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International Journal of Photoenergy
Volume 2012, Article ID 569716, 10 pages
Research Article

Enhanced Visible Light Photocatalytic Activity of Cluster Modified N-Doped for Degradation of Toluene in Air

College of Environmental and Biological Engineering, Key Laboratory of Catalysis Science and Technology of Chongqing Education Commission, Chongqing Technology and Business University, Chongqing 400067, China

Received 2 January 2012; Revised 19 February 2012; Accepted 20 February 2012

Academic Editor: Xuxu Wang

Copyright © 2012 Fan Dong et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


V2O5 cluster-modified N-doped TiO2 (N-TiO2/V2O5) nanocomposites photocatalyst was prepared by a facile impregnation-calcination method. The effects of V2O5 cluster loading content on visible light photocatalytic activity of the as-prepared samples were investigated for degradation of toluene in air. The results showed that the visible light activity of N-doped TiO2 was significantly enhanced by loading V2O5 clusters. The optimal V2O5 loading content was found to be 0.5 wt.%, reaching a removal ratio of 52.4% and a rate constant of 0.027 min−1, far exceeding that of unmodified N-doped TiO2. The enhanced activity is due to the deposition of V2O5 clusters on the surface of N-doped TiO2. The conduction band (CB) potential of V2O5 (0.48 eV) is lower than the CB level of N-doped TiO2 (−0.19 V), which favors the photogenerated electron transfer from CB of N-doped TiO2 to V2O5 clusters. This function of V2O5 clusters helps promote the transfer and separation of photogenerated electrons and holes. The present work not only displays a feasible route for the utilization of low cost V2O5 clusters as a substitute for noble metals in enhancing the photocatalysis but also demonstrates a facile method for preparation of highly active composite photocatalyst for large-scale applications.