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Oxygen Atom Induced Deposition of Silicon Dioxide

Published online by Cambridge University Press:  22 February 2011

Dimitri A. Levedakis
Affiliation:
Department of Chemical, Bio & Materials Engineering and Center for Solid State Electronics, Research Arizona State University Tempe, AZ 85287–6006
Gregory B. Raupp
Affiliation:
Department of Chemical, Bio & Materials Engineering and Center for Solid State Electronics, Research Arizona State University Tempe, AZ 85287–6006
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Abstract

Silicon dioxide was deposited from tetraethylorthosilicate (TEOS) and remote microwave oxygen plasma on a heated silicon substrate in a cold-wall reactor. The deposition rate and film quality were examined as functions of substrate temperature, total pressure, absorbed plasma power and O2:TEOS flow ratio. The deposition reaction exhibited an activation energy of approximately 10 kJ/mol for substrate temperatures in the range of 323–623 K. The deposition rate reached a maximum with increasing total pressure. The rate was found to be a near-linear function of the absorbed microwave power. At fixedabsorbed power the rate reached a maximum with increasing O2:TEOS flow ratio. A one-dimensional mathematical model was developed to predict the oxygen radical concentration at the exit of the afterglow region of the oxygen discharge. Comparisons of the predicted oxygen radical concentrations with the deposition rates at corresponding deposition conditions supports the view that the overall SiO2 deposition reaction is largely controlled by the concentration of oxygen radicals. The average refractive index ofthe deposited films was 1.466 ± 0.011. Fourier transform infra-red (FTIR) transmission spectra showed significant concentrations of hydroxyls in the deposited films.

Type
Research Article
Copyright
Copyright © Materials Research Society 1993

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References

REFERENCES

1. Chang, C., Pai, C. and Hsieh, J., J. Appl. Phys. 67(4) 2119 (1990).Google Scholar
2. Ibbotson, D., Hsieh, J., Flamm, D. and Mucha, J., SPIE Monitoring and Control of Plasma-Enhanced Processing of Semiconductors, 1037 130 (1988).Google Scholar
3. Raupp, G., Cale, T. and Hey, H., J. Vac. Sci. Technol. B 10(1), 37 (1992).Google Scholar
4. Veprek-Heijman, M. and Boutard, D., J. Electrochem. Soc. 138(7), 2042 (1991).Google Scholar
5. Selamoglu, N., Mucha, J., Ibbotson, D. and Flamm, D., J. Vac. Sci. Technol. 7(6), 1345 (1989).Google Scholar
6. Emesh, I., D'Asti, G., Mercier, J. and Leung, P., J. Electrochem. Soc. 136(11), 3404 (1991).Google Scholar
7. Hollahan, J. and Bell, A., Techniques and Applications of Plasma Chemistry, Wiley, New York (1974).Google Scholar
8. Masek, K., Laska, L. and Ruzicka, T., Czech. J. Phys. B 28, 1321 (1978).Google Scholar
9. Wakiya, K., J. Phys. B: Atom. Molec. Phys. 11(22), 3931 (1978).Google Scholar
10. Brake, M. and Kerber, R., J. Plasma Chem. Plasma Process. 3 (1), 79 (1983).Google Scholar
11. Greaves, J. and Linnett, J., Trans. Far. Soc. 55, 1355 (1959).Google Scholar
12. Mearns, A. and Morris, A., CEP Symposium Series 112, 37 (1971).Google Scholar
13. Pai, C. and Chang, C., J. Appl. Phys. 68(2) 793 (1990).Google Scholar
14. Kulisch, W., Lippmann, T. and Kassing, R., Thin Solid Films, 174 57 (1989).Google Scholar