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Rapid Thermal Annealing of Amorphous Silicon Thin Films Grown by Electron Cyclotron Resonance Chemical Vapor Deposition

Published online by Cambridge University Press:  01 February 2011

Pei-Yi Lin
Affiliation:
[email protected], National Central University, Jhongli City, Taiwan, Province of China
Ping-Jung Wu
Affiliation:
[email protected], National Central University, Jhongli City, Taiwan, Province of China
I-Chen Chen
Affiliation:
[email protected], National Central University, Jhongli City, Taiwan, Province of China
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Abstract

Hydrogenated amorphous silicon (a-Si:H) thin films were deposited on pre-oxidized Si wafers by electron cyclotron resonance chemical vapor deposition (ECRCVD). The rapid thermal annealing (RTA) treatments were applied to the as-grown samples in nitrogen atmosphere, and the temperature range for the RTA process is from 450 to 950 °C. The crystallization and grain growth behaviors of the annealed films were investigated by Raman spectroscopy, X-ray diffraction (XRD) and transmission electron microscopy (TEM). The onset temperature for the crystallization and grain growth is around 625 ∼ 650°C. The crystalline fraction of annealed a-Si:H films can reach ∼80%, and a grain size up to 17 nm could be obtained from the RTA treatment at 700 °C. We found that the crystallization continues when the grain growth has stopped.

Type
Research Article
Copyright
Copyright © Materials Research Society 2010

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References

1 Brodsky, M. H., Cardona, M., and Cuomo, J. J., Phys. Rev. B 16, 3556 (1977).Google Scholar
2 Guha, S., Yang, J., Williamson, D. L., Lubianiker, Y., Cohen, J. D., and Mahan, A. H., Appl. Phys. Lett. 74, 1860 (1999).Google Scholar
3 Mahan, A. H., Gedvilas, L. M., and Webb, J. D., J. Appl. Phys. 87, 1650 (2000).Google Scholar
4 Kitagawa, M., Setsune, K., Makabe, Y. and Hirao, T.. Jap. J. App. Phys. 27 (1988).Google Scholar
5 Yue, G., Lorentzen, J. D., Lin, J., Han, D., and Wang, Q., Appl. Phys. Lett. 75, 492 (1999).Google Scholar
6 Smit, C., Swaaij, R. A. C. M. M. van, Donker, H., Petit, A. M. H. N., Kessels, W. M. M., and Sanden, M. C. M. van de, J. Appl. Phys. 94, 3582 (2003).Google Scholar
7 Mahan, A. H., Su, T., Williamson, D. L., Gedvilas, L. M., Ahrenkiel, S. P., Parilla, P. A., Xu, Y., and Ginley, D. A., Adv. Funct. Mater. 19, 1 (2009).Google Scholar
8 Langford, A. A., Fleet, M. L., Nelson, B. P., Lanford, W. A., and Maley, N., Phy. Rev. B 45, 13367 (1992).Google Scholar
9 Smets, A. H. M., Matsui, T., and Kondo, M., Appl. Phys. Lett. 92, 033506 (2008).Google Scholar
10 Johnson, E. V., Kroely, L., and Roca, P. I Cabarrocas, Solar Energy Materials & Solar Cells 93, 1904 (2009).Google Scholar