Wang Jiali, Liu Meng-Ting, Hsu Chia-Shuo, Chu You-Chiuan, Liao Yen-Fa, Pao Chih-Wen, Chan Ting-Shan, Chuang Wei-Tsung, Chen Jeng-Lung, Shao Yu-Cheng, Ishii Hirofumi, Hiraoka Nozomu, Chiang Ching-Yu, Chen Hao Ming
Department of Chemistry, National Taiwan University, Taipei, 10617, Taiwan.
National Synchrotron Radiation Research Center, Hsinchu, 300092, Taiwan.
Adv Mater. 2025 May;37(18):e2418797. doi: 10.1002/adma.202418797. Epub 2025 Mar 24.
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.
尽管已经开发出许多技术来实时了解电化学反应过程中固液界面的动态相互作用,但在过去几十年中,这些方法的进一步发展面临着挑战。随着高亮度同步辐射源的快速发展,原位X射线光谱技术在揭示电催化中的界面特征和催化机制方面越来越受欢迎。然而,所得光谱对X射线辐射、反应环境和采集程序等因素高度敏感,所有这些因素都可能潜在地引入常常被忽视的伪影,从而导致对电催化行为的错误解读。从这个角度出发,本文综述了几种用于电催化研究的新兴硬X射线光谱技术,突出了它们的电子跃迁过程、检测模式和功能互补性。重要的是,基于在不同光束线进行原位X射线吸收光谱的案例研究,通过对典型铜电催化剂进行光子通量密度、剂量和时间依赖性研究,系统地研究了X射线辐照产生的潜在伪影。因此,建立了一个实用的方案,用于在原位电催化研究中进行可靠的X射线光谱测量,以最小化可能影响所得X射线光谱的潜在伪影,从而确保对界面相互作用和电催化机制进行准确解读和更深入的理解。