to enhance the durability of metal halide perovskite solar cells (PSCs). Using density functional theory calculations, we found that phosphine-containing molecules have the strongest binding energy among members of a library of Lewis base molecules studied herein. Experimentally, we found that the best inverted PSC treated with 1,3-bis(diphenylphosphino)propane (DPPP), a diphosphine Lewis base that passivates, binds, and bridges interfaces and GBs, retained a power conversion efficiency (PCE) slightly higher than its initial PCE of similar to 23% after continuous operation under simulated AM1.5 illumination at the maximum power point and at similar to 40 degrees C for >3500 hours. DPPP-treated devices showed a similar increase in PCE after being kept under open-circuit conditions at 85 degrees C for >1500 hours.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 347,
|
|
"Times Cited, All Databases": 357,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "FEB 17",
|
|
"Publication Year": 2023,
|
|
"Volume": 379,
|
|
"Issue": 6633,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 690,
|
|
"End Page": 694,
|
|
"Article Number": null,
|
|
"DOI": "10.1126/science.ade3970",
|
|
"DOI Link": "http://dx.doi.org/10.1126/science.ade3970",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001016371000012",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Yang, Y; Louisia, S; Yu, S; Jin, JB; Roh, I; Chen, CB; Guzman, MVF; Feijóo, J; Chen, PC; Wang, HS; Pollock, CJ; Huang, X; Shao, YT; Wang, C; Muller, DA; Abruña, HD; Yang, PD",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Yang, Yao; Louisia, Sheena; Yu, Sunmoon; Jin, Jianbo; Roh, Inwhan; Chen, Chubai; Fonseca Guzman, Maria V.; Feijoo, Julian; Chen, Peng-Cheng; Wang, Hongsen; Pollock, Christopher J.; Huang, Xin; Shao, Yu-Tsun; Wang, Cheng; Muller, David A.; Abruna, Hector D.; Yang, Peidong",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Operando studies reveal active Cu nullograins for CO2 electroreduction",
|
|
"Source Title": "NATURE",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Carbon dioxide electroreduction facilitates the sustainable synthesis of fuels and chemicals(1). Although Cu enables CO2-to-multicarbon product (C2+) conversion, the nature of the active sites under operating conditions remains elusive(2). Importantly, identifying active sites of high-performance Cu nullocatalysts necessitates nulloscale, time-resolved operando techniques(3-5). Here, we present a comprehensive investigation of the structural dynamics during the life cycle of Cu nullocatalysts. A 7 nm Cu nulloparticle ensemble evolves into metallic Cu nullograins during electrolysis before complete oxidation to single-crystal Cu2O nullocubes following post-electrolysis air exposure. Operando analytical and four-dimensional electrochemical liquid-cell scanning transmission electron microscopy shows the presence of metallic Cu nullograins under CO2 reduction conditions. Correlated high-energy-resolution time-resolved X-ray spectroscopy suggests that metallic Cu, rich in nullograin boundaries, supports undercoordinated active sites for C-C coupling. Quantitative structure-activity correlation shows that a higher fraction of metallic Cu nullograins leads to higher C2+ selectivity. A 7 nm Cu nulloparticle ensemble, with a unity fraction of active Cu nullograins, exhibits sixfold higher C2+ selectivity than the 18 nm counterpart with one-third of active Cu nullograins. The correlation of multimodal operando techniques serves as a powerful platform to advance our fundamental understanding of the complex structural evolution of nullocatalysts under electrochemical conditions.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 400,
|
|
"Times Cited, All Databases": 410,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "FEB 9",
|
|
"Publication Year": 2023,
|
|
"Volume": 614,
|
|
"Issue": 7947,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 262,
|
|
"End Page": "+",
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s41586-022-05540-0",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41586-022-05540-0",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000938818200001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Merchant, A; Batzner, S; Schoenholz, SS; Aykol, M; Cheon, G; Cubuk, ED",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Merchant, Amil; Batzner, Simon; Schoenholz, Samuel S.; Aykol, Muratahan; Cheon, Gowoon; Cubuk, Ekin Dogus",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Scaling deep learning for materials discovery",
|
|
"Source Title": "NATURE",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Novel functional materials enable fundamental breakthroughs across technological applications from clean energy to information processing1-11. From microchips to batteries and photovoltaics, discovery of inorganic crystals has been bottlenecked by expensive trial-and-error approaches. Concurrently, deep- learning models for language, vision and biology have showcased emergent predictive capabilities with increasing data and computation12-14. Here we show that graph networks trained at scale can reach unprecedented levels of generalization, improving the efficiency of materials discovery by an order of magnitude. Building on 48,000 stable crystals identified in continuing studies15-17, improved efficiency enables the discovery of 2.2 million structures below the current convex hull, many of which escaped previous human chemical intuition. Our work represents an order-of-magnitude expansion in stable materials known to humanity. Stable discoveries that are on the final convex hull will be made available to screen for technological applications, as we demonstrate for layered materials and solid-electrolyte candidates. Of the stable structures, 736 have already been independently experimentally realized. The scale and diversity of hundreds of millions of first-principles calculations also unlock modelling capabilities for downstream applications, leading in particular to highly accurate and robust learned interatomic potentials that can be used in condensed-phase molecular-dynamics simulations and high-fidelity zero-shot prediction of ionic conductivity.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 372,
|
|
"Times Cited, All Databases": 397,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "DEC 7",
|
|
"Publication Year": 2023,
|
|
"Volume": 624,
|
|
"Issue": 7990,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 80,
|
|
"End Page": "+",
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s41586-023-06735-9",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41586-023-06735-9",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001169148800004",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Zhang, S; Wu, JH; Zheng, MT; Jin, X; Shen, ZH; Li, ZH; Wang, YJ; Wang, Q; Wang, XB; Wei, H; Zhang, JW; Wang, P; Zhang, SQ; Yu, LY; Dong, LF; Zhu, QS; Zhang, HG; Lu, J",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Zhang, Shuo; Wu, Jianghua; Zheng, Mengting; Jin, Xin; Shen, Zihan; Li, Zhonghua; Wang, Yanjun; Wang, Quan; Wang, Xuebin; Wei, Hui; Zhang, Jiangwei; Wang, Peng; Zhang, Shanqing; Yu, Liyan; Dong, Lifeng; Zhu, Qingshan; Zhang, Huigang; Lu, Jun",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Fe/Cu diatomic catalysts for electrochemical nitrate reduction to ammonia",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Electrochemical conversion of nitrate to ammonia offers an efficient approach to reducing nitrate pollutants and a potential technology for low-temperature and low-pressure ammonia synthesis. However, the process is limited by multiple competing reactions and NO3- adsorption on cathode surfaces. Here, we report a Fe/Cu diatomic catalyst on holey nitrogen-doped graphene which exhibits high catalytic activities and selectivity for ammonia production. The catalyst enables a maximum ammonia Faradaic efficiency of 92.51% (-0.3 V(RHE)) and a high NH3 yield rate of 1.08 mmol h(-1) mg(-1) (at - 0.5 V(RHE)). Computational and theoretical analysis reveals that a relatively strong interaction between NO3- and Fe/Cu promotes the adsorption and discharge of NO3- anions. Nitrogen-oxygen bonds are also shown to be weakened due to the existence of hetero-atomic dual sites which lowers the overall reaction barriers. The dual-site and hetero-atom strategy in this work provides a flexible design for further catalyst development and expands the electrocatalytic techniques for nitrate reduction and ammonia synthesis. Nitrate electroreduction to ammonia can decrease pollutants and produce high-value ammonia. Here, the authors design a Fe/Cu diatomic catalyst on nitrogen-doped graphene, which exhibits high catalytic activities of and selectivity for ammonia.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
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"Funding Text": null,
|
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"Cited Reference Count": null,
|
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"Times Cited, WoS Core": 280,
|
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"Times Cited, All Databases": 283,
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"Publication Date": "JUN 19",
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"Publication Year": 2023,
|
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"Volume": 14,
|
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"Issue": 1,
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"Supplement": null,
|
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"Special Issue": null,
|
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"Meeting Abstract": null,
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"Start Page": null,
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"End Page": null,
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"Article Number": 3634,
|
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"DOI": "10.1038/s41467-023-39366-9",
|
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"DOI Link": "http://dx.doi.org/10.1038/s41467-023-39366-9",
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"Research Areas": "Science & Technology - Other Topics",
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"Pubmed Id": null,
|
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"Open Access Designations": null,
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"Highly Cited Status": "Y",
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"Hot Paper Status": "Y",
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"Date of Export": "2025-04-23",
|
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"UT (Unique WOS ID)": "WOS:001015306500018",
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"Web of Science Record": "View Full Record in Web of Science"
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},
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{
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"Publication Type": "J",
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"Authors": "Li, Z; Sun, XL; Zheng, XP; Li, B; Gao, DP; Zhang, SF; Wu, X; Li, S; Gong, JQ; Luther, JM; Li, ZA; Zhu, ZL",
|
|
"Book Authors": null,
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"Book Editors": null,
|
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"Book Group Authors": null,
|
|
"Author Full Names": "Li, Zhen; Sun, Xianglang; Zheng, Xiaopeng; Li, Bo; Gao, Danpeng; Zhang, Shoufeng; Wu, Xin; Li, Shuai; Gong, Jianqiu; Luther, Joseph M.; Li, Zhong'an; Zhu, Zonglong",
|
|
"Book Author Full Names": null,
|
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"Group Authors": null,
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"Article Title": "Stabilized hole-selective layer for high-performance inverted p-i-n perovskite solar cells",
|
|
"Source Title": "SCIENCE",
|
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"Book Series Title": null,
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"Book Series Subtitle": null,
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"Language": null,
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"Author Keywords": null,
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"Keywords Plus": null,
|
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"Abstract": "P-i-n geometry perovskite solar cells (PSCs) offer simplified fabrication, greater amenability to charge extraction layers, and low-temperature processing over n-i-p counterparts. Self-assembled monolayers (SAMs) can enhance the performance of p-i-n PSCs but ultrathin SAMs can be thermally unstable. We report a thermally robust hole-selective layer comprised of nickel oxide (NiOx) nulloparticle film with a surface-anchored (4-(3,11-dimethoxy-7H-dibenzo[c,g]carbazol-7-yl)butyl)phosphonic acid (MeO-4PADBC) SAM that can improve and stabilize the NiOx/perovskite interface. The energetic alignment and favorable contact and binding between NiOx/MeO-4PADBC and perovskite reduced the voltage deficit of PSCs with various perovskite compositions and led to strong interface toughening effects under thermal stress. The resulting 1.53-electron-volt devices achieved 25.6% certified power conversion efficiency and maintained >90% of their initial efficiency after continuously operating at 65 degrees Celsius for 1200 hours under 1-sun illumination.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
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"ORCIDs": null,
|
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"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 300,
|
|
"Times Cited, All Databases": 311,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "OCT 20",
|
|
"Publication Year": 2023,
|
|
"Volume": 382,
|
|
"Issue": 6668,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 284,
|
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"End Page": 289,
|
|
"Article Number": null,
|
|
"DOI": "10.1126/science.ade9637",
|
|
"DOI Link": "http://dx.doi.org/10.1126/science.ade9637",
|
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"Book DOI": null,
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|
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"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001138559400027",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Hu, HJ; Huang, H; Li, MH; Gao, XX; Yin, L; Qi, RX; Wu, RS; Chen, XJ; Ma, YX; Shi, KR; Li, CH; Maus, TM; Huang, B; Lu, C; Lin, MY; Zhou, S; Lou, ZY; Gu, Y; Chen, YM; Lei, YS; Wang, XY; Wang, RT; Yue, WT; Yang, XY; Bian, YZ; Mu, J; Park, G; Xiang, S; Cai, SQ; Corey, PW; Wang, JS; Xu, S",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Hu, Hongjie; Huang, Hao; Li, Mohan; Gao, Xiaoxiang; Yin, Lu; Qi, Ruixiang; Wu, Ray S.; Chen, Xiangjun; Ma, Yuxiang; Shi, Keren; Li, Chenghai; Maus, Timothy M.; Huang, Brady; Lu, Chengchangfeng; Lin, Muyang; Zhou, Sai; Lou, Zhiyuan; Gu, Yue; Chen, Yimu; Lei, Yusheng; Wang, Xinyu; Wang, Ruotao; Yue, Wentong; Yang, Xinyi; Bian, Yizhou; Mu, Jing; Park, Geonho; Xiang, Shu; Cai, Shengqiang; Corey, Paul W.; Wang, Joseph; Xu, Sheng",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "A wearable cardiac ultrasound imager",
|
|
"Source Title": "NATURE",
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"Book Series Title": null,
|
|
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"Language": null,
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|
|
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|
|
"Abstract": "Continuous imaging of cardiac functions is highly desirable for the assessment of long-term cardiovascular health, detection of acute cardiac dysfunction and clinical management of critically ill or surgical patients(1-4). However, conventional non-invasive approaches to image the cardiac function cannot provide continuous measurements owing to device bulkiness(5-11), and existing wearable cardiac devices can only capture signals on the skin(12-16). Here we report a wearable ultrasonic device for continuous, real-time and direct cardiac function assessment. We introduce innovations in device design and material fabrication that improve the mechanical coupling between the device and human skin, allowing the left ventricle to be examined from different views during motion. We also develop a deep learning model that automatically extracts the left ventricular volume from the continuous image recording, yielding waveforms of key cardiac performance indices such as stroke volume, cardiac output and ejection fraction. This technology enables dynamic wearable monitoring of cardiac performance with substantially improved accuracy in various environments.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
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"Researcher Ids": null,
|
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"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 285,
|
|
"Times Cited, All Databases": 303,
|
|
"180 Day Usage Count": null,
|
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|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JAN 26",
|
|
"Publication Year": 2023,
|
|
"Volume": 613,
|
|
"Issue": 7945,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s41586-022-05498-z",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41586-022-05498-z",
|
|
"Book DOI": null,
|
|
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|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000930959700001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Chen, Y; Deng, HC; Sha, XB; Chen, WJ; Wang, RZ; Chen, YH; Wu, D; Chu, JR; Kivshar, YS; Xiao, SM; Qiu, CW",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Chen, Yang; Deng, Huachun; Sha, Xinbo; Chen, Weijin; Wang, Ruize; Chen, Yu-Hang; Wu, Dong; Chu, Jiaru; Kivshar, Yuri S. S.; Xiao, Shumin; Qiu, Cheng-Wei",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Observation of intrinsic chiral bound states in the continuum",
|
|
"Source Title": "NATURE",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
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|
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|
|
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|
|
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|
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|
|
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|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Photons with spin angular momentum possess intrinsic chirality, which underpins many phenomena including nonlinear optics(1), quantum optics(2), topological photonics(3) and chiroptics(4). Intrinsic chirality is weak in natural materials, and recent theoretical proposals(5-7) aimed to enlarge circular dichroism by resonullt metasurfaces supporting bound states in the continuum that enhance substantially chiral light-matter interactions. Those insightful works resort to three-dimensional sophisticated geometries, which are too challenging to be realized for optical frequencies(8). Therefore, most of the experimental attempts(9-11) showing strong circular dichroism rely on false/extrinsic chirality by using either oblique incidence(9,10) or structural anisotropy(11). Here we report on the experimental realization of true/intrinsic chiral response with resonullt metasurfaces in which the engineered slant geometry breaks both in-plane and out-of-plane symmetries. Our result marks, to our knowledge, the first observation of intrinsic chiral bound states in the continuum with near-unity circular dichroism of 0.93 and a high quality factor exceeding 2,663 for visible frequencies. Our chiral metasurfaces may lead to a plethora of applications in chiral light sources and detectors, chiral sensing, valleytronics and asymmetric photocatalysis.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 286,
|
|
"Times Cited, All Databases": 303,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JAN 19",
|
|
"Publication Year": 2023,
|
|
"Volume": 613,
|
|
"Issue": 7944,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 474,
|
|
"End Page": "+",
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s41586-022-05467-6",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41586-022-05467-6",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000955590300008",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Li, GX; Su, ZH; Canil, L; Hughes, D; Aldamasy, MH; Dagar, J; Trofimov, S; Wang, LY; Zuo, WW; Jeronimo-Rendon, JJ; Byranvand, MM; Wang, CY; Zhu, R; Zhang, ZH; Yang, F; Nasti, G; Naydenov, B; Tsoi, WC; Li, Z; Gao, XY; Wang, ZK; Jia, Y; Unger, E; Saliba, M; Li, M; Abate, A",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Li, Guixiang; Su, Zhenhuang; Canil, Laura; Hughes, Declan; Aldamasy, Mahmoud H.; Dagar, Janardan; Trofimov, Sergei; Wang, Luyao; Zuo, Weiwei; Jeronimo-Rendon, Jose J.; Byranvand, Mahdi Malekshahi; Wang, Chenyue; Zhu, Rui; Zhang, Zuhong; Yang, Feng; Nasti, Giuseppe; Naydenov, Boris; Tsoi, Wing C.; Li, Zhe; Gao, Xingyu; Wang, Zhaokui; Jia, Yu; Unger, Eva; Saliba, Michael; Li, Meng; Abate, Antonio",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Highly efficient p-i-n perovskite solar cells that endure temperature variations",
|
|
"Source Title": "SCIENCE",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Daily temperature variations induce phase transitions and lattice strains in halide perovskites, challenging their stability in solar cells. We stabilized the perovskite black phase and improved solar cell performance using the ordered dipolar structure of beta-poly(1,1-difluoroethylene) to control perovskite film crystallization and energy alignment. We demonstrated p-i-n perovskite solar cells with a record power conversion efficiency of 24.6% over 18 square millimeters and 23.1% over 1 square centimeter, which retained 96 and 88% of the efficiency after 1000 hours of 1-sunmaximum power point tracking at 25 degrees and 75 degrees C, respectively. Devices under rapid thermal cycling between -60 degrees and +80 degrees C showed no sign of fatigue, demonstrating the impact of the ordered dipolar structure on the operational stability of perovskite solar cells.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 318,
|
|
"Times Cited, All Databases": 326,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JAN 27",
|
|
"Publication Year": 2023,
|
|
"Volume": 379,
|
|
"Issue": 6630,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 399,
|
|
"End Page": 403,
|
|
"Article Number": null,
|
|
"DOI": "10.1126/science.add7331",
|
|
"DOI Link": "http://dx.doi.org/10.1126/science.add7331",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001058669200001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Xu, T; Song, Q; Liu, K; Liu, HY; Pan, JJ; Liu, W; Dai, L; Zhang, M; Wang, YX; Si, CL; Du, HS; Zhang, K",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Xu, Ting; Song, Qun; Liu, Kun; Liu, Huayu; Pan, Junjie; Liu, Wei; Dai, Lin; Zhang, Meng; Wang, Yaxuan; Si, Chuanling; Du, Haishun; Zhang, Kai",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "nullocellulose-Assisted Construction of Multifunctional MXene-Based Aerogels with Engineering Biomimetic Texture for Pressure Sensor and Compressible Electrode",
|
|
"Source Title": "nullO-MICRO LETTERS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Multifunctional architecture with intriguing structural design is highly desired for realizing the promising performances in wearable sensors and flexible energy storage devices. Cellulose nullofiber (CNF) is employed for assisting in building conductive, hyperelastic, and ultralight Ti3C2Tx MXene hybrid aerogels with oriented tracheid-like texture. The biomimetic hybrid aerogels are constructed by a facile bidirectional freezing strategy with CNF, carbon nullotube (CNT), and MXene based on synergistic electrostatic interaction and hydrogen bonding. Entangled CNF and CNT mortars bonded with MXene bricks of the tracheid structure produce good interfacial binding, and superior mechanical strength (up to 80% compressibility and extraordinary fatigue resistance of 1000 cycles at 50% strain). Benefiting from the biomimetic texture, CNF/CNT/MXene aerogel shows ultralow density of 7.48 mg cm(-3) and excellent electrical conductivity (similar to 2400 S m(-1)). Used as pressure sensors, such aerogels exhibit appealing sensitivity performance with the linear sensitivity up to 817.3 kPa(-1), which affords their application in monitoring body surface information and detecting human motion. Furthermore, the aerogels can also act as electrode materials of compressive solid-state supercapacitors that reveal satisfactory electrochemical performance (849.2 mF cm(-2) at 0.8 mA cm(-2)) and superior long cycle compression performance (88% after 10,000 cycles at a compressive strain of 30%).",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
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"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
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"Cited Reference Count": null,
|
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"Times Cited, WoS Core": 274,
|
|
"Times Cited, All Databases": 279,
|
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"180 Day Usage Count": null,
|
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"Since 2013 Usage Count": null,
|
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"Publisher": null,
|
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"Publisher Address": null,
|
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"ISSN": null,
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|
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"ISBN": null,
|
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"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "DEC",
|
|
"Publication Year": 2023,
|
|
"Volume": 15,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 98,
|
|
"DOI": "10.1007/s40820-023-01073-x",
|
|
"DOI Link": "http://dx.doi.org/10.1007/s40820-023-01073-x",
|
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"Book DOI": null,
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"Early Access Date": null,
|
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"Number of Pages": null,
|
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"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics; Materials Science; Physics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000968816500005",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Tang, Z; Zhang, R; Wang, HY; Zhou, SY; Pan, ZY; Huang, YC; Sun, D; Tang, YG; Ji, XB; Amine, K; Shao, MH",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Tang, Zheng; Zhang, Rui; Wang, Haiyan; Zhou, Siyu; Pan, Zhiyi; Huang, Yuancheng; Sun, Dan; Tang, Yougen; Ji, Xiaobo; Amine, Khalil; Shao, Minhua",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Revealing the closed pore formation of waste wood-derived hard carbon for advanced sodium-ion battery",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
|
"Book Series Title": null,
|
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"Book Series Subtitle": null,
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"Language": null,
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"Document Type": "Article",
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"Conference Sponsor": null,
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"Conference Host": null,
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"Author Keywords": null,
|
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"Keywords Plus": null,
|
|
"Abstract": "Although the closed pore structure plays a key role in contributing low-voltage plateau capacity of hard carbon anode for sodium-ion batteries, the formation mechanism of closed pores is still under debate. Here, we employ waste wood-derived hard carbon as a template to systematically establish the formation mechanisms of closed pores and their effect on sodium storage performance. We find that the high crystallinity cellulose in nature wood decomposes to long-range carbon layers as the wall of closed pore, and the amorphous component can hinder the graphitization of carbon layer and induce the crispation of long-range carbon layers. The optimized sample demonstrates a high reversible capacity of 430 mAh g-1 at 20 mA g-1 (plateau capacity of 293 mAh g-1 for the second cycle), as well as good rate and stable cycling performances (85.4% after 400 cycles at 500 mA g-1). Deep insights into the closed pore formation will greatly forward the rational design of hard carbon anode with high capacity. It is essential to investigate the formation mechanism of closed pore, which contributes to low-voltage plateau capacity of hard carbon anode in sodium ion batteries. Herein, the authors explore the impact of wood precursor components and carbonization temperature on closed pore formation in hard carbon for enhanced battery performance.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 255,
|
|
"Times Cited, All Databases": 268,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "SEP 27",
|
|
"Publication Year": 2023,
|
|
"Volume": 14,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 6024,
|
|
"DOI": "10.1038/s41467-023-39637-5",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-023-39637-5",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001095471200017",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Zhai, PL; Wang, C; Zhao, YY; Zhang, YX; Gao, JF; Sun, LC; Hou, JA",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Zhai, Panlong; Wang, Chen; Zhao, Yuanyuan; Zhang, Yanxue; Gao, Junfeng; Sun, Licheng; Hou, Jungang",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Regulating electronic states of nitride/hydroxide to accelerate kinetics for oxygen evolution at large current density",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Rational design efficient transition metal-based electrocatalysts for oxygen evolution reaction (OER) is critical for water splitting. However, industrial water-alkali electrolysis requires large current densities at low overpotentials, always limited by intrinsic activity. Herein, we report hierarchical bimetal nitride/hydroxide (NiMoN/NiFe LDH) array as model catalyst, regulating the electronic states and tracking the relationship of structure-activity. As-activated NiMoN/NiFe LDH exhibits the industrially required current density of 1000 mA cm(-2) at overpotential of 266 mV with 250 h stability for OER. Especially, in-situ electrochemical spectroscopic reveals that heterointerface facilitates dynamic structure evolution to optimize electronic structure. Operando electrochemical impedance spectroscopy implies accelerated OER kinetics and intermediate evolution due to fast charge transport. The OER mechanism is revealed by the combination of theoretical and experimental studies, indicating as-activated NiMoN/NiFe LDH follows lattice oxygen oxidation mechanism with accelerated kinetics. This work paves an avenue to develop efficient catalysts for industrial water electrolysis via tuning electronic states. Rational design of efficient electrocatalysts for oxygen evolution reaction is critical for water-alkali electrolysis. Here, the authors fabricate a NiMoN/NiFe layered double hydroxide and show the accelerated oxygen evolution kinetics are due to the heterointerface.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 266,
|
|
"Times Cited, All Databases": 270,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "APR 4",
|
|
"Publication Year": 2023,
|
|
"Volume": 14,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 1873,
|
|
