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Solid-state reactions of the Ag–Cu–Ti thin film–Al2O3 substrate system

Published online by Cambridge University Press:  31 January 2011

Seiichi Suenaga
Affiliation:
Materials and Devices Laboratories, Research and Development Center, Toshiba Corporation, Kawasaki 210, Japan
Miho Koyama
Affiliation:
Materials and Devices Laboratories, Research and Development Center, Toshiba Corporation, Kawasaki 210, Japan
Shinji Arai
Affiliation:
Materials and Devices Laboratories, Research and Development Center, Toshiba Corporation, Kawasaki 210, Japan
Masako Nakahashi
Affiliation:
Materials and Devices Laboratories, Research and Development Center, Toshiba Corporation, Kawasaki 210, Japan
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Abstract

A new interpretation of the reaction mechanism between active metal thin-film filler and ceramic substrate is proposed. The authors predict the possibility of prebonding reactions, prior to melting of the filler, at the interface of the system described above. To prove this, solid-state reactions of Ag–Cu–Ti thin films on sapphire substrates have been studied with Auger electron spectroscopy (AES) and x-ray diffraction (XRD). Reaction process and products have been clarified at the temperature just below the melting point of the filler. It is evident that Cu3Ti3O (diamond structure of Fd3m) is formed by the reaction between Cu3Ti and O which results from the reduction of sapphire. It seems that Cu3Ti3O contributes to bonding between metals and sapphire as an intermediate phase.

Type
Articles
Copyright
Copyright © Materials Research Society 1993

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References

REFERENCES

1Loehman, R.E. and Tomsia, A. P., Ceram. Bull. 67, 375 (1988).Google Scholar
2Yano, T., Suematsu, H., and Iseki, T., J. Mater. Sci. 23, 3362 (1988).Google Scholar
3Chidambaram, P.R., Edwards, G.R., and Olson, D.L., Metall. Trans. 23B, 215 (1992).Google Scholar
4Kritsalis, P., Coudurier, L., and Eustathopoulos, N., J. Mater. Sci. 26, 3400 (1991).Google Scholar
5Santella, M.L., Horton, J.A., and Pak, J.J., J. Am. Ceram. Soc. 73, 1785 (1990).CrossRefGoogle Scholar
6Karlsson, N., Nature 168, 558 (1951).Google Scholar
7Hansen, M. and Anderko, K., Constitution of Binary Alloys, 2nd ed. (McGraw-Hill Book Company, New York, 1985), p. 18.Google Scholar
8Niessen, A. K., Boer, F. R. De, Boom, R., Chatel, P. F. de, Mattens, W. C. M., and Miedema, A.R., CALPHAD 7, 51 (1983).CrossRefGoogle Scholar
9Andersson, S., Acta Chem. Scand. 13, 415 (1959).Google Scholar
10Yoshitake, M. and Yoshihara, K., J. Jpn. Inst. Metals 54, 778 (1990).Google Scholar
11Ohuchi, F.S. and Kohyama, M., J. Am. Ceram. Soc. 74, 1163 (1991).CrossRefGoogle Scholar
12Chamberlain, M.B., J. Vac. Sci. Technol. 15 (2), 240 (1978).Google Scholar
13Karlsson, N., J. Inst. Met. 79, 391 (1951).Google Scholar