Preparation and Visible Light Photocatalytic Activity of Bi2WO6 Hollow Microspheres

Article Preview

Abstract:

Photocatalytic technology as a means of degradation of pollutants had been widespread concerned. In the past three decades, titanium dioxide (TiO2) has become one of the most extensively studied metal oxides because of its excellent photocatalytic activity and photoinduced hydrophilicity [1, . But TiO2 only absorbs wavelengths in the near-UV region (λ<400nm), which is about 3% of the solar spectrum and 53% visible light was can not efficiently utilized for the degradation of organic pollutants. Therefore, it is crucial to explore visible-light-induced photocatalysts. In recent years, in addition to traditional oxides, some complex oxides have been found under visible light driven have a good photocatalytic activity, Such as, N-doped TiO2 [, BiOX (X=Cl, Br, I) [, Bi2MoO6 [ and so on. Nevertheless, such efforts have not achieved satisfactory results aspects of making full use of the visible-light. Therefore, it is still a great challenge to design efficient visible-light driven photocatalysts.

You might also be interested in these eBooks

Info:

Periodical:

Advanced Materials Research (Volumes 864-867)

Pages:

1323-1326

Citation:

Online since:

December 2013

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2014 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

[1] K. I. Katsumata, C. E. J. Cordonier, T. Shichi, et al. J. Am. Chem. Soc. 2009, 131, 3856-3857.

Google Scholar

[2] Y. H. Fu, D. R. Sun, Y. J. Chen, et al. Angew. Chem. Int. Ed. 2012, 51, 3364-3367.

Google Scholar

[3] D. Y Wu, M. Long, ACS Appl. Mater. Interfaces, 2011, 3, 4770-4774.

Google Scholar

[4] X. Zhang, Z. H. Ai, F. L Jia, et al. J. Phys. Chem. C, 2008, 112, 747-753.

Google Scholar

[5] C. Kongmark, R. Coulter, S. Cristol, et al. Crystal Growth & Design, 2012, 12, 5994-6003.

Google Scholar

[6] C. F. Guo, J. M Zhang, Y. Tian, et al. ACS Nano, 2012, 6, 8746-8752.

Google Scholar

[7] J. G. Yu, J. F. Xiong, B. Cheng, et al. J. Solid State Chem. 2005, 178, 1968-(1972).

Google Scholar

[8] M. Shang, W. Z. Wang, S. M. Sun, et al. J. Phys. Chem. C 2008, 112, 10407-10411.

Google Scholar

[9] D. K. Ma, S. M. Huang, W. X. Chen, et al. J. Phys. Chem. C 2009, 113, 4369-4374.

Google Scholar

[10] X. J. Dai, Y. S. Luo, W. D. Zhang, et al. Dalton Trans. 2010, 39, 3426-3432.

Google Scholar

[11] Y. Y. Li, J. P. Liu, X. T. Huang Nanoscale Res. Lett. 20083 365-371.

Google Scholar

[12] S. B. Zhu, T. G. Xu, H. B Fu, et al. Environ. Sci. Technol., 2007, 41 6234-6239.

Google Scholar

[13] D. Q. He, L. L. Wang, D. D. Xu, et al. ACS Appl. Mater. Interfaces, 2011, 3, 3167-3171.

Google Scholar

[14] S. M. Sun, W. Z Wang, L. Zhang J. Phys. Chem. C, 2013, 117, 9113-9120.

Google Scholar

[15] C. Zhang, Y. F. Zhu, Chem. Mater. 2005, 17, 3537-3545.

Google Scholar

[16] J. D. Zhuang, W. X. Dai, P. Liu, Langmuir 2010, 26, 9686-9694.

Google Scholar