1. Site-dependent charge transfer at the Pt(111)-ZnPc interface and the effect of iodine
- Author
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Ahmadi, S., Agnarsson, B., Bidermane, I., Wojek, B. M., Noël, Q., Sun, C. H., and Göthelid, M.
- Subjects
Condensed Matter - Materials Science ,Physics - Chemical Physics - Abstract
The electronic structure of ZnPc, from sub-monolayers to thick films, on bare and iodated Pt(111) is studied by means of X-ray photoelectron spectroscopy (XPS), X-ray absorption spectroscopy (XAS) and scanning tunneling microscopy (STM). Our results suggest that at low coverage ZnPc lies almost parallel to the Pt(111) substrate, in a non-planar configuration induced by Zn-Pt attraction, leading to an inhomogeneous charge distribution within the molecule and charge transfer to the molecule. ZnPc does not form a complete monolayer on the Pt surface, due to a surface-mediated intermolecular repulsion. At higher coverage ZnPc adopts a tilted geometry, due to a reduced molecule-substrate interaction. Our photoemission results illustrate that ZnPc is practically decoupled from Pt, already from the second layer. Pre-deposition of iodine on Pt hinders the Zn-Pt attraction, leading to a non-distorted first layer ZnPc in contact with Pt(111)-I $\left(\sqrt{3}\times\sqrt{3}\right)$ or Pt(111)-I $\left(\sqrt{7}\times\sqrt{7}\right)$, and a more homogeneous charge distribution and charge transfer at the interface. On increased ZnPc thickness iodine is dissolved in the organic film where it acts as an electron acceptor dopant., Comment: 12 pages, 9 figures
- Published
- 2014
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