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Chemistry of Nitrogen-Silane Plasmas

Published online by Cambridge University Press:  25 February 2011

Donald L. Smith
Affiliation:
Xerox Palo Alto Research Center, 3333 Coyote Hill Rd., Palo Alto, CA 94304
Andrew S. Alimonda
Affiliation:
Xerox Palo Alto Research Center, 3333 Coyote Hill Rd., Palo Alto, CA 94304
Frederick J. Von Preissig
Affiliation:
Xerox Palo Alto Research Center, 3333 Coyote Hill Rd., Palo Alto, CA 94304
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Abstract

The N2-SiH4 rf glow-discharge plasma has been analyzed by line-of-sight mass spectrometry of species impinging on the deposition electrode, including N atoms. Properties of SixNyHz films deposited from this plasma have been examined. At high rf power and low SiH4/N2, almost all of the SiH4 is consumed by reaction with N atoms at the film surface and becomes incorporated into the film. No Si-N precursor species are seen in the gas phase. This is in contrast to the NH3-SiH4 plasma, where the Si(NH2)3 radical is the key precursor. If power is insufficient or SiH4 flow is excessive, Si2Hm species are generated in the plasma. Under optimized conditions, films slightly N-rich with no Si-H bonding and only 7% H (as N-H) can be deposited at high rate. The film tensile stress of the NH3 process is absent in the N2 process due to the lesser amount of condensation that takes place during deposition. However, trench coverage is much better in the NH3 process.

Type
Research Article
Copyright
Copyright © Materials Research Society 1989

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References

REFERENCES

1. Smith, D. L., Alimonda, A. S., Chen, C-C., Jackson, W. and Wacker, B. in Amorphous Silicon Technology, edited by Madan, A., Thompson, M. J., Taylor, P. C., LeComber, P. G. and Hamakawa, Y. (Mater. Res. Soc. Proc. 118, Pittsburgh, PA 1988) pp. 107112.Google Scholar
2. Rosler, R. S., Benzing, W. C., and Baldo, J., Solid State Technol., 19 (6), 45 (1976).Google Scholar
3. Chang, M., Wong, J., and Wang, D. N. K., Solid State Technol., May 1988, p. 193.Google Scholar
4. Smith, D. L., Alimonda, A. S., Chen, C-C., Ready, S. E., and Wacker, B., to be published (1989).Google Scholar
5. Baumann, S., Charles Evans & Associates, Redwood City, CA (1988).Google Scholar
6. Lanford, W. A. and Rand, M. J., J. Appl. Phys. 49 (4), 2473 (1978).Google Scholar
7. Doyle, B. L. and Peercy, P. S., Appl. Phys. Lett. 34 (11), 811 (1979).CrossRefGoogle Scholar
8. Levin, R. D. and Lias, S. G., Ionization Potential and Appearance Potential Measurements, 1971–1981 (National Bureau of Standawds, Washington, DC, 1982).Google Scholar
9. Tsu, D. V., Lucovsky, G., and Mantini, M. J., Phys. Rev. B 33 (10), 7069 (1986).CrossRefGoogle Scholar
10. Hasegawa, S., Matuura, M., Anbutu, H. and Kurata, Y., Phil. Mag. B 56 (5), 633 (1987).Google Scholar
11. Chang, C-P., Flamm, D. L., Ibbotson, D. E., and Mucha, J. A., J. Appl. Phys. 62 (4), 1406 (1987).CrossRefGoogle Scholar
12. Dun, H., Pan, P., White, F. R., and Douse, R. W., J. Electrochem. Soc. 128 (7), 1555 (1981).Google Scholar
13. Maeda, M. and Arita, Y., J. Appl. Phys. 53 (10), 6852 (1982).CrossRefGoogle Scholar
14. Zhou, N-S., Fujita, S., and Sasaki, A., J. Electronic Mat. 14 (1), 55 (1985).Google Scholar