电润湿
材料科学
催化作用
氧气
氧化钴
氧化物
化学工程
表面能
析氧
电化学
氧化还原
润湿
接触角
相(物质)
润湿转变
透射电子显微镜
化学
纳米技术
无机化学
电极
物理化学
有机化学
复合材料
冶金
工程类
作者
Tzu‐Hsien Shen,Liam Spillane,Jiayu Peng,Yang Shao‐Horn,Vasiliki Tileli
标识
DOI:10.1038/s41929-021-00723-w
摘要
The surface wettability of catalysts is typically controlled via surface treatments that promote catalytic performance. Here we report on potential-regulated hydrophobicity/hydrophilicity at cobalt-based oxide interfaces with an alkaline solution. The switchable wetting of single particles, directly related to their activity and stability towards the oxygen evolution reaction, was revealed by electrochemical liquid-phase transmission electron microscopy. Analysis of the movement of the liquid in real time revealed distinctive wettability behaviour associated with specific potential ranges. At low potentials, an overall reduction of the hydrophobicity of the oxides was probed. Upon reversible reconstruction towards the surface oxyhydroxide phase, electrowetting was found to cause a change in the interfacial capacitance. At high potentials, the evolution of molecular oxygen, confirmed by operando electron energy-loss spectroscopy, was accompanied by a globally thinner liquid layer. This work directly links the physical wetting with the chemical oxygen evolution reaction of single particles, providing fundamental insights into solid-liquid interfacial interactions of oxygen-evolving oxides.
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