"DOI": "10.1038/s41467-023-37091-x",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-023-37091-x",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000983843800002",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Shao, ZJ; Yin, TY; Jiang, JB; He, Y; Xiang, T; Zhou, SB",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Shao, Zijian; Yin, Tianyu; Jiang, Jinbo; He, Yang; Xiang, Tao; Zhou, Shaobing",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Wound microenvironment self-adaptive hydrogel with efficient angiogenesis for promoting diabetic wound healing",
|
|
"Source Title": "BIOACTIVE MATERIALS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Neovascularization is critical to improve the diabetic microenvironment, deliver abundant nutrients to the wound and promote wound closure. However, the excess of oxidative stress impedes the healing process. Herein, a self-adaptive multifunctional hydrogel with self-healing property and injectability is fabricated through a boronic ester-based reaction between the phenylboronic acid groups of the 3-carboxyl-4-fluorophenylboronic acid -grafted quaternized chitosan and the hydroxyl groups of the polyvinyl alcohol, in which pro-angiogenic drug of desferrioxamine (DFO) is loaded in the form of gelatin microspheres (DFO@G). The boronic ester bonds of the hydrogel can self-adaptively react with hyperglycemic and hydrogen peroxide to alleviate oxidative stress and release DFO@G in the early phase of wound healing. A sustained release of DFO is then realized by responding to overexpressed matrix metalloproteinases. In a full-thickness diabetic wound model, the DFO@G loaded hydrogel accelerates angiogenesis by upregulating expression of hypoxia-inducible factor-1 and angiogenic growth factors, resulting in collagen deposition and rapid wound closure. This multifunctional hydrogel can not only self-adaptively change the microenvironment to a pro-healing state by decreasing oxidative stress, but also respond to matrix metalloproteinases to release DFO. The self-adaptive multifunctional hydrogel has a potential for treating diabetic wounds.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 296,
|
|
"Times Cited, All Databases": 299,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "FEB",
|
|
"Publication Year": 2023,
|
|
"Volume": 20,
|
|
"Issue": null,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 561,
|
|
"End Page": 573,
|
|
"Article Number": null,
|
|
"DOI": "10.1016/j.bioactmat.2022.06.018",
|
|
"DOI Link": "http://dx.doi.org/10.1016/j.bioactmat.2022.06.018",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Engineering; Materials Science",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000826897500002",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Musaelian, A; Batzner, S; Johansson, A; Sun, LX; Owen, CJ; Kornbluth, M; Kozinsky, B",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Musaelian, Albert; Batzner, Simon; Johansson, Anders; Sun, Lixin; Owen, Cameron J.; Kornbluth, Mordechai; Kozinsky, Boris",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Learning local equivariant representations for large-scale atomistic dynamics",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "A simultaneously accurate and computationally efficient parametrization of the potential energy surface of molecules and materials is a long-standing goal in the natural sciences. While atom-centered message passing neural networks (MPNNs) have shown remarkable accuracy, their information propagation has limited the accessible length-scales. Local methods, conversely, scale to large simulations but have suffered from inferior accuracy. This work introduces Allegro, a strictly local equivariant deep neural network interatomic potential architecture that simultaneously exhibits excellent accuracy and scalability. Allegro represents a many-body potential using iterated tensor products of learned equivariant representations without atom-centered message passing. Allegro obtains improvements over state-of-the-art methods on QM9 and revMD17. A single tensor product layer outperforms existing deep MPNNs and transformers on QM9. Furthermore, Allegro displays remarkable generalization to out-of-distribution data. Molecular simulations using Allegro recover structural and kinetic properties of an amorphous electrolyte in excellent agreement with ab-initio simulations. Finally, we demonstrate parallelization with a simulation of 100 million atoms. The paper presents a method that allows scaling machine learning interatomic potentials to extremely large systems, while at the same time retaining the remarkable accuracy and learning efficiency of deep equivariant models. This is obtained with an E(3)- equivariant neural network architecture that combines the high accuracy of equivariant neural networks with the scalability of local methods.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 253,
|
|
"Times Cited, All Databases": 265,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "FEB 3",
|
|
"Publication Year": 2023,
|
|
"Volume": 14,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 579,
|
|
"DOI": "10.1038/s41467-023-36329-y",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-023-36329-y",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000955633400011",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Zhou, YZ; Lu, RH; Tao, XF; Qiu, ZJ; Chen, GB; Yang, J; Zhao, Y; Feng, XL; Müllen, K",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Zhou, Yazhou; Lu, Ruihu; Tao, Xiafang; Qiu, Zijie; Chen, Guangbo; Yang, Juan; Zhao, Yan; Feng, Xinliang; Muellen, Klaus",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Boosting Oxygen Electrocatalytic Activity of Fe-N-C Catalysts by Phosphorus Incorporation",
|
|
"Source Title": "JOURNAL OF THE AMERICAN CHEMICAL SOCIETY",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Nitrogen-doped graphitic carbon materials hosting single-atom iron (Fe-N-C) are major non-precious metal catalysts for the oxygen reduction reaction (ORR). The nitrogen-coordinated Fe sites are described as the first coordination sphere. As opposed to the good performance in ORR, that in the oxygen evolution reaction (OER) is extremely poor due to the sluggish O-O coupling process, thus hampering the practical applications of rechargeable zinc (Zn)-air batteries. Herein, we succeed in boosting the OER activity of Fe-N-C by additionally incorporating phosphorus atoms into the second coordination sphere, here denoted as P/Fe-N-C. The resulting material exhibits excellent OER activity in 0.1 M KOH with an overpotential as low as 304 mV at a current density of 10 mA cm-2. Even more importantly, they exhibit a remarkably small ORR/OER potential gap of 0.63 V. Theoretical calculations using first-principles density functional theory suggest that the phosphorus enhances the electrocatalytic activity by balancing the *OOH/*O adsorption at the FeN4 sites. When used as an air cathode in a rechargeable Zn-air battery, P/Fe-N-C delivers a charge-discharge performance with a high peak power density of 269 mW cm-2, highlighting its role as the state-of-the-art bifunctional oxygen electrocatalyst.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 264,
|
|
"Times Cited, All Databases": 267,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "FEB 15",
|
|
"Publication Year": 2023,
|
|
"Volume": 145,
|
|
"Issue": 6,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 3647,
|
|
"End Page": 3655,
|
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"Article Number": null,
|
|
"DOI": "10.1021/jacs.2c12933",
|
|
"DOI Link": "http://dx.doi.org/10.1021/jacs.2c12933",
|
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"Book DOI": null,
|
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"Early Access Date": "FEB 2023",
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"Number of Pages": null,
|
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|
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|
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"Research Areas": "Chemistry",
|
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"IDS Number": null,
|
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"Pubmed Id": null,
|
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"Open Access Designations": null,
|
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"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000928853600001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Zhang, W; Dai, YH; Chen, RW; Xu, ZM; Li, JW; Zong, W; Li, HX; Li, Z; Zhang, ZY; Zhu, JX; Guo, F; Gao, X; Du, ZJ; Chen, JT; Wang, TL; He, GJ; Parkin, IP",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
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"Author Full Names": "Zhang, Wei; Dai, Yuhang; Chen, Ruwei; Xu, Zhenming; Li, Jianwei; Zong, Wei; Li, Huangxu; Li, Zheng; Zhang, Zhenyu; Zhu, Jiexin; Guo, Fei; Gao, Xuan; Du, Zijuan; Chen, Jintao; Wang, Tianlei; He, Guanjie; Parkin, Ivan P.",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
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"Article Title": "Highly Reversible Zinc Metal Anode in a Dilute Aqueous Electrolyte Enabled by a pH Buffer Additive",
|
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"Source Title": "ANGEWANDTE CHEMIE-INTERNATIONAL EDITION",
|
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"Language": null,
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"Author Keywords": null,
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"Keywords Plus": null,
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"Abstract": "Aqueous zinc-ion batteries have drawn increasing attention due to the intrinsic safety, cost-effectiveness and high energy density. However, parasitic reactions and non-uniform dendrite growth on the Zn anode side impede their application. Herein, a multifunctional additive, ammonium dihydrogen phosphate (NHP), is introduced to regulate uniform zinc deposition and to suppress side reactions. The results show that the NH4+ tends to be preferably absorbed on the Zn surface to form a shielding effect and blocks the direct contact of water with Zn. Moreover, NH4+ and (H2PO4)(-) jointly maintain pH values of the electrode-electrolyte interface. Consequently, the NHP additive enables highly reversible Zn plating/stripping behaviors in Zn//Zn and Zn//Cu cells. Furthermore, the electrochemical performances of Zn//MnO2 full cells and Zn//active carbon (AC) capacitors are improved. This work provides an efficient and general strategy for modifying Zn plating/stripping behaviors and suppressing side reactions in mild aqueous electrolyte.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
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"Email Addresses": null,
|
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"Researcher Ids": null,
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"ORCIDs": null,
|
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"Funding Orgs": null,
|
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"Funding Name Preferred": null,
|
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"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
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"Times Cited, WoS Core": 263,
|
|
"Times Cited, All Databases": 267,
|
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"180 Day Usage Count": null,
|
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"Since 2013 Usage Count": null,
|
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"Publisher": null,
|
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"Publisher City": null,
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"Publisher Address": null,
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"ISSN": null,
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"eISSN": null,
|
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"ISBN": null,
|
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"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JAN 26",
|
|
"Publication Year": 2023,
|
|
"Volume": 62,
|
|
"Issue": 5,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
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"Article Number": null,
|
|
"DOI": "10.1002/anie.202212695",
|
|
"DOI Link": "http://dx.doi.org/10.1002/anie.202212695",
|
|
"Book DOI": null,
|
|
"Early Access Date": "DEC 2022",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000894095400001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Ding, HM; Li, YB; Li, M; Chen, K; Liang, K; Chen, GX; Lu, J; Palisaitis, J; Persson, POA; Eklund, P; Hultman, L; Du, SY; Chai, ZF; Gogotsi, Y; Huang, Q",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Ding, Haoming; Li, Youbing; Li, Mian; Chen, Ke; Liang, Kun; Chen, Guoxin; Lu, Jun; Palisaitis, Justinas; Persson, Per O. A.; Eklund, Per; Hultman, Lars; Du, Shiyu; Chai, Zhifang; Gogotsi, Yury; Huang, Qing",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Chemical scissor-mediated structural editing of layered transition metal carbides",
|
|
"Source Title": "SCIENCE",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
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"Language": null,
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"Keywords Plus": null,
|
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"Abstract": "Intercalated layered materials offer distinctive properties and serve as precursors for important two-dimensional (2D) materials. However, intercalation of non-van der Waals structures, which can expand the family of 2D materials, is difficult. We report a structural editing protocol for layered carbides (MAX phases) and their 2D derivatives (MXenes). Gap-opening and species-intercalating stages were respectively mediated by chemical scissors and intercalants, which created a large family of MAX phases with unconventional elements and structures, as well as MXenes with versatile terminals. The removal of terminals in MXenes with metal scissors and then the stitching of 2D carbide nullosheets with atom intercalation leads to the reconstruction of MAX phases and a family of metal-intercalated 2D carbides, both of which may drive advances in fields ranging from energy to printed electronics.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 265,
|
|
"Times Cited, All Databases": 276,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "MAR 17",
|
|
"Publication Year": 2023,
|
|
"Volume": 379,
|
|
"Issue": 6637,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 1130,
|
|
"End Page": 1135,
|
|
"Article Number": null,
|
|
"DOI": "10.1126/science.add5901",
|
|
"DOI Link": "http://dx.doi.org/10.1126/science.add5901",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000959028800007",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Hossain, MK; Toki, GFI; Kuddus, A; Rubel, MHK; Hossain, MM; Bencherif, H; Rahman, MF; Islam, MR; Mushtaq, M",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Hossain, M. Khalid; Toki, G. F. Ishraque; Kuddus, Abdul; Rubel, M. H. K.; Hossain, M. M.; Bencherif, H.; Rahman, Md. Ferdous; Islam, Md. Rasidul; Mushtaq, Muhammad",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "An extensive study on multiple ETL and HTL layers to design and simulation of high-performance lead-free CsSnCl3-based perovskite solar cells",
|
|
"Source Title": "SCIENTIFIC REPORTS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
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"Document Type": "Article",
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|
"Conference Title": null,
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"Conference Date": null,
|
|
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|
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"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Cesium tin chloride (CsSnCl3) is a potential and competitive absorber material for lead-free perovskite solar cells (PSCs). The full potential of CsSnCl3 not yet been realized owing to the possible challenges of defect-free device fabrication, non-optimized alignment of the electron transport layer (ETL), hole transport layer (HTL), and the favorable device configuration. In this work, we proposed several CsSnCl3-based solar cell (SC) configurations using one dimensional solar cell capacitance simulator (SCAPS-1D) with different competent ETLs like indium-gallium-zinc-oxide (IGZO), tin-dioxide (SnO2), tungsten disulfide (WS2), ceric dioxide (CeO2), titanium dioxide (TiO2), zinc oxide (ZnO), C-60, PCBM, and HTLs of cuprous oxide (Cu2O), cupric oxide (CuO), nickel oxide (NiO), vanadium oxide (V2O5), copper iodide (CuI), CuSCN, CuSbS2, Spiro MeOTAD, CBTS, CFTS, P3HT, PEDOT:PSS. Simulation results revealed that ZnO, TiO2, IGZO, WS2, PCBM, and C-60 ETLs-based halide perovskites with ITO/ETLs/CsSnCl3/CBTS/Au heterostructure exhibited outstanding photoconversion efficiency retaining nearest photovoltaic parameters values among 96 different configurations. Further, for the six best-performing configurations, the effect of the CsSnCl3 absorber and ETL thickness, series and shunt resistance, working temperature, impact of capacitance, Mott-Schottky, generation and recombination rate, current-voltage properties, and quantum efficiency on performance were assessed. We found that ETLs like TiO2, ZnO, and IGZO, with CBTS HTL can act as outstanding materials for the fabrication of CsSnCl3-based high efficiency (eta >= 22%) heterojunction SCs with ITO/ETL/CsSnCl3/CBTS/Au structure. The simulation results obtained by the SCAPS-1D for the best six CsSnCl3-perovskites SC configurations were compared by the wxAMPS (widget provided analysis of microelectronic and photonic structures) tool for further validation. Furthermore, the structural, optical and electronic properties along with electron charge density, and Fermi surface of the CsSnCl3 perovskite absorber layer were computed and analyzed using first-principle calculations based on density functional theory. Thus, this in-depth simulation paves a constructive research avenue to fabricate cost-effective, high-efficiency, and lead-free CsSnCl3 perovskite-based high-performance SCs for a lead-free green and pollution-free environment.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 262,
|
|
"Times Cited, All Databases": 261,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "FEB 13",
|
|
"Publication Year": 2023,
|
|
"Volume": 13,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 2521,
|
|
"DOI": "10.1038/s41598-023-28506-2",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41598-023-28506-2",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000984284300005",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Park, SM; Wei, MY; Xu, J; Atapattu, HR; Eickemeyer, FT; Darabi, K; Grater, L; Yang, Y; Liu, C; Teale, S; Chen, B; Chen, H; Wang, TH; Zeng, LW; Maxwell, A; Wang, ZW; Rao, KR; Cai, ZY; Zakeeruddin, SM; Pham, JT; Risko, CM; Amassian, A; Kanatzidis, MG; Graham, KR; Grätzel, M; Sargent, EH",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Park, So Min; Wei, Mingyang; Xu, Jian; Atapattu, Harindi R.; Eickemeyer, Felix T.; Darabi, Kasra; Grater, Luke; Yang, Yi; Liu, Cheng; Teale, Sam; Chen, Bin; Chen, Hao; Wang, Tonghui; Zeng, Lewei; Maxwell, Aidan; Wang, Zaiwei; Rao, Keerthan R.; Cai, Zhuoyun; Zakeeruddin, Shaik M.; Pham, Jonathan T.; Risko, Chad M.; Amassian, Aram; Kanatzidis, Mercouri G.; Graham, Kenneth R.; Gratzel, Michael; Sargent, Edward H.",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Engineering ligand reactivity enables high-temperature operation of stable perovskite solar cells",
|
|
"Source Title": "SCIENCE",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
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"Document Type": "Article",
|
|
"Conference Title": null,
|
|
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|
|
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|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Perovskite solar cells (PSCs) consisting of interfacial two- and three-dimensional heterostructures that incorporate ammonium ligand intercalation have enabled rapid progress toward the goal of uniting performance with stability. However, as the field continues to seek ever-higher durability, additional tools that avoid progressive ligand intercalation are needed to minimize degradation at high temperatures. We used ammonium ligands that are nonreactive with the bulk of perovskites and investigated a library that varies ligand molecular structure systematically. We found that fluorinated aniliniums offer interfacial passivation and simultaneously minimize reactivity with perovskites. Using this approach, we report a certified quasi-steady-state power-conversion efficiency of 24.09% for inverted-structure PSCs. In an encapsulated device operating at 85 degrees C and 50% relative humidity, we document a 1560-hour T-85 at maximum power point under 1-sun illumination.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 247,
|
|
"Times Cited, All Databases": 253,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JUL 14",
|
|
"Publication Year": 2023,
|
|
"Volume": 381,
|
|
"Issue": 6654,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": "SI",
|
|
"Meeting Abstract": null,
|
|
"Start Page": 209,
|
|
"End Page": 215,
|
|
"Article Number": null,
|
|
"DOI": "10.1126/science.adi4107",
|
|
"DOI Link": "http://dx.doi.org/10.1126/science.adi4107",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001058656200008",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Ji, GJ; Wang, JX; Liang, Z; Jia, K; Ma, J; Zhuang, ZF; Zhou, GM; Cheng, HM",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Ji, Guanjun; Wang, Junxiong; Liang, Zheng; Jia, Kai; Ma, Jun; Zhuang, Zhaofeng; Zhou, Guangmin; Cheng, Hui-Ming",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Direct regeneration of degraded lithium-ion battery cathodes with a multifunctional organic lithium salt",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Sustainable recycle of spent Li ion batteries is an effective strategy to alleviate environmental concerns and support resource conservation. Here, authors report the direct regeneration of LiFePO4 cathode using multifunctional organic lithium salts, leading to high environmental and economic benefits. The recycling of spent lithium-ion batteries is an effective approach to alleviating environmental concerns and promoting resource conservation. LiFePO4 batteries have been widely used in electric vehicles and energy storage stations. Currently, lithium loss, resulting in formation of Fe(III) phase, is mainly responsible for the capacity fade of LiFePO4 cathode. Another factor is poor electrical conductivity that limits its rate capability. Here, we report the use of a multifunctional organic lithium salt (3,4-dihydroxybenzonitrile dilithium) to restore spent LiFePO4 cathode by direct regeneration. The degraded LiFePO4 particles are well coupled with the functional groups of the organic lithium salt, so that lithium fills vacancies and cyano groups create a reductive atmosphere to inhibit Fe(III) phase. At the same time, pyrolysis of the salt produces an amorphous conductive carbon layer that coats the LiFePO4 particles, which improves Li-ion and electron transfer kinetics. The restored LiFePO4 cathode shows good cycling stability and rate performance (a high capacity retention of 88% after 400 cycles at 5 C). This lithium salt can also be used to recover degraded transition metal oxide-based cathodes. A techno-economic analysis suggests that this strategy has higher environmental and economic benefits, compared with the traditional recycling methods.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 241,
|
|
"Times Cited, All Databases": 251,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "FEB 3",
|
|
"Publication Year": 2023,
|
|
"Volume": 14,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 584,
|
|
"DOI": "10.1038/s41467-023-36197-6",
|
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"DOI Link": "http://dx.doi.org/10.1038/s41467-023-36197-6",
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|
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"Number of Pages": null,
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|
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"Web of Science Index": null,
|
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"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
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"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
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"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
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"UT (Unique WOS ID)": "WOS:000955633400015",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Szymanski, NJ; Rendy, B; Fei, YX; Kumar, RE; He, TJ; Milsted, D; McDermott, MJ; Gallant, M; Cubuk, ED; Merchant, A; Kim, H; Jain, A; Bartel, CJ; Persson, K; Zeng, Y; Ceder, G",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
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"Book Group Authors": null,
|
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"Author Full Names": "Szymanski, Nathan J.; Rendy, Bernardus; Fei, Yuxing; Kumar, Rishi E.; He, Tanjin; Milsted, David; McDermott, Matthew J.; Gallant, Max; Cubuk, Ekin Dogus; Merchant, Amil; Kim, Haegyeom; Jain, Anubhav; Bartel, Christopher J.; Persson, Kristin; Zeng, Yan; Ceder, Gerbrand",
|
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"Book Author Full Names": null,
|
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"Group Authors": null,
|
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"Article Title": "An autonomous laboratory for the accelerated synthesis of novel materials",
|
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"Source Title": "NATURE",
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"Book Series Title": null,
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"Book Series Subtitle": null,
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"Author Keywords": null,
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"Keywords Plus": null,
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"Abstract": "To close the gap between the rates of computational screening and experimental realization of novel materials1,2, we introduce the A-Lab, an autonomous laboratory for the solid-state synthesis of inorganic powders. This platform uses computations, historical data from the literature, machine learning (ML) and active learning to plan and interpret the outcomes of experiments performed using robotics. Over 17 days of continuous operation, the A-Lab realized 41 novel compounds from a set of 58 targets including a variety of oxides and phosphates that were identified using large-scale ab initio phase-stability data from the Materials Project and Google DeepMind. Synthesis recipes were proposed by natural-language models trained on the literature and optimized using an active-learning approach grounded in thermodynamics. Analysis of the failed syntheses provides direct and actionable suggestions to improve current techniques for materials screening and synthesis design. The high success rate demonstrates the effectiveness of artificial-intelligence-driven platforms for autonomous materials discovery and motivates further integration of computations, historical knowledge and robotics.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
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"Researcher Ids": null,
|
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"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 237,
|
|
"Times Cited, All Databases": 250,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "DEC 7",
|
|
"Publication Year": 2023,
|
|
"Volume": 624,
|
|
"Issue": 7990,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 86,
|
|
"End Page": "+",
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s41586-023-06734-w",
|
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"DOI Link": "http://dx.doi.org/10.1038/s41586-023-06734-w",
|
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"Book DOI": null,
|
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"Early Access Date": null,
|
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"Number of Pages": null,
|
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"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001169148800005",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Cheng, SM; Lou, ZR; Zhang, L; Guo, HT; Wang, ZT; Guo, CF; Fukuda, K; Ma, SH; Wang, GQ; Someya, T; Cheng, HM; Xu, XM",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Cheng, Simin; Lou, Zirui; Zhang, Lan; Guo, Haotian; Wang, Zitian; Guo, Chuanfei; Fukuda, Kenjiro; Ma, Shaohua; Wang, Guoqing; Someya, Takao; Cheng, Hui-Ming; Xu, Xiaomin",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Ultrathin Hydrogel Films toward Breathable Skin-Integrated Electronics",
|
|
"Source Title": "ADVANCED MATERIALS",
|
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"Book Series Title": null,
|
|
"Book Series Subtitle": null,
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"Language": null,
|
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"Document Type": "Article",
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"Conference Sponsor": null,
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|
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"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "On-skin electronics that offer revolutionary capabilities in personalized diagnosis, therapeutics, and human-machine interfaces require seamless integration between the skin and electronics. A common question remains whether an ideal interface can be introduced to directly bridge thin-film electronics with the soft skin, allowing the skin to breathe freely and the skin-integrated electronics to function stably. Here, an ever-thinnest hydrogel is reported that is compliant to the glyphic lines and subtle minutiae on the skin without forming air gaps, produced by a facile cold-lamination method. The hydrogels exhibit high water-vapor permeability, allowing nearly unimpeded transepidermal water loss and free breathing of the skin underneath. Hydrogel-interfaced flexible (opto)electronics without causing skin irritation or accelerated device performance deterioration are demonstrated. The long-term applicability is recorded for over one week. With combined features of extreme mechanical compliance, high permeability, and biocompatibility, the ultrathin hydrogel interface promotes the general applicability of skin-integrated electronics.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 216,
|
|
"Times Cited, All Databases": 221,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JAN",
|
|
"Publication Year": 2023,
|
|
"Volume": 35,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": null,
|
|
"DOI": "10.1002/adma.202206793",
|
|
"DOI Link": "http://dx.doi.org/10.1002/adma.202206793",
|
|
"Book DOI": null,
|
|
"Early Access Date": "NOV 2022",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry; Science & Technology - Other Topics; Materials Science; Physics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000888665600001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Deng, BW; Zhong, PC; Jun, K; Riebesell, J; Han, K; Bartel, CJ; Ceder, G",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Deng, Bowen; Zhong, Peichen; Jun, KyuJung; Riebesell, Janosh; Han, Kevin; Bartel, Christopher J.; Ceder, Gerbrand",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "CHGNet as a pretrained universal neural network potential for charge-informed atomistic modelling",
|
|
