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Abstract
The metal-free phthalocyanine interface formation on rutile TiO 2(1 1 0) is investigated using scanning tunneling microscopy and photoelectron spectroscopy. The molecules are adsorbed flat on the surface, centered on the substrate oxygen rows. High-resolution core-level C1s spectroscopy indicates a strong difference between the second layer and the first monolayer bonding to the surface. The C1s core-level from the second layer has a bulk-like line shape whereas the first layer shows a strongly modified line profile. Upon thermal treatment, changes in the N1s core level line profile points to dehydrogenation of the center of the molecule.
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