X射线光电子能谱
钝化
电解质
电化学
碳化钨
氧化物
催化作用
钨
化学
化学工程
无机化学
碳化物
材料科学
电极
纳米技术
物理化学
图层(电子)
有机化学
工程类
作者
Christoph Grießer,S. Díaz-Coello,Matteo Olgiati,Wanderson Ferraz do Valle,Toni Moser,Andrea Auer,Elena Pastor,Markus Valtiner,Julia Kunze‐Liebhäuser
标识
DOI:10.1002/anie.202500965
摘要
Tungsten carbide (WC) is a renowned compound catalyst material for electrochemical water splitting, and its high electrocatalytic activity towards the hydrogen evolution reaction (HER) has been repeatedly reported. However, its susceptibility to oxidation raises the fundamental question of the underlying reason for its high activity, especially since passivation and thus potential deactivation can occur not only in air but also during reaction. Hence, the investigation of the surface chemistry under true operating conditions is crucial for a fundamental understanding of the electrocatalytic process. In this work we use electrochemical X‐ray photoelectron spectroscopy (EC‐XPS) to revisit the surface chemistry of WC powder electrodes in alkaline electrolyte in‐situ and under full potential control. Our results show that although the surface is initially covered with oxide, this passive film dissolves in the electrolyte under electrochemical reaction conditions. This clarifies the active surface termination during the HER and highlights the potential of laboratory‐based EC‐XPS to study applied energy conversion materials.
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