"Source Title": "NATURE MACHINE INTELLIGENCE",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Large-scale simulations with complex electron interactions remain one of the greatest challenges for atomistic modelling. Although classical force fields often fail to describe the coupling between electronic states and ionic rearrangements, the more accurate ab initio molecular dynamics suffers from computational complexity that prevents long-time and large-scale simulations, which are essential to study technologically relevant phenomena. Here we present the Crystal Hamiltonian Graph Neural Network (CHGNet), a graph neural network-based machine-learning interatomic potential (MLIP) that models the universal potential energy surface. CHGNet is pretrained on the energies, forces, stresses and magnetic moments from the Materials Project Trajectory Dataset, which consists of over 10 years of density functional theory calculations of more than 1.5 million inorganic structures. The explicit inclusion of magnetic moments enables CHGNet to learn and accurately represent the orbital occupancy of electrons, enhancing its capability to describe both atomic and electronic degrees of freedom. We demonstrate several applications of CHGNet in solid-state materials, including charge-informed molecular dynamics in LixMnO2, the finite temperature phase diagram for LixFePO4 and Li diffusion in garnet conductors. We highlight the significance of charge information for capturing appropriate chemistry and provide insights into ionic systems with additional electronic degrees of freedom that cannot be observed by previous MLIPs.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 220,
|
|
"Times Cited, All Databases": 230,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "SEP",
|
|
"Publication Year": 2023,
|
|
"Volume": 5,
|
|
"Issue": 9,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 1031,
|
|
"End Page": 1041,
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s42256-023-00716-3",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s42256-023-00716-3",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Computer Science",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001085170400007",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Jin, HY; Liu, XY; An, PF; Tang, C; Yu, HM; Zhang, QH; Peng, HJ; Gu, L; Zheng, Y; Song, TS; Davey, K; Paik, U; Dong, JC; Qiao, SZ",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Jin, Huanyu; Liu, Xinyan; An, Pengfei; Tang, Cheng; Yu, Huimin; Zhang, Qinghua; Peng, Hong-Jie; Gu, Lin; Zheng, Yao; Song, Taeseup; Davey, Kenneth; Paik, Ungyu; Dong, Juncai; Qiao, Shi-Zhang",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Dynamic rhenium dopant boosts ruthenium oxide for durable oxygen evolution",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Heteroatom-doping is a practical means to boost RuO2 for acidic oxygen evolution reaction (OER). However, a major drawback is conventional dopants have static electron redistribution. Here, we report that Re dopants in Re0.06Ru0.94O2 undergo a dynamic electron accepting-donating that adaptively boosts activity and stability, which is different from conventional dopants with static dopant electron redistribution. We show Re dopants during OER, (1) accept electrons at the on-site potential to activate Ru site, and (2) donate electrons back at large overpotential and prevent Ru dissolution. We confirm via in situ characterizations and first-principle computation that the dynamic electron-interaction between Re and Ru facilitates the adsorbate evolution mechanism and lowers adsorption energies for oxygen intermediates to boost activity and stability of Re0.06Ru0.94O2. We demonstrate a high mass activity of 500 A g(cata.)(-1) (7811 A g(Re-Ru)(-1)) and a high stability number of S-number = 4.0 x 10(6) n(oxygen) n(Ru)(-1) to outperform most electrocatalysts. We conclude that dynamic dopants can be used to boost activity and stability of active sites and therefore guide the design of adaptive electrocatalysts for clean energy conversions. RuO2 is a promising anode catalyst for proton exchange membrane water electrolyzers but suffers from poor catalytic stability. Here the authors present a rhenium-doped RuO2 with a unique dynamic electron accepting-donating that adaptively boosts activity and stability in acidic water oxidation.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 218,
|
|
"Times Cited, All Databases": 225,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JAN 21",
|
|
"Publication Year": 2023,
|
|
"Volume": 14,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 354,
|
|
"DOI": "10.1038/s41467-023-35913-6",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-023-35913-6",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000953220800003",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Yang, CY; Xia, JL; Cui, CY; Pollard, TP; Vatamanu, J; Faraone, A; Dura, JA; Tyagi, M; Kattan, A; Thimsen, E; Xu, JJ; Song, WT; Hu, EY; Ji, X; Hou, SY; Zhang, XY; Ding, MS; Hwang, S; Su, D; Ren, Y; Yang, XQ; Wang, H; Borodin, O; Wang, CS",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Yang, Chongyin; Xia, Jiale; Cui, Chunyu; Pollard, Travis P.; Vatamanu, Jenel; Faraone, Antonio; Dura, Joseph A.; Tyagi, Madhusudan; Kattan, Alex; Thimsen, Elijah; Xu, Jijian; Song, Wentao; Hu, Enyuan; Ji, Xiao; Hou, Singyuk; Zhang, Xiyue; Ding, Michael S. S.; Hwang, Sooyeon; Su, Dong; Ren, Yang; Yang, Xiao-Qing; Wang, Howard; Borodin, Oleg; Wang, Chunsheng",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "All-temperature zinc batteries with high-entropy aqueous electrolyte",
|
|
"Source Title": "NATURE SUSTAINABILITY",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Electrification of transportation and rising demand for grid energy storage continue to build momentum around batteries across the globe. However, the supply chain of Li-ion batteries is exposed to the increasing challenges of resourcing essential and scarce materials. Therefore, incentives to develop more sustainable battery chemistries are growing. Here we show an aqueous ZnCl2 electrolyte with introduced LiCl as supporting salt. Once the electrolyte is optimized to Li2ZnCl4.9H(2)O, the assembled Zn-air battery can sustain stable cycling over the course of 800 hours at a current density of 0.4 mA cm-2 between -60 degrees C and +80 degrees C, with 100% Coulombic efficiency for Zn stripping/plating. Even at -60 degrees C, > 80% of room-temperature power density can be retained. Advanced characterization and theoretical calculations reveal a high-entropy solvation structure that is responsible for the excellent performance. The strong acidity allows ZnCl2 to accept donated Cl- ions to form ZnCl42- anions, while water molecules remain within the free solvent network at low salt concentration or coordinate with Li ions. Our work suggests an effective strategy for the rational design of electrolytes that could enable next-generation Zn batteries.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 215,
|
|
"Times Cited, All Databases": 223,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "MAR",
|
|
"Publication Year": 2023,
|
|
"Volume": 6,
|
|
"Issue": 3,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 325,
|
|
"End Page": 335,
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s41893-022-01028-x",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41893-022-01028-x",
|
|
"Book DOI": null,
|
|
"Early Access Date": "JAN 2023",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics; Environmental Sciences & Ecology",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000913832800005",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Wu, D; Guo, CG; Zeng, LH; Ren, XY; Shi, ZF; Wen, L; Chen, Q; Zhang, M; Li, XJ; Shan, CX; Jie, JS",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Wu, Di; Guo, Chenguang; Zeng, Longhui; Ren, Xiaoyan; Shi, Zhifeng; Wen, Long; Chen, Qin; Zhang, Meng; Li, Xin Jian; Shan, Chong-Xin; Jie, Jiansheng",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Phase-controlled van der Waals growth of wafer-scale 2D MoTe2 layers for integrated high-sensitivity broadband infrared photodetection",
|
|
"Source Title": "LIGHT-SCIENCE & APPLICATIONS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
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"Conference Title": null,
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|
"Conference Date": null,
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"Conference Location": null,
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"Conference Sponsor": null,
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|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Being capable of sensing broadband infrared (IR) light is vitally important for wide-ranging applications from fundamental science to industrial purposes. Two-dimensional (2D) topological semimetals are being extensively explored for broadband IR detection due to their gapless electronic structure and the linear energy dispersion relation. However, the low charge separation efficiency, high noise level, and on-chip integration difficulty of these semimetals significantly hinder their further technological applications. Here, we demonstrate a facile thermal-assisted tellurization route for the van der Waals (vdW) growth of wafer-scale phase-controlled 2D MoTe2 layers. Importantly, the type-II Weyl semimetal 1T'-MoTe2 features a unique orthorhombic lattice structure with a broken inversion symmetry, which ensures efficient carrier transportation and thus reduces the carrier recombination. This characteristic is a key merit for the well-designed 1T'-MoTe2/Si vertical Schottky junction photodetector to achieve excellent performance with an ultrabroadband detection range of up to 10.6 mu m and a large room temperature specific detectivity of over 10(8) Jones in the mid-infrared (MIR) range. Moreover, the large-area synthesis of 2D MoTe2 layers enables the demonstration of high-resolution uncooled MIR imaging capability by using an integrated device array. This work provides a new approach to assembling uncooled IR photodetectors based on 2D materials.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 215,
|
|
"Times Cited, All Databases": 221,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JAN 2",
|
|
"Publication Year": 2023,
|
|
"Volume": 12,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s41377-022-01047-5",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41377-022-01047-5",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Optics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000906375800001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Qiao, LP; Liang, YP; Chen, JY; Huang, Y; Alsareii, SA; Alamri, AM; Harraz, FA; Guo, BL",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Qiao, Lipeng; Liang, Yongping; Chen, Jueying; Huang, Ying; Alsareii, Saeed A.; Alamri, Abdulrahman Manaa; Harraz, Farid A.; Guo, Baolin",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Antibacterial conductive self-healing hydrogel wound dressing with dual dynamic bonds promotes infected wound healing",
|
|
"Source Title": "BIOACTIVE MATERIALS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "In clinical applications, there is a lack of wound dressings that combine efficient resistance to drug-resistant bacteria with good self-healing properties. In this study, a series of adhesive self-healing conductive antibacte-rial hydrogel dressings based on oxidized sodium alginate-grafted dopamine/carboxymethyl chitosan/Fe3+ (OSD/CMC/Fe hydrogel)/polydopamine-encapsulated poly(thiophene-3-acetic acid) (OSD/CMC/Fe/PA hydro-gel) were prepared for the repair of infected wound. The Schiff base and Fe3+ coordination bonds of the hydrogel structure are dynamic bonds that can be repaired automatically after the hydrogel network is disrupted. Macroscopically, the hydrogel exhibits self-healing properties, allowing the hydrogel dressing to adapt to complex wound surfaces. The OSD/CMC/Fe/PA hydrogel showed good conductivity and photothermal anti-bacterial properties under near-infrared (NIR) light irradiation. In addition, the hydrogels exhibit tunable rheological properties, suitable mechanical properties, antioxidant properties, tissue adhesion properties and hemostatic properties. Furthermore, all hydrogel dressings improved wound healing in the infected full-thickness defect skin wound repair test in mice. The wound size repaired by OSD/CMC/Fe/PA3 hydrogel + NIR was much smaller (12%) than the control group treated with TegadermTM film after 14 days. In conclusion, the hydrogels have high antibacterial efficiency, suitable conductivity, great self-healing properties, good biocompatibility, hemostasis and antioxidant properties, making them promising candidates for wound healing dressings for the treatment of infected skin wounds.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 231,
|
|
"Times Cited, All Databases": 237,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "DEC",
|
|
"Publication Year": 2023,
|
|
"Volume": 30,
|
|
"Issue": null,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 129,
|
|
"End Page": 141,
|
|
"Article Number": null,
|
|
"DOI": "10.1016/j.bioactmat.2023.07.015",
|
|
"DOI Link": "http://dx.doi.org/10.1016/j.bioactmat.2023.07.015",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Engineering; Materials Science",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001053110100001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Zeng, YH; Xia, ZC; Kang, KF; Zhu, JC; Knueppel, P; Vaswani, C; Watanabe, K; Taniguchi, T; Mak, KF; Shan, J",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Zeng, Yihang; Xia, Zhengchao; Kang, Kaifei; Zhu, Jiacheng; Knueppel, Patrick; Vaswani, Chirag; Watanabe, Kenji; Taniguchi, Takashi; Mak, Kin Fai; Shan, Jie",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Thermodynamic evidence of fractional Chern insulator in moiré MoTe2",
|
|
"Source Title": "NATURE",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Chern insulators, which are the lattice analogues of the quantum Hall states, can potentially manifest high-temperature topological orders at zero magnetic field to enable next-generation topological quantum devices(1-3). Until now, integer Chern insulators have been experimentally demonstrated in several systems at zero magnetic field(3-8), whereas fractional Chern insulators have been reported in only graphene-based systems under a finite magnetic field(9,10). The emergence of semiconductor moire materials(11), which support tunable topological flat bands(12,13), provides an opportunity to realize fractional Chern insulators(13-16). Here we report thermodynamic evidence of both integer and fractional Chern insulators at zero magnetic field in small-angle twisted bilayer MoTe2 by combining the local electronic compressibility and magneto-optical measurements. At hole filling factor nu = 1 and 2/3, the system is incompressible and spontaneously breaks time-reversal symmetry. We show that they are integer and fractional Chern insulators, respectively, from the dispersion of the state in the filling factor with an applied magnetic field. We further demonstrate electric-field-tuned topological phase transitions involving the Chern insulators. Our findings pave the way for the demonstration of quantized fractional Hall conductance and anyonic excitation and braiding17 in semiconductor moire materials.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 213,
|
|
"Times Cited, All Databases": 221,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "OCT 5",
|
|
"Publication Year": 2023,
|
|
"Volume": 622,
|
|
"Issue": 7981,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s41586-023-06452-3",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41586-023-06452-3",
|
|
"Book DOI": null,
|
|
"Early Access Date": "JUL 2023",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001078346100001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Qin, CC; Wu, XD; Tang, L; Chen, XH; Li, M; Mou, Y; Su, B; Wang, SB; Feng, CY; Liu, JW; Yuan, XZ; Zhao, YL; Wang, H",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Qin, Chencheng; Wu, Xiaodong; Tang, Lin; Chen, Xiaohong; Li, Miao; Mou, Yi; Su, Bo; Wang, Sibo; Feng, Chengyang; Liu, Jiawei; Yuan, Xingzhong; Zhao, Yanli; Wang, Hou",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Dual donor-acceptor covalent organic frameworks for hydrogen peroxide photosynthesis",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Constructing photocatalytically active and stable covalent organic frameworks containing both oxidative and reductive reaction centers remain a challenge. In this study, benzotrithiophene-based covalent organic frameworks with spatially separated redox centers are rationally designed for the photocatalytic production of hydrogen peroxide from water and oxygen without sacrificial agents. The triazine-containing framework demonstrates high selectivity for H2O2 photogeneration, with a yield rate of 2111 mu Mh(-1) (21.11 mu mol h(-1) and 1407 mu mol g(-1) h(-1)) and a solar-to-chemical conversion efficiency of 0.296%. Codirectional charge transfer and large energetic differences between linkages and linkers are verified in the double donor-acceptor structures of periodic frameworks. The active sites are mainly concentrated on the electron-acceptor fragments near the imine bond, which regulate the electron distribution of adjacent carbon atoms to optimally reduce the Gibbs free energy of O-2* and OOH* intermediates during the formation of H2O2.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 213,
|
|
"Times Cited, All Databases": 216,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "AUG 28",
|
|
"Publication Year": 2023,
|
|
"Volume": 14,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 5238,
|
|
"DOI": "10.1038/s41467-023-40991-7",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-023-40991-7",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001057573200013",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Kang, X; Yang, FN; Zhang, ZY; Liu, HM; Ge, SY; Hu, SQ; Li, SH; Luo, YT; Yu, QM; Liu, ZB; Wang, Q; Ren, WC; Sun, CH; Cheng, HM; Liu, BL",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Kang, Xin; Yang, Fengning; Zhang, Zhiyuan; Liu, Heming; Ge, Shiyu; Hu, Shuqi; Li, Shaohai; Luo, Yuting; Yu, Qiangmin; Liu, Zhibo; Wang, Qiang; Ren, Wencai; Sun, Chenghua; Cheng, Hui-Ming; Liu, Bilu",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "A corrosion-resistant RuMoNi catalyst for efficient and long-lasting seawater oxidation and anion exchange membrane electrolyzer",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Direct seawater electrolysis is promising for sustainable hydrogen production but suffers severe side reactions and corrosion. Here, the authors report a corrosion-resistant electrocatalyst with in situ-formed chloride-ion-repelling cation layer for efficient and long-lasting seawater oxidation. Direct seawater electrolysis is promising for sustainable hydrogen gas (H-2) production. However, the chloride ions in seawater lead to side reactions and corrosion, which result in a low efficiency and poor stability of the electrocatalyst and hinder the use of seawater electrolysis technology. Here we report a corrosion-resistant RuMoNi electrocatalyst, in which the in situ-formed molybdate ions on its surface repel chloride ions. The electrocatalyst works stably for over 3000 h at a high current density of 500 mA cm(-2) in alkaline seawater electrolytes. Using the RuMoNi catalyst in an anion exchange membrane electrolyzer, we report an energy conversion efficiency of 77.9% and a current density of 1000 mA cm(-2) at 1.72 V. The calculated price per gallon of gasoline equivalent (GGE) of the H-2 produced is $ 0.85, which is lower than the 2026 technical target of $ 2.0/GGE set by the United Stated Department of Energy, thus, suggesting practicability of the technology.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 216,
|
|
"Times Cited, All Databases": 216,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JUN 17",
|
|
"Publication Year": 2023,
|
|
"Volume": 14,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 3607,
|
|
"DOI": "10.1038/s41467-023-39386-5",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-023-39386-5",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
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"Open Access Designations": null,
|
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"Highly Cited Status": "Y",
|
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"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001009499200009",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Sun, X; Qiu, Y; Jiang, B; Chen, ZY; Zhao, CH; Zhou, H; Yang, L; Fan, LS; Zhang, Y; Zhang, NQ",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Sun, Xun; Qiu, Yue; Jiang, Bo; Chen, Zhaoyu; Zhao, Chenghao; Zhou, Hao; Yang, Li; Fan, Lishuang; Zhang, Yu; Zhang, Naiqing",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
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"Article Title": "Isolated Fe-Co heteronuclear diatomic sites as efficient bifunctional catalysts for high-performance lithium-sulfur batteries",
|
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"Source Title": "NATURE COMMUNICATIONS",
|
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"Book Series Title": null,
|
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"Book Series Subtitle": null,
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"Language": null,
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"Document Type": "Article",
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"Author Keywords": null,
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"Keywords Plus": null,
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"Abstract": "The slow redox kinetics of polysulfides and the difficulties in decomposition of Li2S are two serious obstacles to lithium-sulfur batteries. Here, the authors report an isolated Fe-Co heteronuclear diatomic catalyst to achieve high efficiency bifunctional catalysis for lithium-sulfur batteries. The slow redox kinetics of polysulfides and the difficulties in decomposition of Li2S during the charge and discharge processes are two serious obstacles to the practical application of lithium-sulfur batteries. Herein, we construct the Fe-Co diatomic catalytic materials supported by hollow carbon spheres to achieve high-efficiency catalysis for the conversion of polysulfides and the decomposition of Li2S simultaneously. The Fe atom center is beneficial to accelerate the discharge reaction process, and the Co atom center is favorable for charging process. Theoretical calculations combined with experiments reveal that this excellent bifunctional catalytic activity originates from the diatomic synergy between Fe and Co atom. As a result, the assembled cells exhibit the high rate performance (the discharge specific capacity achieves 688 mAh g(-1) at 5 C) and the excellent cycle stability (the capacity decay rate is 0.018% for 1000 cycles at 1 C).",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
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"Researcher Ids": null,
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"ORCIDs": null,
|
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"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
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"Cited Reference Count": null,
|
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"Times Cited, WoS Core": 205,
|
|
"Times Cited, All Databases": 207,
|
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"180 Day Usage Count": null,
|
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"Since 2013 Usage Count": null,
|
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"Publisher": null,
|
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"Publisher City": null,
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"Publisher Address": null,
|
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"ISSN": null,
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"eISSN": null,
|
|
"ISBN": null,
|
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"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JAN 18",
|
|
"Publication Year": 2023,
|
|
"Volume": 14,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
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"Article Number": 291,
|
|
"DOI": "10.1038/s41467-022-35736-x",
|
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"DOI Link": "http://dx.doi.org/10.1038/s41467-022-35736-x",
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"Number of Pages": null,
|
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"WoS Categories": null,
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"Web of Science Index": null,
|
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"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
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"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001006189100004",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Yang, GX; Gong, ZG; Luo, XL; Chen, LH; Shuai, L",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
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"Author Full Names": "Yang, Guangxu; Gong, Zhenggang; Luo, Xiaolin; Chen, Lihui; Shuai, Li",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
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"Article Title": "Bonding wood with uncondensed lignins as adhesives",
|
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"Source Title": "NATURE",
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"Book Series Title": null,
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"Book Series Subtitle": null,
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"Keywords Plus": null,
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"Abstract": "Plywood is widely used in construction, such as for flooring and interior walls, as well as in the manufacture of household items such as furniture and cabinets. Such items are made of wood veneers that are bonded together with adhesives such as urea-formaldehyde and phenol-formaldehyde resins1,2. Researchers in academia and industry have long aimed to synthesize lignin-phenol-formaldehyde resin adhesives using biomass-derived lignin, a phenolic polymer that can be used to substitute the petroleum-derived phenol3-6. However, lignin-phenol-formaldehyde resin adhesives are less attractive to plywood manufacturers than urea-formaldehyde and phenol-formaldehyde resins owing to their appearance and cost. Here we report a simple and practical strategy for preparing lignin-based wood adhesives from lignocellulosic biomass. Our strategy involves separation of uncondensed or slightly condensed lignins from biomass followed by direct application of a suspension of the lignin and water as an adhesive on wood veneers. Plywood products with superior performances could be prepared with such lignin adhesives at a wide range of hot-pressing temperatures, enabling the use of these adhesives as promising alternatives to traditional wood adhesives in different market segments. Mechanistic studies indicate that the adhesion mechanism of such lignin adhesives may involve softening of lignin by water, filling of vessels with softened lignin and crosslinking of lignins in adhesives with those in the cell wall. A straightforward strategy for preparing lignin-based wood adhesives from lignocellulosic biomass is described, with the resulting adhesives demonstrating performance attractive for plywood manufacture.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
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"Researcher Ids": null,
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"ORCIDs": null,
|
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"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 206,
|
|
"Times Cited, All Databases": 208,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "SEP 21",
|
|
"Publication Year": 2023,
|
|
"Volume": 621,
|
|
"Issue": 7979,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 511,
|
|
"End Page": "+",
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s41586-023-06507-5",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41586-023-06507-5",
|
|
"Book DOI": null,
|
|
"Early Access Date": "AUG 2023",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001059705300001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Cao, QH; Gao, Y; Pu, J; Zhao, X; Wang, YX; Chen, JP; Guan, C",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Cao, Qinghe; Gao, Yong; Pu, Jie; Zhao, Xin; Wang, Yuxuan; Chen, Jipeng; Guan, Cao",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Gradient design of imprinted anode for stable Zn-ion batteries",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
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"Document Type": "Article",
|
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|
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|
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"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Zinc metal anodes suffer from electrolyte corrosion and dendrite growth issues during electrochemical cycling. Here, the authors propose a gradient design to imprint the zinc anode, which both prohibits side reactions and alleviates zinc deposition behaviour. Achieving long-term stable zinc anodes at high currents/capacities remains a great challenge for practical rechargeable zinc-ion batteries. Herein, we report an imprinted gradient zinc electrode that integrates gradient conductivity and hydrophilicity for long-term dendrite-free zinc-ion batteries. The gradient design not only effectively prohibits side reactions between the electrolyte and the zinc anode, but also synergistically optimizes electric field distribution, zinc ion flux and local current density, which induces preferentially deposited zinc in the bottom of the microchannels and suppresses dendrite growth even under high current densities/capacities. As a result, the imprinted gradient zinc anode can be stably cycled for 200 h at a high current density/capacity of 10 mA cm(-2)/10 mAh cm(-2), with a high cumulative capacity of 1000 mAh cm(-2), which outperforms the none-gradient counterparts and bare zinc. The imprinted gradient design can be easily scaled up, and a high-performance large-area pouch cell (4*5 cm(2)) is also demonstrated.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 211,
|
|
"Times Cited, All Databases": 214,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "FEB 6",
|
|
"Publication Year": 2023,
|
|
"Volume": 14,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s41467-023-36386-3",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-023-36386-3",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000954587000010",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Zhang, SC; Tan, CH; Yan, RP; Zou, XF; Hu, FL; Mi, Y; Yan, C; Zhao, SL",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Zhang, Shucong; Tan, Chunhui; Yan, Ruipeng; Zou, Xifei; Hu, Fei-Long; Mi, Yan; Yan, Cheng; Zhao, Shenlong",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Constructing Built-in Electric Field in Heterogeneous nullowire Arrays for Efficient Overall Water Electrolysis",
|
|
