Abstract
Electrochemical impedance spectroscopy, photoelectron spectroscopy, and Kelvin probe measurements on various TiO2 single-crystal surfaces show that the position of the Fermi level and the conduction band minimum depend significantly on the sample environment (vacuum, air, water vapor, and aqueous or aprotic electrolyte solutions). In most cases, the conduction-band minimum increases in the series: anatase < rutile < brookite.
The offset between anatase and rutile indicates a type H staggered alignment if the environment is vacuum, air, water vapor, or aprotic electrolyte solution, but a type IV aligned configuration is found in an aqueous electrolyte solution. The photoelectron spectra in water vapor reveal a strong upshift of the conduction band, which is nearly reversible in the early stages of water/titania interactions.
Our results rationalize various earlier contradictions and highlight the need for proper analytical techniques and experimental conditions for investigation of the band energetics, which is relevant to practical applications of titania materials.