Identifying Trapped Electronic Holes at the Aqueous TiO2 Interface

Jun Cheng, Joost VandeVondele, Michiel Sprik

Research output: Contribution to journalArticle

42 Citations (Scopus)

Abstract

Trapping of photogenerated holes near or at the surface is believed to be a crucial step in the photo-oxidation of water and organic pollutants by TiO2. The detailed nature of these localized states is however still a matter of debate. Here, we investigate this question for the rutile TiO2(110) water interface using ab initio molecular dynamics simulation methods based on a state-of-the-art hybrid density functional. We identify the reactive surface trapped holes as the OH• on five-coordinated terminal Ti and its deprotonated O•–. Our calculations show that the large reorganization energies hold the key to reconciling some of the conflicting interpretations of spectroscopic and thermodynamic measurements reported in the literature. We also observe an asymmetry in reorganization energies owing to the pinning of the valence band of TiO2. This has important implications for the understanding of the heterogeneous electron transfer kinetics driving photo-oxidation.
Original languageEnglish
Pages (from-to)5437-5444
Number of pages8
JournalThe Journal of Physical Chemistry C
Volume118
Issue number10
Early online date24 Feb 2014
DOIs
Publication statusPublished - 13 Mar 2014

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Photooxidation
photooxidation
Water
Organic pollutants
Valence bands
electronics
rutile
water
Interfaces (computer)
contaminants
Molecular dynamics
electron transfer
trapping
asymmetry
Thermodynamics
molecular dynamics
valence
thermodynamics
Kinetics
energy

Cite this

Identifying Trapped Electronic Holes at the Aqueous TiO2 Interface. / Cheng, Jun; VandeVondele, Joost; Sprik, Michiel.

In: The Journal of Physical Chemistry C, Vol. 118, No. 10, 13.03.2014, p. 5437-5444.

Research output: Contribution to journalArticle

Cheng, Jun ; VandeVondele, Joost ; Sprik, Michiel. / Identifying Trapped Electronic Holes at the Aqueous TiO2 Interface. In: The Journal of Physical Chemistry C. 2014 ; Vol. 118, No. 10. pp. 5437-5444.
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