OAK

in-situ electrochemical extended X-ray absorption fine structure spectroscopy study on the reactivation of Pd electrocatalyst in formic acid oxidation

Metadata Downloads
Author(s)
Jeon, HongraeJeong, BeomgyunChoun, MyounghoonLee, Jae Young
Type
Article
Citation
ELECTROCHIMICA ACTA, v.140, pp.525 - 528
Issued Date
2014-09
Abstract
Palladium (Pd) has been considered as an excellent option to replace platinum-based electrocatalysts in formic acid oxidation owing to its superb catalytic activity to Pt and cheaper material price. However, unstable catalytic activity of Pd is the most critical obstacle in the development of Pd-based electrocatalysts for formic acid oxidation, and the fundamental understanding on Pd deactivation is still incomplete. In this study, the activity of deactivated Pd in a formic acid oxidation was recovered to 93% by applying a cathodic bias potential of -0.2V vs. RHE. Based on in-situ electrochemical extended X-ray absorption fine structure spectroscopy analysis we show that cathodic polarization of Pd/C electrode could remove the adsorption of poisoning species by increasing bond length of Pd-Pd and further discuss on the origin of reactivation mechanism of Pd. (C) 2014 Elsevier Ltd. All rights reserved.
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
ISSN
0013-4686
DOI
10.1016/j.electacta.2014.06.093
URI
https://scholar.gist.ac.kr/handle/local/15048
공개 및 라이선스
  • 공개 구분공개
파일 목록
  • 관련 파일이 존재하지 않습니다.

Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.