CO tolerant Pt/WC methanol electro-oxidation catalyst

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Platinum supported on WC (Pt/WC) catalyst (20 wt.% Pt) was synthesized as a new methanol electro-oxidation catalyst. Particle size of 7.5 nm was obtained from X-ray diffraction results and a uniform distribution of particles was observed by transmission electron microscopy. In cyclic voltammetry (CV) measurement, the reduction peak potential of NO increased from 0.72 V in commercial Pt/C to 0.76 V in Pt/WC. By combining the CV and CO stripping results, spill-over of H+ from Pt to WC was observed. Electrochemically active surface area calculated from the desorption area of H+ were 11.2 and 5.74 m(2)/g catalyst for Pt/WC and Pt/C, while those obtained from the desorption area of CO were 4.42 and 6.40 m(2)/g catalyst, respectively. CO electro-oxidation peak potential greatly decreased from 0.80 V in Pt/C to 0.68 V in Pt/WC. The reaction of WC with water to produce WC-OH could lower to CO electro-oxidation peak potential. Specific activity for methanol electro-oxidation increased from 144 mA/m(2) in Pt/C to 188 mA/m(2) in Pt/WC. (C) 2007 Elsevier B.V. All rights reserved.
Publisher
ELSEVIER SCIENCE INC
Issue Date
2007-11
Language
English
Article Type
Article
Keywords

TUNGSTEN CARBIDE; CARBON SUPPORT; FUEL-CELLS; OXIDATION; ELECTROCATALYSTS; ELECTRODE

Citation

ELECTROCHEMISTRY COMMUNICATIONS, v.9, no.11, pp.2692 - 2695

ISSN
1388-2481
DOI
10.1016/j.elecom.2007.09.001
URI
http://hdl.handle.net/10203/18276
Appears in Collection
CBE-Journal Papers(저널논문)
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