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

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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.
Author(s)
Jeon, HongraeJeong, BeomgyunChoun, MyounghoonLee, Jae Young
Issued Date
2014-09
Type
Article
DOI
10.1016/j.electacta.2014.06.093
URI
https://scholar.gist.ac.kr/handle/local/15048
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Citation
ELECTROCHIMICA ACTA, v.140, pp.525 - 528
ISSN
0013-4686
Appears in Collections:
Department of Environment and Energy Engineering > 1. Journal Articles
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