6533b7dafe1ef96bd126e1e4

RESEARCH PRODUCT

Reversible oxidation of WOx and MoOx nano phases

Z. LiStéphanie BruyèreK. SchierbaumSylvie BourgeoisBruno Domenichini

subject

Materials scienceAnnealing (metallurgy)Inorganic chemistryAnalytical chemistrychemistry.chemical_elementCATALYSTS02 engineering and technologyTungsten010402 general chemistryTIO2(110) SURFACE01 natural sciencesSTOICHIOMETRYCatalysisTUNGSTEN-OXIDE[ CHIM.OTHE ] Chemical Sciences/OtherMonolayerWork functionHEXACARBONYL ADSORPTIONSOL-GELVISIBLE-LIGHT IRRADIATIONTIO2 110MOLYBDENUMGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical scienceschemistryMolybdenumPhotocatalysisPHOTOCATALYSIS[CHIM.OTHE]Chemical Sciences/Other0210 nano-technologyStoichiometryTitanium

description

International audience; WOx and MoOx nano phases were prepared on TiO2(1 1 0) surfaces by a CVD procedure consisting of adsorption and decomposition of W(CO)(6) or Mo(CO)(6) precursors followed by annealing under UHV. Metal amount involved in each elaborated sample is in the fractional range from 0.1 to 0.35 equivalent monolayer (eqML) of W or Mo. Evolution of sample stoichiometry as a function of subsequent treatment is followed by valence band and core level photoemission as well as work function measurement. In each case, exposure of samples to molecular oxygen at room temperature induces an increase of sample work function in a range of several tenth of eV. Such a work function change is related to oxidation of sample involving both titanium and tungsten (or molybdenum) ions. Such an oxidation is reversible through an annealing under UHV at 470 K for molybdenum oxide and 670 K for tungsten oxide. Several cycles of exposure/annealing are possible without changes in work function or stoichiometry. (C) 2011 Elsevier B.V. All rights reserved.

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