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Characterizing Coverage of Phosphoric Acid on Carbon-Supported Platinum Nanoparticles Using In Situ Extended X-Ray Absorption Fine Structure Spectroscopy and Cyclic Voltammetry

Authors
Park, Hee-YoungAhn, Sang HyunKim, Soo-KilKim, Hyoung-JuhnHenkensmeier, DirkKim, Jin YoungYoo, Sung JongJang, Jong Hyun
Issue Date
2016
Publisher
ELECTROCHEMICAL SOC INC
Citation
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, v.163, no.3, pp F210 - F215
Journal Title
JOURNAL OF THE ELECTROCHEMICAL SOCIETY
Volume
163
Number
3
Start Page
F210
End Page
F215
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/8656
DOI
10.1149/2.0651603jes
ISSN
0013-4651
1945-7111
Abstract
Using extended X-ray absorption fine structure (EXAFS) spectroscopy and cyclic voltammetry (CV) in combination, the fraction of surface Pt atoms poisoned by the phosphoric acid adsorbed (theta(PA)) on Pt/C was analyzed for various electrode potentials (0.35, 0.60, and 0.8 V). The theta(PA) values at 0.35 V, 0.6 V, and 0.8 V were determined to be 0.32, 0.45, and 0.38, respectively. The differences in the theta(PA) values determined using EXAFS spectroscopy in this study and those estimated from the relative number of phosphoric acid molecules adsorbed are probably attributable to an increase in the number of Pt-O bonds per adsorbed phosphoric acid molecule. This, in turn, is owing to an increase in the degree of electrochemical adsorption with an increase in the potential. That the theta(PA) value for the Pt(111) surface at 0.35 V as determined using EXAFS spectroscopy was higher than that estimated through the CV analysis was because of the chemical adsorption and/or electrochemical adsorption of phosphoric acid on the (100) facets and edge sites of the Pt/C surfaces. (C) 2015 The Electrochemical Society. All rights reserved.
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