Hostname: page-component-8448b6f56d-sxzjt Total loading time: 0 Render date: 2024-04-24T05:24:29.941Z Has data issue: false hasContentIssue false

Preparation and Characterization of Nanocomposite Composed of TiO2 as Active Matrix

Published online by Cambridge University Press:  10 February 2011

T. Sasaki
Affiliation:
National Institute of Materials and Chemical Research (NIMC), Agency of Industrial Science and Technology, MITI, 1–1 Higashi, Tsukuba, Ibaraki 305, Japan.
R. Rozbicki
Affiliation:
College of Engineering, Boston University, MA 02215
Y. Matsumoto
Affiliation:
Department of Applied Chemistry and Biochemistry, Faculty of Engineering, Kumamoto University, 2–39–1 Kurokami, Kumamoto 860, Japan.
N. Koshizaki
Affiliation:
National Institute of Materials and Chemical Research (NIMC), Agency of Industrial Science and Technology, MITI, 1–1 Higashi, Tsukuba, Ibaraki 305, Japan.
S. Terauchi
Affiliation:
National Institute of Materials and Chemical Research (NIMC), Agency of Industrial Science and Technology, MITI, 1–1 Higashi, Tsukuba, Ibaraki 305, Japan.
H. Umehara
Affiliation:
National Institute of Materials and Chemical Research (NIMC), Agency of Industrial Science and Technology, MITI, 1–1 Higashi, Tsukuba, Ibaraki 305, Japan.
Get access

Abstract

Pt/TiO2 nanocomposite films were deposited on quartz glass and ITO glass substrates by the co-sputtering method. As-deposited composite films were amorphous and content of Pt in the films could be easily controlled by the amount Pt wire placed on the TiO2 target. Pt/Ti atomic ratio in the nanocomposite increased as the length of Pt wire on the TiO2 target increased. It was determined by XPS that the chemical states of Pt in as-deposited nanocomposites were Pt metal, Pt-O-Ti and PtO2, which were dependent on the Pt/Ti atomic ratio in the nanocomposite. The size of Pt nanoparticles in the composite films increased as the temperature of heat-treatment and Pt/Ti atomic ratio in the composite films increased. Pt nanoparticles in the nanocomposite films inhibited grain growth of TiO2 during heat-treatment.

Type
Research Article
Copyright
Copyright © Materials Research Society 1997

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. Hache, F., Ricard, D., Flytzanis, C. and Kreigig, U., Appl. Phys., A47, 347(1988).Google Scholar
2. Kineri, T., Mori, M, Kadono, K., Sakaguchi, T., Miya, M., Wakabayashi, H. and Tsuchiya, T., J. Ceram. Soc. Jpn., 101, 1340(1993).Google Scholar
3. Ohtsuka, S., Koyama, K. and Tanaka, S., Extended Abstracta Inter. Sympo. Nonlinear Photonics Mater., Tokyo, 207 (1994).Google Scholar
4. Yoshida, S., Hanada, T., Tanabe, S. and Soga, N., Jpn. J. Appl. Phys., 35, 2694(1996).Google Scholar
5. Hayashi, S., Kataoka, M. and Yamamoto, K., Jpn. J. Appl. Phys., 32, L274(1993).Google Scholar
6. Maeda, Y., Tsukamoto, N., Yazawa, Y., Kanemitsu, Y and Masumoto, Y., Appl. Phys. Lett., 59, 3168(1991).Google Scholar
7. Koshizaki, N., Yasumoto, K. and Terauchi, S., Jpn. J. Appl. Phys., 34, Suppl. 34–1, 119(1994).Google Scholar
8. Tabata, S., Nishida, H., Masaki, Y and Tabata, K., Catalysis Lett., 34, 245(1995).Google Scholar
9. Avalle, L., Santos, E., Leiva, E. and Macagno, V., Thin Solid Films, 219, 7(1992).Google Scholar
10. Takahashi, M., Mita, K. and Toyuki, H., J. Mater. Sci., 24, 243(1989).Google Scholar
11. Davidson, M., Hofiund, G., Niinisto, L. and Laitinen, H., J. Electroanal. Chem., 228, 471(1987).Google Scholar
12. Perrin, S. and Bardolle, C., J. Microsc. Spectrosc. Electron, 1, 175(1976).Google Scholar
13. McDaniel, C. L., J. Solid State Chem., 9, 139(1974).Google Scholar