完整後設資料紀錄
DC 欄位語言
dc.contributor.authorRaja, Duraisamy Senthilen_US
dc.contributor.authorHuang, Chun-Lungen_US
dc.contributor.authorChen, Yu-Anen_US
dc.contributor.authorChoi, YongManen_US
dc.contributor.authorLu, Shih-Yuanen_US
dc.date.accessioned2020-10-05T02:01:55Z-
dc.date.available2020-10-05T02:01:55Z-
dc.date.issued2020-12-15en_US
dc.identifier.issn0926-3373en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.apcatb.2020.119375en_US
dc.identifier.urihttp://hdl.handle.net/11536/155339-
dc.description.abstractEngineering synergistic effects of multi-component catalysts is the key for breakthrough catalyst design. Here, a maximized-entropy approach was proposed to maximize the synergistic effects for maximum enhancements in electrocatalytic efficiencies of multi-component catalysts. Accordingly, composition-balanced iron, cobalt, and nickel based trimetallic MOFs was developed and demonstrated outstanding oxygen evolution reaction (OER) performances with ultra-low overpotentials of 196 and 284 mV achieved at current densities of 10 and 1000 mA cm(-2), respectively, as well as an ultra-low Tafel slope of 29.5 mV dec(-1) in alkaline aqueous media. The catalyst was ultra-stable even when operated at ultra-high current densities, experiencing only 5% loss in current densities, when chronoamperometrically tested at an industrially relevant current density of 1000 mA cm(-2) for over 50 h. in situ Raman spectroscopy study and density functional theory simulations were conducted to explore the OER mechanism and to illustrate the validity of the proposed maximized-entropy approach.en_US
dc.language.isoen_USen_US
dc.subjectWater electrolysisen_US
dc.subjectMetal-organic framework (MOF)en_US
dc.subjectLarge current densityen_US
dc.subjectWater oxidationen_US
dc.subjectNickel foamen_US
dc.titleComposition-balanced trimetallic MOFs as ultra-efficient electrocatalysts for oxygen evolution reaction at high current densitiesen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.apcatb.2020.119375en_US
dc.identifier.journalAPPLIED CATALYSIS B-ENVIRONMENTALen_US
dc.citation.volume279en_US
dc.citation.spage0en_US
dc.citation.epage0en_US
dc.contributor.department光電學院zh_TW
dc.contributor.departmentCollege of Photonicsen_US
dc.identifier.wosnumberWOS:000566454400002en_US
dc.citation.woscount0en_US
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