纳米材料基催化剂
溶解
电催化剂
铜
电化学
化学
聚结(物理)
材料科学
X射线吸收光谱法
化学工程
吸收光谱法
无机化学
纳米技术
电极
催化作用
物理化学
冶金
工程类
物理
天体生物学
量子力学
生物化学
作者
Jan Vávra,Tzu‐Hsien Shen,Dana Stoian,Vasiliki Tileli,Raffaella Buonsanti
标识
DOI:10.1002/ange.202011137
摘要
Abstract Size, morphology, and surface sites of electrocatalysts have a major impact on their performance. Understanding how, when, and why these parameters change under operating conditions is of importance for designing stable, active, and selective catalysts. Herein, we study the reconstruction of a Cu‐based nanocatalysts during the startup phase of the electrochemical CO 2 reduction reaction by combining results from electrochemical in situ transmission electron microscopy with operando X‐ray absorption spectroscopy. We reveal that dissolution followed by redeposition, rather than coalescence, is the mechanism responsible for the size increase and morphology change of the electrocatalyst. Furthermore, we point out the key role played by the formation of copper oxides in the process. Understanding of the underlying processes opens a pathway to rational design of Cu electro (re)deposited catalysts and to stability improvement for catalysts fabricated by other methods.
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