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Nanostrukturen und Grenzflächen Poster: Do., 13:00–15:30 D-P303<br />

Growth and Oxidation of Pd/α-Al2O3(0001) Nanoparticles studied with<br />

Synchrotron X-ray Diffraction<br />

Philipp Nolte 1 , N. Kasper 1 , A. Stierle 1 , H. Dosch 1<br />

1 Max Planck Instute for Metals Research, Heisenbergstr. 3, 70569 Stuttgart<br />

Supported transition metal nanoparticles are used as model catalysts. The oxidation<br />

of such systems is of great interest as not only the pure metal, but also its oxides<br />

can be involved in a catalytic process. In addition to bulk single crystal surfaces, the<br />

oxidation properties of nanoparticles can be expected to depend on the support, the<br />

orientation and the particle size. In-situ x-ray diffraction is an appropriate method to<br />

follow structural changes of oxygen induced phase transformations and simultaneously<br />

allows to bridge the pressure gap of UHV based surface analysis techniques.<br />

Pd nanoparticles were grown on α-Al2O3(0001) by electron beam evaporation in UHV<br />

and were studied with SXRD at the MPI-MF beamline at the synchrotron ANKA (FZ<br />

Karlsruhe). It was observed that the particles mainly grow (111)-oriented and epitaxially<br />

with a typical height of 2 nm and a lateral diameter of 4 nm in coexistence with<br />

particles in (110)-orientation. Oxidation experiments were performed in a temperature<br />

range between room temperature and 350 ◦ C.<br />

Applying UHV near oxygen pressures, it could be observed a reversible decrease of<br />

intensity and a broadening of the Pd Bragg peaks. At 350 ◦ C, the formation of bulk<br />

oxide could be observed at an oxygen pressure of 5 mbar. This indicates a structural<br />

change at the Pd particle surface at low oxygen pressures which acts as a kinetic barrier<br />

for the formation of the thermodynamically stable bulk oxide.<br />

Financial support of this work is acknowledged from the European Union under contract<br />

no. NMP3-CT-2003-505670 (NANO2).

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