Numéro |
J. Phys. IV France
Volume 132, March 2006
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|
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Page(s) | 11 - 15 | |
DOI | https://doi.org/10.1051/jp4:2006132004 | |
Publié en ligne | 11 mars 2006 |
C. Girardeaux, et al.
J. Phys. IV France 132 (2006) 11-15
DOI: 10.1051/jp4:2006132004
Soft X-ray photoelectron spectroscopy of metal-phthalocyanines on the (001) surface of GaAs and Ge
G. Cabailh1, 0, B.N. Holland1, C. Stephens1, I.T. McGovern1, C. McGuinness1, A. Cafolla2, A.R. Vearey-Roberts3 and D.A. Evans31 Physics Dept., Trinity College Dublin 2, Ireland
2 School of Physical Sciences, Dublin City University, Dublin 9, Ireland
3 Institute of Mathematical and Physical Sciences, University of Wales, Aberystwyth SY23 3BZ, UK
Abstract
The interaction between selected metal-phthalocyanine (MPc)
molecules and the clean (001) surfaces of gallium arsenide and
germanium is probed by soft x-ray photoelectron spectroscopy (SXPS)
using synchrotron radiation. As-3d and Ga-3d core spectra show no
significant change when approximately one monolayer of any of three
MPc molecules is deposited; also, the metal atom spectrum comprises
a single component. In some contrast, deposition on the Ge(001)
surface leads to changes in both substrate and deposit core spectra.
Upon deposition of approximately one monolayer of any of three MPc
molecules, approximately 50% of the `up' dimer-atom intensity is
shifted to higher binding energy, indicative of an electron-removing
interaction. A corresponding electron-receiving shift to lower
binding energy is observed in the metal core spectra of
two of the three molecules, SnPc and PbPc;
significantly, MgPc shows no such satellite feature. Since MgPc is
planar while SnPc and PbPc are non-planar, it seems reasonable to
attribute the two component spectrum of the latter to the two
possible geometries of metal atom in `contact' and `non-contact'
with the surface.
© EDP Sciences 2006