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Abstract

A method combining cyclic voltammetry (CV) with x-ray absorption fine structure (XAFS) spectroscopy, viz. CV-XAFS, has been developed to enable in situ real-time investigation of atomic and electronic structures related to electrochemical reactions. We use this method to study the reaction of a Pt/C cathode catalyst in the oxygen reduction reaction (ORR) in an alkaline electrolyte, using x-ray energies near the Pt LIII edge for XAFS measurements. It was found that the current induced by the ORR was first observed at approximately 0.08 V versus Hg/HgO, although the Pt valence, which is reflected in the oxidation states, remained almost unchanged. The electronic structure of the catalytic surface in the ORR was observed to be different in the negative and positive scan directions of CV measurements. Hydrogen adsorption is also discussed on the basis of the observation of this spectral change. We have demonstrated that CV-XAFS provides dynamical structural and electronic information related to electrochemical reactions and can be used for in situ real-time measurements of a catalyst.

Details

Title
Study of Catalytic Reaction at Electrode-Electrolyte Interfaces by a CV-XAFS Method
Author
Kusano, Shogo 1 ; Matsumura, Daiju 2 ; Asazawa, Koichiro 3 ; Kishi, Hirofumi 3 ; Sakamoto, Tomokazu 3 ; Yamaguchi, Susumu 3 ; Tanaka, Hirohisa 4 ; Mizuki, Jun'ichiro 5 

 Graduate School of Science and Technology, Kwansei Gakuin University, Sanda, Hyogo, Japan 
 Materials Sciences Research Center, Japan Atomic Energy Agency, Sayo, Hyogo, Japan 
 Research and Development Division, Daihatsu Motor Co., Ltd., Gamo, Shiga, Japan 
 Graduate School of Science and Technology, Kwansei Gakuin University, Sanda, Hyogo, Japan; Research and Development Division, Daihatsu Motor Co., Ltd., Gamo, Shiga, Japan 
 Graduate School of Science and Technology, Kwansei Gakuin University, Sanda, Hyogo, Japan; Materials Sciences Research Center, Japan Atomic Energy Agency, Sayo, Hyogo, Japan 
Pages
3634-3638
Publication year
2017
Publication date
Jun 2017
Publisher
Springer Nature B.V.
ISSN
0361-5235
e-ISSN
1543-186X
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
1899618214
Copyright
Journal of Electronic Materials is a copyright of Springer, 2017.