Hostname: page-component-78c5997874-g7gxr Total loading time: 0 Render date: 2024-11-18T03:19:30.815Z Has data issue: false hasContentIssue false

(110)-oriented diamond films synthesized by microwave chemical-vapor deposition

Published online by Cambridge University Press:  31 January 2011

Koji Kobashi
Affiliation:
Electronics Research Laboratory, Kobe Steel, Ltd., 1-5-5, Takatsukadai, Nishi-ku, Kobe 673-02, Japan
Kozo Nishimura
Affiliation:
Electronics Research Laboratory, Kobe Steel, Ltd., 1-5-5, Takatsukadai, Nishi-ku, Kobe 673-02, Japan
Koichi Miyata
Affiliation:
Electronics Research Laboratory, Kobe Steel, Ltd., 1-5-5, Takatsukadai, Nishi-ku, Kobe 673-02, Japan
Kazuo Kumagai
Affiliation:
Electronics Research Laboratory, Kobe Steel, Ltd., 1-5-5, Takatsukadai, Nishi-ku, Kobe 673-02, Japan
Akimitsu Nakaue
Affiliation:
Electronics Research Laboratory, Kobe Steel, Ltd., 1-5-5, Takatsukadai, Nishi-ku, Kobe 673-02, Japan
Get access

Abstract

Bilayer diamond films were deposited on Si substrates by microwave-plasma chemical-vapor deposition (CVD) using a methane-hydrogen gas mixture. The first layer was deposited for 3 h using a reaction gas which was composed of 2.5 vol. % methane and 97.5 vol.% hydrogen. The deposited film consisted of very weakly (110)-oriented microcrystalline diamonds as well as amorphous carbon and graphite. In order to remove non-diamond carbons from the film surface, the specimen was treated in hydrogen plasma for 1 h. Finally, a second layer was deposited on the first layer for 14 h using a methane concentration of between 0.2 and 1.6 vol.%. It was found that the x-ray intensity of the (220) diffraction of the bilayer films was much greater than that of the (111) diffraction, indicating that the diamond grains in the second layer were strongly oriented with their crystallographic (110) planes parallel to the substrate surface. X-ray diffraction spectra of bilayer films in which the second layer was deposited for 7, 14, 21, and 35 h using two different methane concentrations, 0.3 and 1.2 vol.%, showed that within periods of up to 21 h, the (220) intensity increased with the deposition time much more quickly than the (111) intensity, indicating that the degree of (110) orientation was further enhanced as the second layer thickness increased. However, the (220) intensity decreased after 21 h, presumably due to thermal randomization. Results of scanning electron microscopy, electron diffraction, and Raman spectroscopy of the bilayer films are also presented.

Type
Diamond and Diamond-Like Materials
Copyright
Copyright © Materials Research Society 1990

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

1Kobashi, K., Nishimura, K., Kawate, Y., and Horiuchi, T., Phys. Rev. B 38, 4067 (1988).CrossRefGoogle Scholar
2Setaka, N., Research Report No. 39, National Institute for Research in Inorganic Materials (1984).Google Scholar
3Wada, N. and Solin, S.A., Physica B + C 105B, 353 (1981).CrossRefGoogle Scholar
4Solin, S.A. and Ramadas, A. K., Phys. Rev. B 1, 1687 (1970).CrossRefGoogle Scholar
5Dillon, R. O., Woollam, J. A., and Katkanant, V., Phys. Rev. B 29, 3482 (1984).CrossRefGoogle Scholar
6Ishida, H., Fukuda, H., Katagiri, G., and Ishitani, S., Appl. Speciose. 40, 322 (1986).CrossRefGoogle Scholar
7Tuinstra, F. and Koenig, J.L., J. Chem. Phys. 53, 1126 (1970).CrossRefGoogle Scholar
8Shirakawa, H., Ito, T., and Ikeda, S., Polymer J. 4, 460 (1973).CrossRefGoogle Scholar
9Baruya, A., Macromolecules 16, 578 (1983).CrossRefGoogle Scholar
10Knight, D. S. and White, W. B., J. Mater. Res. 4, 385 (1989).CrossRefGoogle Scholar
11Nemanich, R. J., Glass, J.T., Lukovsky, G., and Shroder, R. E., J. Vac. Sci. Technol. 6, 1783 (1988).CrossRefGoogle Scholar
12Glass, J.T., Williams, B. E., Davis, R. F., and Kobashi, K., Abstracts of the 1st Int. Conf. on the New Diamond Sci. Technol. (Tokyo, 1988), p. 164.Google Scholar
13Davis, R. F., Williams, B.E., Glass, J.T., and Kobashi, K., Extended Abstracts of the 175th Meeting of the Electrochemical Society (Los Angeles, CA, 1989), p. 130.Google Scholar
14Srivatsa, A. R., Narayan, J., and Ravi, K.V., Extended Abstracts of the 175th Meeting of the Electrochemical Society (Los Angeles, CA, 1989), p. 131.Google Scholar