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@ARTICLE{Krger:16362,
author = {Kröger, I. and Stadtmüller, B. and Kleimann, C. and
Rajput, P. and Kumpf, C.},
title = {{N}ormal-incidence x-ray standing-wave study of copper
phthalocyanine submonolayers on {C}u(111) and {A}u(111)},
journal = {Physical review / B},
volume = {83},
number = {19},
issn = {1098-0121},
address = {College Park, Md.},
publisher = {APS},
reportid = {PreJuSER-16362},
pages = {195414},
year = {2011},
note = {We would like to thank the ESRF and their staff members
Yanyu Mi, Blanka Detlefs, and Jorg Zegenhagen for enabling
the NIXSW experiments and their permanent support during the
beamtime. We also acknowledge Patrick Bayersdorfer and
Giuseppe Mercurio for their help, as well as Marc Haming,
Johannes Ziroff, and Christoph Stadler for stimulating
discussions. This work was supported by the Deutsche
Forschungsgemeinschaft (KU 1531/2-1).},
abstract = {Understanding the adsorption and growth mechanisms of large
pi-conjugated molecules on noblemetal surfaces is a crucial
aspect for designing and optimizing electronic devices based
on organic materials. The investigation of adsorption
heights for these molecules on different surfaces can be a
direct measure for the strength of the adsorbate-substrate
interaction, and gives insight into the fundamental bonding
mechanisms. However, the adsorption strength is often also
influenced by intermolecular (lateral) interactions which
cause, e. g., island formation in the submonolayer regime
and influence the adsorption geometry of individual
molecules. The lateral structure can then dominate the
vertical structure formation and influence the
adsorbate-substrate interaction. In this context, the
adsorption of copper-phthalocyanines on noble metal surfaces
[Au(111), Ag(111), and Cu(111)] represents an ideal model
system since the lateral structure formation, as well as the
molecular adsorption geometries, strongly depend on coverage
and temperature, and hence can be tuned easily. We
demonstrate that for CuPc/Au(111), a system dominated by
physisorption, the adsorption height of the molecules is
independent from the lateral adsorption geometry. In
contrast, a strong chemisorption of CuPc on Cu(111) shows a
clear gradient in the interaction strength: Individual
molecules in diluted phases are significantly stronger
bonded than molecules in dense phases. This finding
quantifies the increase of the exchange correlation in the
binding process, which goes along with the tendency to a
more site-specific adsorption geometry at small coverages.},
keywords = {J (WoSType)},
cin = {PGI-3 / JARA-FIT},
ddc = {530},
cid = {I:(DE-Juel1)PGI-3-20110106 / $I:(DE-82)080009_20140620$},
pnm = {Grundlagen für zukünftige Informationstechnologien},
pid = {G:(DE-Juel1)FUEK412},
shelfmark = {Physics, Condensed Matter},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000290307700005},
doi = {10.1103/PhysRevB.83.195414},
url = {https://juser.fz-juelich.de/record/16362},
}