Defect-Induced Water Bilayer Growth on Anatase TiO2(101)

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Preparing an anatase TiO2(101) surface with a high density of oxygen vacancies and associated reduced Ti species in the near-surface region results in drastic changes in the water adsorption chemistry compared to adsorption on a highly stoichiometric surface. Using synchrotron radiation excited photoelectron spectroscopy, we observe a change in the water growth mode, from layer-by-layer growth on the highly stoichiometric surface to bilayer growth on the reduced surface. Furthermore, we have been able to observe Ti3+ enrichment at the surface upon water adsorption. The Ti3+ enrichment occurs concomitant with effective water dissociation into hydroxyls with a very high thermal stability. The water bilayer on the reduced surface is thermally more stable than that on the stoichiometric surface, and it is more efficient in promoting further water dissociation upon heating. The results thus show how the presence of subsurface defects can alter the wetting mechanism of an oxide surface.


  • A. Schaefer
  • V. Lanzilotto
  • U. B. Cappel
  • P. Uvdal
  • A. Borg
  • A. Sandell
Enheter & grupper
Externa organisationer
  • Chalmers University of Technology
  • Uppsala universitet, Historiska institutionen
  • Norwegian University of Science and Technology

Ämnesklassifikation (UKÄ) – OBLIGATORISK

  • Materialkemi
Sidor (från-till)10856-10864
Antal sidor9
StatusPublished - 2018
Peer review utfördJa