Models for the Photoelectrolytic Decomposition of Water at Semiconducting Oxide Anodes.

Abstract

Surface states at semiconducting TiO2/electrolyte interfaces are believed to play an important role in charge transfer and thereby the efficiency of photoelectrochemical processes at such interfaces. Theoretical calculations were therefore performed using the SCF-Xalpha-SW method to determine the position and character of surface states at various characteristic interfaces. At the TiO2/water interface, antibonding surface states were found which when occupied would explain the experimentally observed dissociation of water into hydroxyl groups at n-type semiconducting TiO2 surfaces. Similarly, antibonding surface states were found at the TiO2/OH interface which when occupied would tend to destabilize the OH bond. A likely mechanism for the dissociation of water and decomposition of certain photoanodes in photoelectrochemical cells based on the above results is presented. The effects of surface reconstruction at heavily reduced TiO2 surfaces on the validity of our calculations are also discussed. (Author)

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Document Details

Document Type
Technical Report
Publication Date
Dec 31, 1979
Accession Number
ADA079469

Entities

People

  • Harry L Tuller
  • J. M. Kowalski
  • Keith H. Johnson

Organizations

  • Massachusetts Institute of Technology

Tags

Communities of Interest

  • Energy and Power Technologies

DTIC Thesaurus Topics

  • Auger Electron Spectroscopy
  • Band Gaps
  • Band Theory Of Solids
  • Charge Transfer
  • Decomposition
  • Dissociation
  • Electrons
  • Energy Bands
  • Energy Gaps
  • Energy Levels
  • Materials
  • Materials Science
  • Oxides
  • Photoelectrochemical Cells
  • Solid State Physics
  • Titanium
  • Valence Bands

Fields of Study

  • Materials science

Readers

  • Electrochemical Engineering/ Fuel Cell Technologies
  • Materials Science and Engineering.
  • Quantum Chemistry