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International Journal of Hydrogen EnergyVolume 37, Issue 14, July 2012, Pages 10671-10679

Core-shell structured tungsten-tungsten carbide as a Pt catalyst support and its activity for methanol electrooxidation(Article)

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  • aInstitute of Chemistry, Technology and Metallurgy, University of Belgrade, Njegoševa 12, 11000 Belgrade, Serbia
  • bVinča Institute of Nuclear Sciences, University of Belgrade, P. O. Box 522, 11001 Belgrade, Serbia
  • cFaculty of Technology and Metallurgy, University of Belgrade, Karnegijeva 4, 11120 Belgrade, Serbia

Abstract

Tungsten carbide was synthesized by calcination of carbon cryogel containing tungsten in a form of metatungstate. Characterization by X-ray diffraction and transmission electron microscopy indicated core-shell structure of the particles with tungsten core and tungsten carbide shell, attached to graphitized carbon. Pt nanoparticles were deposited on this material and most of them were nucleated on tungsten carbide. Cyclic voltammetry of W-C support and Pt/W-C catalyst indicated hydrogen intercalation in surface hydrous tungsten oxide. Oxidation of CO ads on Pt/W-C commences earlier than on Pt/C for about 100 mV. The onset potentials of MOR on Pt/W-C and Pt/C are the same, but at more positive potentials Pt/W-C catalyst is more active. It was proposed that promotion of MOR is based on bifunctional mechanism that facilitates CO ads removal. Stability test was performed by potential cycling of Pt/W-C and Pt/C in the supporting electrolyte and in the presence of methanol. Pt surface area loss observed in the supporting electrolyte of both catalysts after 250 cycles was about 20%. Decrease in the activity for methanol oxidation was 30% for Pt/W-C, but even 48% for Pt/C. The difference was explained by the presence of hydrous tungsten oxide on Pt in Pt/W-C catalyst, which reduces accumulation of poisoning CO ads. © 2012, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.

Author keywords

CO oxidationElectrocatalysisFuel cellMethanol oxidationPlatinumTungsten carbide

Indexed keywords

Engineering uncontrolled termsBifunctional mechanismsCo oxidationCore shell structureCore-shellCryogelsGraphitized carbonsHydrogen intercalationMeta-tungstateMethanol electrooxidationMethanol OxidationOnset potentialOxidation of COPositive potentialPotential cyclingPt catalystsPt nanoparticlesStability testsSupporting electrolyteSurface areaTungsten oxide
Engineering controlled terms:CalcinationCarbonCatalyst poisoningCatalyst supportsCyclic voltammetryElectrocatalysisElectrolytesElectrooxidationFuel cellsHydrogenMethanolOxidationOxidesPlatinumPlatinum alloysTransmission electron microscopyTungstenX ray diffraction
Engineering main heading:Tungsten carbide

Funding details

Funding sponsor Funding number Acronym
Basic Energy SciencesBES
European Commission
See opportunities by EC
EC
Office of Science
See opportunities by SC
SC
Seventh Framework Programme245916FP7
U.S. Department of Energy
See opportunities by USDOE
DE-AC02-05CH11231USDOE
ON 172054
172054
  • 1

    This work was financially supported by the Ministry of Science, Republic of Serbia , Contract No. ON 172054 . V.R.R acknowledges support of Nanotechnology and Functional Materials Center , funded by the European FP7 project No. 245916 . Electron microscopy was performed at the National Center for Electron Microscopy, which is supported by the Office of Science, Office of Basic Energy Sciences , of the U.S. Department of Energy under Contract No. DE-AC02-05CH11231 .

  • ISSN: 03603199
  • CODEN: IJHED
  • Source Type: Journal
  • Original language: English
  • DOI: 10.1016/j.ijhydene.2012.04.114
  • Document Type: Article

  Gojković, S.L.; Faculty of Technology and Metallurgy, University of Belgrade, Karnegijeva 4, Serbia;
© Copyright 2012 Elsevier B.V., All rights reserved.

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