Hostname: page-component-76fb5796d-22dnz Total loading time: 0 Render date: 2024-04-25T15:04:27.621Z Has data issue: false hasContentIssue false

Effect of the Crystallographic Orientation of Underlying Poly-Si on the Thermal Stability of the TiSi2 Film

Published online by Cambridge University Press:  25 February 2011

Y. W. Kim
Affiliation:
R&D Center, Samsung Electronics Co., Suwon P.O. Box #107, Korea.
I. K. Kim
Affiliation:
R&D Center, Samsung Electronics Co., Suwon P.O. Box #107, Korea.
N. I. Lee
Affiliation:
R&D Center, Samsung Electronics Co., Suwon P.O. Box #107, Korea.
J. W. Ko
Affiliation:
R&D Center, Samsung Electronics Co., Suwon P.O. Box #107, Korea.
S. T. Ahn
Affiliation:
R&D Center, Samsung Electronics Co., Suwon P.O. Box #107, Korea.
M. Y. Lee
Affiliation:
R&D Center, Samsung Electronics Co., Suwon P.O. Box #107, Korea.
J. G. Lee
Affiliation:
R&D Center, Samsung Electronics Co., Suwon P.O. Box #107, Korea.
Get access

Abstract

The effect of the crystallographic orientation of underlying poly-Si film on the thermal stability of the TiSi2 film was studied. Different preferred orientations of the poly-Si film were obtained by annealing poly-Si or amorphous Si films at various temperatures. The TiSi2 film was formed by the solid-state reaction of the Ti film sputtered on the poly-Si film. The thermal stability of the TiSi2 film was evaluated by changes in the sheet resistance and microstructural evolution during furnace anneals. The TiSi2 film on poly-Si with the <110> preferred orientation shows more stable conductivity during high temperature anneals than with the <111> orientation. The surface energy of underlying poly-Si is expected to influence the thermal stability of the TiSi2/poly-Si structure significantly. Better thermal stability of the TiSi2 film can be obtained by the higher surface energy of underlying poly-Si.

Type
Research Article
Copyright
Copyright © Materials Research Society 1993

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

Ting, C.Y., d'Heurle, F.M., Iyer, S.S., and Fryer, P.M., J. Electrochem. Soc. 133, 2621 (1986)CrossRefGoogle Scholar
2. Nolan, T.P., Sinclair, R., and Beyers, R., J. Appl. Phys. 71, 720 (1992)Google Scholar
3. Joubert, P., Loisel, B., Chouan, Y., and Haji, L., J. Electrochem. Soc. 134, 2541 (1987)Google Scholar
4. Mullins, W.W. and Shewmon, P.G., Acta Metall. 7, 163 (1959)Google Scholar
5. Mullins, W.W., J. Appl. Phys. 28, 333 (1957)Google Scholar
6. Srolovitz, D.J. and Safran, S.A., J. Appl. Phys. 60, 247 (1986)Google Scholar
7. Miller, K.T., Lange, F.F., and Marshall, D.B., J. Mater. Res. 5, 151 (1990)Google Scholar
8. Jiran, E. and Thompson, C.V., J. Elect. Mater. 19, 1153 (1990)CrossRefGoogle Scholar
9. Jaccodine, R.J., J. Electrochem. Soc. 110, 524 (1963)CrossRefGoogle Scholar