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An Approach to Nanoglasses through Anodic Oxidation of Sputtered Aluminum on Glass Surface

Published online by Cambridge University Press:  11 February 2011

Satoru Inoue
Affiliation:
National Institute for Materials Science, Advanced Materials Laboratory, Namiki 1–1, Tsukuba, Ibaraki, 305–0044, Japan
Song-Zhu Chu
Affiliation:
National Institute for Materials Science, Advanced Materials Laboratory, Namiki 1–1, Tsukuba, Ibaraki, 305–0044, Japan
Kenji Wada
Affiliation:
National Institute for Materials Science, Advanced Materials Laboratory, Namiki 1–1, Tsukuba, Ibaraki, 305–0044, Japan
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Abstract

The new processes for the preparation of nanoglasses have been developed through anodic oxidation. The aluminum thin film sputtered on the ITO thin film on the glass surface was decomposed into alumina by anodic oxidation technique. The alumina layer possessed nanometer size pore array standing on the glass surface. The sizes of the pore was widened by acid etching from 10∼20nm to a few hundred nm. The glass substrate having the alumina nanostructures on the surface could transmit the UV and visible light at the wavelength range of 200 ∼ 800nm. The TiO2 sol was impregnated into the pores of alumina layer and the sample was heated at ∼ 400 °C for 2 hr, converted into TiO2 nanotubes of anatase phase. The acid etching could remove the alumina skeletons, leaving the TiO2 nanotube array on the glass surface. These glasses were transparent to the light in UV-visible region. The electro deposition technique was applied to the introduction of Ni metal into pores, giving Ni nanorod array on the glass surface. The glass samples possessing TiO2 nanotube array showed very good catalytic function on the decomposition of acetaldehyde gas under the irradiation of UV light. The effect of the dimensions of the Ni nanorods on the magnetization was investigated.

Type
Research Article
Copyright
Copyright © Materials Research Society 2003

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References

REFERENCES

1. Huczko, A., Appl. Phys. 70, 365 (2000).Google Scholar
2. Kyotani, T. and Tomita, A., Bull. Chem. Soc. Jpn. 72, 1957 (1999).Google Scholar
3. Zhang, M., Bando, Y, Wada, K. and Kurashima, K., J. Mater. Sci. Lett. 18, 1911 (1999).Google Scholar
4. Lakshmi, B. B., Dorhout, P. K. and Martin, C. R., Chem. Mater. 9, 857 (1997).Google Scholar
5. Masuda, H. and Fukuda, K., Science 268, 1466 (1995).Google Scholar
6. for example; Mozalev, A., Surganov, A. and Imai, H., Electrochim. Acta 46, 2825 (2001).Google Scholar
7. for example; Crouse, D., Lo, Y, Miller, A. E. and Crouse, M., Appl. Phys. Lett. 76, 49 (2000).Google Scholar
8. Chu, S. Z., Wada, K., Inoue, S. and Todoroki, S., J. Electrochem. Soc. 149(7), B321 (2002).Google Scholar
9. Chu, S. Z., Wada, K., Inoue, S. and Todoroki, S., Chem Mater. 14, 266 (2002).Google Scholar
10. Chu, S. Z., Wada, K. and Inoue, S., Advanced Materials, 14[23], 1752 (2002)Google Scholar
11. Chu, S. Z., Inoue, S., Wada, K., Li, Di and Haneda, H., J. Mater. Chem., (in press) (2003), also published as an Advanced Article on the RSC web site (http://www.rsc.org/is/journals/current/jmc/mappub.htm) onFeb.7, 2003.Google Scholar
12. Chu, S. Z., Wada, K., Inoue, S. and Todoroki, S., Chem. Mater, 14, 4595 (2002).Google Scholar