AVS 58th Annual International Symposium and Exhibition
    Surface Science Division Tuesday Sessions
       Session SS-TuP

Paper SS-TuP5
Characterization and Chemical Activity of Pt-Au and Ni-Au Bimetallic Clusters on TiO2(110)

Tuesday, November 1, 2011, 6:00 pm, Room East Exhibit Hall

Session: Surface Science Poster Session
Presenter: Samuel Tenney, University of South Carolina
Authors: S.A. Tenney, University of South Carolina
B.A. Cagg, University of South Carolina
W. He, University of South Carolina
M.S. Levine, University of South Carolina
R.P. Galhenage, University of South Carolina
D.A. Chen, University of South Carolina
Correspondent: Click to Email

Oxide-supported bimetallic Pt-Au and Ni-Au clusters were studied as model catalysts for low temperature oxidation reactions. The growth, composition, and chemical activity of Ni-Au and Pt-Au clusters deposited at 300 K on TiO2(110) were investigated using scanning tunneling microscopy (STM), low energy ion scattering (LEIS), X-ray photoelectron spectroscopy (XPS), and temperature programmed desorption (TPD). The importance of the Au-titania interface for low temperature oxidation was illustrated by a series of TPD and STM experiments that show a direct correlation between the number of Au-titania interfacial sites and the activity on the surface. Bimetallic clusters were grown by first depositing Ni or Pt onto the surface in order to seed the more mobile Au at existing Ni or Pt clusters. The surfaces of the bimetallic clusters are significantly enriched in Au and are almost entirely pure Au for clusters with > 50% bulk Au composition. TPD of methanol and CO on bimetallic clusters that are highly enriched in Au at the surface still show significant activity characteristic of Ni or Pt at the surface, suggesting that methanol and CO are able to induce the diffusion of Ni and Pt to the surface of the clusters. Heating the bimetallic clusters above 600 K results in the selective encapsulation of Pt or Ni by a thin film of titania. Pre-annealed Pt-Au and Ni-Au bimetallic clusters show promise for enhanced activity towards the conversion of methanol to formaldehyde.