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Enhanced activity for supported Au clusters: Methanol oxidation on Au/TiO2(110)
Authors:Samuel A Tenney  Brett A Cagg  Mara S Levine  Wei He  Kedar Manandhar  Donna A Chen
Institution:Department of Chemistry and Biochemistry, University of South Carolina, Columbia, SC 29208, United States
Abstract:Gold clusters supported on TiO2(110) exhibit unusual activity for the oxidation of methanol to formaldehyde. Temperature programmed desorption studies of methanol on Au clusters show that both Au and titania sites are necessary for methanol reaction. Isotopic labeling experiments with CD3OH demonstrate that reaction occurs via Osingle bondH bond scission to form a methoxy intermediate. When the TiO2 surface is oxidized with 18O2 before or after Au deposition, methanol reaction produces H218O below 300 K, indicating that oxygen from titania promotes Osingle bondH bond scission and is incorporated into desorbing products. XPS experiments provide additional evidence that during methanol reaction on the Au/TiO2 surface, methanol adsorption occurs on TiO2, given that the titania support becomes slightly oxidized after exposure to methanol in the presence of Au clusters. While the role of TiO2 is to dissociate the Osingle bondH bond and form the reactive methoxy intermediate, the role of the Au sites is to remove hydrogen from the surface as H2, thus preventing the recombination of methoxy and hydrogen to methanol. The decrease in formaldehyde yield with increasing Au coverage above 0.25 ML suggests that reaction occurs at Au–titania interfacial sites; scanning tunneling microscopy images of various Au coverages confirm that the number of interfacial sites at the perimeter of the Au clusters decreases as the Au coverage is increased between 0.25 and 5 ML.
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