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Visualization of Electrooxidation on Palladium Single Crystal Surfaces via In Situ Raman Spectroscopy.
Sun, Yu-Lin; Ji, Xu; Wang, Xue; He, Quan-Feng; Dong, Jin-Chao; Le, Jia-Bo; Li, Jian-Feng.
Afiliação
  • Sun YL; Xiamen University, College of Chemistry and Chemical Engineering, CHINA.
  • Ji X; Ningbo Institute of Materials Technology and Engineering CAS, Key Laboratory of Advanced Fuel Cells and Electrolyzers Technology of Zhejiang Province, CHINA.
  • Wang X; Ningbo Institute of Materials Technology and Engineering CAS, Key Laboratory of Advanced Fuel Cells and Electrolyzers Technology of Zhejiang Province, CHINA.
  • He QF; Xiamen University, College of Chemistry and Chemical Engineering, CHINA.
  • Dong JC; Xiamen University, College of Energy, CHINA.
  • Le JB; Ningbo Institute of Materials Technology and Engineering CAS, Key Laboratory of Advanced Fuel Cells and Electrolyzers Technology of Zhejiang Province, CHINA.
  • Li JF; Xiamen University, Chemistry, No. 422, Simingnan Road, 361005, Xiamen, CHINA.
Angew Chem Int Ed Engl ; : e202408736, 2024 Aug 06.
Article em En | MEDLINE | ID: mdl-39107260
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 ClO4- ions facilitate the deprotonation process, leading to the formation of PdOx. Subsequently, under deep electrooxidation potential range, the oxygen atoms within PdOx contribute to creating surface-bound peroxide species, ultimately resulting in oxygen generation. The adsorption strength of *OH and the coverage of ClO4- 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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China