"Source Title": "ANGEWANDTE CHEMIE-INTERNATIONAL EDITION",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Efficient bifunctional electrocatalysts for hydrogen and oxygen evolution reactions are key to water electrolysis. Herein, we report a built-in electric field (BEF) strategy to fabricate heterogeneous nickel phosphide-cobalt nullowire arrays grown on carbon fiber paper (Ni2P-CoCH/CFP) with large work function difference (Delta phi) as bifunctional electrocatalysts for overall water splitting. Impressively, Ni2P-CoCH/CFP exhibits a remarkable catalytic activity for hydrogen and oxygen evolution reactions to obtain 10 mA cm(-2), respectively. Moreover, the assembled lab-scale electrolyzer driven by an AAA battery delivers excellent stability after 50 h electrocatalysis with a 100 % faradic efficiency. Computational calculations combining with experiments reveal the interface-induced electric field effect facilitates asymmetrical charge distributions, thereby regulating the adsorption/desorption of the intermediates during reactions. This work offers an avenue to rationally design high-performance heterogeneous electrocatalysts.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 201,
|
|
"Times Cited, All Databases": 202,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JUN 26",
|
|
"Publication Year": 2023,
|
|
"Volume": 62,
|
|
"Issue": 26,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": null,
|
|
"DOI": "10.1002/anie.202302795",
|
|
"DOI Link": "http://dx.doi.org/10.1002/anie.202302795",
|
|
"Book DOI": null,
|
|
"Early Access Date": "MAY 2023",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000989587300001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Huang, W; Chen, JH; Yao, Y; Zheng, D; Ji, XD; Feng, LW; Moore, D; Glavin, NR; Xie, M; Chen, Y; Pankow, RM; Surendran, A; Wang, Z; Xia, Y; Bai, LB; Rivnay, J; Ping, JF; Guo, XG; Cheng, YH; Marks, TJ; Facchetti, A",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Huang, Wei; Chen, Jianhua; Yao, Yao; Zheng, Ding; Ji, Xudong; Feng, Liang-Wen; Moore, David; Glavin, Nicholas R.; Xie, Miao; Chen, Yao; Pankow, Robert M.; Surendran, Abhijith; Wang, Zhi; Xia, Yu; Bai, Libing; Rivnay, Jonathan; Ping, Jianfeng; Guo, Xugang; Cheng, Yuhua; Marks, Tobin J.; Facchetti, Antonio",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Vertical organic electrochemical transistors for complementary circuits",
|
|
"Source Title": "NATURE",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Organic electrochemical transistors (OECTs) and OECT-based circuitry offer great potential in bioelectronics, wearable electronics and artificial neuromorphic electronics because of their exceptionally low driving voltages (< 1 V), low power consumption (< 1 mu W), high transconductances (> 10 mS) and biocompatibility(1-5). However, the successful realization of critical complementary logic OECTs is currently limited by temporal and/or operational instability, slow redox processes and/or switching, incompatibility with high-density monolithic integration and inferior n-type OECT performance(6-8). Here we demonstrate p- and n-type vertical OECTs with balanced and ultra-high performance by blending redox-active semiconducting polymers with a redox-inactive photocurable and/or photopatternable polymer to form an ion-permeable semiconducting channel, implemented in a simple, scalable vertical architecture that has a dense, impermeable top contact. Footprint current densities exceeding 1 kA cm(-2) at less than +/- 0.7 V, transconductances of 0.2-0.4 S, short transient times of less than 1 ms and ultra-stable switching (> 50,000 cycles) are achieved in, to our knowledge, the first vertically stacked complementary vertical OECT logic circuits. This architecture opens many possibilities for fundamental studies of organic semiconductor redox chemistry and physics in nulloscopically confined spaces, without macroscopic electrolyte contact, as well as wearable and implantable device applications.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 200,
|
|
"Times Cited, All Databases": 212,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JAN 19",
|
|
"Publication Year": 2023,
|
|
"Volume": 613,
|
|
"Issue": 7944,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 496,
|
|
"End Page": 502,
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s41586-022-05592-2",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41586-022-05592-2",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000922739000002",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Rao, MY; Tang, H; Wu, JB; Song, WH; Zhang, MX; Yin, WB; Zhuo, Y; Kiani, F; Chen, BJM; Jiang, XQ; Liu, HF; Chen, HY; Midya, R; Ye, F; Jiang, H; Wang, ZR; Wu, MC; Hu, M; Wang, H; Xia, QF; Ge, N; Li, J; Yang, JJ",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Rao, Mingyi; Tang, Hao; Wu, Jiangbin; Song, Wenhao; Zhang, Max; Yin, Wenbo; Zhuo, Ye; Kiani, Fatemeh; Chen, Benjamin; Jiang, Xiangqi; Liu, Hefei; Chen, Hung-Yu; Midya, Rivu; Ye, Fan; Jiang, Hao; Wang, Zhongrui; Wu, Mingche; Hu, Miao; Wang, Han; Xia, Qiangfei; Ge, Ning; Li, Ju; Yang, J. Joshua",
|
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"Book Author Full Names": null,
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"Group Authors": null,
|
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"Article Title": "Thousands of conductance levels in memristors integrated on CMOS",
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"Source Title": "NATURE",
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"Book Series Title": null,
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"Book Series Subtitle": null,
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"Author Keywords": null,
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"Keywords Plus": null,
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"Abstract": "Neural networks based on memristive devices(1-3) have the ability to improve throughput and energy efficiency for machine learning(4,5) and artificial intelligence(6), especially in edge applications(7-21). Because training a neural network model from scratch is costly in terms of hardware resources, time and energy, it is impractical to do it individually on billions of memristive neural networks distributed at the edge. A practical approach would be to download the synaptic weights obtained from the cloud training and program them directly into memristors for the commercialization of edge applications. Some post-tuning in memristor conductance could be done afterwards or during applications to adapt to specific situations. Therefore, in neural network applications, memristors require high-precision programmability to guarantee uniform and accurate performance across a large number of memristive networks(22-28). This requires many distinguishable conductance levels on each memristive device, not only laboratory-made devices but also devices fabricated in factories. Analog memristors with many conductance states also benefit other applications, such as neural network training, scientific computing and even `mortal computing'(25,29,30.) Here we report 2,048 conductance levels achieved with memristors in fully integrated chips with 256 x 256 memristor arrays monolithically integrated on complementary metal-oxide-semiconductor (CMOS) circuits in a commercial foundry. We have identified the underlying physics that previously limited the number of conductance levels that could be achieved in memristors and developed electrical operation protocols to avoid such limitations. These results provide insights into the fundamental understanding of the microscopic picture of memristive switching as well as approaches to enable high-precision memristors for various applications.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
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"Email Addresses": null,
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"Researcher Ids": null,
|
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"ORCIDs": null,
|
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"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 204,
|
|
"Times Cited, All Databases": 216,
|
|
"180 Day Usage Count": null,
|
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"Since 2013 Usage Count": null,
|
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"Publisher": null,
|
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"Publisher City": null,
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"Publisher Address": null,
|
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"ISSN": null,
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"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "MAR 30",
|
|
"Publication Year": 2023,
|
|
"Volume": 615,
|
|
"Issue": 7954,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 823,
|
|
"End Page": 829,
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s41586-023-05759-5",
|
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"DOI Link": "http://dx.doi.org/10.1038/s41586-023-05759-5",
|
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"Book DOI": null,
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"Early Access Date": null,
|
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"Number of Pages": null,
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"WoS Categories": null,
|
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"Web of Science Index": null,
|
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"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000961772700001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Wang, YB; Li, Q; Hong, H; Yang, S; Zhang, R; Wang, XQ; Jin, X; Xiong, B; Bai, SC; Zhi, CY",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
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"Author Full Names": "Wang, Yanbo; Li, Qing; Hong, Hu; Yang, Shuo; Zhang, Rong; Wang, Xiaoqi; Jin, Xu; Xiong, Bo; Bai, Shengchi; Zhi, Chunyi",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Lean-water hydrogel electrolyte for zinc ion batteries",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
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"Book Series Title": null,
|
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"Book Series Subtitle": null,
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"Language": null,
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"Document Type": "Article",
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"Conference Title": null,
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"Conference Date": null,
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"Conference Location": null,
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"Conference Sponsor": null,
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"Conference Host": null,
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|
"Author Keywords": null,
|
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"Keywords Plus": null,
|
|
"Abstract": "Solid polymer electrolytes (SPEs) and hydrogel electrolytes were developed as electrolytes for zinc ion batteries (ZIBs). Hydrogels can retain water molecules and provide high ionic conductivities; however, they contain many free water molecules, inevitably causing side reactions on the zinc anode. SPEs can enhance the stability of anodes, but they typically possess low ionic conductivities and result in high impedance. Here, we develop a lean water hydrogel electrolyte, aiming to balance ion transfer, anode stability, electrochemical stability window and resistance. This hydrogel is equipped with a molecular lubrication mechanism to ensure fast ion transportation. Additionally, this design leads to a widened electrochemical stability window and highly reversible zinc plating/ stripping. The full cell shows excellent cycling stability and capacity retentions at high and low current rates, respectively. Moreover, superior adhesion ability can be achieved, meeting the needs of flexible devices. Excess water in hydrogel-based zinc ion batteries causes side reactions, but reduced water content results in low conductivities. Here, authors develop a lean-water hydrogel based on molecular lubrication mechanism for fast ion transportation, extended stability, and reversible Zinc plating/stripping.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
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"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 212,
|
|
"Times Cited, All Databases": 215,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JUL 1",
|
|
"Publication Year": 2023,
|
|
"Volume": 14,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 3890,
|
|
"DOI": "10.1038/s41467-023-39634-8",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-023-39634-8",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001022536900008",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Yokoyama, T; Nagashima, K; Nakai, I; Young, ED; Abe, Y; Aleon, J; Alexander, CMO; Amari, S; Amelin, Y; Bajo, KI; Bizzarro, M; Bouvier, A; Carlson, RW; Chaussidon, M; Choi, BG; Dauphas, N; Davis, AM; Di Rocco, T; Fujiya, W; Fukai, R; Gautam, I; Haba, MK; Hibiya, Y; Hidaka, H; Homma, H; Hoppe, P; Huss, GR; Ichida, K; Iizuka, T; Ireland, TR; Ishikawa, A; Ito, M; Itoh, S; Kawasaki, N; Kita, NT; Kitajima, K; Kleine, T; Komatani, S; Krot, AN; Liu, MC; Masuda, Y; McKeegan, KD; Morita, M; Motomura, K; Moynier, F; Nguyen, A; Nittler, L; Onose, M; Pack, A; Park, C; Piani, L; Qin, LP; Russell, SS; Sakamoto, N; Schoenbaechler, M; Tafla, L; Tang, HL; Terada, K; Terada, Y; Usui, T; Wada, S; Wadhwa, M; Walker, RJ; Yamashita, K; Yin, QZ; Yoneda, S; Yui, H; Zhang, AC; Connolly, HC Jr; Lauretta, DS; Nakamura, T; Naraoka, H; Noguchi, T; Okazaki, R; Sakamoto, K; Yabuta, H; Abe, M; Arakawa, M; Fujii, A; Hayakawa, M; Hirata, N; Hirata, N; Honda, R; Honda, C; Hosoda, S; Iijima, Y; Ikeda, H; Ishiguro, M; Ishihara, Y; Iwata, T; Kawahara, K; Kikuchi, S; Kitazato, K; Matsumoto, K; Matsuoka, M; Michikami, T; Mimasu, Y; Miura, A; Morota, T; Nakazawa, S; Namiki, N; Noda, H; Noguchi, R; Ogawa, N; Ogawa, K; Okada, T; Okamoto, C; Ono, G; Ozaki, M; Saiki, T; Sakatani, N; Sawada, H; Senshu, H; Shimaki, Y; Shirai, K; Sugita, S; Takei, Y; Takeuchi, H; Tanaka, S; Tatsumi, E; Terui, F; Tsuda, Y; Tsukizaki, R; Wada, K; Watanabe, SI; Yamada, M; Yamada, T; Yamamoto, Y; Yano, H; Yokota, Y; Yoshihara, K; Yoshikawa, M; Yoshikawa, K; Furuya, S; Hatakeda, K; Hayashi, T; Hitomi, Y; Kumagai, K; Miyazaki, A; Nakato, A; Nishimura, M; Soejima, H; Suzuki, A; Yada, T; Yamamoto, D; Yogata, K; Yoshitake, M; Tachibana, S; Yurimoto, H",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Yokoyama, Tetsuya; Nagashima, Kazuhide; Nakai, Izumi; Young, Edward D.; Abe, Yoshinari; Aleon, Jerome; Alexander, Conel M. O'D.; Amari, Sachiko; Amelin, Yuri; Bajo, Ken-ichi; Bizzarro, Martin; Bouvier, Audrey; Carlson, Richard W.; Chaussidon, Marc; Choi, Byeon-Gak; Dauphas, Nicolas; Davis, Andrew M.; Di Rocco, Tommaso; Fujiya, Wataru; Fukai, Ryota; Gautam, Ikshu; Haba, Makiko K.; Hibiya, Yuki; Hidaka, Hiroshi; Homma, Hisashi; Hoppe, Peter; Huss, Gary R.; Ichida, Kiyohiro; Iizuka, Tsuyoshi; Ireland, Trevor R.; Ishikawa, Akira; Ito, Motoo; Itoh, Shoichi; Kawasaki, Noriyuki; Kita, Noriko T.; Kitajima, Kouki; Kleine, Thorsten; Komatani, Shintaro; Krot, Alexander N.; Liu, Ming-Chang; Masuda, Yuki; McKeegan, Kevin D.; Morita, Mayu; Motomura, Kazuko; Moynier, Frederic; Nguyen, Ann; Nittler, Larry; Onose, Morihiko; Pack, Andreas; Park, Changkun; Piani, Laurette; Qin, Liping; Russell, Sara S.; Sakamoto, Naoya; Schoenbaechler, Maria; Tafla, Lauren; Tang, Haolan; Terada, Kentaro; Terada, Yasuko; Usui, Tomohiro; Wada, Sohei; Wadhwa, Meenakshi; Walker, Richard J.; Yamashita, Katsuyuki; Yin, Qing-Zhu; Yoneda, Shigekazu; Yui, Hiroharu; Zhang, Ai-Cheng; Connolly Jr, Harold C.; Lauretta, Dante S.; Nakamura, Tomoki; Naraoka, Hiroshi; Noguchi, Takaaki; Okazaki, Ryuji; Sakamoto, Kanako; Yabuta, Hikaru; Abe, Masanao; Arakawa, Masahiko; Fujii, Atsushi; Hayakawa, Masahiko; Hirata, Naoyuki; Hirata, Naru; Honda, Rie; Honda, Chikatoshi; Hosoda, Satoshi; Iijima, Yu-ichi; Ikeda, Hitoshi; Ishiguro, Masateru; Ishihara, Yoshiaki; Iwata, Takahiro; Kawahara, Kosuke; Kikuchi, Shota; Kitazato, Kohei; Matsumoto, Koji; Matsuoka, Moe; Michikami, Tatsuhiro; Mimasu, Yuya; Miura, Akira; Morota, Tomokatsu; Nakazawa, Satoru; Namiki, Noriyuki; Noda, Hirotomo; Noguchi, Rina; Ogawa, Naoko; Ogawa, Kazunori; Okada, Tatsuaki; Okamoto, Chisato; Ono, Go; Ozaki, Masanobu; Saiki, Takanao; Sakatani, Naoya; Sawada, Hirotaka; Senshu, Hiroki; Shimaki, Yuri; Shirai, Kei; Sugita, Seiji; Takei, Yuto; Takeuchi, Hiroshi; Tanaka, Satoshi; Tatsumi, Eri; Terui, Fuyuto; Tsuda, Yuichi; Tsukizaki, Ryudo; Wada, Koji; Watanabe, Sei-ichiro; Yamada, Manabu; Yamada, Tetsuya; Yamamoto, Yukio; Yano, Hajime; Yokota, Yasuhiro; Yoshihara, Keisuke; Yoshikawa, Makoto; Yoshikawa, Kent; Furuya, Shizuho; Hatakeda, Kentaro; Hayashi, Tasuku; Hitomi, Yuya; Kumagai, Kazuya; Miyazaki, Akiko; Nakato, Aiko; Nishimura, Masahiro; Soejima, Hiromichi; Suzuki, Ayako; Yada, Toru; Yamamoto, Daiki; Yogata, Kasumi; Yoshitake, Miwa; Tachibana, Shogo; Yurimoto, Hisayoshi",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Samples returned from the asteroid Ryugu are similar to Ivuna-type carbonaceous meteorites",
|
|
"Source Title": "SCIENCE",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
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"Language": null,
|
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"Document Type": "Article",
|
|
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|
|
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|
|
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|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Carbonaceous meteorites are thought to be fragments of C-type (carbonaceous) asteroids. Samples of the C-type asteroid (162173) Ryugu were retrieved by the Hayabusa2 spacecraft. We measured the mineralogy and bulk chemical and isotopic compositions of Ryugu samples. The samples are mainly composed of materials similar to those of carbonaceous chondrite meteorites, particularly the CI (Ivuna-type) group. The samples consist predominulltly of minerals formed in aqueous fluid on a parent planetesimal. The primary minerals were altered by fluids at a temperature of 37 degrees +/- 10 degrees C, about 5.2(-0.7)(+0.8) million (statistical) or 5.2(-2.1)(+1.6) million (systematic) years after the formation of the first solids in the Solar System. After aqueous alteration, the Ryugu samples were likely never heated above similar to 100 degrees C. The samples have a chemical composition that more closely resembles that of the Sun's photosphere than other natural samples do.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 208,
|
|
"Times Cited, All Databases": 211,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "FEB 24",
|
|
"Publication Year": 2023,
|
|
"Volume": 379,
|
|
"Issue": 6634,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 786,
|
|
"End Page": "+",
|
|
"Article Number": "eabn7850",
|
|
"DOI": "10.1126/science.abn7850",
|
|
"DOI Link": "http://dx.doi.org/10.1126/science.abn7850",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000981670800001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Mao, ML; Ji, X; Wang, QY; Lin, ZJ; Li, MY; Liu, T; Wang, CL; Hu, YS; Li, H; Huang, XJ; Chen, LQ; Suo, LM",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Mao, Minglei; Ji, Xiao; Wang, Qiyu; Lin, Zejing; Li, Meiying; Liu, Tao; Wang, Chengliang; Hu, Yong-Sheng; Li, Hong; Huang, Xuejie; Chen, Liquan; Suo, Liumin",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Anion-enrichment interface enables high-voltage anode-free lithium metal batteries",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Aggressive chemistry involving Li metal anode (LMA) and high-voltage LiNi0.8Mn0.1Co0.1O2 (NCM811) cathode is deemed as a pragmatic approach to pursue the desperate 400 Wh kg(-1). Yet, their implementation is plagued by low Coulombic efficiency and inferior cycling stability. Herein, we propose an optimally fluorinated linear carboxylic ester (ethyl 3,3,3-trifluoropropanoate, FEP) paired with weakly solvating fluoroethylene carbonate and dissociated lithium salts (LiBF4 and LiDFOB) to prepare a weakly solvating and dissociated electrolyte. An anion-enrichment interface prompts more anions' decomposition in the inner Helmholtz plane and higher reduction potential of anions. Consequently, the anion-derived interface chemistry contributes to the compact and columnar-structure Li deposits with a high CE of 98.7% and stable cycling of 4.6 V NCM811 and LiCoO2 cathode. Accordingly, industrial anode-free pouch cells under harsh testing conditions deliver a high energy of 442.5 Wh kg(-1) with 80% capacity retention after 100 cycles. The implementation of Li metal anode with high-voltage Ni/Co rich cathode is plagued by low coulombic efficiency and inferior cycling stability. Here authors propose an anion-enriched interface to facilitate the columnar-structure of Li deposits to solve this issue.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 190,
|
|
"Times Cited, All Databases": 197,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "FEB 25",
|
|
"Publication Year": 2023,
|
|
"Volume": 14,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 1082,
|
|
"DOI": "10.1038/s41467-023-36853-x",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-023-36853-x",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001002656000019",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Su, JJ; Musgrave, CB; Song, Y; Huang, LB; Liu, Y; Li, G; Xin, YE; Xiong, P; Li, MMJ; Wu, HR; Zhu, MH; Chen, HM; Zhang, JY; Shen, HC; Tang, BZ; Robert, M; Goddard, W ; Ye, RQ",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Su, Jianjun; Musgrave, Charles B.; Song, Yun; Huang, Libei; Liu, Yong; Li, Geng; Xin, Yinger; Xiong, Pei; Li, Molly Meng-Jung; Wu, Haoran; Zhu, Minghui; Chen, Hao Ming; Zhang, Jianyu; Shen, Hanchen; Tang, Ben Zhong; Robert, Marc; Goddard, William A., III; Ye, Ruquan",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Strain enhances the activity of molecular electrocatalysts via carbon nullotube supports",
|
|
"Source Title": "NATURE CATALYSIS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
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"Language": null,
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"Document Type": "Article",
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"Conference Title": null,
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"Conference Date": null,
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"Conference Location": null,
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"Conference Sponsor": null,
|
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"Conference Host": null,
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"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Support-induced strain engineering is useful for modulating the properties of two-dimensional materials. However, controlling strain of planar molecules is technically challenging due to their sub-2 nm lateral size. Additionally, the effect of strain on molecular properties remains poorly understood. Here we show that carbon nullotubes (CNTs) are ideal substrates for inducing optimum properties through molecular curvature. In a tandem-flow electrolyser with monodispersed cobalt phthalocyanine (CoPc) on single-walled CNTs (CoPc/SWCNTs) for CO2 reduction, we achieve a methanol partial current density of >90 mA cm(-2) with >60% selectivity, surpassing wide multiwalled CNTs at 16.6%. We report vibronic and X-ray spectroscopies to unravel the distinct local geometries and electronic structures induced by the strong molecule-support interactions. Grand canonical density functional theory confirms that curved CoPc/SWCNTs improve *CO binding to enable subsequent reduction, whereas wide multiwalled CNTs favour CO desorption. Our results show the important role of SWCNTs beyond catalyst dispersion and electron conduction.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 195,
|
|
"Times Cited, All Databases": 200,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "SEP",
|
|
"Publication Year": 2023,
|
|
"Volume": 6,
|
|
"Issue": 9,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 818,
|
|
"End Page": 828,
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s41929-023-01005-3",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41929-023-01005-3",
|
|
"Book DOI": null,
|
|
"Early Access Date": "AUG 2023",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001048827200001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Zhang, ZL; Skripka, A; Dahl, JC; Dun, CC; Urban, JJ; Jaque, D; Schuck, PJ; Cohen, BE; Chan, EM",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Zhang, Zhuolei; Skripka, Artiom; Dahl, Jakob C.; Dun, Chaochao; Urban, Jeffrey J.; Jaque, Daniel; Schuck, P. James; Cohen, Bruce E.; Chan, Emory M.",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Tuning Phonon Energies in Lanthanide-doped Potassium Lead Halide nullocrystals for Enhanced Nonlinearity and Upconversion",
|
|
"Source Title": "ANGEWANDTE CHEMIE-INTERNATIONAL EDITION",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Optical applications of lanthanide-doped nulloparticles require materials with low phonon energies to minimize nonradiative relaxation and promote nonlinear processes like upconversion. Heavy halide hosts offer low phonon energies but are challenging to synthesize as nullocrystals. Here, we demonstrate the size-controlled synthesis of low-phonon-energy KPb2X5 (X=Cl, Br) nulloparticles and the ability to tune nullocrystal phonon energies as low as 128 cm(-1). KPb2Cl5 nulloparticles are moisture resistant and can be efficiently doped with lighter lanthanides. The low phonon energies of KPb2X5 nulloparticles promote upconversion luminescence from higher lanthanide excited states and enable highly nonlinear, avalanche-like emission from KPb2Cl5 : Nd3+ nulloparticles. The realization of nulloparticles with tunable, ultra-low phonon energies facilitates the discovery of nullomaterials with phonon-dependent properties, precisely engineered for applications in nulloscale imaging, sensing, luminescence thermometry and energy conversion.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 194,
|
|
"Times Cited, All Databases": 193,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JAN 2",
|
|
"Publication Year": 2023,
|
|
"Volume": 62,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": null,
|
|
"DOI": "10.1002/anie.202212549",
|
|
"DOI Link": "http://dx.doi.org/10.1002/anie.202212549",
|
|
"Book DOI": null,
|
|
"Early Access Date": "DEC 2022",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000898399100001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Liu, MQ; Wu, F; Gong, YT; Li, Y; Li, Y; Feng, X; Li, QJ; Wu, C; Bai, Y",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Liu, Mingquan; Wu, Feng; Gong, Yuteng; Li, Yu; Li, Ying; Feng, Xin; Li, Qiaojun; Wu, Chuan; Bai, Ying",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Interfacial-Catalysis-Enabled Layered and Inorganic-Rich SEI on Hard Carbon Anodes in Ester Electrolytes for Sodium-Ion Batteries",
|
|
"Source Title": "ADVANCED MATERIALS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Constructing a homogenous and inorganic-rich solid electrolyte interface (SEI) can efficiently improve the overall sodium-storage performance of hard carbon (HC) anodes. However, the thick and heterogenous SEI derived from conventional ester electrolytes fails to meet the above requirements. Herein, an innovative interfacial catalysis mechanism is proposed to design a favorable SEI in ester electrolytes by reconstructing the surface functionality of HC, of which abundant C(sic)O (carbonyl) bonds are accurately and homogenously implanted. The C(sic)O (carbonyl) bonds act as active centers that controllably catalyze the preferential reduction of salts and directionally guide SEI growth to form a homogenous, layered, and inorganic-rich SEI. Therefore, excessive solvent decomposition is suppressed, and the interfacial Na+ transfer and structural stability of SEI on HC anodes are greatly promoted, contributing to a comprehensive enhancement in sodium-storage performance. The optimal anodes exhibit an outstanding reversible capacity (379.6 mAh g(-1)), an ultrahigh initial Coulombic efficiency (93.2%), a largely improved rate capability, and an extremely stable cycling performance with a capacity decay rate of 0.0018% for 10 000 cycles at 5 A g(-1). This work provides novel insights into smart regulation of interface chemistry to realize high-performance HC anodes for sodium storage.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 185,
|
|
"Times Cited, All Databases": 191,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JUL",
|
|
"Publication Year": 2023,
|
|
"Volume": 35,
|
|
"Issue": 29,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": null,
|
|
"DOI": "10.1002/adma.202300002",
|
|
"DOI Link": "http://dx.doi.org/10.1002/adma.202300002",
|
|
"Book DOI": null,
|
|
"Early Access Date": "MAY 2023",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry; Science & Technology - Other Topics; Materials Science; Physics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000995947700001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Li, SJ; Wang, CC; Dong, KX; Zhang, P; Chen, XB; Li, X",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Li, Shijie; Wang, Chunchun; Dong, Kexin; Zhang, Peng; Chen, Xiaobo; Li, Xin",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "MIL-101(Fe)/BiOBr S-scheme photocatalyst for promoting photocatalytic abatement of Cr(VI) and enrofloxacin antibiotic: Performance and mechanism",
|
|
"Source Title": "CHINESE JOURNAL OF CATALYSIS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "The development of highly active, economical, and robust bifunctional photocatalysts is a priority for sustainable photocatalytic water remediation. Inadequately available reactive sites and sluggish interface photocarrier transfer and separation remain significant challenges in the photoreaction progress. In this study, the Fe-containing metal-organic framework (MOF) MIL-101(Fe) was inte-grated with BiOBr microspheres to form a competent S-scheme heterostructure for the photocatalytic mitigation of Cr(VI) and enrofloxacin (ENR) antibiotics. The optimal MIL-101(Fe)/BiOBr ex-hibited the highest photoactivity, with 99.4% of Cr(VI) and 84.4% of ENR eliminated upon visi-ble-light illumination in a single-pollutant system. The photoactivity of MIL-101(Fe)/BiOBr in the decontamination of the Cr(VI)-ENR co-existence system exhibited a substantial enhancement when compared to that in a single system, owing to the improved utilization of electrons and holes resulting from the synergism between Cr(VI), ENR, and the photocatalyst. The enhanced photoactivity is attributed to two aspects: (1) the incorporation of MIL-101(Fe) results in an increased number of available reactive sites and improved solar harvesting properties; and (2) the S-scheme mechanism enables the effective spatial disassociation of photoexcited carriers and optimization of the pho-to-redox capability of the system. Through scavenging experiments, electron spin resonullce characterization, liquid chromatography-tandem mass spectrometry analysis, and T.E.S.T. theoretical estimation, the catalytic mechanism, antibiotic degradation process, and biotoxicities of the de-graded products were analyzed and confirmed. This study provides a viable strategy for building competent MOF-inorganic semiconductor S-scheme photocatalysts with superior photocatalytic decontamination performance.(c) 2023, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 192,
|
|
"Times Cited, All Databases": 201,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "AUG",
|
|
"Publication Year": 2023,
|
|
