电催化剂
材料科学
同步辐射
纳米技术
X射线吸收光谱法
同步加速器
电化学
吸收光谱法
纳米材料
电极
化学
物理化学
光学
物理
作者
Jiali Wang,Meng-Ting Liu,Chia‐Shuo Hsu,You‐Chiuan Chu,Yen‐Fa Liao,Chih‐Wen Pao,Ting‐Shan Chan,Wei‐Tsung Chuang,Jeng‐Lung Chen,Yu‐Cheng Shao,Hirofumi Ishii,Nozomu Hiraoka,Ching‐Yu Chiang,Hao Ming Chen
标识
DOI:10.1002/adma.202418797
摘要
Although numerous techniques are developed to enable real-time understanding of dynamic interactions at the solid-liquid interface during electrochemical reactions, further progress in the development of these methods over the last several decades has faced challenges. With the rapid development of high-brilliance synchrotron sources, operando X-ray spectroscopies have become increasingly popular for revealing interfacial features and catalytic mechanisms in electrocatalysis. Nevertheless, the resulting spectra are highly sensitive to factors such as X-ray radiation, reaction environment, and acquisition procedures, all of which may potentially introduce artifacts that are often overlooked, leading to misinterpretations of electrocatalytic behaviors. In this perspective, several emerging hard X-ray spectroscopies used in electrocatalysis research are reviewed, highlighting their electronic transition processes, detection modes, and functional complementarity. Significantly, based on a case study of operando X-ray absorption spectroscopy at various beamlines, potential artifacts generated by X-ray irradiation are systematically investigated through photon-flux density-, dose-, and time-dependent studies of typical copper electrocatalysts. Accordingly, a practical protocol for conducting reliable X-ray spectroscopic measurements in operando electrocatalytic studies to minimize potential artifacts that can affect the resulting X-ray spectra, thereby ensuring accurate interpretation and a deeper understanding of interfacial interactions and electrocatalytic mechanisms, is established.
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