Methanol on anatase TiO2(101): Mechanistic insights into photocatalysis

M. Setvin, X. Shi, J. Hulva, T. Simschitz, G. S. Parkinson, M. Schmid, C. Di Valentin, A. Selloni, U. Diebold

Institut für Angewandte Physik, TU Wien, 1040 Wien, Austria
Department of Chemistry, Princeton University, Frick Laboratory, Princeton, New Jersey 08544, U. S. A.
Dipartimento dei Scienza dei Materiali, Universita di Milano-Bicocca, 20125 Milano, Italy

ACS Catalysis 7 (2017) 7081-7091

The photoactivity of methanol adsorbed on the anatase TiO2(101) surface was studied by a combination of scanning tunneling microscopy (STM), temperature-programmed desorption (TPD), X-ray photoemission spectroscopy (XPS), and density functional theory (DFT) calculations. Isolated methanol molecules adsorbed at the anatase (101) surface show a negligible photoactivity. Two ways of methanol activation were found. First, methoxy groups formed by reaction of methanol with coadsorbed O2 molecules or terminal OH groups are photoactive, and they turn into formaldehyde upon UV illumination. The methoxy species show an unusual C 1s core-level shift of 1.4 eV compared to methanol; their chemical assignment was verified by DFT calculations with inclusion of final-state effects. The second way of methanol activation opens at methanol coverages above 0.5 monolayer (ML), and methyl formate is produced in this reaction pathway. The adsorption of methanol in the coverage regime from 0 to 2 ML is described in detail; it is key for understanding the photocatalytic behavior at high coverages. There, a hydrogen-bonding network is established in the adsorbed methanol layer, and consequently, methanol dissociation becomes energetically more favorable. DFT calculations show that dissociation of the methanol molecule is always the key requirement for hole transfer from the substrate to the adsorbed methanol. We show that the hydrogen-bonding network established in the methanol layer dramatically changes the kinetics of proton transfer during the photoreaction.

Corresponding author: Martin Setvin (setvin at iap_tuwien_ac_at).

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