"Volume": 51,
|
|
"Issue": null,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 101,
|
|
"End Page": 112,
|
|
"Article Number": null,
|
|
"DOI": "10.1016/S1872-2067(23)64479-1",
|
|
"DOI Link": "http://dx.doi.org/10.1016/S1872-2067(23)64479-1",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry; Engineering",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001136853100001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Shen, Y; Ren, CJ; Zheng, LR; Xu, XY; Long, R; Zhang, WQ; Yang, Y; Zhang, YC; Yao, YF; Chi, HQ; Wang, JL; Shen, Q; Xiong, YJ; Zou, ZG; Zhou, Y",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Shen, Yan; Ren, Chunjin; Zheng, Lirong; Xu, Xiaoyong; Long, Ran; Zhang, Wenqing; Yang, Yong; Zhang, Yongcai; Yao, Yingfang; Chi, Haoqiang; Wang, Jinlan; Shen, Qing; Xiong, Yujie; Zou, Zhigang; Zhou, Yong",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Room-temperature photosynthesis of propane from CO2 with Cu single atoms on vacancy-rich TiO2",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "A photocatalyst for CO2 reduction to C3H8 is prepared by implanting Cu single atoms on vacancy rich TiO2 single layers. Key reaction intermediates, *CHOCO and *CH2OCOCO, are stabilized on the catalyst which promotes C-C bond formation. Photochemical conversion of CO2 into high-value C2+ products is difficult to achieve due to the energetic and mechanistic challenges in forming multiple C-C bonds. Herein, an efficient photocatalyst for the conversion of CO2 into C3H8 is prepared by implanting Cu single atoms on Ti0.91O2 atomically-thin single layers. Cu single atoms promote the formation of neighbouring oxygen vacancies (V(O)s) in Ti0.91O2 matrix. These oxygen vacancies modulate the electronic coupling interaction between Cu atoms and adjacent Ti atoms to form a unique Cu-Ti-V-O unit in Ti0.91O2 matrix. A high electron-based selectivity of 64.8% for C3H8 (product-based selectivity of 32.4%), and 86.2% for total C2+ hydrocarbons (product-based selectivity of 50.2%) are achieved. Theoretical calculations suggest that Cu-Ti-V-O unit may stabilize the key *CHOCO and *CH2OCOCO intermediates and reduce their energy levels, tuning both C-1-C-1 and C-1-C-2 couplings into thermodynamically-favourable exothermal processes. Tandem catalysis mechanism and potential reaction pathway are tentatively proposed for C3H8 formation, involving an overall (20e(-) - 20H(+)) reduction and coupling of three CO2 molecules at room temperature.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 191,
|
|
"Times Cited, All Databases": 198,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "FEB 27",
|
|
"Publication Year": 2023,
|
|
"Volume": 14,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 1117,
|
|
"DOI": "10.1038/s41467-023-36778-5",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-023-36778-5",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000942107800020",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Li, MB; Sun, RM; Chang, JX; Dong, JJ; Tian, QS; Wang, HZ; Li, ZH; Yang, PH; Shi, HK; Yang, C; Wu, ZC; Li, RZ; Yang, YG; Wang, AF; Zhang, ST; Wang, FF; Huang, W; Qin, TS",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Li, Mubai; Sun, Riming; Chang, Jingxi; Dong, Jingjin; Tian, Qiushuang; Wang, Hongze; Li, Zihao; Yang, Pinghui; Shi, Haokun; Yang, Chao; Wu, Zichao; Li, Renzhi; Yang, Yingguo; Wang, Aifei; Zhang, Shitong; Wang, Fangfang; Huang, Wei; Qin, Tianshi",
|
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"Book Author Full Names": null,
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"Group Authors": null,
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"Article Title": "Orientated crystallization of FA-based perovskite via hydrogen-bonded polymer network for efficient and stable solar cells",
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"Source Title": "NATURE COMMUNICATIONS",
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"Abstract": "Incorporating mixed ion is a frequently used strategy to stabilize black-phase formamidinum lead iodide perovskite for high-efficiency solar cells. However, these devices commonly suffer from photoinduced phase segregation and humidity instability. Herein, we find that the underlying reason is that the mixed halide perovskites generally fail to grow into homogenous and highcrystalline film, due to the multiple pathways of crystal nucleation originating from various intermediate phases in the film-forming process. Therefore, we design a multifunctional fluorinated additive, which restrains the complicated intermediate phases and promotes orientated crystallization of a-phase of perovskite. Furthermore, the additives in-situ polymerize during the perovskite film formation and form a hydrogen-bonded network to stabilize aphase. Remarkably, the polymerized additives endow a strongly hydrophobic effect to the bare perovskite film against liquid water for 5min. The unencapsulated devices achieve 24.10% efficiency and maintain >95% of the initial efficiency for 1000 h under continuous sunlight soaking and for 2000 h at air ambient of similar to 50% humid, respectively.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
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"Reprint Addresses": null,
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"Email Addresses": null,
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"Researcher Ids": null,
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"ORCIDs": null,
|
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"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
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"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
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"Times Cited, WoS Core": 191,
|
|
"Times Cited, All Databases": 195,
|
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"180 Day Usage Count": null,
|
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"Since 2013 Usage Count": null,
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"Publisher": null,
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"Publisher City": null,
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"Publisher Address": null,
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"ISSN": null,
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|
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|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "FEB 2",
|
|
"Publication Year": 2023,
|
|
"Volume": 14,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
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"End Page": null,
|
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"Article Number": 573,
|
|
"DOI": "10.1038/s41467-023-36224-6",
|
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"DOI Link": "http://dx.doi.org/10.1038/s41467-023-36224-6",
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"Web of Science Index": null,
|
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"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
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"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001076389000015",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Yang, TH; Gao, LL; Lu, J; Ma, C; Du, YC; Wang, PJ; Ding, ZC; Wang, SQ; Xu, P; Liu, DL; Li, HJ; Chang, XM; Fang, JJ; Tian, WM; Yang, YG; Liu, SZ; Zhao, K",
|
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"Book Authors": null,
|
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"Author Full Names": "Yang, Tinghuan; Gao, Lili; Lu, Jing; Ma, Chuang; Du, Yachao; Wang, Peijun; Ding, Zicheng; Wang, Shiqiang; Xu, Peng; Liu, Dongle; Li, Haojin; Chang, Xiaoming; Fang, Junjie; Tian, Wenming; Yang, Yingguo; Liu, Shengzhong (Frank); Zhao, Kui",
|
|
"Book Author Full Names": null,
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"Group Authors": null,
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"Article Title": "One-stone-for-two-birds strategy to attain beyond 25% perovskite solar cells",
|
|
"Source Title": "NATURE COMMUNICATIONS",
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"Book Series Title": null,
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"Language": null,
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"Abstract": "Even though the perovskite solar cell has been so popular for its skyrocketing power conversion efficiency, its further development is still roadblocked by its overall performance, in particular long-term stability, large-area fabrication and stable module efficiency. In essence, the soft component and ionic-electronic nature of metal halide perovskites usually chaperonage large number of anion vacancy defects that act as recombination centers to decrease both the photovoltaic efficiency and operational stability. Herein, we report a one-stone-for-two-birds strategy in which both anion-fixation and associated undercoordinated-Pb passivation are in situ achieved during crystallization by using a single amidino-based ligand, namely 3-amidinopyridine, for metal-halide perovskite to overcome above challenges. The resultant devices attain a power conversion efficiency as high as 25.3% (certified at 24.8%) with substantially improved stability. Moreover, the device without encapsulation retained 92% of its initial efficiency after 5000 h exposure in ambient and the device with encapsulation retained 95% of its initial efficiency after >500 h working at the maximum power point under continuous light irradiation in ambient. It is expected this one-stone-for-two-birds strategy will benefit large-area fabrication that desires for simplicity. Long-term stability and stable efficiency are essential for large-area fabrication of perovskite solar cells. Here, the authors achieve in situ anion-fixation and undercoordinated-Pb passivation using amidino-based ligand, realizing maximum power conversion efficiency of 25.3% with T95 over 500 h.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
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"Researcher Ids": null,
|
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"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 200,
|
|
"Times Cited, All Databases": 201,
|
|
"180 Day Usage Count": null,
|
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"Since 2013 Usage Count": null,
|
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"Publisher": null,
|
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"Publisher City": null,
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"Publisher Address": null,
|
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"ISSN": null,
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|
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|
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"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "FEB 15",
|
|
"Publication Year": 2023,
|
|
"Volume": 14,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 839,
|
|
"DOI": "10.1038/s41467-023-36229-1",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-023-36229-1",
|
|
"Book DOI": null,
|
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"Early Access Date": null,
|
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"Number of Pages": null,
|
|
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|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000940806000012",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Lv, HL; Yao, YX; Li, SC; Wu, GL; Zhao, B; Zhou, XD; Dupont, RL; Kara, UI; Zhou, YM; Xi, SB; Liu, B; Che, RC; Zhang, JC; Xu, HB; Adera, S; Wu, RB; Wang, XG",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
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|
|
"Author Full Names": "Lv, Hualiang; Yao, Yuxing; Li, Shucong; Wu, Guanglei; Zhao, Biao; Zhou, Xiaodi; Dupont, Robert L.; Kara, Ufuoma I.; Zhou, Yimin; Xi, Shibo; Liu, Bo; Che, Renchao; Zhang, Jincang; Xu, Hongbin; Adera, Solomon; Wu, Renbing; Wang, Xiaoguang",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Staggered circular nulloporous graphene converts electromagnetic waves into electricity",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
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"Language": null,
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"Author Keywords": null,
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|
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"Abstract": "The electromagnetic (EM) energy released by electronic devices in the environment is largely wasted and contributes to EM pollution. Here, the authors report the synthesis of staggered circular nulloporous graphene enabling the absorption and conversion of EM waves into electricity via the thermoelectric effect. Harvesting largely ignored and wasted electromagnetic (EM) energy released by electronic devices and converting it into direct current (DC) electricity is an attractive strategy not only to reduce EM pollution but also address the ever-increasing energy crisis. Here we report the synthesis of nulloparticle-templated graphene with monodisperse and staggered circular nullopores enabling an EM-heat-DC conversion pathway. We experimentally and theoretically demonstrate that this staggered nulloporous structure alters graphene's electronic and phononic properties by synergistically manipulating its intralayer nullostructures and interlayer interactions. The staggered circular nulloporous graphene exhibits an anomalous combination of properties, which lead to an efficient absorption and conversion of EM waves into heat and in turn an output of DC electricity through the thermoelectric effect. Overall, our results advance the fundamental understanding of the structure-property relationships of ordered nulloporous graphene, providing an effective strategy to reduce EM pollution and generate electric energy.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 184,
|
|
"Times Cited, All Databases": 189,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
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|
|
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|
|
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|
|
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|
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|
|
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|
|
"Publication Date": "APR 8",
|
|
"Publication Year": 2023,
|
|
"Volume": 14,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 1982,
|
|
"DOI": "10.1038/s41467-023-37436-6",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-023-37436-6",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000980800100009",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Zheng, XH; Liu, ZC; Sun, JF; Luo, RH; Xu, K; Si, MY; Kang, J; Yuan, Y; Liu, S; Ahmad, T; Jiang, TL; Chen, N; Wang, MM; Xu, Y; Chuai, M; Zhu, ZX; Peng, Q; Meng, YH; Zhang, K; Wang, WP; Chen, W",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Zheng, Xinhua; Liu, Zaichun; Sun, Jifei; Luo, Ruihao; Xu, Kui; Si, Mingyu; Kang, Ju; Yuan, Yuan; Liu, Shuang; Ahmad, Touqeer; Jiang, Taoli; Chen, Na; Wang, Mingming; Xu, Yan; Chuai, Mingyan; Zhu, Zhengxin; Peng, Qia; Meng, Yahan; Zhang, Kai; Wang, Weiping; Chen, Wei",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Constructing robust heterostructured interface for anode-free zinc batteries with ultrahigh capacities",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
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"Language": null,
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|
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|
|
"Abstract": "The development of Zn-free anodes to inhibit Zn dendrite formation and modulate high-capacity Zn batteries is highly applauded yet very challenging. Here, we design a robust two-dimensional antimony/antimony-zinc alloy heterostructured interface to regulate Zn plating. Benefiting from the stronger adsorption and homogeneous electric field distribution of the Sb/Sb2Zn3-heterostructured interface in Zn plating, the Zn anode enables an ultrahigh areal capacity of 200 mAh cm(-2) with an overpotential of 112 mV and a Coulombic efficiency of 98.5%. An anode-free Zn-Br-2 battery using the Sb/Sb2Zn3-heterostructured interface@Cu anode shows an attractive energy density of 274 Wh kg(-1) with a practical pouch cell energy density of 62 Wh kg(-1). The scaled-up Zn-Br-2 battery in a capacity of 500 mAh exhibits over 400 stable cycles. Further, the Zn-Br-2 battery module in an energy of 9 Wh (6 V, 1.5 Ah) is integrated with a photovoltaic panel to demonstrate the practical renewable energy storage capabilities. Our superior anode-free Zn batteries enabled by the heterostructured interface enlighten an arena towards large-scale energy storage applications. The development of dendrite-free, Zn-free anodes is challenging. Here, the authors design a two-dimensional antimony/antimony-zinc alloy heterostructured interface to achieve dendrite-free Zn deposition with areal capacity of 200 mAh cm(-2), and energy density of around 270 Wh kg(-1) for anode-free zinc-bromine battery.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 182,
|
|
"Times Cited, All Databases": 187,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JAN 5",
|
|
"Publication Year": 2023,
|
|
"Volume": 14,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 76,
|
|
"DOI": "10.1038/s41467-022-35630-6",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-022-35630-6",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000940650100013",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Lin, Y; Kang, Q; Liu, YJ; Zhu, YK; Jiang, PK; Mai, YW; Huang, XY",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Lin, Ying; Kang, Qi; Liu, Yijie; Zhu, Yingke; Jiang, Pingkai; Mai, Yiu-Wing; Huang, Xingyi",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Flexible, Highly Thermally Conductive and Electrically Insulating Phase Change Materials for Advanced Thermal Management of 5G Base Stations and Thermoelectric Generators",
|
|
"Source Title": "nullO-MICRO LETTERS",
|
|
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|
|
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|
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"Language": null,
|
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|
|
"Abstract": "Thermal management has become a crucial problem for high-power-density equipment and devices. Phase change materials (PCMs) have great prospects in thermal management applications because of their large capacity of heat storage and isothermal behavior during phase transition. However, low intrinsic thermal conductivity, ease of leakage, and lack of flexibility severely limit their applications. Solving one of these problems often comes at the expense of other performance of the PCMs. In this work, we report core-sheath structured phase change nullocomposites (PCNs) with an aligned and interconnected boron nitride nullosheet network by combining coaxial electrospinning, electrostatic spraying, and hot-pressing. The advanced PCN films exhibit an ultrahigh thermal conductivity of 28.3 W m(-1) K-1 at a low BNNS loading (i.e., 32 wt%), which thereby endows the PCNs with high enthalpy (> 101 J g(-1)), outstanding ductility (> 40%) and improved fire retardancy. Therefore, our core-sheath strategies successfully balance the trade-off between thermal conductivity, flexibility, and phase change enthalpy of PCMs. Further, the PCNs provide powerful cooling solutions on 5G base station chips and thermoelectric generators, displaying promising thermal management applications on high-power-density equipment and thermoelectric conversion devices.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 179,
|
|
"Times Cited, All Databases": 190,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "DEC",
|
|
"Publication Year": 2023,
|
|
"Volume": 15,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 31,
|
|
"DOI": "10.1007/s40820-022-01003-3",
|
|
"DOI Link": "http://dx.doi.org/10.1007/s40820-022-01003-3",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics; Materials Science; Physics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000911314100002",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Zhou, JZ; Xu, X; Wu, HJ; Wang, JL; Lou, LC; Yin, K; Gong, YC; Shi, JJ; Luo, YH; Li, DM; Xin, H; Meng, QB",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
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"Author Full Names": "Zhou, Jiazheng; Xu, Xiao; Wu, Huijue; Wang, Jinlin; Lou, Licheng; Yin, Kang; Gong, Yuancai; Shi, Jiangjian; Luo, Yanhong; Li, Dongmei; Xin, Hao; Meng, Qingbo",
|
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"Book Author Full Names": null,
|
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"Group Authors": null,
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"Article Title": "Control of the phase evolution of kesterite by tuning of the selenium partial pressure for solar cells with 13.8% certified efficiency",
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"Source Title": "NATURE ENERGY",
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"Book Series Title": null,
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"Abstract": "The control of the phase evolution during the selenization of kesterite Cu2ZnSn(S,Se)(4) (CZTSSe) is crucial for efficient solar cells. Here, we regulate the phase-evolution kinetics of Ag-alloyed CZTSSe by applying a positive pressure in the reaction chamber at the initial stage of the annealing process. The partial pressure of Se decreases, reducing the collision probability between selenium molecules and the kesterite precursor during the initial formation of the crystals. This results in the precursor transforming into CZTSSe in a single step, without the formation of secondary phases. CZTSSe forms at relatively higher temperature than conventional methods, leading to high-crystallinity kesterite films with fewer defects. We demonstrate solar cells with a total area efficiency of 14.1% and a certified total area efficiency of 13.8%. This work provides insights into the selenization mechanism and phase evolution of kesterite absorbers, enabling efficient solar cells. Secondary phases or multi-step phase formation lead to poorly crystallized and defective kesterite films. Now Zhou et al. convert precursors into kesterite in a single step, using low partial pressure of selenium, and achieve solar cells with 13.8% certified efficiency.",
|
|
"Addresses": null,
|
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"Affiliations": null,
|
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"Reprint Addresses": null,
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"Email Addresses": null,
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"Researcher Ids": null,
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"ORCIDs": null,
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"Funding Orgs": null,
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"Funding Name Preferred": null,
|
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"Funding Text": null,
|
|
"Cited References": null,
|
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"Cited Reference Count": null,
|
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"Times Cited, WoS Core": 190,
|
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"Times Cited, All Databases": 191,
|
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"180 Day Usage Count": null,
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"ISSN": null,
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"ISBN": null,
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|
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"Journal ISO Abbreviation": null,
|
|
"Publication Date": "MAY",
|
|
"Publication Year": 2023,
|
|
"Volume": 8,
|
|
"Issue": 5,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
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"Start Page": 526,
|
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"End Page": "+",
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"Article Number": null,
|
|
"DOI": "10.1038/s41560-023-01251-6",
|
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"DOI Link": "http://dx.doi.org/10.1038/s41560-023-01251-6",
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"Book DOI": null,
|
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"Early Access Date": "APR 2023",
|
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"Number of Pages": null,
|
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"WoS Categories": null,
|
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"Web of Science Index": null,
|
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"Research Areas": "Energy & Fuels; Materials Science",
|
|
"IDS Number": null,
|
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"Pubmed Id": null,
|
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"Open Access Designations": null,
|
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"Highly Cited Status": "Y",
|
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"Hot Paper Status": "Y",
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"Date of Export": "2025-04-23",
|
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"UT (Unique WOS ID)": "WOS:000968306600002",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Liu, YF; Liu, SD; Xie, XS; Li, ZC; Wang, PJ; Lu, BA; Liang, SQ; Tang, Y; Zhou, J",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
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"Book Group Authors": null,
|
|
"Author Full Names": "Liu, Yanfen; Liu, Shude; Xie, Xuesong; Li, Zhicheng; Wang, Pinji; Lu, Bingan; Liang, Shuquan; Tang, Yan; Zhou, Jiang",
|
|
"Book Author Full Names": null,
|
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"Group Authors": null,
|
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"Article Title": "A functionalized separator enables dendrite-free Zn anode via metal-polydopamine coordination chemistry",
|
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"Source Title": "INFOMAT",
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"Book Series Title": null,
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"Book Series Subtitle": null,
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"Language": null,
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"Document Type": "Article",
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"Conference Sponsor": null,
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"Author Keywords": null,
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"Keywords Plus": null,
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"Abstract": "Designing a multifunctional separator with abundant ion migration paths is crucial for tuning the ion transport in rocking-chair-type batteries. Herein, a polydopamine-functionalized PVDF (PVDF@PDA) nullofibrous membrane is designed to serve as a separator for aqueous zinc-ion batteries (AZIBs). The functional groups (-OH and -NH-) in PDA facilitate the formation of Zn-O and Zn-N coordination bonds with Zn ions, homogenizing the Zn-ion flux and thus enabling dendrite-free Zn deposition. Moreover, the PVDF@PDA separator effectively inhibits the shuttling of V-species through the formation of V-O coordination bonds. As a result, the Zn/NH4V4O10 battery with the PVDF@PDA separator exhibits enhanced cycling stability (92.3% after 1000 cycles at 5 A g(-1)) and rate capability compared to that using a glass fiber separator. This work provides a new avenue to design functionalized separators for high-performance AZIBs.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
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"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 184,
|
|
"Times Cited, All Databases": 184,
|
|
"180 Day Usage Count": null,
|
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"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
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"Publisher City": null,
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"Publisher Address": null,
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"ISSN": null,
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"eISSN": null,
|
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"ISBN": null,
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"Journal Abbreviation": null,
|
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"Journal ISO Abbreviation": null,
|
|
"Publication Date": "MAR",
|
|
"Publication Year": 2023,
|
|
"Volume": 5,
|
|
"Issue": 3,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
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"Article Number": null,
|
|
"DOI": "10.1002/inf2.12374",
|
|
"DOI Link": "http://dx.doi.org/10.1002/inf2.12374",
|
|
"Book DOI": null,
|
|
"Early Access Date": "OCT 2022",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Materials Science",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000863843500001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Fei, CB; Li, NX; Wang, MR; Wang, XM; Gu, HY; Chen, B; Zhang, Z; Ni, ZY; Jiao, HY; Xu, WZ; Shi, ZF; Yan, YF; Huang, JS",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Fei, Chengbin; Li, Nengxu; Wang, Mengru; Wang, Xiaoming; Gu, Hangyu; Chen, Bo; Zhang, Zhao; Ni, Zhenyi; Jiao, Haoyang; Xu, Wenzhan; Shi, Zhifang; Yan, Yanfa; Huang, Jinsong",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Lead-chelating hole-transport layers for efficient and stable perovskite minimodules",
|
|
"Source Title": "SCIENCE",
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"Book Series Title": null,
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"Book Series Subtitle": null,
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"Language": null,
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"Abstract": "The defective bottom interfaces of perovskites and hole-transport layers (HTLs) limit the performance of p-i-n structure perovskite solar cells. We report that the addition of lead chelation molecules into HTLs can strongly interact with lead(II) ion (Pb2+), resulting in a reduced amorphous region in perovskites near HTLs and a passivated perovskite bottom surface. The minimodule with an aperture area of 26.9 square centimeters has a power conversion efficiency (PCE) of 21.8% (stabilized at 21.1%) that is certified by the National Renewable Energy Laboratory (NREL), which corresponds to a minimal small-cell efficiency of 24.6% (stabilized 24.1%) throughout the module area. Small-area cells and large-area minimodules with lead chelation molecules in HTLs had a light soaking stability of 3010 and 2130 hours, respectively, at an efficiency loss of 10% from the initial value under 1-sun illumination and open-circuit voltage conditions.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
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"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 192,
|
|
"Times Cited, All Databases": 199,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "MAY 26",
|
|
"Publication Year": 2023,
|
|
"Volume": 380,
|
|
"Issue": 6647,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 823,
|
|
"End Page": 829,
|
|
"Article Number": null,
|
|
"DOI": "10.1126/science.ade9463",
|
|
"DOI Link": "http://dx.doi.org/10.1126/science.ade9463",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001001476900004",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Wang, CX; Liu, Y; Jia, ZR; Zhao, WR; Wu, GL",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Wang, Chenxi; Liu, Yue; Jia, Zirui; Zhao, Wanru; Wu, Guanglei",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Multicomponent nulloparticles Synergistic One-Dimensional nullofibers as Heterostructure Absorbers for Tunable and Efficient Microwave Absorption",
