4.6 Article

Synergic effect of cation doping and phase composition on the photocatalytic performance of TiO2 under visible light

Journal

CATALYSIS COMMUNICATIONS
Volume 51, Issue -, Pages 46-52

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.catcom.2014.03.024

Keywords

Cation doping; Phase composition; Titanium dioxide; Synergic effect; Visible light; Photocatalyst

Funding

  1. Chinese Academy of Sciences for 100 Talents Project
  2. National Natural Science Foundation of China [11079036]
  3. Natural Science Foundation of Liaoning Province [20092173]

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The synergic effect of cation doping and phase composition for the further improvement of the photocatalytic activity of TiO2 under visible light is reported for the first time. Fe3+ and Sn4+ co-doped TiO2 with optimized phase composition were synthesized through a simple soft-chemical solution method. The visible-light-driven photocatalytic activity of Fe3+ and Sn4+ co-doped TiO2 was 5 times of that of Evonik P25 TiO2 using degradation of methylene blue as model reaction. The synthesized photocatalysts were characterized by powder X-ray diffraction, UV-Vis diffuse reflectance spectroscopy, X-ray photoelectron spectroscopy, Sn-119 Mossbauer spectroscopy, and X-ray absorption fine structure spectroscopy. It is indicated that Sn4+ doping can facilitate the phase transition from anatase to rutile. The different ratios of anatase and rutile can be achieved by tuning the amount of Se4+ doped into the lattice. Furthermore, the doping of Se4+ into TiO2 lattice can stabilize the phase composition when Fe3+ is co-doped. In the Fe3+ and Se4+ co-doped TiO2, Sn4+ is mainly used to tune and stabilize the phase composition of TiO2 and Fe3+ acts as a doping cation to narrow the band gap of TiO2. Both band gap and phase composition of TiO2 can be tuned effectively by the simultaneous introduction of Fe3+ and Sn4+. The synergic effect of optimized phase composition (anatase/rutile = 25/75) and narrowed band gap should be the two main reasons for the promoted photocatalytic activity of TiO2 under visible light. (C) 2014 Elsevier B.V. All rights reserved.

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