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Synthesis of New Copper(I) β-Diketonate Compounds for CVD of Copper

Published online by Cambridge University Press:  25 February 2011

H.K. Shin
Affiliation:
Departments of Chemistry, Los Alamos National Laboratories, Los Alamos, NM 87545
K.-M. Chi
Affiliation:
Departments of Chemistry, Los Alamos National Laboratories, Los Alamos, NM 87545
M.J. Hampden-Smith
Affiliation:
Departments of Chemistry, Los Alamos National Laboratories, Los Alamos, NM 87545
T.T. Kodas
Affiliation:
Chemical Engineering; and Los Alamos National Laboratories, Los Alamos, NM 87545
J.D. Farr
Affiliation:
Chemical Engineering; and Los Alamos National Laboratories, Los Alamos, NM 87545
M.F. Paffeif
Affiliation:
Center for Micro-Engineered Ceramics, University of New Mexico, Albuquerque, NM 87131 CLS-1, Los Alamos National Laboratories, Los Alamos, NM 87545
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Abstract

A series of (0β-diketonate) copper(l) trimethylphosphine compounds has been prepared. These species exist either as liquids or low-melting solids at room temperature. The utility of these compounds as precursors for Chemical Vapor Deposition (CVD) of copper has been examined under a variety of conditions. High purity films with low resistivities have been deposited under a variety of conditions. Selective copper deposition was observed as a function of the substrate, precursor and substrate temperature. Evidence consistent with thermallyinduced disproportionation of the title compounds to form copper metal and copper(II) (β-diketonate)2 during deposition was observed.

Type
Research Article
Copyright
Copyright © Materials Research Society 1991

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References

REFERENCES

1. Murarka, S. and Peckerar, M. C., “Electronic Materials Science and Technology”, Academic Press, 1989.Google Scholar
2. Hess, D.W. and Jensen, K.F., “Microelectronics Processing, Chemical Engineering Aspects”, Adv. in Chem. Series, 1989, Vol. 221.Google Scholar
3. Gilliard, J., Hasson, R. and Oudar, J., J. Cryst. Growth, 2, 149, 1968.Google Scholar
4. a. Houle, F.A., Jones, C.R., Baum, T.H., Pico, C. and Kovac, C.A., Appl. Physi Lett. 1985, 46, 204. b: C.Oehr and H. Suhr, Appl. Phys., A., 45, 151, 1988. c. D. Temple and A. Reisman, Technical report number 4, Microelectronic Center of North Carolina, July 2 8 th, 1988.Google Scholar
5. Jeffries, P.M. and Girolami, G.S., Chem. Mater., 1, 8, 1989.Google Scholar
6. Dupuy, C.G., Beach, D.B., Hurst, J.E. and Jasinski, J.M., Chem. Mater., 1, 16, 1989.Google Scholar
7. Beach, D.B., LeGoues, F.K. and Hu, C.-K., Chem. Mater. 2, 216, 1990 Google Scholar
8. Hampden-Smith, M.J., Kodas, T.T., Paffett, M., Farr, J.D. and Shin, H.K., Chem. Mater, 2, 636, 1990.Google Scholar
9. Shin, H.-K., Hampden-Smith, M.J., Kodas, T., Farr, J.D. and Paffett, M., Proc. Mat. Res. Soc. Symp. J., Spring Meeting, San Fransisco 1990, in press.Google Scholar
10. Shin, H.K., Hampden-Smith, M.J., Kodas, T.T. and Duesler, E.N., Polyhedron, in Press.Google Scholar
11. Wolf, W.R., Sievers, R.E. and Brown, G.H., Inorg. Chem., 11, 1995, 1972.Google Scholar
12. Moss, R.H. and Evans, J.S., J. Cryst. Growth, 55, 129, 1981.Google Scholar