|
|
"Source Title": "nullO-MICRO LETTERS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
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"Language": null,
|
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"Document Type": "Article",
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"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Application of novel radio technologies and equipment inevitably leads to electromagnetic pollution. One-dimensional polymer-based composite membrane structures have been shown to be an effective strategy to obtain high-performance microwave absorbers. Herein, we reported a one-dimensional N-doped carbon nullofibers material which encapsulated the hollow Co3SnC0.7 nullocubes in the fiber lumen by electrospinning. Space charge stacking formed between nulloparticles can be channeled by longitudinal fibrous structures. The dielectric constant of the fibers is highly related to the carbonization temperature, and the great impedance matching can be achieved by synergetic effect between Co3SnC0.7 and carbon network. At 800 & DEG;C, the necklace-like Co3SnC0.7/CNF with 5% low load achieves an excellent RL value of - 51.2 dB at 2.3 mm and the effective absorption bandwidth of 7.44 GHz with matching thickness of 2.5 mm. The multiple electromagnetic wave (EMW) reflections and interfacial polarization between the fibers and the fibers internal contribute a major effect to attenuating the EMW. These strategies for regulating electromagnetic performance can be expanded to other electromagnetic functional materials which facilitate the development of emerging absorbers.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 173,
|
|
"Times Cited, All Databases": 184,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "DEC",
|
|
"Publication Year": 2023,
|
|
"Volume": 15,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 13,
|
|
"DOI": "10.1007/s40820-022-00986-3",
|
|
"DOI Link": "http://dx.doi.org/10.1007/s40820-022-00986-3",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics; Materials Science; Physics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000899513300001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Rehan, AI; Rasee, AI; Awual, ME; Waliullah, RM; Hossain, MS; Kubra, KT; Salman, MS; Sheikh, MC; Marwani, HM; Khaleque, MA; Islam, A; Awual, MR",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Rehan, Ariyan Islam; Rasee, Adiba Islam; Awual, Mrs Eti; Waliullah, R. M.; Hossain, Mohammed Sohrab; Kubra, Khadiza Tul; Salman, Md. Shad; Sheikh, Md. Chanmiya; Marwani, Hadi M.; Khaleque, Md. Abdul; Islam, Aminul; Awual, Md. Rabiul",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Improving toxic dye removal and remediation using novel nullocomposite fibrous adsorbent",
|
|
"Source Title": "COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Materials with regulated nulloscale morphology provide capabilities to remove dangerous pollutants from wastewater, by adsorption. In this study, the chitosan-based composite fibrous adsorbent was fabricated and used as a novel and facile eliminator in the process of removing cationic methyl orange (MO) from the water medium. Different methods were applied to check the properties of the desired composite fibrous adsorbent. The removal value showed that the chitosan-embedded composite fibrous adsorbent has super characteristics and can be removed the organic dye from the water. The influence of pH, time, temperature, eliminator quantity, and MO content was explored. With increasing time and eliminator quantity, the adsorption efficiency increased. The composite fibrous adsorbent with the advantage of its high functionality and combined micro-nullomorphology features, has emerged as a very promising candidate for obtaining versatile and robust adsorbents. This work presents how the tunned synthesis of composite fibrous adsorbent tailored their nulloarchitecture giving rise to adsorption capacities toward cleaning aqueous samples polluted with MO dye. The composite fibrous adsorbent was prepared by the direct immobilization method, with normal aging temperature, in order to study the effect of synthesis conditions on the adsorption properties of MO dye. The solution acidity was exhibited as the key factor, and a suitable pH of 5.50 was selected based on the efficiency. The competing ions were not adversely affected in the dye adsorption as defined by the stable bonding mechanism. The adsorption data were highly fitted with the Langmuir adsorption model with monolayer coverage. The determined maximum adsorption was 175.45 mg/g, which was comparable with the other forms of materials. The adsorbed MO dye elution was evaluated using ethanol and then the composite fibrous adsorbent was ready to use for MO dye adsorption after washing with water without significant loss in its functionality. Therefore, we explored the tunned morphology of composite fibrous adsorbent for obtaining performant adsorbents for the elimination of refractory pollutants in wastewater.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 190,
|
|
"Times Cited, All Databases": 191,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "SEP 20",
|
|
"Publication Year": 2023,
|
|
"Volume": 673,
|
|
"Issue": null,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 131859,
|
|
"DOI": "10.1016/j.colsurfa.2023.131859",
|
|
"DOI Link": "http://dx.doi.org/10.1016/j.colsurfa.2023.131859",
|
|
"Book DOI": null,
|
|
"Early Access Date": "JUN 2023",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001144186400001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Wang, YY; Wang, ZJ; Pang, WK; Lie, W; Yuwono, JA; Liang, GM; Liu, SL; D' Angelo, AM; Deng, JJ; Fan, YM; Davey, K; Li, BH; Guo, ZP",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Wang, Yanyan; Wang, Zhijie; Pang, Wei Kong; Lie, Wilford; Yuwono, Jodie A.; Liang, Gemeng; Liu, Sailin; D' Angelo, Anita M.; Deng, Jiaojiao; Fan, Yameng; Davey, Kenneth; Li, Baohua; Guo, Zaiping",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Solvent control of water O-H bonds for highly reversible zinc ion batteries",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
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"Conference Location": null,
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"Abstract": "Aqueous Zn-ion batteries have attracted increasing research interest; however, the development of these batteries has been hindered by several challenges, including dendrite growth, Zn corrosion, cathode material degradation, limited temperature adaptability and electrochemical stability window, which are associated with water activity and the solvation structure of electrolytes. Here we report that water activity is suppressed by increasing the electron density of the water protons through interactions with highly polar dimethylacetamide and trimethyl phosphate molecules. Meanwhile, the Zn corrosion in the hybrid electrolyte is mitigated, and the electrochemical stability window and the operating temperature of the electrolyte are extended. The dimethylacetamide alters the surface energy of Zn, guiding the (002) plane dominated deposition of Zn. Molecular dynamics simulation evidences Zn2+ ions are solvated with fewer water molecules, resulting in lower lattice strain in the NaV3O8 center dot 1.5H(2)O cathode during the insertion of hydrated Zn2+ ions, boosting the lifespan of Zn|| NaV3O8 center dot 1.5H(2)O cell to 3000 cycles. The electrochemical performance of aqueous zinc ion batteries is limited by water activity. Here, the authors propose a hybrid electrolyte that incorporate strongly polar molecules to strengthen the water O-H bonds, thus reduce water activity and improve the electrochemical performance of the batteries.",
|
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"Addresses": null,
|
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"Affiliations": null,
|
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"Reprint Addresses": null,
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"Funding Name Preferred": null,
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"Funding Text": null,
|
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"Cited References": null,
|
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"Cited Reference Count": null,
|
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"Times Cited, WoS Core": 182,
|
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"Times Cited, All Databases": 184,
|
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"180 Day Usage Count": null,
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|
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"Publication Date": "MAY 11",
|
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"Publication Year": 2023,
|
|
"Volume": 14,
|
|
"Issue": 1,
|
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"Part Number": null,
|
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"Supplement": null,
|
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"Special Issue": null,
|
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"Meeting Abstract": null,
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"Start Page": null,
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"End Page": null,
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"Article Number": 2720,
|
|
"DOI": "10.1038/s41467-023-38384-x",
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"DOI Link": "http://dx.doi.org/10.1038/s41467-023-38384-x",
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"Number of Pages": null,
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"Web of Science Index": null,
|
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"Research Areas": "Science & Technology - Other Topics",
|
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"IDS Number": null,
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"Pubmed Id": null,
|
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"Open Access Designations": null,
|
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"Highly Cited Status": "Y",
|
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"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
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"UT (Unique WOS ID)": "WOS:000992465700007",
|
|
"Web of Science Record": "View Full Record in Web of Science"
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|
},
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|
{
|
|
"Publication Type": "J",
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|
"Authors": "Kim, SC; Wang, JY; Xu, R; Zhang, P; Chen, YL; Huang, ZJ; Yang, YF; Yu, Z; Oyakhire, ST; Zhang, WB; Greenburg, LC; Kim, MS; Boyle, DT; Sayavong, P; Ye, YS; Qin, J; Bao, ZA; Cui, Y",
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"Book Authors": null,
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"Book Editors": null,
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"Author Full Names": "Kim, Sang Cheol; Wang, Jingyang; Xu, Rong; Zhang, Pu; Chen, Yuelang; Huang, Zhuojun; Yang, Yufei; Yu, Zhiao; Oyakhire, Solomon T.; Zhang, Wenbo; Greenburg, Louisa C.; Kim, Mun Sek; Boyle, David T.; Sayavong, Philaphon; Ye, Yusheng; Qin, Jian; Bao, Zhenull; Cui, Yi",
|
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"Book Author Full Names": null,
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"Group Authors": null,
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"Article Title": "High-entropy electrolytes for practical lithium metal batteries",
|
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"Source Title": "NATURE ENERGY",
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"Book Series Title": null,
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"Abstract": "Electrolyte engineering is crucial for improving battery performance, particularly for lithium metal batteries. Recent advances in electrolytes have greatly improved cyclability by enhancing electrochemical stability at the electrode interfaces, but concurrently achieving high ionic conductivity has remained challenging. Here we report an electrolyte design strategy for enhanced lithium metal batteries by increasing the molecular diversity in electrolytes, which essentially leads to high-entropy electrolytes. We find that, in weakly solvating electrolytes, the entropy effect reduces ion clustering while preserving the characteristic anion-rich solvation structures, which is characterized by synchrotron-based X-ray scattering and molecular dynamics simulations. Electrolytes with smaller-sized clusters exhibit a twofold improvement in ionic conductivity compared with conventional weakly solvating electrolytes, enabling stable cycling at high current densities up to 2C (6.2 mA cm(-2)) in anode-free LiNi0.6Mn0.2Co0.2 (NMC622)||Cu pouch cells. The efficacy of the design strategy is verified by performance improvements in three disparate weakly solvating electrolyte systems. Electrolyte engineering has proven an effective approach to enhance the performance of lithium metal batteries. Here the authors propose a strategy by using multiple solvents in weakly solvating electrolytes-dubbed as high-entropy electrolytes-to improve the ionic conductivity while maintaining electrochemical stability, leading to high-performance batteries.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
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"Email Addresses": null,
|
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"Researcher Ids": null,
|
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"ORCIDs": null,
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"Funding Orgs": null,
|
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"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
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"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 173,
|
|
"Times Cited, All Databases": 177,
|
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"180 Day Usage Count": null,
|
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"Since 2013 Usage Count": null,
|
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"Publisher": null,
|
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"Publisher City": null,
|
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"Publisher Address": null,
|
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"ISSN": null,
|
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"eISSN": null,
|
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"ISBN": null,
|
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"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "AUG",
|
|
"Publication Year": 2023,
|
|
"Volume": 8,
|
|
"Issue": 8,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 814,
|
|
"End Page": 826,
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s41560-023-01280-1",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41560-023-01280-1",
|
|
"Book DOI": null,
|
|
"Early Access Date": "JUL 2023",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Energy & Fuels; Materials Science",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001023405800005",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Zhang, DF; Li, MN; Yong, X; Song, HQ; Waterhouse, GIN; Yi, YF; Xue, BJ; Zhang, DL; Liu, BZ; Lu, SY",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Zhang, Dafeng; Li, Mengnull; Yong, Xue; Song, Haoqiang; Waterhouse, Geoffrey I. N.; Yi, Yunfei; Xue, Bingjie; Zhang, Dongliang; Liu, Baozhong; Lu, Siyu",
|
|
"Book Author Full Names": null,
|
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"Group Authors": null,
|
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"Article Title": "Construction of Zn-doped RuO2 nullowires for efficient and stable water oxidation in acidic media",
|
|
"Source Title": "NATURE COMMUNICATIONS",
|
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"Book Series Title": null,
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"Language": null,
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"Document Type": "Article",
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"Keywords Plus": null,
|
|
"Abstract": "Oxygen evolution reaction catalysts capable of working efficiently in acidic media are highly demanded for the commercialization of proton exchange membrane water electrolysis. Herein, we report a Zn-doped RuO2 nullowire array electrocatalyst with outstanding catalytic performance for the oxygen evolution reaction under acidic conditions. Overpotentials as low as 173, 304, and 373 mV are achieved at 10, 500, and 1000 mA cm(-2), respectively, with robust stability reaching to 1000 h at 10 mA cm(-2). Experimental and theoretical investigations establish a clear synergistic effect of Zn dopants and oxygen vacancies on regulating the binding configurations of oxygenated adsorbates on the active centers, which then enables an alternative Ru-Zn dual-site oxide path of the reaction. Due to the change of reaction pathways, the energy barrier of rate-determining step is reduced, and the over-oxidation of Ru active sites is alleviated. As a result, the catalytic activity and stability are significantly enhanced. Ru-based materials are promising catalysts for oxygen evolution reaction in acidic condition, but their catalytic performance needs to be further improved. Here, the authors report Zn-RuO2 nullowires with a Ru-Zn dual-site oxide reaction pathway with enhanced activity and stability for acidic oxygen evolution reaction.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
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"Researcher Ids": null,
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"ORCIDs": null,
|
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|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 178,
|
|
"Times Cited, All Databases": 181,
|
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"180 Day Usage Count": null,
|
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"Since 2013 Usage Count": null,
|
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"Publisher": null,
|
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"Publisher City": null,
|
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|
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"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
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"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "MAY 2",
|
|
"Publication Year": 2023,
|
|
"Volume": 14,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 2517,
|
|
"DOI": "10.1038/s41467-023-38213-1",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-023-38213-1",
|
|
"Book DOI": null,
|
|
"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000980689000020",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Kumar, P; Kannimuthu, K; Zeraati, AS; Roy, S; Wang, X; Wang, XY; Samanta, S; Miller, KA; Molina, M; Trivedi, D; Abed, J; Mata, AC; Al-Mahayni, H; Baltrusaitis, J; Shimizu, G; Wu, YA; Seifitokaldani, A; Sargent, EH; Ajayan, PM; Hu, JG; Kibria, MG",
|
|
"Book Authors": null,
|
|
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|
|
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|
|
"Author Full Names": "Kumar, Pawan; Kannimuthu, Karthick; Zeraati, Ali Shayesteh; Roy, Soumyabrata; Wang, Xiao; Wang, Xiyang; Samanta, Subhajyoti; Miller, Kristen A.; Molina, Maria; Trivedi, Dhwanil; Abed, Jehad; Mata, Astrid Campos; Al-Mahayni, Hasan; Baltrusaitis, Jonas; Shimizu, George; Wu, Yimin A.; Seifitokaldani, Ali; Sargent, Edward H.; Ajayan, Pulickel M.; Hu, Jinguang; Kibria, Md Golam",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "High-Density Cobalt Single-Atom Catalysts for Enhanced Oxygen Evolution Reaction",
|
|
"Source Title": "JOURNAL OF THE AMERICAN CHEMICAL SOCIETY",
|
|
"Book Series Title": null,
|
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"Language": null,
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|
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"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Single atom catalysts (SACs) possess unique catalytic properties due to low-coordination and unsaturated active sites. However, the demonstrated performance of SACs is limited by low SAC loading, poor metal-support interactions, and nonstable performance. Herein, we report a macromolecule-assisted SAC synthesis approach that enabled us to demonstrate high-density Co single atoms (10.6 wt % Co SAC) in a pyridinic N-rich graphenic network. The highly porous carbon network (surface area of similar to 186 m(2) g(-1)) with increased conjugation and vicinal Co site decoration in Co SACs significantly enhanced the electrocatalytic oxygen evolution reaction (OER) in 1 M KOH (eta(10) at 351 mV; mass activity of 2209 mA mg(Co)(-1) at 1.65 V) with more than 300 h stability. Operando X-ray absorption near-edge structure demonstrates the formation of electron-deficient Co-O coordination intermediates, accelerating OER kinetics. Density functional theory (DFT) calculations reveal the facile electron transfer from cobalt to oxygen speciesaccelerated OER.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 178,
|
|
"Times Cited, All Databases": 180,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "APR 12",
|
|
"Publication Year": 2023,
|
|
"Volume": 145,
|
|
"Issue": 14,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 8052,
|
|
"End Page": 8063,
|
|
"Article Number": null,
|
|
"DOI": "10.1021/jacs.3c00537",
|
|
"DOI Link": "http://dx.doi.org/10.1021/jacs.3c00537",
|
|
"Book DOI": null,
|
|
"Early Access Date": "MAR 2023",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000967668600001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Zheng, XP; Li, Z; Zhang, Y; Chen, M; Liu, T; Xiao, CX; Gao, DP; Patel, JB; Kuciauskas, D; Magomedov, A; Scheidt, RA; Wang, XM; Harvey, SP; Dai, ZH; Zhang, CL; Morales, D; Pruett, H; Wieliczka, BM; Kirmani, AR; Padture, NP; Graham, KR; Yan, YF; Nazeeruddin, MK; McGehee, MD; Zhu, ZL; Luther, JM",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Zheng, Xiaopeng; Li, Zhen; Zhang, Yi; Chen, Min; Liu, Tuo; Xiao, Chuanxiao; Gao, Danpeng; Patel, Jay B.; Kuciauskas, Darius; Magomedov, Artiom; Scheidt, Rebecca A.; Wang, Xiaoming; Harvey, Steven P.; Dai, Zhenghong; Zhang, Chunlei; Morales, Daniel; Pruett, Henry; Wieliczka, Brian M.; Kirmani, Ahmad R.; Padture, Nitin P.; Graham, Kenneth R.; Yan, Yanfa; Nazeeruddin, Mohammad Khaja; McGehee, Michael D.; Zhu, Zonglong; Luther, Joseph M.",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Co-deposition of hole-selective contact and absorber for improving the processability of perovskite solar cells",
|
|
"Source Title": "NATURE ENERGY",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
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"Document Type": "Article",
|
|
"Conference Title": null,
|
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|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Simplifying the manufacturing processes of renewable energy technologies is crucial to lowering the barriers to commercialization. In this context, to improve the manufacturability of perovskite solar cells (PSCs), we have developed a one-step solution-coating procedure in which the hole-selective contact and perovskite light absorber spontaneously form, resulting in efficient inverted PSCs. We observed that phosphonic or carboxylic acids, incorporated into perovskite precursor solutions, self-assemble on the indium tin oxide substrate during perovskite film processing. They form a robust self-assembled monolayer as an excellent hole-selective contact while the perovskite crystallizes. Our approach solves wettability issues and simplifies device fabrication, advancing the manufacturability of PSCs. Our PSC devices with positive-intrinsic-negative (p-i-n) geometry show a power conversion efficiency of 24.5% and retain >90% of their initial efficiency after 1,200 h of operating at the maximum power point under continuous illumination. The approach shows good generality as it is compatible with different self-assembled monolayer molecular systems, perovskites, solvents and processing methods. Improving the manufacturability of perovskite solar cells is key to their deployment. Zheng et al. report a one-step deposition of the hole-selective and absorber layers that addresses wettability issues and simplifies the fabrication process.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 178,
|
|
"Times Cited, All Databases": 183,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "MAY",
|
|
"Publication Year": 2023,
|
|
"Volume": 8,
|
|
"Issue": 5,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 462,
|
|
"End Page": "+",
|
|
"Article Number": null,
|
|
"DOI": "10.1038/s41560-023-01227-6",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41560-023-01227-6",
|
|
"Book DOI": null,
|
|
"Early Access Date": "MAR 2023",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Energy & Fuels; Materials Science",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000950511100003",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Li, XW; Yu, X; Zhao, M; Li, ZD; Wang, ZG; Zhai, W",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Li, Xinwei; Yu, Xiang; Zhao, Miao; Li, Zhendong; Wang, Zhonggang; Zhai, Wei",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Multi-Level Bioinspired Microlattice with Broadband Sound-Absorption Capabilities and Deformation-Tolerant Compressive Response",
|
|
"Source Title": "ADVANCED FUNCTIONAL MATERIALS",
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"Abstract": "Owing to the omnipresent noise and crash hazards, multifunctional sound-absorbing, and deformation-tolerant materials are highly sought-after for practical engineering design. However, challenges lie with designing such a material. Herein, leveraging the inherent mechanical robustness of the biological cuttlebone, by introducing dissipative pores, a high-strength microlattice is presented which is also sound-absorbing. Its absorption bandwidth and deformation tolerance are further enhanced by introducing another level of bioinspiration, based on geometrical heterogeneities amongst the building cells. A high-fidelity microstructure-based model is developed to predict and optimize properties. Across a broad range of frequencies from 1000 to 6300 Hz, at a low thickness of 21 mm, the optimized microlattice displays a high experimentally measured average absorption coefficient of 0.735 with 68% of the points higher than 0.7. The absorption mechanism attributes to the resonating air frictional loss whilst its broadband characteristics attribute to the multiple resonullce modes working in tandem. The heterogeneous architecture also enables the microlattice to deform with a deformation-tolerant plateau behavior not observed in its uniform counterpart, which thereby leads to a 30% improvement in the specific energy absorption. Overall, this work presents an effective approach to the design of sound and energy-absorbing materials by modifying state-of-the-art bioinspired structures.",
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"Addresses": null,
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"Times Cited, WoS Core": 182,
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"Publication Date": "JAN",
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"Volume": 33,
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"DOI": "10.1002/adfm.202210160",
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"DOI Link": "http://dx.doi.org/10.1002/adfm.202210160",
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"Early Access Date": "NOV 2022",
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"Highly Cited Status": "Y",
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},
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{
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"Publication Type": "J",
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"Authors": "Xue, TT; Yang, Y; Yu, DY; Wali, Q; Wang, ZY; Cao, XS; Fan, W; Liu, TX",
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"Author Full Names": "Xue, Tiantian; Yang, Yi; Yu, Dingyi; Wali, Qamar; Wang, Zhenyu; Cao, Xuesong; Fan, Wei; Liu, Tianxi",
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"Article Title": "3D Printed Integrated Gradient-Conductive MXene/CNT/Polyimide Aerogel Frames for Electromagnetic Interference Shielding with Ultra-Low Reflection",
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"Source Title": "nullO-MICRO LETTERS",
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"Abstract": "Construction of advanced electromagnetic interference (EMI) shielding materials with miniaturized, programmable structure and low reflection are promising but challenging. Herein, an integrated transition-metal carbides/carbon nullotube/polyimide (gradient-conductive MXene/CNT/PI, GCMCP) aerogel frame with hierarchical porous structure and gradient-conductivity has been constructed to achieve EMI shielding with ultra-low reflection. The gradient-conductive structures are obtained by continuous 3D printing of MXene/CNT/poly (amic acid) inks with different CNT contents, where the slightly conductive top layer serves as EM absorption layer and the highly conductive bottom layer as reflection layer. In addition, the hierarchical porous structure could extend the EM dissipation path and dissipate EM by multiple reflections. Consequently, the GCMCP aerogel frames exhibit an excellent average EMI shielding efficiency (68.2 dB) and low reflection (R = 0.23). Furthermore, the GCMCP aerogel frames with miniaturized and programmable structures can be used as EMI shielding gaskets and effectively block wireless power transmission, which shows a prosperous application prospect in defense industry and aerospace.",
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"Addresses": null,
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"Affiliations": null,
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"Times Cited, WoS Core": 166,
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"Times Cited, All Databases": 180,
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"Publication Date": "DEC",
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"Publication Year": 2023,
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"Volume": 15,
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"Issue": 1,
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"Start Page": null,
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"Article Number": 45,
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"DOI": "10.1007/s40820-023-01017-5",
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"DOI Link": "http://dx.doi.org/10.1007/s40820-023-01017-5",
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"Highly Cited Status": "Y",
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"Hot Paper Status": "Y",
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"Date of Export": "2025-04-23",
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"UT (Unique WOS ID)": "WOS:000931727400001",
|
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"Web of Science Record": "View Full Record in Web of Science"
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},
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|
{
|
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"Publication Type": "J",
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"Authors": "Zheng, ZL; Zhang, OF; Borgs, C; Chayes, JT; Yaghi, OM",
