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Deactivation of Pd particles supported on Nb2O5/Cu3Au(100): SFG and TPD studies from UHV to 100 mbar

MPG-Autoren
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Höbel,  Frank
Chemical Physics, Fritz Haber Institute, Max Planck Society;

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Bandara,  Athula
Chemical Physics, Fritz Haber Institute, Max Planck Society;

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Rupprechter,  Günther
Chemical Physics, Fritz Haber Institute, Max Planck Society;

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Freund,  Hans-Joachim
Chemical Physics, Fritz Haber Institute, Max Planck Society;

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Zitation

Höbel, F., Bandara, A., Rupprechter, G., & Freund, H.-J. (2006). Deactivation of Pd particles supported on Nb2O5/Cu3Au(100): SFG and TPD studies from UHV to 100 mbar. Surface science: a journal devoted to the physics and chemistry of interfaces, 600(4), 963-970. doi:10.1016/j.susc.2005.12.039.


Zitierlink: https://hdl.handle.net/11858/00-001M-0000-0011-0560-5
Zusammenfassung
Structural changes that occur on Pd-Nb2O5/Cu3Au(100) model catalysts upon thermal annealing were followed by sum frequency generation (SFG) and temperature-programmed desorption (TPD) using CO as probe molecule. SFG experiments were performed both under ultrahigh vacuum and mbar pressure. Heating the catalyst to temperatures above 300 K lead to an irreversible 50% decrease in the CO adsorption capacity and modified the remaining adsorption sites. Alterations of the phase between resonant and non-resonant SFG signals upon annealing indicate a change in the electronic structure of the surface, which excludes Pd sintering or migration of Nb2O5 over Pd particles to cause the observed effect and rather suggests the formation of "mixed Pd-NbOx" sites. The same changes in surface properties also occur during CO hydrogenation at 1 bar and high temperature, pointing to an involvement of "mixed Pd-NbOx" sites in catalytic reactions.