X-ray absorption and photoemission spectroscopy of zinc protoporphyrin adsorbed on rutile TiO2(110) prepared by in situ electrospray deposition

Summary, in English

Zinc-protoporphyrin, adsorbed on the rutile TiO2(110) surface, has been studied using photoemission spectroscopy and near-edge absorption fine structure spectroscopy to deduce the nature of the molecule-surface bonding and the chemical environment of the central metal atom. To overcome the difficulties associated with sublimation of the porphyrin molecules, samples were prepared in situ using ultrahigh vacuum electrospray deposition, a technique which facilitates the deposition of nonvolatile and fragile molecules. Monolayers of Zn protoporphyrin are found to bond to the surface via the oxygen atoms of the deprotonated carboxyl groups. The molecules initially lie largely parallel to the surface, reorienting to an upright geometry as the coverage is increased up to a monolayer. For those molecules directly chemisorbed to the surface, the interaction is sufficiently strong to pull the central metal atom out of the molecule. (C) 2010 American Institute of Physics.

• Author: Anna Rienzo; Louise C. Mayor; Graziano Magnano; Christopher J. Satterley; Evren Ataman; Joachim Schnadt; Karina Schulte; James N. O'Shea
• Department/s: Synchrotron Radiation Research; MAX IV Laboratory
• Publishing year: 2010
• Language: English
• Publication/Series: Journal of Chemical Physics
• Volume: 132
• Issue: 8
• Links: http://dx.doi.org/10.1063/1.3336747
• Document type: Journal article
• Publisher: American Institute of Physics (AIP)
• Topic: Physical Sciences; Atom and Molecular Physics and Optics; Natural Sciences
• Status: Published
• ISBN/ISSN/Other: ISSN: 0021-9606