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"Book Authors": null,
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"Book Editors": null,
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"Author Full Names": "Zheng, Zhiling; Zhang, Oufan; Borgs, Christian; Chayes, Jennifer T.; Yaghi, Omar M.",
|
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"Article Title": "ChatGPT Chemistry Assistant for Text Mining and the Prediction of MOF Synthesis",
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"Source Title": "JOURNAL OF THE AMERICAN CHEMICAL SOCIETY",
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"Abstract": "We use prompt engineering to guide ChatGPT in the automationoftext mining of metal-organic framework (MOF) synthesis conditionsfrom diverse formats and styles of the scientific literature. Thiseffectively mitigates ChatGPT's tendency to hallucinate information,an issue that previously made the use of large language models (LLMs)in scientific fields challenging. Our approach involves the developmentof a workflow implementing three different processes for text mining,programmed by ChatGPT itself. All of them enable parsing, searching,filtering, classification, summarization, and data unification withdifferent trade-offs among labor, speed, and accuracy. We deploy thissystem to extract 26 257 distinct synthesis parameters pertainingto approximately 800 MOFs sourced from peer-reviewed research articles.This process incorporates our ChemPrompt Engineering strategy to instructChatGPT in text mining, resulting in impressive precision, recall,and F1 scores of 90-99%. Furthermore, with the data set builtby text mining, we constructed a machine-learning model with over87% accuracy in predicting MOF experimental crystallization outcomesand preliminarily identifying important factors in MOF crystallization.We also developed a reliable data-grounded MOF chatbot to answer questionsabout chemical reactions and synthesis procedures. Given that theprocess of using ChatGPT reliably mines and tabulates diverse MOFsynthesis information in a unified format while using only narrativelanguage requiring no coding expertise, we anticipate that our ChatGPTChemistry Assistant will be very useful across various other chemistrysubdisciplines.",
|
|
"Addresses": null,
|
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|
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"Times Cited, WoS Core": 170,
|
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"Times Cited, All Databases": 176,
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|
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|
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"Publication Date": "AUG 7",
|
|
"Publication Year": 2023,
|
|
"Volume": 145,
|
|
"Issue": 32,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
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|
|
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|
|
"Start Page": 18048,
|
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"End Page": 18062,
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"Article Number": null,
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"DOI": "10.1021/jacs.3c05819",
|
|
"DOI Link": "http://dx.doi.org/10.1021/jacs.3c05819",
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|
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"Highly Cited Status": "Y",
|
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"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
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"UT (Unique WOS ID)": "WOS:001052894400001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Zeng, JL; Xie, WH; Guo, Y; Zhao, T; Zhou, H; Wang, QY; Li, HD; Guo, ZH; Bin Xu, B; Gu, HB",
|
|
"Book Authors": null,
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"Author Full Names": "Zeng, Junling; Xie, Wenhao; Guo, Ying; Zhao, Tong; Zhou, Heng; Wang, Qiaoying; Li, Handong; Guo, Zhanhu; Bin Xu, Ben; Gu, Hongbo",
|
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"Book Author Full Names": null,
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"Article Title": "Magnetic field facilitated electrocatalytic degradation of tetracycline in wastewater by magnetic porous carbonized phthalonitrile resin",
|
|
"Source Title": "APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY",
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"Abstract": "Herein, the magnetic field facilitated electrocatalytic degradation of tetracycline is reported for the first time. A magnetic porous carbonized phthalonitrile resin electrocatalyst has been prepared through directly annealing phthalonitrile monomer, polyaniline coated barium ferrite and potassium hydroxide. The tetracycline degradation percentage (DP%) by such electrocatalyst is significantly increased up to 37.42% under magnetic field with the optimal pH value of 5.0 and bias voltage of 1.0 V (vs. SCE). The mechanism of this phenomenon is explained by the spin-selective electron removal process in the reaction between metal-oxygen species and tetracycline on the electrocatalyst. The comparison of degradation pathways for tetracycline with and without magnetic field confirms the improvement of tetracycline DP%. This work opens a new direction for the application of an external magnetic field in the electrocatalytic degradation of antibiotics in wastewater.",
|
|
"Addresses": null,
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|
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|
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"Publication Date": "JAN",
|
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"Publication Year": 2024,
|
|
"Volume": 340,
|
|
"Issue": null,
|
|
"Part Number": null,
|
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|
|
"Special Issue": null,
|
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|
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"Start Page": null,
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"End Page": null,
|
|
"Article Number": 123225,
|
|
"DOI": "10.1016/j.apcatb.2023.123225",
|
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"DOI Link": "http://dx.doi.org/10.1016/j.apcatb.2023.123225",
|
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|
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"Early Access Date": "AUG 2023",
|
|
"Number of Pages": null,
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|
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"Research Areas": "Chemistry; Engineering",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
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"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001069094400001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Ding, SC; Barr, JA; Lyu, Z; Zhang, FY; Wang, MY; Tieu, P; Li, X; Engelhard, MH; Feng, ZX; Beckman, SP; Pan, XQ; Li, JC; Du, D; Lin, YH",
|
|
"Book Authors": null,
|
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|
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"Author Full Names": "Ding, Shichao; Barr, Jordan Alysia; Lyu, Zhaoyuan; Zhang, Fangyu; Wang, Maoyu; Tieu, Peter; Li, Xin; Engelhard, Mark H.; Feng, Zhenxing; Beckman, Scott P.; Pan, Xiaoqing; Li, Jin-Cheng; Du, Dan; Lin, Yuehe",
|
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"Book Author Full Names": null,
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"Article Title": "Effect of Phosphorus Modulation in Iron Single-Atom Catalysts for Peroxidase Mimicking",
|
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"Source Title": "ADVANCED MATERIALS",
|
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"Book Series Title": null,
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"Abstract": "Fe-N-C single-atom catalysts (SACs) exhibit excellent peroxidase (POD)-like catalytic activity, owing to their well-defined isolated iron active sites on the carbon substrate, which effectively mimic the structure of natural peroxidase's active center. To further meet the requirements of diverse biosensing applications, SAC POD-like activity still needs to be continuously enhanced. Herein, a phosphorus (P) heteroatom is introduced to boost the POD-like activity of Fe-N-C SACs. A 1D carbon nullowire (FeNCP/NW) catalyst with enriched Fe-N-4 active sites is designed and synthesized, and P atoms are doped in the carbon matrix to affect the Fe center through long-range interaction. The experimental results show that the P-doping process can boost the POD-like activity more than the non-P-doped one, with excellent selectivity and stability. The mechanism analysis results show that the introduction of P into SAC can greatly enhance POD-like activity initially, but its effect becomes insignificant with increasing amount of P. As a proof of concept, FeNCP/NW is employed in an enzyme cascade platform for highly sensitive colorimetric detection of the neurotransmitter acetylcholine.",
|
|
"Addresses": null,
|
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"Affiliations": null,
|
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"Reprint Addresses": null,
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|
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"Funding Text": null,
|
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|
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"Cited Reference Count": null,
|
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"Times Cited, WoS Core": 113,
|
|
"Times Cited, All Databases": 113,
|
|
"180 Day Usage Count": null,
|
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|
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|
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|
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|
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|
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|
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|
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|
|
"Publication Date": "MAR",
|
|
"Publication Year": 2024,
|
|
"Volume": 36,
|
|
"Issue": 10,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": "SI",
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
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"End Page": null,
|
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"Article Number": null,
|
|
"DOI": "10.1002/adma.202209633",
|
|
"DOI Link": "http://dx.doi.org/10.1002/adma.202209633",
|
|
"Book DOI": null,
|
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"Early Access Date": "MAR 2023",
|
|
"Number of Pages": null,
|
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"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry; Science & Technology - Other Topics; Materials Science; Physics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000948326900001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Wang, ML; Lu, YP; Lan, JG; Wang, TM; Zhang, C; Cao, ZQ; Li, TJ; Liaw, PK",
|
|
"Book Authors": null,
|
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"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Wang, Mingliang; Lu, Yiping; Lan, Jinggang; Wang, Tongmin; Zhang, Chuan; Cao, Zhiqiang; Li, Tingju; Liaw, Peter K.",
|
|
"Book Author Full Names": null,
|
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"Group Authors": null,
|
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"Article Title": "Lightweight, ultrastrong and high thermal-stable eutectic high-entropy alloys for elevated-temperature applications",
|
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"Source Title": "ACTA MATERIALIA",
|
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"Book Series Title": null,
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"Language": null,
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"Document Type": "Article",
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"Keywords Plus": null,
|
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"Abstract": "Eutectic high-entropy alloys (EHEAs) that combine the advantages of HEAs and eutectic alloys are promising candidates for high-temperature applications. However, currently developed EHEAs still exhibit high densities and low high-temperature strengths, which limit their usage. Here we propose a strategy to design lightweight, strong, and high thermal-stable EHEAs by introducing an extremely stable Heusler-type ordered phase (L21 phase) containing a high-content of low-density elements and constructing a low lattice misfit eutectic-phase interface, which can lead to generate ultrafine and stable lamellar structures and high-density of coherent nulloprecipitates. As a manifestation of this strategy, a novel bulk Al17Ni34Ti17V32 EHEA was designed to consist of L21 and body-centered-cubic (BCC) phases (interlamellar spacing -320 nm) with a lattice misfit only 2.4%. This alloy has one of the lowest densities (-6.2 g/cm3) among all EHEAs reported previously and exhibits much higher high-temperature hardness and specific yield strengths than most reported refractory HEAs (RHEAs), lightweight HEAs (LWHEAs), EHEAs, and conventional superalloys. This work paves the way to develop light EHEAs with excellent high-temperature properties.",
|
|
"Addresses": null,
|
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"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
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"Researcher Ids": null,
|
|
"ORCIDs": null,
|
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"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 172,
|
|
"Times Cited, All Databases": 176,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
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"Publisher": null,
|
|
"Publisher City": null,
|
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"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "APR 15",
|
|
"Publication Year": 2023,
|
|
"Volume": 248,
|
|
"Issue": null,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 118806,
|
|
"DOI": "10.1016/j.actamat.2023.118806",
|
|
"DOI Link": "http://dx.doi.org/10.1016/j.actamat.2023.118806",
|
|
"Book DOI": null,
|
|
"Early Access Date": "MAR 2023",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Materials Science; Metallurgy & Metallurgical Engineering",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000952487500001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Bai, B; Chen, J; Bai, F; Nie, QK; Jia, XX",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Bai, Bing; Chen, Jing; Bai, Fan; Nie, Qingke; Jia, Xiangxin",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Corrosion effect of acid/alkali on cementitious red mud-fly ash materials containing heavy metal residues",
|
|
"Source Title": "ENVIRONMENTAL TECHNOLOGY & INNOVATION",
|
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"Book Series Title": null,
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"Book Series Subtitle": null,
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"Language": null,
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"Document Type": "Article",
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"Conference Title": null,
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"Conference Date": null,
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"Conference Location": null,
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"Conference Sponsor": null,
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"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "High-strength cementitious red mud-fly ash materials (RFMs) were formed from sodium hydroxide and water glass mixed solutions, and their abilities to solidify heavy metal ions (HMs, e. g., copper and cadmium) were assessed. The mechanism for precipitation of the HMs by corrosive acid/alkali solutions was explored via toxicity leaching tests, as well as SEM, XRD, FT-IR and XPS. The results showed that when the added alkaline activator was not fully consumed, the presence of small amounts of HMs consumed the excess alkaline ions to form hydroxide precipitates that filled the pores of the RFM, so the compressive strength of the RFM increased. Otherwise, the presence of excess HMs reduced the compactness of the RFM and eventually resulted in a highly porous structure, leading to weakening of the material. Additionally, small amounts of anhydrite phases were produced in the RFM. In neutral and alkaline environments, the HMs formed precipitates or coordination complexes with hydroxyl groups, and the solidification efficiencies exceeded 99%. In acidic environments, the HMs converted from their original precipitated forms or ion-hydroxide complexes to free cations. As a result, the HMs were more likely to be separated from the RFMs. Moreover, the RFMs were more prone to disaggregation under acidic conditions, which led to destruction of the RFM microstructure and rerelease of the HMs fixed in the microstructure.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 155,
|
|
"Times Cited, All Databases": 158,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "FEB",
|
|
"Publication Year": 2024,
|
|
"Volume": 33,
|
|
"Issue": null,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 103485,
|
|
"DOI": "10.1016/j.eti.2023.103485",
|
|
"DOI Link": "http://dx.doi.org/10.1016/j.eti.2023.103485",
|
|
"Book DOI": null,
|
|
"Early Access Date": "DEC 2023",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Biotechnology & Applied Microbiology; Engineering; Environmental Sciences & Ecology",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001145912100001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Razaq, R; Din, MMU; Småbråten, DR; Eyupoglu, V; Janakiram, S; Sunde, TO; Allahgoli, N; Rettenwander, D; Deng, LY",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Razaq, Rameez; Din, Mir Mehraj Ud; Smabraten, Didrik Rene; Eyupoglu, Volkan; Janakiram, Saravanull; Sunde, Tor Olav; Allahgoli, Nima; Rettenwander, Daniel; Deng, Liyuan",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Synergistic Effect of Bimetallic MOF Modified Separator for Long Cycle Life Lithium-Sulfur Batteries",
|
|
"Source Title": "ADVANCED ENERGY MATERIALS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Severe polysulfide dissolution and shuttling are the main challenges that plague the long cycle life and capacity retention of lithium-sulfur (Li-S) batteries. To address these challenges, efficient separators are designed and modified with a dual functional bimetallic metal-organic framework (MOF). Flower-shaped bimetallic MOFs (i.e., Fe-ZIF-8) with nullostructured pores are synthesized at 35 degrees C in water by introducing dopant metal sites (Fe), which are then coated on a polypropylene (PP) separator to provide selective channels, thereby effectively inhibiting the migration of lithium polysulfides while allowing homogeneous transport of Li-ions. The active sites of the Fe-ZIF-8 enable electrocatalytic conversion, facilitating the conversion of lithium polysulfides. Moreover, the developed separator can prevent dendrite formation due to the uniform pore size and hence the even Li-ion transport and deposition. A coin cell using a Fe-ZIF-8/PP separator with S-loaded carbon cathode displayed a high cycle life of 1000 cycles with a high initial discharge capacity of 863 mAh g-1 at 0.5 C and a discharge capacity of 746 mAh g-1 at a high rate of 3 C. Promising specific capacity has been documented even under high sulfur loading of 5.0 mg cm-2 and electrolyte to the sulfur ratio (E/S) of 5 mu L mg-1. A multifunctional bimetallic MOF-based separator is designed specifically for lithium-sulfur batteries that can selectively block and convert polysulfides while providing even transport of lithium ions. Remarkably higher catalytic activity is found for the conversion of polysulfides by the Fe-doped MOF (ZIF-8) compared to the parent ZIF-8. Meanwhile, the incorporation of Fe (II) centers into the ZIF framework dramatically improves the specific capacity and rate capability.image",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 145,
|
|
"Times Cited, All Databases": 145,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JAN",
|
|
"Publication Year": 2024,
|
|
"Volume": 14,
|
|
"Issue": 3,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": null,
|
|
"DOI": "10.1002/aenm.202302897",
|
|
"DOI Link": "http://dx.doi.org/10.1002/aenm.202302897",
|
|
"Book DOI": null,
|
|
"Early Access Date": "NOV 2023",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry; Energy & Fuels; Materials Science; Physics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001105691300001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Wang, SJ; Zhang, X; Tang, YX; Hao, SY; Zheng, SA; Qiao, J; Wang, Z; Wu, LL; Liu, JR; Wang, FL",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Wang, Shijie; Zhang, Xue; Tang, Yunxiang; Hao, Shuyan; Zheng, Sinull; Qiao, Jing; Wang, Zhou; Wu, Lili; Liu, Jiurong; Wang, Fenglong",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Facile fabrication of biomass chitosan-derived magnetic carbon aerogels as multifunctional and high-efficiency electromagnetic wave absorption materials",
|
|
"Source Title": "CARBON",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "Biomass chitosan-derived porous carbon-based materials take the advantage of light weight, adjustable intrinsic conductivity, and environmental friendliness, attracting more attention in the field of electromagnetic compatibility. However, exploring a facile fabrication method to achieve rational structure design and electrical-magnetic coupling for electromagnetic absorption performance enhancement still remains challenging. Here, a unique honeycomb-like porous cobalt/carbon aerogel is fabricated through the directional freezing-drying and carbonization process, and abundant and even-distributed cobalt particles in-situ grow on the carbon skeletons. The aerogel exhibits an impressive electromagnetic wave absorption performance of a-75.8-dB absorption intensity and a-256.9-dB mm-1 specific reflection loss at a low filling content (10%), as well as an 8.53-GHz effective absorption bandwidth. Besides, the aerogel also demonstrates classy radar stealth and thermal insu-lation performance. The eco-friendly, easily fabricated, and high-performance cobalt/carbon aerogel suggests broad application prospects for electromagnetic compatibility and protection, thermal management, and multifarious electron devices.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 132,
|
|
"Times Cited, All Databases": 133,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JAN 5",
|
|
"Publication Year": 2024,
|
|
"Volume": 216,
|
|
"Issue": null,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 118528,
|
|
"DOI": "10.1016/j.carbon.2023.118528",
|
|
"DOI Link": "http://dx.doi.org/10.1016/j.carbon.2023.118528",
|
|
"Book DOI": null,
|
|
"Early Access Date": "OCT 2023",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry; Materials Science",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001092870600001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Tang, YQ; Mak, CH; Zhang, J; Jia, GH; Cheng, KC; Song, HS; Yuan, MJ; Zhao, SJ; Kai, JJ; Colmenares, JC; Hsu, HY",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Tang, Yunqi; Mak, Chun Hong; Zhang, Jun; Jia, Guohua; Cheng, Kuan-Chen; Song, Haisheng; Yuan, Mingjian; Zhao, Shijun; Kai, Ji-Jung; Colmenares, Juan Carlos; Hsu, Hsien-Yi",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Unravelling the Interfacial Dynamics of Bandgap Funneling in Bismuth-Based Halide Perovskites",
|
|
"Source Title": "ADVANCED MATERIALS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "An environmentally friendly mixed-halide perovskite MA(3)Bi(2)Cl(9-)(x)I(x) with a bandgap funnel structure has been developed. However, the dynamic interfacial interactions of bandgap funneling in MA(3)Bi(2)Cl(9-)(x)I(x) perovskites in the photoelectrochemical (PEC) system remain ambiguous. In light of this, single- and mixed-halide lead-free bismuth-based hybrid perovskites-MA(3)Bi(2)Cl(9-)(y)I(y) and MA(3)Bi(2)I(9) (named MBCl-I and MBI)-in the presence and absence of the bandgap funnel structure, respectively, are prepared. Using temperature-dependent transient photoluminescence and electrochemical voltammetric techniques, the photophysical and (photo)electrochemical phenomena of solid-solid and solid-liquid interfaces for MBCl-I and MBI halide perovskites are therefore confirmed. Concerning the mixed-halide hybrid perovskites MBCl-I with a bandgap funnel structure, stronger electronic coupling arising from an enhanced overlap of electronic wavefunctions results in more efficient exciton transport. Besides, MBCl-I's effective diffusion coefficient and electron-transfer rate demonstrate efficient heterogeneous charge transfer at the solid-liquid interface, generating improved photoelectrochemical hydrogen production. Consequently, this combination of photophysical and electrochemical techniques opens up an avenue to explore the intrinsic and interfacial properties of semiconductor materials for elucidating the correlation between material characterization and device performance.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 177,
|
|
"Times Cited, All Databases": 177,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JAN 12",
|
|
"Publication Year": 2023,
|
|
"Volume": 35,
|
|
"Issue": 2,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": null,
|
|
"DOI": "10.1002/adma.202207835",
|
|
"DOI Link": "http://dx.doi.org/10.1002/adma.202207835",
|
|
"Book DOI": null,
|
|
"Early Access Date": "NOV 2022",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry; Science & Technology - Other Topics; Materials Science; Physics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000888939100001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Li, XM; Dong, QB; Li, F; Zhu, QH; Tian, QY; Tian, L; Zhu, YY; Pan, B; Padervand, M; Wang, CY",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Li, Ximing; Dong, Qibing; Li, Fei; Zhu, Qiuhui; Tian, Qingyun; Tian, Lin; Zhu, Yiyin; Pan, Bao; Padervand, Mohsen; Wang, Chuanyi",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Defective Bi@BiOBr/C microrods derived from Bi-MOF for efficient photocatalytic NO abatement: Directional regulation of interfacial charge transfer via carbon-loading",
|
|
"Source Title": "APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "The implementation of precisely directional electron transfer at the interface of catalysts is still considered a huge challenge. Herein, hierarchical Bi@BiOBr/C microrods derived from a novel Bi-MOF were employed as a model to precisely construct the atomic-level interface electrons transfer channels via carbon-bismuth bonding. The optimized Bi@BiOBr/C with plasmonic Bi and oxygen vacancies exhibited a photocatalytic removal efficiency of 69.5 % for ppb-level atmospheric NO, which is 3.5 times higher than that of pure BiOBr (19.8 %). The enhanced photocatalytic performance is owing to precisely constructed electron transport channels with loaded graphitic carbon as a bridge (i.e., BiOBr -> graphitic carbon -> Bi nulloparticles). Further DFT calculations demonstrated the built-in graphitic carbon reconstructs an Ohmic contact with BiOBr and eliminates the Schottky barrier between BiOBr and Bi nulloparticles, enhancing the photoelectron transfer efficiency. This research represents an exciting case for the modulation of photoelectron transfer at the catalysts interface for air purification.",
|
|
"Addresses": null,
|
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"Affiliations": null,
|
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"Reprint Addresses": null,
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"Funding Orgs": null,
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"Funding Name Preferred": null,
|
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"Funding Text": null,
|
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"Cited References": null,
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"Cited Reference Count": null,
|
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"Times Cited, WoS Core": 71,
|
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"Times Cited, All Databases": 72,
|
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"180 Day Usage Count": null,
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"Since 2013 Usage Count": null,
|
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"Publisher": null,
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"ISBN": null,
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"Journal Abbreviation": null,
|
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"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JAN",
|
|
"Publication Year": 2024,
|
|
"Volume": 340,
|
|
"Issue": null,
|
|
"Part Number": null,
|
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"Supplement": null,
|
|
"Special Issue": null,
|
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"Meeting Abstract": null,
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"Start Page": null,
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"End Page": null,
|
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"Article Number": 123238,
|
|
"DOI": "10.1016/j.apcatb.2023.123238",
|
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"DOI Link": "http://dx.doi.org/10.1016/j.apcatb.2023.123238",
|
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"Book DOI": null,
|
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"Early Access Date": "SEP 2023",
|
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"Number of Pages": null,
|
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"WoS Categories": null,
|
|
"Web of Science Index": null,
|
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"Research Areas": "Chemistry; Engineering",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
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"Open Access Designations": null,
|
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"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001076231400001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Zhang, X; Su, H; Cui, PX; Cao, YY; Teng, ZY; Zhang, QT; Wang, Y; Feng, YB; Feng, R; Hou, JX; Zhou, XY; Ma, PJ; Hu, HW; Wang, KW; Wang, C; Gan, LY; Zhao, YX; Liu, QH; Zhang, TR; Zheng, K",
|
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"Book Authors": null,
|
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"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Zhang, Xu; Su, Hui; Cui, Peixin; Cao, Yongyong; Teng, Zhenyuan; Zhang, Qitao; Wang, Yang; Feng, Yibo; Feng, Ran; Hou, Jixiang; Zhou, Xiyuan; Ma, Peijie; Hu, Hanwen; Wang, Kaiwen; Wang, Cong; Gan, Liyong; Zhao, Yunxuan; Liu, Qinghua; Zhang, Tierui; Zheng, Kun",
|
|
"Book Author Full Names": null,
|
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"Group Authors": null,
|
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"Article Title": "Developing Ni single-atom sites in carbon nitride for efficient photocatalytic H2O2 production",
|
|
"Source Title": "NATURE COMMUNICATIONS",
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"Book Series Title": null,
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"Book Series Subtitle": null,
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"Language": null,
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"Document Type": "Article",
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"Conference Date": null,
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"Conference Sponsor": null,
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"Author Keywords": null,
