Hostname: page-component-cd9895bd7-gbm5v Total loading time: 0 Render date: 2024-12-27T02:23:05.863Z Has data issue: false hasContentIssue false

Hydrogen Content of a-Si:H and a-Si:H,F as a Function of Chemical Annealing

Published online by Cambridge University Press:  01 January 1993

J.N. Bullock
Affiliation:
Department of Electrical Engineering, Princeton University,, Princeton,, NJ 08544
K. Rim
Affiliation:
Department of Electrical Engineering, Princeton University,, Princeton,, NJ 08544
S. Wagner
Affiliation:
Department of Electrical Engineering, Princeton University,, Princeton,, NJ 08544
Get access

Abstract

Chemical annealing, the periodic exposure of the growing amorphous silicon surface to H radicals, has evoked much interest because of its potential for modifying the film properties during the crucial process of sub-surface restructuring. We report the results of measurements of H content in chemically annealed a-Si:H and a-Si:H,F films.

We prepared a-Si:H and a-Si:H,F in a dc-triode reactor from SiH4 and SiF4 plus H2, respectively. We chemically anneal with a H2 discharge by switching off the Si bearing gas and switching on the H2 flow after 7 s of deposition. We measure the H content with a differential pressure effusion apparatus. We also report the opto-electronic properties of these films, including the defect density after light-soaking.

The key parameter of chemical annealing is the anneal duty cycle, which we specify as the fraction of the time that the H2 discharge is on. In the silane samples, we find that the H content is independent of chemical annealing. For the fluorinated samples we observe that the H content starts out at about 5 at.% without chemical annealing, rises to 10-15 at.% at 0.5 to 0.7 annealing duty cycle, and then decays to 6-7 at.% at 0.9 duty cycle. Although not fully understood, we offer evidence that these effects are due to the physics of the glow-discharge rather than surface reactions.

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

1. Shirai, Hajime, Das, Debajyoti, Hanna, Jun-ichi and Shimzu, Isamu, Appl. Phys. Lett. 59 (9), 1096 (1991).Google Scholar
2. Li, Y.M., An, I., Gunes, M., Dawson, R.M., Collins, R.W. and Wronski, C.R., Mat. Res. Soc. Proc. 258, 57 (1992).Google Scholar
3. Miyachi, K., Koyama, M., Tanaka, H., Ashida, Y., Fukuda, N. and Nitta, A., Intern. PVSEC-5, 63 (1990).Google Scholar
4. Chambouleyron, I., Lloret, A., Roca i Cabarrocas, P., Sardin, O. and Andreu, J., Proc. 7th E.C. Photovoltaic Solar Energy Conf., 155 (1987).Google Scholar
5. Slobodin, D., PhD Thesis, Princeton University, 1987.Google Scholar
6. Madan, A., Ovshinsky, S.R. and Benn, E., Philos. Mag. B 40, 259 (1979).Google Scholar
7. Chou, S.F., Schwarz, R., Okada, Y., Slobodin, D. and Wagner, S., Mat. Res. Soc. Symp. Proc. 95, 165 (1987).Google Scholar
8. Tauc, J., Grigorivici, R. and Vancu, A., Phys. Stat. Solidi 15, 627 (1966).Google Scholar
9. Vanacek, M., Kocka, J., Stuchlik, J. and Triska, A., Sol. State Comm. 39, 1199 (1981).Google Scholar
10. Wang, N.W.., Morin, P.A., Chu, V. and Wagner, S., Mat. Res. Soc. Symp. Proc. 258, 589 (1992).Google Scholar
11. Gleskova, H., Morin, P.A. and Wagner, S., this volume.Google Scholar
12. Collins, R.W., (private communication).Google Scholar