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Chemical Vapor Deposition of Highly Transparent and Conductive Boron Doped Zinc Oxide Thin Films

Published online by Cambridge University Press:  25 February 2011

Jianhua Hu
Affiliation:
Department of Chemistry, Harvard University, Cambridge, MA 02138
Roy G. Gordon
Affiliation:
Department of Chemistry, Harvard University, Cambridge, MA 02138
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Abstract

Boron doped zinc oxide films have been successfully deposited from a gas mixture of 0.05% diethyl zinc, 2.3% ethanol and various diborane concentrations in the temperature range 300°C to 430°C in an atmospheric pressure chemical vapor deposition reactor. The dopant diborane was found to decrease the film growth rate. The crystallite sizes of doped films were smaller than those of undoped films. Hall coefficient and resistance measurements at room temperatures gave conductivities between 250 and 1700 Ω-1, electron densities between 1.4×1020 and 6.7×1020 cm-3, and mobilities between 7 and 23 cm2/V-s. Optical measurements showed that a film with a sheet resistance of 8.8 Ω/square has an average visible absorption of about 8% and maximum infrared reflectance close to 85%. The ratio of conductivity to absorption coefficient is between 0.05 Ω-1 and 0.55 Ω-1. The band gap of doped film was widened and followed the Burstein-Moss relation.

Type
Research Article
Copyright
Copyright © Materials Research Society 1992

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References

REFERENCES

1. Jin, Z.-C., Hamberg, I., and Granqvist, C. G., J. Appl. Phys. 64, 5117 (1988).Google Scholar
2. Schropp, R. E. I. and Madan, A., J. Appl. Phys. 66, 2027 (1989).CrossRefGoogle Scholar
3. Yoo, J. B., Fahrenbruch, A. L., and Bube, R. H., J. Appl. Phys. 68, 4694 (1990).Google Scholar
4. Banerjee, R., Ray, S., Basu, N., Batabyal, A. K., and Barua, A. K., J. Appl. Phys. 62, 912 (1987).Google Scholar
5. Minami, T., Sato, H., Nanto, H., and Takata, S., Thin Solid Films 176, 277 (1989).Google Scholar
6. Hu, J. and Gordon, R. G., Solar Cells 20, 437 (1991).Google Scholar
7. Hu, J. and Gordon, R. G., Mater. Res. Soc. Symp. Proc. 202, 457 (1991).Google Scholar
8. Wenas, W. W., Yamada, A., Konagai, M., and Takahashi, K., Jpn. J. App1. Phys. 30, 1441 (1991).Google Scholar
9. Choi, B. H., Im, H. B., Song, J. S. and Yoon, K. H., Thin Solid Films 194, 712 (1990).Google Scholar
10. Qiu, S. N., Qiu, C. X. and Shih, I., Solar Energy Mater. 15, 261 (1987).Google Scholar
11. Oda, S., Tokunaga, H., Kitajima, N., Hanna, J., Shimizu, I., and Kokado, H., Jpn. J. Appl. Phys. 24, 1607 (1985).Google Scholar
12. Smith, F. T. J., Appl. Phys. Lett. 43, 1108 (1983).Google Scholar
13. Strickler, D. A., Ph. D. thesis, Harvard University, 1989.Google Scholar
14. Hamberg, I. and Granqvist, C. G., J. Appl. Phys. 60, R123 (1986).Google Scholar