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CO-Tolerant PtMo/C Fuel Cell Catalyst for H-2 Oxidation

Title
CO-Tolerant PtMo/C Fuel Cell Catalyst for H-2 Oxidation
Author(s)
Bang, Jin HoKim, Hasuck
Issued Date
2011-10
Citation
Bulletin of the Korean Chemical Society, v.32, no.10, pp.3660 - 3665
Type
Article
Author Keywords
CO electro-oxidationFuel cellH2 oxidationPtMo electrocatalystX-ray absorption spectroscopy
Keywords
ABSORPTIONAbsorption SpectroscopyActive Oxygen SpeciesALLOY CATALYSTALLOY CATALYSTSALLOYSCARBON-MONOXIDECatalyst ActivityCatalytic OxidationCo Electro-OxidationCo ElectrooxidationCo OxidationColloidal MethodsCyclic VoltammetryDensity Functional TheoryElectrocatalystsELECTROCATALYTIC ACTIVITYElectrochemical StudiesElectronic PropertiesElectronic StructureELECTROOXIDATIONEnhanced Catalytic ActivityFacile FormationFuel CellFuel Cell CatalystsFuel CellsH-2 OxidationInvestmentsIonization of GasesMIXTURESMolybdenumOXIDATIONOxygenPlatinumPlatinum AlloysPT-RUPtmo ElectrocatalystROTATING-DISK ELECTRODESpectroscopic AnalysisSPECTROSCOPYSynergetic EffectWeak InteractionsX-RAY-ABSORPTIONX-Ray Absorption SpectroscopyX Ray AbsorptionX Ray Absorption Spectroscopy
ISSN
0253-2964
Abstract
CO-tolerant PtMo/C alloy electrocatalyst was prepared by a colloidal method, and its electrocatalytic activity toward CO oxidation was investigated. Electrochemical study revealed that the alloy catalyst significantly enhanced catalytic activity toward the electro-oxidation of CO compared to Pt/C counterpart. Cyclic voltammetry suggested that Mo plays an important role in promoting CO electro-oxidation by facilitating the formation of active oxygen species. The effect of Mo on the electronic structure of Pt was investigated using X-ray absorption spectroscopy to elucidate the synergetic effect of alloying. Our in-depth spectroscopic analysis revealed that CO is less strongly adsorbed on PtMo/C catalyst than on Pt/C catalyst due to the modulation of the electronic structure of Pt d-band. Our investigation shows that the enhanced CO electrooxidation in PtMo alloy electrocatalyst is originated from two factors; one comes from the facile formation of active oxygen species, and the other from the weak interaction between Pt and CO.
URI
http://hdl.handle.net/20.500.11750/56409
DOI
10.5012/bkcs.2011.32.10.3660
Publisher
Korean Chemical Society
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