Universal dependence of hydrogen oxidation and evolution reaction activity of platinum-group metals on pH and hydrogen binding energy
Author(s) -
Jie Zheng,
Wenchao Sheng,
Zhongbin Zhuang,
Bingjun Xu,
Yushan Yan
Publication year - 2016
Publication title -
science advances
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.928
H-Index - 146
ISSN - 2375-2548
DOI - 10.1126/sciadv.1501602
Subject(s) - hydrogen , platinum group , platinum , binding energy , chemistry , inorganic chemistry , biochemistry , catalysis , organic chemistry , atomic physics , physics
Publisher's PDFUnderstanding how pH affects the activity of hydrogen oxidation reaction (HOR) and hydrogen evolution reaction
(HER) is key to developing active, stable, and affordable HOR/HER catalysts for hydroxide exchange membrane fuel
cells and electrolyzers. A common linear correlation between hydrogen binding energy (HBE) and pH is observed
for four supported platinum-group metal catalysts (Pt/C, Ir/C, Pd/C, and Rh/C) over a broad pH range (0 to 13),
suggesting that the pH dependence of HBE is metal-independent. A universal correlation between exchange current
density and HBE is also observed on the four metals, indicating that they may share the same elementary steps
and rate-determining steps and that the HBE is the dominant descriptor for HOR/HER activities. The onset potential
of CO stripping on the four metals decreases with pH, indicating a stronger OH adsorption, which provides evidence
against the promoting effect of adsorbed OH on HOR/HER.University of Delaware. Department of Chemical & Biomolecular Engineering.University of Delaware. Center for Catalytic Science & Technology
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