Surface electronic structure of TiO2: Atomic geometry, ligand coordination, and the effect of adsorbed hydrogen
The intrinsic electronic surface-state structure in the region of the bulk band gap for the (110), (100), and (001) surfaces of TiO2 (rutile) has been determined by fracturing single-crystal samples in ultrahigh vacuum and measuring their ultraviolet photoemission spectra. None of the faces exhibits an appreciable density of surface states in the bulk band gap, in disagreement with recent calculations for the TiO2(001) surface by Kasowski and Tait. The atomic geometry of both perfect and defect surfaces is examined, and the incomplete screening of pairs of surface cations at defect sites is suggested to give rise to occupied band-gap surface states rather than the coordinative unsaturation of surface cations. Hydrogen-exposure experiments indicate that TiO2 surfaces may not interact as strongly with hydrogen as has been suggested. © 1981 The American Physical Society.
Publication Source (Journal or Book title)
Physical Review B
Henrich, V., & Kurtz, R. (1981). Surface electronic structure of TiO2: Atomic geometry, ligand coordination, and the effect of adsorbed hydrogen. Physical Review B, 23 (12), 6280-6287. https://doi.org/10.1103/PhysRevB.23.6280