铟
钴
金属间化合物
材料科学
化学工程
纳米颗粒
氧气
无机化学
氧还原反应
浸出(土壤学)
冶金
电极
电化学
纳米技术
化学
物理化学
有机化学
环境科学
合金
土壤科学
土壤水分
工程类
作者
J. Niklas Hausmann,Marten L. P. Ashton,Stefan Mebs,Carsten Walter,Sören Selve,Michael Haumann,Tobias Sontheimer,Holger Dau,Matthias Drieß,Prashanth W. Menezes
出处
期刊:Small
[Wiley]
日期:2024-02-17
卷期号:20 (29): e2309749-e2309749
被引量:11
标识
DOI:10.1002/smll.202309749
摘要
Merely all transition-metal-based materials reconstruct into similar oxyhydroxides during the electrocatalytic oxygen evolution reaction (OER), severely limiting the options for a tailored OER catalyst design. In such reconstructions, initial constituent p-block elements take a sacrificial role and leach into the electrolyte as oxyanions, thereby losing the ability to tune the catalyst's properties systematically. From a thermodynamic point of view, indium is expected to behave differently and should remain in the solid phase under alkaline OER conditions. However, the structural behavior of transition metal indium phases during the OER remains unexplored. Herein, are synthesized intermetallic cobalt indium (CoIn3) nanoparticles and revealed by in situ X-ray absorption spectroscopy and scanning transmission microscopy that they undergo phase segregation to cobalt oxyhydroxide and indium hydroxide. The obtained cobalt oxyhydroxide outperforms a metallic-cobalt-derived one due to more accessible active sites. The observed phase segregation shows that indium behaves distinctively differently from most p-block elements and remains at the electrode surface, where it can form lasting interfaces with the active metal oxo phases.
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