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Molecular Evidence for the Catalytic Process of Cobalt Porphyrin Catalyzed Oxygen Evolution Reaction in Alkaline Solution.
Wang, Xiang; Cai, Zhen-Feng; Wang, Dong; Wan, Li-Jun.
Afiliação
  • Wang X; CAS Key Laboratory of Molecular Nanostructure and Nanotechnology, CAS Research/Education Center for Excellence in Molecular Sciences, Beijing National Laboratory for Molecular Science (BNLMS), Institute of Chemistry, Chinese Academy of Sciences , Beijing 100190 , China.
  • Cai ZF; University of Chinese Academy of Sciences , Beijing 100049 , China.
  • Wang D; CAS Key Laboratory of Molecular Nanostructure and Nanotechnology, CAS Research/Education Center for Excellence in Molecular Sciences, Beijing National Laboratory for Molecular Science (BNLMS), Institute of Chemistry, Chinese Academy of Sciences , Beijing 100190 , China.
  • Wan LJ; University of Chinese Academy of Sciences , Beijing 100049 , China.
J Am Chem Soc ; 141(19): 7665-7669, 2019 May 15.
Article em En | MEDLINE | ID: mdl-31050417
ABSTRACT
We report an electrochemical scanning tunneling microscopy (ECSTM) study of the 5,10,15,20-tetraphenyl-21 H,23 H-porphyrin cobalt(II) (CoTPP) catalyzed oxygen evolution reaction (OER). A highly ordered self-assembled monolayer of CoTPP is formed on the Au(111) electrode. Cyclic voltammetry results show the OER activity of the electrode is enhanced with the increasing alkalinity of the electrolytes. The CoTPP molecules appear as two symmetric bright spots in STM images in alkaline solution, which is in sharp contrast to that in acidic solution. The molecular contour changes are attributed to the formation of the CoTPP-OH- species before OER, which is further confirmed by UV-vis absorption spectroscopy. In situ ECSTM results reveal the evolution from the CoTPP-OH- species to CoTPP molecules during OER.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article