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Understanding Photocatalytic Activity of S- and P-Doped TiO2 under Visible Light from First-Principles

Yang, Kesong, Dai, Ying, Huang, Baibiao·2007·The Journal of Physical Chemistry C

Abstract

Substitutional S- and P-doped anatase and rutile TiO 2 crystals have been investigated by first-principles calculations on the basis of density functional theory (DFT). The results obtained show that S anion-doped anatase and rutile polymorphs of TiO 2 exhibit different modifications of electronic band structure at ultrahigher and realtively lower S concentration. In S cation-doped anatase and rutile TiO 2, the band gap has few changes but some mixing states of S 3s and O 2p are localized in the band gap, resulting in the reduction of photon absorption energy. In P anion-doped anatase TiO 2, the band gap has a slight narrowing and some P 3p states locate in it, which is consistent with experimental absorption spectra measurements in P-doped anatase TiO 2 . In P anion-doped rutile TiO 2, some of P 3p states locate in the band gap but it has little narrowing. Our electronic structure calculations for P cation-doped anatase and rutile TiO 2 also indicate that the band gap has few modifications and no impurity energy levels, which favor recent experimental observations that higher photocatalytic activity in P cation-doped TiO 2 results from the large surface area and the crystallinity of TiO 2 rather than impurity energy levels in the band gap. In addition, our results indicate that S (P) anion-doped TiO 2 is chemically more favored under Ti-rich condition while S (P) cation-doped TiO 2 is preferred to be synthesized under O-rich condition.

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Metadata

Authors
Yang, K., Dai, Y., & Huang, B.
Venue
The Journal of Physical Chemistry C
Published
2007-12-01
Volume
111
Issue
51
Pages
18985-18994
ISSN
  • 1932-7447 (ISSN-L)
  • 1932-7455
OpenAlex
W1980653269
Cited by
258
References
35
FWCI
7.12
Type
journal article
Language
en
Open access
closed

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