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Dehydrogenation and Polymerization of TiOxHy Films in Obtaining Anatase Coating at Low Temperature

Published online by Cambridge University Press:  11 February 2011

Kouichi Takayama
Affiliation:
Department of Chemistry, Nagaoka University of Technology, 1603–1, Kamitomioka, Nagaoka, Niigata 940–2188, Japan
Shigeo Ohshio
Affiliation:
Department of Chemistry, Nagaoka University of Technology, 1603–1, Kamitomioka, Nagaoka, Niigata 940–2188, Japan
Hidetoshi Saitoh
Affiliation:
Department of Chemistry, Nagaoka University of Technology, 1603–1, Kamitomioka, Nagaoka, Niigata 940–2188, Japan
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Abstract

Chemical-vapor-deposition of titanium tetra-isopropoxide (TTIP) under the atmosphere at low temperature has been conducted. The structure of the obtained films was assessed using Fourier transform infrared spectroscopy, X-ray diffractometry and Raman spectroscopy. These analyses indicated that amorphous TiOxHy films were obtained at gas temperatures in the range of 150–300 °C, and crystalline anatase-TiO2 film was formed at 350 °C. This distinction is accounted for by plausible chemical reactions as follows; the hydroxyl reaction of TTIP below 350 °C promotes the formation of the amorphous TiOxHy. As the temperature goes up to 350 °C, dehydrogenation of the TiOxHy films promotes to form crystalline TiO2. Also the obtained amorphous films were annealed for 10 min under the atmosphere in assessing the transformation proceeding in the solid state. The structural change is shown at 350 °C, indicating that the crystalline phase would be formed via dehydrogenation and polymerization on the surface of the amorphous phase under the atmosphere. The crystal size of the annealed films was evaluated in assessment for the transformation.

Type
Research Article
Copyright
Copyright © Materials Research Society 2003

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References

REFERENCES

1. Chen, D., Sol. Energy Mater. & Sol. Cells 68, 313 (2001).Google Scholar
2. Shirai, M., Umeda, S., Tsunooka, M. and Matsuo, T., Eur. Polym. J. 34, 1295 (1998).Google Scholar
3. Straumal, B., Vershinin, N., Filonov, K., Dimitriou, R. and Gust, W., Thin SolidFilms 351, 204 (1999).Google Scholar
4. Satoh, M., Tanaka, N., Ueda, Y, Ohshio, S. and Saitoh, H., Jpn. J. Appl. Phys. 38, L586 (1999).Google Scholar
5. Saitoh, H., Satoh, M., Tanaka, N., Ueda, Y and Ohshio, S., Jpn. J. Appl. Phys. 38, 6873 (1999).Google Scholar
6. Tanaka, N., Ohshio, S. and Saitoh, H., J. Ceram. Soc. Jpn. 105, 551 (1997).Google Scholar
7. Saitoh, H., Sunayama, H., Tanaka, N. and Ohshio, S., J. Ceram. Soc. Jpn. 106, 1051 (1998).Google Scholar
8. Tokita, S., Tanaka, N. and Saitoh, H., Jpn. J. Appl. Phys. 39, Ll 69 (2000).Google Scholar
9. Saitoh, H., Namioka, Y, Sugata, H. and Ohshio, S., Jpn. J. Appl. Phys. 40, 6024 (2001).Google Scholar
10. Brasseur-Tilmant, J., Chhor, K., Jestin, P. and Pommier, C., Mater. Res. Bull. 34, 2013 (1999).Google Scholar
11. Katagiri, Y, Nasu, H., Matsuoka, J. and Kamiya, K., J. Am. Ceram. Soc. 77, 673 (1994).Google Scholar
12. Fukui, T., J. Sol-Gel Sci. Tech. 11, 31 (1998).Google Scholar
13. Ohsaka, T., Izumi, F. and Fujiki, Y, J Raman Spectrosc. 7, 321 (1978).Google Scholar
14. Wang, W. -C., Lin, M.-H and Liu, H. -S., J Mater. Res. 14, 196 (1999).Google Scholar