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Molecular-driven substrate reconstruction in the two-dimensional serf-organization of Fe-phthalocyanines on Au(110)

Fortuna Sara
•
Gargiani P.
•
Betti M. G.
altro
Fabris S.
2012
  • journal article

Periodico
JOURNAL OF PHYSICAL CHEMISTRY. C
Abstract
The structural patterns formed by molecular self-assembly at surfaces are usually controlled by the relative strengths of the intermolecular and molecule-substrate interactions. An additional steering neffect is present when the substrate can easily reconstruct upon molecular adsorption, which therefore drives a self-templating effect on the metal support. This is here demonstrated for the model case of Fe-Phthalocyanine molecules adsorbed on the Au(110) surface. Scanning Tunneling Microscopy shows that molecular adsorption promotes a local (1×5) surface reconstruction, which drives the assembly of molecular chains along the [1 ̄10] direction. The order and periodicity of the molecular assemblies are determined with Low Energy Electron Diffraction patterns. Density Functional Theory calculations reveal the energetic origins of the molecule-driven substrate reconstruction.
DOI
10.1021/jp211036m
WOS
WOS:000301509600036
Archivio
https://hdl.handle.net/11390/1314872
info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84858315196
http://pubs.acs.org/doi/abs/10.1021/jp211036m
https://ricerca.unityfvg.it/handle/11390/1314872
Diritti
closed access
license:non pubblico
license uri:iris.2.pri01
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