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Crabb, E.M.; Ravikumar, M.K.; Qian, Y.; Russell, A.E.; Maniquet, S.; Yao, J.; Thompsett, D.; Hurford, M. and Ball, S.C.
(2002).
DOI: https://doi.org/10.1149/1.1419703
URL: http://ecsdl.org/vsearch/servlet/VerityServlet?KEY...
Abstract
A carbon-supported platinum electrocatalyst was modified with molybdenum using surface organometallic chemistry. The catalyst was characterized using transmission electron microscopy, cyclic voltammetry (CV), polarization studies, and in situ fluorescence extended X-ray absorption fine structure (EXAFS) studies. The CV and polarization studies show that CO oxidation starts at low overpotentials, similar to those of a conventially prepared PtCoMo/C electrocatalyst. EXAFS at the Mo K edge recorded at 0.65 V show that the Mo exists as an oxide species associated with the Pt surface with a Mo-O distance of 1.75 Å. At 0.05 V this oxide is reduced with the formation of a metal-metal bond between the Mo and Pt, with a bond distance of 2.63 Å. ©2001 The Electrochemical Society. All rights reserved.