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DOI | 10.1039/d0ee00755b |
In situ structural evolution of the multi-site alloy electrocatalyst to manipulate the intermediate for enhanced water oxidation reaction | |
Wang B.; Zhao K.; Yu Z.; Sun C.; Wang Z.; Feng N.; Mai L.; Wang Y.; Xia Y. | |
发表日期 | 2020 |
ISSN | 17545692 |
起始页码 | 2200 |
结束页码 | 2208 |
卷号 | 13期号:7 |
英文摘要 | Investigating the reaction mechanism and the rational design of highly efficient electrocatalysts for the oxygen evolution reaction play a key role in renewable energy applications. Here, we report a homogeneous multi-metal-site oxyhydroxide electrocatalyst (consisting of Fe doped NiOOH and Cu doped NiOOH) obtained by in situ electrochemical dealloying of the multi-metal-site alloy (consisting of FeNi3 and NiCu alloys). The in situ structural evolution process manipulates the intermediate and enhances the water oxidation performance. After dealloying, the electrochemically dealloyed catalyst exhibits a small overpotential at large current density (250 mV at 100 mA cm-2), low Tafel slope (34 mV dec-1), remarkably increased ECSA (8-fold larger than before), and superior durability for 200 h at 100 mA cm-2. This electrocatalyst presents one of the best performances among all reported transition metal-based electrocatalysts, and is even superior to the benchmark RuO2. Operando ATR FT-IR reveals that the electrochemically dealloyed electrocatalyst could manipulate the reaction path based on direct O2 evolution mechanism (DOEM) and facilitate the formation of O-O bonds. This fundamental understanding will contribute to the identification and design of the active structure of oxygen evolution electrocatalysts. © 2020 The Royal Society of Chemistry. |
英文关键词 | Binary alloys; Dealloying; Electrocatalysts; Electrolysis; Oxygen; Oxygen evolution reaction; Ruthenium compounds; Transition metals; Active structures; Large current density; Oxygen evolution; Rational design; Reaction mechanism; Renewable energy applications; Structural evolution; Water oxidation; Reaction intermediates; alloy; catalysis; catalyst; concentration (composition); electrochemistry; oxidation; performance assessment |
语种 | 英语 |
来源期刊 | Energy & Environmental Science
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文献类型 | 期刊论文 |
条目标识符 | http://gcip.llas.ac.cn/handle/2XKMVOVA/189615 |
作者单位 | Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Institute of New Energy, IChEM (Collaborative Innovation Center of Chemistry for Energy Materials), Fudan University, Shanghai, 200433, China; State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, State Key Laboratory of Silicate Materials for Architectures, International School of Materials Science and Engineering, Wuhan University of Technology, Wuhan, 430070, China; NRC (Nanostructure Research Centre), Wuhan University of Technology, Wuhan, 430070, China |
推荐引用方式 GB/T 7714 | Wang B.,Zhao K.,Yu Z.,et al. In situ structural evolution of the multi-site alloy electrocatalyst to manipulate the intermediate for enhanced water oxidation reaction[J],2020,13(7). |
APA | Wang B..,Zhao K..,Yu Z..,Sun C..,Wang Z..,...&Xia Y..(2020).In situ structural evolution of the multi-site alloy electrocatalyst to manipulate the intermediate for enhanced water oxidation reaction.Energy & Environmental Science,13(7). |
MLA | Wang B.,et al."In situ structural evolution of the multi-site alloy electrocatalyst to manipulate the intermediate for enhanced water oxidation reaction".Energy & Environmental Science 13.7(2020). |
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