Hostname: page-component-77c89778f8-swr86 Total loading time: 0 Render date: 2024-07-24T01:22:59.662Z Has data issue: false hasContentIssue false

Nitrogen and Fluorine Roles in Visible-Light-Driven Anion-Doped TiO2 Photocatalysis

Published online by Cambridge University Press:  01 February 2011

Li Di
Affiliation:
LI.Di@nims.go.jp, National Institute for Materials Science, Advanced Materials Lab, 1-1 Namiki, Tsukuba, Ibaraki, 305-0044, Japan, +81-29-851-3354 ext 8608, +81-29-855-1196
Naoki Ohashi
Affiliation:
OHASHI.Naoki@nims.go.jp, National Institute for Materials Science, Advanced materials Laboratory, Japan
Shunichi Hishita
Affiliation:
HISHITA.Shunichi@nims.go.jp, National Institute for Materials Science, Advanced materials Laboratory
Taras Kolodiazhnyi
Affiliation:
KOLODIAZHNYI.Taras@nims.go.jp, National Institute for Materials Science, Advanced materials Laboratory, Japan
Hajime Haneda
Affiliation:
HANEDA.Hajime@nims.go.jp, National Institute for Materials Science, Advanced materials Laboratory, Japan
Get access

Abstract

This paper describes the synthesis of N-doped, F-doped, and N-F-codoped TiO2 powders (NTO, FTO, NFTO) by spray pyrolysis (SP). An overall comparative study was carried out on these anion-doped powders in order to elucidate the roles of N and F played in visible-light (Vis)-driven photocatalysis. The comparisons in their characteristics were based on the analysis of UV-Vis, PL, NH3-TPD and ESR spectra. As the results, N-doping into TiO2 resulted in both the improvement of Vis absorption and the creation of surface oxygen vacancies (OVs). F-doping produced several beneficial effects including the creation of surface OVs, the enhancement of surface acidity and the increase of Ti3+ ions. The photocatalytic tests indicated that the NFTO demonstrated the highest Vis activity for decomposition of both acetaldehyde and trichloroethylene. This high activity was ascribed to a synergetic consequence of doped N and F.

Type
Research Article
Copyright
Copyright © Materials Research Society 2006

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

[1] Asahi, R., Morikawa, T., Ohwaki, T., Aoki, K., Taga, Y., Science 293, 269 (2001).Google Scholar
[2] Li, D., Haneda, H., Hishita, S., Ohashi, N., Mater. Sci. Eng. B 117, 67 (2005).Google Scholar
[2] Li, D., Haneda, H., Labhsetwar, N. K., Hishita, S., Ohashi, N., Chem. Phys. Lett. 401, 579 (2005).Google Scholar
[4] Li, D., Haneda, H., Hishita, S., Ohashi, N., Chem. Mater. 17, 2588 (2005).Google Scholar
[5] Li, D., Haneda, H., Hishita, S., Ohashi, N., Chem. Mater. 17, 2596 (2005).Google Scholar
[6] Stashans, A., Lunell, S., Grimes, R.W., J. Phys. Chem. Solids 57, 1293 (1996).Google Scholar
[7] Saraf, L.V., Patil, S.I., Ogale, S.B., Sainkar, S.R., Kshirsager, S.T., Int. J. Mod. Phys. B 12, 2635 (1998).Google Scholar
[8] Serpone, N., Lawless, D., Khairutdinov, R., J. Phys. Chem. 99, 16646 (1995).Google Scholar
[9] Keller, V., Bernhardt, P., Garin, F., J. Catal. 215, 129 (2003).Google Scholar
[10] Meriaudeau, P., Vedrine, J.C., J. Chem. Soc., Faraday Trans. II 72, 472 (1976).Google Scholar
[11] Howe, R.F., Grätzel, M., J. Phys. Chem. 89, 4495 (1985).Google Scholar
[12] Yu, J.C., Yu, J., Ho, W., Jiang, Z., Zhang, L., Chem. Mater. 14, 3808 (2002).Google Scholar
[13] Martyanov, I.N., Uma, S., Rodrigues, S., Klabunde, K.J., Chem. Comm., 2476 (2004).Google Scholar
[14] Henderson, M.A., Epling, W.S., Perkins, C.L., Peden, C.H.F., J. Phys. Chem. B. 103, 5328 (1999)Google Scholar