Hostname: page-component-848d4c4894-nmvwc Total loading time: 0 Render date: 2024-06-21T08:11:43.215Z Has data issue: false hasContentIssue false

Nucleation and Growth of Polycrystalline Silicon Films in an Ultra high Vacuum Rapid Thermal Chemical Vapor Deposition Reactor Using Disilane and Hydrogen

Published online by Cambridge University Press:  15 February 2011

Katherine E. Violette
Affiliation:
North Carolina State University, Department of Electrical and Computer Engineering, Box 7911, Raleigh, NC 27695–7911
Mehmet C. Öztürk
Affiliation:
North Carolina State University, Department of Electrical and Computer Engineering, Box 7911, Raleigh, NC 27695–7911
Gari Harris
Affiliation:
North Carolina State University, Department of Materials Science and Engineering, Box 7916, Raleigh, NC 27695–7916
Mahesh K. Sanganeria
Affiliation:
North Carolina State University, Department of Electrical and Computer Engineering, Box 7911, Raleigh, NC 27695–7911
Archie Lee
Affiliation:
North Carolina State University, Department of Materials Science and Engineering, Box 7916, Raleigh, NC 27695–7916
Dennis M. Maher
Affiliation:
North Carolina State University, Department of Materials Science and Engineering, Box 7916, Raleigh, NC 27695–7916
Get access

Abstract

A study of Si nucleation and deposition on SiO2 was performed using disilane and hydrogen in an ultra high vacuum rapid thermal chemical vapor deposition reactor in pressure and temperature ranges of 0.1 – 1.5 Torr and 625 – 750°C. The film analysis was carried out using scanning electron microscopy, transmission electron microscopy and atomic force microscopy. At lower pressures, an incubation time exists which leads to a retardation in film nucleation. At 750°C, the incubation time is 10s at 0.1 Torr and decreases to less than Is at 1.5 Torr. The nuclei grow and form three dimensional islands on S1O2, and as they coalesce, result in a rough surface morphology. At higher pressures, the inherent selectivity is lost resulting in a higher nucleation density and smoother surface morphology. For ˜ 2000 Å thick films, the root-mean-square surface roughness at 750ÅC ranges from 110Å at 0.1 Torr to 40Å at 1.5 Torr. Temperature also strongly influences the film structure through surface mobility and grain growth. At 1 Torr, the roughness ranges from 3Å at 625°C to 60Å at 750°C. The grain structure at 625°C/1Torr appears to be amorphous, whereas at 750°C the structure is columnar. The growth rate at 625°C/1.5 Torr is 1200 Å/min provides a surface roughness on the order of atomic dimensions which is comparable to or better than amorphous silicon deposited in LPCVD furnaces.

Type
Research Article
Copyright
Copyright © Materials Research Society 1994

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. Kamins, T.I., Polycrystalline Silicon for Integrated Circuit Applications. The Kluwer International Series in Engineering and Computer Science, ed. Allen, J.. 1988, Norwell, MA: Kluwer Academic Publishers. 280.Google Scholar
2. Cobiani, C., Popa, O., and Dascalu, D., IEEE Electron Device Letters, 1993. 14(5): p. 213215.Google Scholar
3. Ibok, E. and Garg, S., Journal of the Electrochemical Society, 1993. 140(10): p. 29272937.Google Scholar
4. Burggraaf, P., . 1992, p. 71–74.CrossRefGoogle Scholar
5. Ren, X., et al, Journal of Vacuum Science Technology B, 1992. 10(3): p. 1081–1086.CrossRefGoogle Scholar
6. Sadamoto, M., Comfort, J.H., and Reif, R., Journal of Electronic Materials, 1990. 19(12): p. 1395.Google Scholar
7. Nakazawa, K., Journal of Applied Physics, 1991. 69(3): p. 17031706.Google Scholar
8. Voutsas, A.T. and Hatalis, M.K., Journal of the Electrochemical Society, 1993. 140(3): p. 871877.Google Scholar
9. Nakayama, S., Kawashima, I., and Murota, J., Journal of the Electrochemical Society, 1986. 133(8): p. 17211724.Google Scholar
10. Madsen, L.D. and Weaver, L., Journal of the Electrochemical Society, 1990. 137(7): p. 22462251.Google Scholar
11. Bloem, J., Journal of Crystal Growth, 1980. 50: p. 581604.CrossRefGoogle Scholar
12. Xu, X.-L., et al, Journal of Electronic Materials, 1993. 22(11): p. 13451351.Google Scholar
13. Voutsas, A.T. and Hatalis, M.K., Journal of the Electrochemical Society, 1993. 140(1): p. 282288.CrossRefGoogle Scholar
14. Sanganeria, M.K., Violette, K.E., and Öztürk, M.C., Applied Physics Letters, 1993. 63(9): p. 1225–127.Google Scholar
15. Harbeke, G., et al., Journal of the Electrochemical Society, 1984. 131(3): p. 675682.Google Scholar
16. Foster, D., Learn, A., and Kamins, T., Solid State Technology, 1986. (May): p. 227232.Google Scholar
17. Kamins, T.I., Solid State Technology, 1990. (April): p. 80–82.Google Scholar
18. Violette, K.E., Sanganeria, M.K., and Öztürk, M.C., Journal of the Electrochemical Society,Google Scholar
19. Gates, S.M. and Kulkarni, S.K., Applied Physics Letters, 1992. 60(1): p. 5355.Google Scholar