The DOI matches its Crossref record; 35 of the 35 references it cites were found in a registry or an index.
Understanding Photocatalytic Activity of S- and P-Doped TiO2 under Visible Light from First-Principles
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
- Publisher
- American Chemical Society (ACS)
- 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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