Hostname: page-component-cd9895bd7-p9bg8 Total loading time: 0 Render date: 2024-12-27T02:26:30.754Z Has data issue: false hasContentIssue false

Chemical Vapor Deposition of Copper from an Organometallic Source

Published online by Cambridge University Press:  25 February 2011

David B. Beach
Affiliation:
IBM Research Division, Thomas J. Watson Research Center, P.O. Box 218, Yorktown Heights, NY 10598.
William F. Kane
Affiliation:
IBM Research Division, Thomas J. Watson Research Center, P.O. Box 218, Yorktown Heights, NY 10598.
Francoise K. Legoues
Affiliation:
IBM Research Division, Thomas J. Watson Research Center, P.O. Box 218, Yorktown Heights, NY 10598.
Christopher J. Knors
Affiliation:
IBM General Technology Division, East Fishkill, Hopewell Junction, NY, 12533.
Get access

Abstract

High purity copper has been deposited from trialkyl phosphine complexes of cyclopentadienyl and methylcyclopentadienyl copper(I) by thermal chemical vapor deposition (CVD). Films as thick as 4.4 μm have been deposited at growth rates of up to 2000 Å/min with resistivites typically 2.0 μΩ cm, just slightly higher than bulk copper. Depositions were carried out at substrate temperatures between 150 and 220 °C on a variety of substrates including Si, SiO2, polyimide, and Cr/Cu. At low substrate temperatures, copper film growth appears to show some selectivity for transition metal surfaces. An activation energy of 18 kcal/mole has been measured for film growth on Cu seeded substrates. CVD copper films have been characterized by Auger spectroscopy which showed that carbon and oxygen levels are below the limits of detection. Transmission electron microscopy revealed that the copper grain size was ∼0.6μm and the grain boundaries are free of precipitates. Films show good conformality.

Type
Research Article
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

1. Kaloyeros, A. E., Feng, A., Garhart, J., Brooks, K. C., and Luehrs, F., J. Electron. Mater. 19, 271 (1990).Google Scholar
2. Cotton, F. A. and Tatakas, J., J. Amer. Chem. Soc. 92, 2353 (1970).Google Scholar
3. Hara, K., Kojima, T. and Kukimoto, H., Jpn. J. Appl. Phys. 26, L1107 (1987).CrossRefGoogle Scholar
4. Dupuy, C. G., Beach, D. B., Hurst, J. E. and Jasinski, J. M., Chem. of Mater. 1, 16 (1989).Google Scholar
5. Beach, D. B., LeGoues, F. K. and Hu, C. K., Chem. of Mater. 2, 0000 (1990).Google Scholar
6. Cotton, F. A. and Marks, T. J., J. Amer. Chem. Soc. 92, 5114 (1970).Google Scholar
7. Ziling, X., Strouse, M. J., Shuh, D. K., Knobler, C. B., Kaesz, H. D., Hicks, R. F. and Williams, W. R., J. Amer. Chem. Soc. 111, 8779 (1989).Google Scholar