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Photocatalytic Hydrogen Production from Gas-phase Methanol and Water with Nanocrystalline TiO2 Thin Films in High Vacuum

Published online by Cambridge University Press:  01 February 2011

Kei Noda
Affiliation:
[email protected], Kyoto University, Electronic Science & Engineering, Katsura, Nishikyo, Kyoto, 615-8510, Japan, 81753832307, 81753832308
Masashi Hattori
Affiliation:
[email protected], Kyoto University, Electronic Science & Engineering, Katsura, Nishikyo, Kyoto, 615-8510, Japan
Kouichi Amari
Affiliation:
[email protected], Kyoto University, Electronic Science & Engineering, Katsura, Nishikyo, Kyoto, 615-8510, Japan
Kei Kobayashi
Affiliation:
[email protected], Kyoto University, Innovative Collaboration Center(ICC), Katsura, Nishikyo, Kyoto, 615-8520, Japan
Toshihisa Horiuchi
Affiliation:
[email protected], Kyoto University, Innovative Collaboration Center(ICC), Katsura, Nishikyo, Kyoto, 615-8520, Japan
Kazumi Matsushige
Affiliation:
[email protected], Advanced Software Technology and Mechanics Research Institute (ASTEM), Shimogyo, Kyoto, 600-8813, Japan
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Abstract

Photocatalytic hydrogen production with gas-phase reactions in high vacuum was examined for nanocrystalline anatase-type titanium dioxide (TiO2) thin films. The hydrogen generation process on platinized TiO2 specimens was investigated using a quadrupole mass spectrometer at a real-time scale under various partial pressures of gaseous methanol and water. As a result, hydrogen generation was successfully detected under ultraviolet ray (UV) illumination even in high vacuum (∼ 10−7 Torr). And the amount of produced H2 largely depends on the temperature of TiO2 samples, probably due to different surface states of TiO2. This study suggests the possibility of new high-speed H2 production system with gas-phase photocatalytic reactions.

Type
Research Article
Copyright
Copyright © Materials Research Society 2008

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References

REFERENCES

1 O'Regan, B. and Grätzel, M., Nature 353, 737 (1991).Google Scholar
2 Kawai, M., Naito, S., Tamaru, K. and Kawai, T., Chem. Phys. Lett. 98, 377 (1983).Google Scholar
3 Nosaka, A. Y., Nishino, J., Fujiwara, T., Ikegami, T., Yagi, H., Akutsu, H., Nosaka, Y., J. Phys. Chem. B 110, 8380 (2006).Google Scholar
4 Anpo, M., Catalysis Survey from Japan 1, 169 (1997).Google Scholar
5 Fujishima, A. and Honda, K., Nature 238, 37 (1972).Google Scholar
6 Sato, S., New. J. Chem. 12, 859 (1988).Google Scholar
7 Noda, K., Hattori, M., Amari, K., Kobayashi, K., Horiuchi, T. and Matsushige, K., Jpn. J. Appl. Phys. Part2 46, L749 (2007).Google Scholar
8 Jiu, J., Isoda, S., Adachi, M., Wang, F., J. Photochem. Photobiol. A: Chem. 189, 314 (2007).Google Scholar
9 Bard, A. J., J. Photochem. 10, 59 (1979).Google Scholar
10 Herman, G. S., Dohnalek, Z., Ruzycki, N. and Diebold, U., J. Phys. Chem. B 107, 2788 (2003).Google Scholar