Structure of 3,4,9,10-perylene-tetracarboxylic-dianhydride grown on reconstructed and unreconstructed Au(100)

Citation
T. Schmitz-hubsch et al., Structure of 3,4,9,10-perylene-tetracarboxylic-dianhydride grown on reconstructed and unreconstructed Au(100), SURF SCI, 437(1-2), 1999, pp. 163-172
Citations number
32
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
SURFACE SCIENCE
ISSN journal
00396028 → ACNP
Volume
437
Issue
1-2
Year of publication
1999
Pages
163 - 172
Database
ISI
SICI code
0039-6028(19990820)437:1-2<163:SO3GOR>2.0.ZU;2-R
Abstract
The growth of 3,4,9,10-perylene-tetracarboxylic-dianhydride (PTCDA) has bee n characterized on Au(100) from the submonolayer range to multilayer films by scanning tunneling microscopy (STM) in ultrahigh vacuum (UHV) and under ambient conditions. Two different structures of PTCDA are found, one of whi ch is the well-known herringbone structure, with the plane of the molecule flat-lying on the substrate surface. This structure is point-online coincid ent with the Au( 100) lattice. The second structure which is predominant on this surface consists of closely spaced rods, each rod consisting of close ly packed PTCDA molecules. We propose that this structure is associated wit h the (010) bulk plane of the alpha-polymorph of PTCDA. The reason for the different growth behavior compared to PTCDA on Au(111) at the very same gro wth conditions can be found in the nanoscopic structure of the reconstructe d Au(100)(hex) surface. This reconstruction of the Au(100) surface provides trenches along the Au[011] azimuth which act as a specific adsorption site for PTCDA, leading to very low diffusion rates of this molecule following its deposition. The diffusion rate of first-deposited PTCDA was low enough to enable us to image single molecules at room temperature. These findings, in comparison with results on the reconstructed Au(111) surface, show that not only the substrate material and the symmetry, but also the surface str ucture on the nanoscopic scale can rule the growth of the organic overlayer . (C) 1999 Elsevier Science B.V. All rights reserved.