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   <subfield code="a">Adsorption and reaction of CO on vanadium oxide-Pd(111) &quot;inverse” model catalysts: an HREELS study</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[M. Sock, S. Surnev, M.G. Ramsey, F.P. Netzer]</subfield>
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   <subfield code="a">The room temperature adsorption and reaction of CO on Pd(111) surfaces decorated with submonolayer coverages of vanadium oxide - so-called &quot;inverse” model catalysts - have been studied by high-resolution electron energy loss spectroscopy (HREELS) and X-ray photoelectron spectroscopy (XPS). The HREELS surface phonon spectra of the V oxide phases have been measured and used to monitor the changes in the oxide as a result of the interaction with CO. The intramolecular C-O stretching frequency of CO adsorbed on the V-oxide/Pd(111) surfaces displays two vibrational loss components as a function of CO coverage as it has been observed on the clean Pd(111) surface. The relative intensities of the two vibrational features as a function of V oxide coverage however suggest that the balance of CO adsorption sites is modified as compared to clean Pd(111) by the presence of the V oxide-Pd phase boundary. Preferential population of high coordination adsorption sites by CO in the vicinity of the oxide-metal interface is proposed. The analysis of the V oxide phonon spectra indicates that adsorbed CO partially reduces the V oxide at the boundaries of the oxide islands to the Pd metal. The reduction of V oxide by CO is dependent on the oxygen content of the V oxide phase. The reduction of V oxide is confirmed by the XPS V 2p core level shifts.</subfield>
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