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通过原位拉曼光谱对钯单晶表面电氧化的可视化研究

Visualization of Electrooxidation on Palladium Single Crystal Surfaces via In Situ Raman Spectroscopy.

作者信息

Sun Yu-Lin, Ji Xu, Wang Xue, He Quan-Feng, Dong Jin-Chao, Le Jia-Bo, Li Jian-Feng

机构信息

State Key Laboratory of Physical Chemistry of Solid Surfaces, iChEM, College of Chemistry and Chemical Engineering, College of Energy, College of Materials, Xiamen University, 361005, Xiamen, China.

Key Laboratory of Advanced Fuel Cells and Electrolyzers Technology of Zhejiang Province, Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, Key Laboratory of Advanced Marine Materials, Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, 315201, Ningbo, China.

出版信息

Angew Chem Int Ed Engl. 2024 Oct 24;63(44):e202408736. doi: 10.1002/anie.202408736. Epub 2024 Sep 24.

Abstract

The electrooxidation of catalyst surfaces is across various electrocatalytic reactions, directly impacting their activity, stability and selectivity. Precisely characterizing the electrooxidation on well-defined surfaces is essential to understanding electrocatalytic reactions comprehensively. Herein, we employed in situ Raman spectroscopy to monitor the electrooxidation process of palladium single crystal. Our findings reveal that the Pd surface's initial electrooxidation process involves forming *OH intermediate and ClO ions facilitate the deprotonation process, leading to the formation of PdO. Subsequently, under deep electrooxidation potential range, the oxygen atoms within PdO contribute to creating surface-bound peroxide species, ultimately resulting in oxygen generation. The adsorption strength of *OH and the coverage of ClO can be adjusted by the controllable electronic effect, resulting in different oxidation rates. This study offers valuable insights into elucidating the electrooxidation mechanisms underlying a range of electrocatalytic reactions, thereby contributing to the rational design of catalysts.

摘要

催化剂表面的电氧化作用贯穿于各种电催化反应中,直接影响其活性、稳定性和选择性。精确表征在明确界定的表面上的电氧化作用对于全面理解电催化反应至关重要。在此,我们采用原位拉曼光谱来监测钯单晶的电氧化过程。我们的研究结果表明,钯表面的初始电氧化过程涉及形成*OH中间体,并且ClO离子促进去质子化过程,导致形成PdO。随后,在深度电氧化电位范围内,PdO中的氧原子有助于产生表面结合的过氧化物物种,最终导致氧气生成。*OH的吸附强度和ClO的覆盖度可通过可控的电子效应进行调节,从而导致不同的氧化速率。这项研究为阐明一系列电催化反应背后的电氧化机制提供了有价值的见解,从而有助于催化剂的合理设计。

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