X射线吸收精细结构
电催化剂
扩展X射线吸收精细结构
氧烷
X射线吸收光谱法
吸收光谱法
化学物理
过渡金属
化学
吸收(声学)
纳米技术
电子结构
催化作用
材料科学
光谱学
电化学
物理化学
电极
计算化学
光学
物理
生物化学
量子力学
复合材料
作者
Wen Cheng,Peng Fan,Wei Jin
标识
DOI:10.1002/cssc.202401306
摘要
Abstract As the global energy structure evolves and clean energy technologies advance, electrocatalysis has become a focal point as a critical conversion pathway in the new energy sector. Transitional metal electrocatalysts (TMEs) with their distinctive electronic structures and redox properties show great potential in electrocatalytic reactions. However, complex reaction mechanisms and kinetic limitations hinder the improvement of energy conversion efficiency, highlighting the necessity for comprehensive studies on structure and performance of electrocatalysts. X‐ray Absorption Fine Structure (XAFS) spectra stand out as a robust tool for examining the electrocatalyst′s structures and performance due to its atomic selectivity and sensitivity to local environments. This review delves into the application of XAFS technology in characterizing TMEs, providing in‐depth analyses of X‐ray Absorption Near‐Edge Structure (XANES) spectra, and Extended XAFS (EXAFS) spectra in both R‐space and k ‐space. These analyses reveal intrinsic structural information, electronic interactions, catalyst stability, and aggregation morphology. Furthermore, the paper examines advancements in in‐situ XAFS techniques for real‐time monitoring of active site changes, capturing critical intermediate and transitional states, and elucidating the evolution of active species during electrocatalytic reactions. These insights deepen our understanding on structure‐activity relationship of electrocatalysts and offer valuable guidance for designing and developing highly active and stable electrocatalysts.
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