Photochemistry on TiO2: Mechanisms Behind the Surface Chemistry

Abstract

Photochemistry from TiO2 surfaces is described for two cases: The UV-induced photodesorption of O2 from TiO2(110) - 1 x 1; and the hydrophilic effect caused by UV irradiation on TiO2. In both cases fundamental information about how these processes occur has been found. In the case of the O2 photodesorption kinetics, it has been found that the rate of the process is proportional to the square root of the UV flux, showing that second-order electron?hole pair recombination is dominant in governing the photodesorption rate. In addition these measurements provide an estimate of the concentration of hole traps in the TiO2 crystal. In other measurements of the UV-induced hydrophilicity, starting with the atomically-clean TiO2 surface, it has been shown that the effect occurs suddenly at a critical point during irradiation as a result of photooxidation of a monolayer of hydrocarbon (n-hexane) at equilibrium with ppm concentration of n-hexane in O2 at 1 atmosphere pressure.

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Document Details

Document Type
Technical Report
Publication Date
Jan 21, 2009
Accession Number
ADA518004

Entities

People

  • John Yates

Organizations

  • University of Virginia

Tags

Communities of Interest

  • Energy and Power Technologies
  • Materials and Manufacturing Processes

DTIC Thesaurus Topics

  • Band Gaps
  • Charge Carriers
  • Charge Transfer
  • Chemical Reaction Properties
  • Chemical Reactions
  • Chemistry
  • Desorption
  • Electrons
  • Energy
  • Energy Bands
  • Energy Gaps
  • Hydrophilic Properties
  • Measurement
  • Photochemistry
  • Quantum Yields
  • Semiconductors
  • Surface Chemistry

Readers

  • Aerospace Research.
  • Materials Science and Engineering.
  • Thin Film Deposition Science.

Technology Areas

  • Microelectronics
  • Microelectronics - Graphene