纳米技术
电化学
同步加速器
反应动力学
电化学能量转换
材料科学
计算机科学
生化工程
化学
物理
电极
有机化学
光学
工程类
物理化学
分子
作者
Yao Yang,Julian Feijóo,Valentín Briega‐Martos,Qihao Li,Mihail R. Krumov,Stefan Merkens,Giuseppe De Salvo,Andrey Chuvilin,Jianbo Jin,Haowei Huang,Christopher J. Pollock,Miquel Salmerón,Cheng Wang,David A. Muller,Héctor D. Abruña,Peidong Yang
标识
DOI:10.1016/j.coelec.2023.101403
摘要
One of the grand challenges facing electrochemistry is to directly resolve the complex nature of (electro)catalyst active sites and capture real-time “movies” of reaction dynamics, i.e. “watching chemistry in action”. The need for such fundamental understanding has stimulated the development of operando/in situ methods, which have greatly enhanced our ability to identify activity descriptors of electrocatalysts and establish structure–property relationships of energy materials. This review summarizes the frontiers of operando electrochemical liquid-cell scanning transmission electron microscopy and correlative synchrotron X-ray methods, which are complementary tools to comprehensively investigate reaction dynamics across multiple spatiotemporal scales. In an effort to encourage greater adoption of advanced operando methods by the general electrochemistry community, this review points out the need to benchmark electrochemistry in confined and heterogenous liquid environment with minimal beam-induced damage. We anticipate that multimodal operando methods will become indispensable for understanding interfacial reaction mechanisms for the broad chemistry and energy materials communities.
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