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Photoemission from Size-Selected Pt-Clusters Deposited on Silver Films

  • H. V. Roy
  • P. Fayet
  • F. Patthey
  • W. D. Schneider
Part of the NATO ASI Series book series (NSSB, volume 283)

Abstract

When atoms are brought close together to form a solid their outer wave functions overlap and the energy levels of the individual atoms broaden and become the energy bands of condensed matter. The observation of the evolution of this process from the single atom to the bulk as a function of the number of atoms involved would in principle give insight into the size dependence of many properties of condensed matter, for example the onset of metallic behavior, the critical size for a heterogeneous catalytic reaction or the behavior of the melting temperature. Up to now most of the experimental studies of the electronic structure of supported small particles were carried out on evaporated or sputtered thin films when only some average particle size distribution could be achieved.1–5,9. Only recently photoemission data have been obtained from monosize Au and Pt-clusters mass selected and deposited onto amorphous carbon and/or naturally oxidized Si-wafers6,7. The following observations were made: (i) the 4f core-levels of Pt and Au shift to higher binding energies with decreasing cluster size, indicating that the cluster is charged in the photoemission final state8,(ii) for the Au-clusters the valence band width decreases with cluster size as expected for a decreasing coordination number6, (iii) for the Pt-clusters different valence band onsets for different cluster sizes (1–6 atoms) have been observed, where the trend is towards higher binding energies with decreasing cluster size7.

Keywords

Quadrupole Mass Spectrometer High Binding Energy Silver Film Photoemission Spectrum Cluster Beam 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Plenum Press, New York 1992

Authors and Affiliations

  • H. V. Roy
    • 1
  • P. Fayet
    • 1
  • F. Patthey
    • 1
  • W. D. Schneider
    • 1
  1. 1.Institut de Physique ExpérimentaleUniversité de LausanneLausanneSwitzerland

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