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"Keywords Plus": null,
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"Abstract": "Photocatalytic two-electron oxygen reduction to produce high-value hydrogen peroxide (H2O2) is gaining popularity as a promising avenue of research. However, structural evolution mechanisms of catalytically active sites in the entire photosynthetic H2O2 system remains unclear and seriously hinders the development of highly-active and stable H2O2 photocatalysts. Herein, we report a high-loading Ni single-atom photocatalyst for efficient H2O2 synthesis in pure water, achieving an apparent quantum yield of 10.9% at 420nm and a solar-to-chemical conversion efficiency of 0.82%. Importantly, using in situ synchrotron X-ray absorption spectroscopy and Raman spectroscopy we directly observe that initial Ni-N-3 sites dynamically transform into high-valent O-1-Ni-N-2 sites after O-2 adsorption and further evolve to form a key *OOH intermediate before finally forming HOO-Ni-N-2. Theoretical calculations and experiments further reveal that the evolution of the active sites structure reduces the formation energy barrier of *OOH and suppresses the O=O bond dissociation, leading to improved H2O2 production activity and selectivity.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
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"Researcher Ids": null,
|
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"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 172,
|
|
"Times Cited, All Databases": 175,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
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"Publisher Address": null,
|
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"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "NOV 6",
|
|
"Publication Year": 2023,
|
|
"Volume": 14,
|
|
"Issue": 1,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 7115,
|
|
"DOI": "10.1038/s41467-023-42887-y",
|
|
"DOI Link": "http://dx.doi.org/10.1038/s41467-023-42887-y",
|
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"Book DOI": null,
|
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"Early Access Date": null,
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001142811000024",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Awual, E; Salman, MS; Hasan, MM; Hasan, MN; Kubra, KT; Sheikh, MC; Rasee, AI; Rehan, AI; Waliullah, RM; Hossain, MS; Marwani, HM; Asiri, AM; Rahman, MM; Islam, A; Khaleque, MA; Awual, MR",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Awual, Eti; Salman, Md Shad; Hasan, Md Munjur; Hasan, Md Nazmul; Kubra, Khadiza Tul; Sheikh, Md Chanmiya; Rasee, Adiba Islam; Rehan, Ariyan Islam; Waliullah, R. M.; Hossain, Mohammed Sohrab; Marwani, Hadi M.; Asiri, Abdullah M.; Rahman, Mohammed M.; Islam, Aminul; Khaleque, Md Abdul; Awual, Md Rabiul",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Ligand imprinted composite adsorbent for effective Ni(II) ion monitoring and removal from contaminated water",
|
|
"Source Title": "JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY",
|
|
"Book Series Title": null,
|
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"Book Series Subtitle": null,
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"Language": null,
|
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"Document Type": "Article",
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"Conference Title": null,
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"Conference Date": null,
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"Conference Location": null,
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"Conference Sponsor": null,
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"Conference Host": null,
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|
"Author Keywords": null,
|
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"Keywords Plus": null,
|
|
"Abstract": "Heavy metal especially nickel (Ni(II)) is the most pernicious kind of pollution since it is both poisonous and difficult to break down in nature and can cause many human disorders and diseases. The monitoring and removal of Ni(II) ions optically is required to enhance the quality of the water and make it appropriate for drinking as well as other uses around the residence. Therefore, the goal of the current work was to synthesize ligand imprinted composite adsorbent (MCA) and utilize it as an adsorbent to monitor and remove Ni(II) ions from the water. Based on the findings gathered, the MCA that was synthesized had a large particle size with a high surface area even after the ligand impregnation. The MCA was enhanced significantly in color with the contact of Ni(II) ion with limit detection at 0.35 mu g/L. The maximum level of Ni(II) ions was eliminated (99 %) when the pH was adjusted to 5.50. The Langmuir model was also used to study the adsorption equilibrium data and the maximum adsorption capacity was 167.55 mg/g. Additionally, the method can selectively detect and remove Ni(II) even in the presence of diverse metal ions. Overall, the MCA offers an ideal platform for the on-site monitoring and removal of heavy metal ions, especially in resource-limited areas.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 164,
|
|
"Times Cited, All Databases": 168,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "MAR 25",
|
|
"Publication Year": 2024,
|
|
"Volume": 131,
|
|
"Issue": null,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 585,
|
|
"End Page": 592,
|
|
"Article Number": null,
|
|
"DOI": "10.1016/j.jiec.2023.10.062",
|
|
"DOI Link": "http://dx.doi.org/10.1016/j.jiec.2023.10.062",
|
|
"Book DOI": null,
|
|
"Early Access Date": "DEC 2023",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry; Engineering",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001142454000001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Zhu, HH; Qin, G; Zhou, W; Li, Y; Zhou, XB",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Zhu, Henghai; Qin, Gang; Zhou, Wei; Li, Yang; Zhou, Xiaobing",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Constructing flake-like ternary rare earth Pr3Si2C2 ceramic on SiC whiskers to enhance electromagnetic wave absorption properties",
|
|
"Source Title": "CERAMICS INTERNATIONAL",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "In this work, flaky-like ternary Pr3Si2C2 was successfully coated in SiC whiskers (SiCw) via a molten salt process to augment the electromagnetic wave absorption (EWA) efficiency and expand the application potential of ternary rare earth silicate (RE3Si2C2) materials. Comprehensive investigations into the phase composition, morphological characteristics, EWA capacity, and corresponding mechanisms of the material were conducted. Furthermore, the electric field distribution is simulated and calculated for both vertical and horizontal incidence of the electromagnetic wave (EMW) on the specimens. Results showed that the incorporation of Pr3Si2C2 coating on SiC whiskers induces the development of heterogeneous interfaces and conductive networks, thereby augmenting polarization loss and conductive polarization, correspondingly enhancing the EWA performance of the material. In synergy with excellent attenuation ability and enhanced impedance matching, the Pr3Si2C2/SiCw composite demonstrates superior EWA performance in comparison to pristine SiCw. The minimum reflection loss (RLmin) of Pr3Si2C2/SiCw composites was achieved -48.117 dB accompanied by the effective absorption bandwidth (EAB) of 5.04 GHz at a thin thickness of merely 2.71 mm in the frequency range of 2-18 GHz. This research will serve as a valuable reference for the investigation of ternary rare earth ceramic-based EWA material.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 65,
|
|
"Times Cited, All Databases": 67,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JAN 1",
|
|
"Publication Year": 2024,
|
|
"Volume": 50,
|
|
"Issue": 1,
|
|
"Part Number": "A",
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 134,
|
|
"End Page": 142,
|
|
"Article Number": null,
|
|
"DOI": "10.1016/j.ceramint.2023.10.050",
|
|
"DOI Link": "http://dx.doi.org/10.1016/j.ceramint.2023.10.050",
|
|
"Book DOI": null,
|
|
"Early Access Date": "DEC 2023",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Materials Science",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001131768000001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Yang, SY; Wang, KL; Chen, Q; Wu, Y",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Yang, Songyu; Wang, Kailin; Chen, Qiao; Wu, Yan",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Enhanced photocatalytic hydrogen production of S-scheme TiO2/g-C3 N 4 heterojunction loaded with single-atom Ni",
|
|
"Source Title": "JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
|
"Language": null,
|
|
"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "S-scheme heterostructure photocatalysts can achieve highly efficient solar energy utilization. Here, singleatom Ni species were deposited onto TiO 2 /g-C 3 N 4 (TCN) composite photocatalyst with an S-scheme heterojunction for highly efficient photocatalytic water splitting to produce hydrogen. Under solar irradiation, it realized the hydrogen production activity of 134 mu mol g -1 h -1 , about 5 times higher than the TCN without atomic Ni. In-situ Kelvin probe force microscopy characterization and the density functional calculation certify that by forming the S-scheme heterojunction, the photo-excited electrons from the TiO 2 combine with the photogenerated holes at the coupled g-C 3 N 4 driven by a built-in electric field. More importantly, the single-atom Ni species stabilized the photogenerated electrons from the g-C 3 N 4 could effectively enhance the charge separation between the holes on the valence band of TiO 2 and electrons at the conduction band of g-C 3 N 4 . Meanwhile, the Ni atoms act as the surface catalytic centers for the water reduction reaction, which greatly improves the reactivity of the photocatalyst. The present work provides a new approach for developing noble metal-free heterojunctions for high-efficiency photocatalysis. (c) 2023 Published by Elsevier Ltd on behalf of The editorial office of Journal of Materials Science & Technology.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
|
"Researcher Ids": null,
|
|
"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 82,
|
|
"Times Cited, All Databases": 83,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "MAR 10",
|
|
"Publication Year": 2024,
|
|
"Volume": 175,
|
|
"Issue": null,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": 104,
|
|
"End Page": 114,
|
|
"Article Number": null,
|
|
"DOI": "10.1016/j.jmst.2023.07.044",
|
|
"DOI Link": "http://dx.doi.org/10.1016/j.jmst.2023.07.044",
|
|
"Book DOI": null,
|
|
"Early Access Date": "SEP 2023",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Materials Science; Metallurgy & Metallurgical Engineering",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001079213500001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Hui, SC; Zhou, X; Zhang, LM; Wu, HJ",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Hui, Shengchong; Zhou, Xu; Zhang, Limin; Wu, Hongjing",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Constructing Multiphase-Induced Interfacial Polarization to Surpass Defect-Induced Polarization in Multielement Sulfide Absorbers",
|
|
"Source Title": "ADVANCED SCIENCE",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
|
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"Language": null,
|
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"Document Type": "Article",
|
|
"Conference Title": null,
|
|
"Conference Date": null,
|
|
"Conference Location": null,
|
|
"Conference Sponsor": null,
|
|
"Conference Host": null,
|
|
"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "The extremely weak heterointerface construction of high-entropy materials (HEM) hinders them being the electromagnetic wave (EMW) absorbers with ideal properties. To address this issue, this study proposes multiphase interfacial engineering and results in a multiphase-induced interfacial polarization loss in multielement sulfides. Through the selection of atoms with diverse reaction activities, the multiphase interfacial components of CuS (1 0 5), Fe0.5Ni0.5S2 (2 1 0), and CuFe2S3 (2 0 0) are constructed to enhance the interfacial polarization loss in multielement Cu-based sulfides. Compared with single-phase high-entropy Zn-based sulfides (ZnFeCoNiCr-S), the multiphase Cu-based sulfides (CuFeCoNiCr-S) possess optimized EMW absorption properties (effective absorption bandwidth (EAB) of 6.70 GHz at 2.00 mm) due to the existence of specific interface of CuS (1 0 5)/CuFe2S3 (2 0 0) with proper EM parameters. Furthermore, single-phase ZnFeCoNiCr-S into FeNi2S4 (3 1 1)/(Zn, Fe)S (1 1 1) heterointerface through 400 degrees C heat-treated is decomposed. The EMW absorption properties are enhanced by strong interfacial polarization (EAB of 4.83 GHz at 1.45 mm). This work reveals the reasons for the limited EMW absorption properties of high-entropy sulfides and proposes multiphase interface engineering to improve charge accumulation and polarization between specific interfaces, leading to the enhanced EMW absorption properties. This work shows that the weak electron exchange effect induced by high conformational entropy adversely affects microwave absorption. Constructing the heterointerfaces with significantly different work functions in multi-element sulfides can effectively enhance the phase interface polarization and eliminate these negative effects. This is expected to serve as a new design guideline for microwave absorbers.image",
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|
"Addresses": null,
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"Affiliations": null,
|
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"Reprint Addresses": null,
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"Researcher Ids": null,
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"Funding Name Preferred": null,
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"Funding Text": null,
|
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"Cited References": null,
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"Cited Reference Count": null,
|
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"Times Cited, WoS Core": 70,
|
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"Times Cited, All Databases": 71,
|
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"180 Day Usage Count": null,
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"Since 2013 Usage Count": null,
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"Publisher": null,
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"ISSN": null,
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"ISBN": null,
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|
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"Journal ISO Abbreviation": null,
|
|
"Publication Date": "FEB",
|
|
"Publication Year": 2024,
|
|
"Volume": 11,
|
|
"Issue": 6,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
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"Start Page": null,
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"End Page": null,
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"Article Number": null,
|
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"DOI": "10.1002/advs.202307649",
|
|
"DOI Link": "http://dx.doi.org/10.1002/advs.202307649",
|
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"Book DOI": null,
|
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"Early Access Date": "DEC 2023",
|
|
"Number of Pages": null,
|
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"WoS Categories": null,
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"Web of Science Index": null,
|
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"Research Areas": "Chemistry; Science & Technology - Other Topics; Materials Science",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
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"Highly Cited Status": "Y",
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"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001113438000001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Ye, RP; Ma, LX; Hong, XL; Reina, TR; Luo, WH; Kang, LQ; Feng, G; Zhang, RB; Fan, MH; Zhang, RG; Liu, J",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Ye, Runping; Ma, Lixuan; Hong, Xiaoling; Reina, Tomas Ramirez; Luo, Wenhao; Kang, Liqun; Feng, Gang; Zhang, Rongbin; Fan, Maohong; Zhang, Riguang; Liu, Jian",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Boosting Low-Temperature CO2 Hydrogenation over Ni-based Catalysts by Tuning Strong Metal-Support Interactions",
|
|
"Source Title": "ANGEWANDTE CHEMIE-INTERNATIONAL EDITION",
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"Book Series Title": null,
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"Language": null,
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"Document Type": "Article",
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"Conference Sponsor": null,
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"Author Keywords": null,
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"Keywords Plus": null,
|
|
"Abstract": "Rational design of low-cost and efficient transition-metal catalysts for low-temperature CO2 activation is significant and poses great challenges. Herein, a strategy via regulating the local electron density of active sites is developed to boost CO2 methanation that normally requires >350 degrees C for commercial Ni catalysts. An optimal Ni/ZrO2 catalyst affords an excellent low-temperature performance hitherto, with a CO2 conversion of 84.0 %, CH4 selectivity of 98.6 % even at 230 degrees C and GHSV of 12,000 mL g(-1) h(-1) for 106 h, reflecting one of the best CO2 methanation performance to date on Ni-based catalysts. Combined a series of in situ spectroscopic characterization studies reveal that re-constructing monoclinic-ZrO2 supported Ni species with abundant oxygen vacancies can facilitate CO2 activation, owing to the enhanced local electron density of Ni induced by the strong metal-support interactions. These findings might be of great aid for construction of robust catalysts with an enhanced performance for CO2 emission abatement and beyond.",
|
|
"Addresses": null,
|
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"Affiliations": null,
|
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"Reprint Addresses": null,
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"Email Addresses": null,
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"Researcher Ids": null,
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"ORCIDs": null,
|
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"Funding Orgs": null,
|
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"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 89,
|
|
"Times Cited, All Databases": 89,
|
|
"180 Day Usage Count": null,
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"Since 2013 Usage Count": null,
|
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"Publisher": null,
|
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"Publisher City": null,
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"Publisher Address": null,
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"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
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"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JAN 15",
|
|
"Publication Year": 2024,
|
|
"Volume": 63,
|
|
"Issue": 3,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": null,
|
|
"DOI": "10.1002/anie.202317669",
|
|
"DOI Link": "http://dx.doi.org/10.1002/anie.202317669",
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"Book DOI": null,
|
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"Early Access Date": "DEC 2023",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
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"Web of Science Index": null,
|
|
"Research Areas": "Chemistry",
|
|
"IDS Number": null,
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"Pubmed Id": null,
|
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"Open Access Designations": null,
|
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"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "Y",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001117638400001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Deng, ZX; Zhang, H; Priimagi, A; Zeng, H",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Deng, Zixuan; Zhang, Hang; Priimagi, Arri; Zeng, Hao",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Light-Fueled Nonreciprocal Self-Oscillators for Fluidic Transportation and Coupling",
|
|
"Source Title": "ADVANCED MATERIALS",
|
|
"Book Series Title": null,
|
|
"Book Series Subtitle": null,
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"Language": null,
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"Document Type": "Article",
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"Conference Sponsor": null,
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"Author Keywords": null,
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"Keywords Plus": null,
|
|
"Abstract": "Light-fueled self-oscillators based on soft actuating materials have triggered novel designs for small-scale robotic constructs that self-sustain their motion at non-equilibrium states and possess bioinspired autonomy and adaptive functions. However, the motions of most self-oscillators are reciprocal, which hinders their use in sophisticated biomimetic functions such as fluidic transportation. Here, an optically powered soft material strip that can perform nonreciprocal, cilia-like, self-sustained oscillation under water is reported. The actuator is made of planar-aligned liquid crystal elastomer responding to visible light. Two laser beams from orthogonal directions allow for piecewise control over the strip deformation, enabling two self-shadowing effects coupled in one single material to yield nonreciprocal strokes. The nonreciprocity, stroke pattern and handedness are connected to the fluidic pumping efficiency, which can be controlled by the excitation conditions. Autonomous microfluidic pumping in clockwise and anticlockwise directions, translocation of a micro-object by liquid propulsion, and coupling between two oscillating strips through liquid medium interaction are demonstrated. The results offer new concepts for non-equilibrium soft actuators that can perform bio-like functions under water.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
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|
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|
|
"Funding Text": null,
|
|
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|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 86,
|
|
"Times Cited, All Databases": 86,
|
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"180 Day Usage Count": null,
|
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|
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|
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|
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|
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|
|
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|
|
"ISBN": null,
|
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|
|
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|
|
"Publication Date": "MAR",
|
|
"Publication Year": 2024,
|
|
"Volume": 36,
|
|
"Issue": 12,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": "SI",
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": null,
|
|
"DOI": "10.1002/adma.202209683",
|
|
"DOI Link": "http://dx.doi.org/10.1002/adma.202209683",
|
|
"Book DOI": null,
|
|
"Early Access Date": "JAN 2023",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry; Science & Technology - Other Topics; Materials Science; Physics",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:000906511900001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Xu, MF; Ni, XX; Liu, QW; Chen, CC; Deng, XH; Wang, X; Yu, RR",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Xu, Mingfeng; Ni, Xiangxiang; Liu, Qiwei; Chen, Chengcheng; Deng, Xiaohong; Wang, Xiu; Yu, Rongrong",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Ultra-high pressure improved gelation and digestive properties of Tai Lake whitebait myofibrillar protein",
|
|
"Source Title": "FOOD CHEMISTRY-X",
|
|
"Book Series Title": null,
|
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"Book Series Subtitle": null,
|
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"Language": null,
|
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"Document Type": "Article",
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"Author Keywords": null,
|
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"Keywords Plus": null,
|
|
"Abstract": "This study investigated the effects of ultra-high pressure (UHP) at different levels on the physicochemical properties, gelling properties, and in vitro digestion characteristics of myofibrillar protein (MP) in Tai Lake whitebait. The alpha-helix gradually unfolded and transformed into beta-sheet as the pressure increased from 0 to 400 MPa. In addition, the elastic modulus (G') and viscous modulus (G) of the 400 MPa-treated MP samples increased by 4.8 and 3.8 times, respectively, compared with the control group. The gel properties of the MP also increased significantly after UHP treatment, e.g., the gel strength increased by a 4.8-fold when the pressure reached 400 Mpa, compared with the control group. The results of in vitro simulated digestion showed that the 400 MPa-treated MP gel samples showed a 1.8-fold increase in digestibility and a 69.6 % decrease in digestible particle size compared with the control group.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
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|
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|
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|
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|
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"Times Cited, WoS Core": 55,
|
|
"Times Cited, All Databases": 55,
|
|
"180 Day Usage Count": null,
|
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"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
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|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "MAR 30",
|
|
"Publication Year": 2024,
|
|
"Volume": 21,
|
|
"Issue": null,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 101061,
|
|
"DOI": "10.1016/j.fochx.2023.101061",
|
|
"DOI Link": "http://dx.doi.org/10.1016/j.fochx.2023.101061",
|
|
"Book DOI": null,
|
|
"Early Access Date": "DEC 2023",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Chemistry; Food Science & Technology",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001137691700001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
},
|
|
{
|
|
"Publication Type": "J",
|
|
"Authors": "Luo, D; Wu, ZH; Yan, YY; Cao, J; Yang, XL; Zhao, YL; Cao, BY",
|
|
"Book Authors": null,
|
|
"Book Editors": null,
|
|
"Book Group Authors": null,
|
|
"Author Full Names": "Luo, Ding; Wu, Zihao; Yan, Yuying; Cao, Jin; Yang, Xuelin; Zhao, Yulong; Cao, Bingyang",
|
|
"Book Author Full Names": null,
|
|
"Group Authors": null,
|
|
"Article Title": "Performance investigation and design optimization of a battery thermal management system with thermoelectric coolers and phase change materials",
|
|
"Source Title": "JOURNAL OF CLEANER PRODUCTION",
|
|
"Book Series Title": null,
|
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"Book Series Subtitle": null,
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"Language": null,
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"Document Type": "Article",
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"Conference Date": null,
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"Conference Location": null,
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"Conference Sponsor": null,
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|
"Conference Host": null,
|
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"Author Keywords": null,
|
|
"Keywords Plus": null,
|
|
"Abstract": "In this work, a novel battery thermal management system (BTMS) integrated with thermoelectric coolers (TECs) and phase change materials (PCMs) is developed to ensure the temperature working environment of batteries, where a fin framework is adopted to enhance the heat transfer. By establishing a transient thermal-electric-fluid multi-physics field numerical model, the thermal performance of the BTMS is thoroughly examined in two cases. The findings demonstrate that increasing the TEC input current, fin length, and thickness is beneficial for reducing the maximum temperature and PCM liquid fraction. Nevertheless, although the increase in fin length can lower the temperature difference, the influence of fin thickness and TEC input current on the temperature difference is tiny. Based on the numerical findings, the optimal fin length and thickness of 7 mm and 3 mm are obtained. In this situation, when the TEC input current is 3 A, the maximum temperature, temperature difference, and PCM liquid fraction in Case 1 are 315.10 K, 2.39 K, and 0.002, respectively, and those are respectively 318.24 K, 3.60 K, and 0.181 in Case 2. The configuration of Case 1 outperforms that of Case 2, due to the fewer TECs and greater distance from the battery pack to the TEC within Case 2. When experiencing a higher battery discharge rate, the TEC input current should also be correspondingly increased to ensure the temperature performance of the battery. The relative findings contribute to new insights into battery thermal management.",
|
|
"Addresses": null,
|
|
"Affiliations": null,
|
|
"Reprint Addresses": null,
|
|
"Email Addresses": null,
|
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"Researcher Ids": null,
|
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"ORCIDs": null,
|
|
"Funding Orgs": null,
|
|
"Funding Name Preferred": null,
|
|
"Funding Text": null,
|
|
"Cited References": null,
|
|
"Cited Reference Count": null,
|
|
"Times Cited, WoS Core": 60,
|
|
"Times Cited, All Databases": 61,
|
|
"180 Day Usage Count": null,
|
|
"Since 2013 Usage Count": null,
|
|
"Publisher": null,
|
|
"Publisher City": null,
|
|
"Publisher Address": null,
|
|
"ISSN": null,
|
|
"eISSN": null,
|
|
"ISBN": null,
|
|
"Journal Abbreviation": null,
|
|
"Journal ISO Abbreviation": null,
|
|
"Publication Date": "JAN 1",
|
|
"Publication Year": 2024,
|
|
"Volume": 434,
|
|
"Issue": null,
|
|
"Part Number": null,
|
|
"Supplement": null,
|
|
"Special Issue": null,
|
|
"Meeting Abstract": null,
|
|
"Start Page": null,
|
|
"End Page": null,
|
|
"Article Number": 139834,
|
|
"DOI": "10.1016/j.jclepro.2023.139834",
|
|
"DOI Link": "http://dx.doi.org/10.1016/j.jclepro.2023.139834",
|
|
"Book DOI": null,
|
|
"Early Access Date": "NOV 2023",
|
|
"Number of Pages": null,
|
|
"WoS Categories": null,
|
|
"Web of Science Index": null,
|
|
"Research Areas": "Science & Technology - Other Topics; Engineering; Environmental Sciences & Ecology",
|
|
"IDS Number": null,
|
|
"Pubmed Id": null,
|
|
"Open Access Designations": null,
|
|
"Highly Cited Status": "Y",
|
|
"Hot Paper Status": "N",
|
|
"Date of Export": "2025-04-23",
|
|
"UT (Unique WOS ID)": "WOS:001130014000001",
|
|
"Web of Science Record": "View Full Record in Web of Science"
|
|
}
|
|
] |