Methanol adsorption and reactivity on clean and hydroxylated anatase(101) surfaces

Antonio Tilocca, Annabella Selloni

Research output: Contribution to journalArticlepeer-review

104 Scopus citations


The adsorption and reactivity of methanol on TiO 2 anatase(101) surfaces are studied through first-principles total energy calculations and Car-Parrinello molecular dynamics simulations. The effects of different methanol coverages up to one monolayer and different surface oxidation states are investigated. The most stable monolayer state involves two different molecular adsorption states, with specific vibrational and electronic properties. Molecular adsorption is always favored on the stoichiometric surface, even though dissociation becomes increasingly more favorable with increasing coverage. Oxygen vacancies shift the energy balance in favor of the dissociated state, whereas dissociative and molecular adsorption appear competitive on the hydroxylaled surface. On the latter, a specific molecular adsorption mode, not available on the clean surface, turns out to be stable. The vibrational and electronic properties of adsorbed methanol and methoxy are determined and compared to available experimental data.

Original languageEnglish (US)
Pages (from-to)19314-19319
Number of pages6
JournalJournal of Physical Chemistry B
Issue number50
StatePublished - Dec 16 2004

All Science Journal Classification (ASJC) codes

  • Materials Chemistry
  • Surfaces, Coatings and Films
  • Physical and Theoretical Chemistry


Dive into the research topics of 'Methanol adsorption and reactivity on clean and hydroxylated anatase(101) surfaces'. Together they form a unique fingerprint.

Cite this