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Hydrogen electrocatalysis by carbon supported Pt and Pt alloys: An in situ X-ray absorption study

Journal Article · · Journal of the Electrochemical Society
DOI:https://doi.org/10.1149/1.1836995· OSTI ID:367778
;  [1]
  1. Brookhaven National Lab., Upton, NY (United States)

In situ X-ray absorption spectroscopy (XAS) in 1 M HClO{sub 4} was used to examine the electronic and structural effects of hydrogen adsorption on carbon supported Pt (Pt/C) and Pt alloyed with first row transition metals (Cr, Mn, Fe, Co, and Ni). In the case of Pt/C, potential excursions from the double layer region (0.54 V vs RHE) to 0.0 V caused significant changes in the XAS spectra whereas none was observed for the alloys. The L{sub 3} and L{sub 2} X-ray absorption near edge structure indicated the generation of empty electronic states in the vicinity of the Fermi level due to adsorption of hydrogen, and the L{sub 3} extended X-ray absorption fine structure indicated an increase in the coordination number of the first Pt-Pt shell from 9 to 11. The latter was attributed to a reversible surface restructuring process. Alloying of the Pt suppresses both the electronic and structural effects at 0.0 V. A comparison of the electrochemical kinetics for hydrogen oxidation by these electrocatalysts in a proton exchange membrane fuel cell indicated that alloying of the Pt had insignificant effects on the kinetics.

Research Organization:
Brookhaven National Laboratory (BNL), Upton, NY
DOE Contract Number:
AC02-76CH00016
OSTI ID:
367778
Journal Information:
Journal of the Electrochemical Society, Journal Name: Journal of the Electrochemical Society Journal Issue: 7 Vol. 143; ISSN 0013-4651; ISSN JESOAN
Country of Publication:
United States
Language:
English