Advanced X-ray spectroscopies: Unveiling chemical reaction mechanism in photo/electrocatalytic water splitting

被引:0
作者
Shen, Lifu [1 ]
Yu, Pengfei [2 ]
Meng, Jianwei [2 ]
Liu, Xiaosong [3 ]
Weng, Tsu-Chien [1 ,2 ]
机构
[1] ShanghaiTech Univ, Sch Phys Sci & Technol, Shanghai 200100, Peoples R China
[2] ShanghaiTech Univ, Ctr Transformat Sci, Shanghai 200100, Peoples R China
[3] Univ Sci & Technol China, Natl Synchrotron Radiat Lab, Hefei 230029, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
X-ray spectroscopy; In-situ / operando measurement; Spectroscopic imaging; Photo/electrocatalysis; Water splitting; HYDROGEN-EVOLUTION REACTION; PHOTOELECTRON-SPECTROSCOPY; ELECTRONIC-STRUCTURE; OXYGEN REDUCTION; WORKING CATALYST; TRANSITION-METAL; TOOL; ELECTROCHEMISTRY; SPECTRA; SURFACE;
D O I
10.1016/j.mtchem.2024.102397
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The challenge of detecting intermediates in photo/electrocatalytic water splitting hinges critically on a profound understanding of processes across multiple spatial and temporal scales, encompassing electron excitation, electron transfer, interfacial reaction kinetics and so on. Advanced X-ray spectroscopies are powerful tools for analyzing complex processes at various scales. They offer non-destructive insights into electron dynamics, local structures, crystal lattices, and material distributions through absorption and imaging. This article provides an overview of the diverse applications of X-ray spectroscopies in the study of photo/electrocatalytic water splitting. It begins by introducing the fundamental principles of photo/electrocatalytic reactions for water splitting. Subsequently, it discusses the successful application of X-ray spectroscopic tools on the scales of energy resolution, temporal resolution, and spatial resolution in elucidating the mechanisms of chemical reactions in photo/ electrocatalytic water splitting. Finally, the review looks forward to the development of advanced X-ray spectroscopies and their potential applications in catalytic water splitting reactions.
引用
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页数:28
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