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Book of Abstracts Book of Abstracts - Universität Konstanz

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A - 45<br />

Morphologies Studies <strong>of</strong> Mass Selected Au Clusters on Rutile TiO2 as a<br />

Function <strong>of</strong> Impact Energy and Surface Temperature<br />

P. Convers, R. Vallotton, R. Monot, W. Harbich<br />

Institut de Physique des Nanostructures,<br />

Ecole polytechnique Fédérale de Lausanne (EPFL),<br />

CH-1015 Lausanne<br />

In 1989 Haruta and coworkers have shown that small gold particles (diameter < 4 nm) are<br />

catalytically active [1]. Gold was found to be even more efficient for temperatures below 400°C<br />

than Pt, usually used for CO oxydation [2, 3]. More recent studies by Heiz et al. (Mass selected<br />

Aun deposited on MgO) and Anderson et al. (Mass selected Aun deposited on TiO2) report a<br />

pronounced size dependence <strong>of</strong> the catalytic activity [4, 5]. However informations on the<br />

morphology <strong>of</strong> the clusters is sparse. Wahlström et al. showed that atomic Au thermally<br />

deposited on a surface <strong>of</strong> TiO2(110) form clusters that are stabilized by oxygen vacancies at the<br />

surface [6]. The clusters are small enough for catalysis, however a temperature increase causes a<br />

sintering <strong>of</strong> the clusters and probably decreases the catalytic efficiency.<br />

To understand the clusters morphology as a function <strong>of</strong> temperature, we deposit mass-selected<br />

gold clusters with defined kinetic energy on a TiO2(110). The morphology is then studied by<br />

STM after different heating cycles up to 1000 K. We observe that large cluster sizes (n = 7) and<br />

high deposition energy (up to 4500 eV ) stabilize gold on the surface. Figure 1 is a typical STM<br />

image <strong>of</strong> a deposit <strong>of</strong> Au7 on TiO2 at 20 eV after a heating cycle at 800 K.<br />

References<br />

Figure 1. Au 7/TiO 2 at 20eV after annealing at 800K<br />

[1] M. Haruta, N. Yamada, T. Kobayashi, and S. Iijima, Journal <strong>of</strong> Catalysis 115, 301 (1989).<br />

[2] M. Haruta, Catalysis Today 36, 153 (1997).<br />

[3] M. Valden, X. Lai, and D. W. Goodman, Science 281, 1647 (1998).<br />

[4] A. Sanchez, S. Abbet, U. Heiz, W.-D. Schneider, H. Häkkinen, R. N. Barnett, and U. Landman, J.<br />

Phys. Chem. A 103, 9573 (1999).<br />

[5] S. Lee, C. Fan, T. Wu, and S. L. Anderson, J. Am. Chem. Soc. 126, 5682 (2004).<br />

[6] E. Wahlstrom, N. Lopez, R. Schaub, P. Thostrup, A. Ronnau, C. Africh, E. Laegsgaard, J.<br />

Norskov, and F. Besenbacher, Phys. Rev. Lett. 90, 026101 (2003).<br />

163

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