Pinning mass-selected Agn clusters on the TiO2(110)-1x1 surface via deposition at high kinetic energy |
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Authors: | Tong Xiao Benz Lauren Chrétien Steeve Kemper Paul Kolmakov Andrei Metiu Horia Bowers Michael T Buratto Steven K |
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Affiliation: | Department of Chemistry and Biochemistry, University of California, Santa Barbara, CA 93106, USA. |
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Abstract: | We present the first scanning tunneling microscopy (STM) study of the deposition of mass-selected silver clusters (Ag(n),n=1, 2, 3) on a rutile TiO(2)(110)-1x1 surface at room temperature under hard-landing conditions. Under hard-landing conditions, only small features are observed on the surface in all cases without sintering or surface damage. This suggests that the high impact energy of the clusters mainly dissipates as thermal energy in the substrate, resulting in the recovery of any initial impact-induced surface damage and the formation of bound clusters on the surface near the impact point. STM images indicate that Ag(1) binds on the bridging oxygen rows twice as often as on the Ti rows. Density-functional Theory (DFT) calculations are consistent with Ag(1) binding at either bridging oxygen vacancies or with two adjacent bridging oxygen atoms in the same bridging oxygen row. STM images of Ag(2) and Ag(3) depositions indicate almost exclusive binding centered on the Ti-atom rows. DFT calculations suggest that the Ag(2) and Ag(3) clusters are bound between two bridging oxygen rows, which is consistent with the STM observations. |
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