A shell model for atomistic simulation of charge transfer in titania

Sebastien Kerisit, N. Aaron Deskins, Kevin M. Rosso, Michel Dupuis

Research output: Contribution to journalArticle

35 Citations (Scopus)

Abstract

The derivation of atomistic potential parameters, based on electronic structure calculations, for modeling electron and hole polarons in titania polymorphs is presented. The potential model is a polarizable version of the Matsui and Akaogi model (Matsui, M.; Akaogi, M. Mol. Simul. 1991, 6, 239) that makes use of a shell model to account for the polarizability of oxygen ions. The -1 and +1 formal charges of the electron and hole polarons, respectively, are modeled by delocalizing the polaron's charge over a titanium or oxygen ion, respectively, and its first nearest-neighbors. The charge distributions and the oxygen polarizability were fitted to the reorganization energies of a series of electron and hole polaron transfers in rutile and anatase obtained from electronic structure calculations at zero Kelvin and validated against lattice deformation due to both types of polaron. Good agreement was achieved for both properties. In addition, the potential model yields an accurate representation of a range of bulk properties of several TiO2 polymorphs as well as Ti2O3. The model thus derived enables us to consider systems large enough to investigate how the charge transfer properties at titania surfaces and interfaces differ from those in the bulk. For example, reorganization energies and free energies of charge transfer were computed as a function of depth below vacuum-terminated rutile (110) and anatase (001) surfaces using a mapping approach first introduced by Warshel (Warshel, A. J. Phys. Chem. 1982, 86, 2218). These calculations indicate that deviations from bulk values at the surface are substantial but limited to the first couple of surface atomic layers and that polarons are generally repelled from the surface. Moreover, attractive subsurface sites may be found as is predicted for hole polarons at the rutile (110) surface. Finally, several charge transfers from under-coordinated surface sites were found to be in the so-called Marcus inverted-region.

Original languageEnglish
Pages (from-to)7678-7688
Number of pages11
JournalJournal of Physical Chemistry C
Volume112
Issue number20
DOIs
Publication statusPublished - May 22 2008

Fingerprint

Charge transfer
titanium
Titanium
charge transfer
Polarons
polarons
Gene Conversion
rutile
simulation
Oxygen
oxygen ions
Polymorphism
anatase
Titanium dioxide
Electronic structure
Electrons
Ions
electronic structure
electrons
Charge distribution

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Electronic, Optical and Magnetic Materials
  • Surfaces, Coatings and Films
  • Energy(all)

Cite this

A shell model for atomistic simulation of charge transfer in titania. / Kerisit, Sebastien; Aaron Deskins, N.; Rosso, Kevin M.; Dupuis, Michel.

In: Journal of Physical Chemistry C, Vol. 112, No. 20, 22.05.2008, p. 7678-7688.

Research output: Contribution to journalArticle

Kerisit, Sebastien ; Aaron Deskins, N. ; Rosso, Kevin M. ; Dupuis, Michel. / A shell model for atomistic simulation of charge transfer in titania. In: Journal of Physical Chemistry C. 2008 ; Vol. 112, No. 20. pp. 7678-7688.
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