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Si and Ge Nanocrystallites Embedded in CaF2 by Molecular Beam Epitaxy (MBE)

Published online by Cambridge University Press:  25 February 2011

A. P. Taylor
Affiliation:
Physics Department and Center for Integrated Electronics, Rensselaer Polytechnic Institute, Troy, New York 12180
B. M. Kim
Affiliation:
Physics Department and Center for Integrated Electronics, Rensselaer Polytechnic Institute, Troy, New York 12180
P. D. Persans
Affiliation:
Physics Department and Center for Integrated Electronics, Rensselaer Polytechnic Institute, Troy, New York 12180
L. J. Schowalter
Affiliation:
Physics Department and Center for Integrated Electronics, Rensselaer Polytechnic Institute, Troy, New York 12180
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Abstract

Thin films of CaF2 containing layers of Si and Ge nanocrystallites were grown epitaxially on Si( 111) substrates by MBE while varying the substrate temperature. The sticking coefficient of both Si and Ge to CaF2 are less than unity at the temperatures studied. Evidence that chemical reactions are minimal between Si and CaF2 leading to the formation of volatile species such as SiFx is presented and it is surmised that the dominant mechanism for re-evaporation is thermal desorption. Both Si and Ge sticking coefficients vary exponentially with 1/T and activation energies are determined. A cluster growth model describing the evolution of the amount of Si in clusters over time is given. Solving in the limit of low cluster coverage, a solution that varies linearly with time and exponentially with 1/T is obtained. Weak room temperature photoluminescence from Si nanocrystallites in CaF2 is seen, however, it is unclear whether the luminescence is coming from the Si nanocrystallites or the CaF2. Second harmonic generation is observed from samples containing single layers of Ge in CaF2.

Type
Research Article
Copyright
Copyright © Materials Research Society 1993

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References

[1] Wang, Y. and Herron, N., J. Phys. Chem., 95, 525, 1991.CrossRefGoogle Scholar
[2] Brus, L., Appl. Phys. A 53, 465, 1991.Google Scholar
[3] See for example, Mat. Res. Soc. Symp. vol. 256, editors, Iyer, S. S., Collins, R. T., and Canham, L. T., 1992.Google Scholar
[4] Taylor, A. P., Stokes, K., Wu, Z. C., Persans, P. D., Schowalter, L. J., and LeGoues, F. K., in Mat. Res. Soc. Symp. vol. 283, 1993.Google Scholar
[5] Taylor, A. P., Yang, K., and Schowalter, L. J., J. Vac. Sci. Technol. A 9, 3181, 1991.CrossRefGoogle Scholar
[6] Asano, T. and Ishiwara, H., J. Appl. Phys., 55, 3566, 1984.Google Scholar
[7] Zinke-Allmang, M., Scan. Microscopy, 4, 523, 1990.Google Scholar
[8] Himpsel, F. J., Karlsson, U. O., Morar, J. F., Rieger, D., and Yarnoff, J. A., Phys. Rev. Lett., 56, 1497, 1986.CrossRefGoogle Scholar