Hostname: page-component-76fb5796d-45l2p Total loading time: 0 Render date: 2024-04-26T07:18:57.571Z Has data issue: false hasContentIssue false

Growth and Characterization of Highly Oxygen-Doped GaAs

Published online by Cambridge University Press:  25 February 2011

M.S. Goorsky
Affiliation:
IBM Research Division T.J.Watson Research Center, P.O.Box 218, Yorktown Heights, NY, 10598
T.F. Kuech
Affiliation:
IBM Research Division T.J.Watson Research Center, P.O.Box 218, Yorktown Heights, NY, 10598
P.M. Mooney
Affiliation:
IBM Research Division T.J.Watson Research Center, P.O.Box 218, Yorktown Heights, NY, 10598
F. Cardone
Affiliation:
IBM Research Division T.J.Watson Research Center, P.O.Box 218, Yorktown Heights, NY, 10598
R.M. Potemski
Affiliation:
IBM Research Division T.J.Watson Research Center, P.O.Box 218, Yorktown Heights, NY, 10598
Get access

Abstract

High levels (≃ 1018cm-3) of oxygen were introduced into GaAs by using dimethyl aluminum methoxide (DMAlM0) as an oxygen-bearing precursor during metalorganic vapor phase epitaxy. Layers co-doped with oxygen and intentionally added silicon, both to concentrations of ≃ 1018 cm-3, were depleted of free carriers and had no measurable luminescence. Deep levels were present in layers grown with lower oxygen incorporation, but the compensation mechanism due to oxygen incorporation is not apparently tied to a specific defect level. The material with the electronic deep levels also possessed deep luminescence energy lines. All layers exhibited excellent surface morphology. For comparison, other layers were grown by introducing low levels of 02 and trimethyl aluminum during GaAs growth. The surface morphology of these layers was usually hazy and the layers did not exhibit the same well defined electrical and optical characteristics as the layers grown with DMAlMO.

Type
Research Article
Copyright
Copyright © Materials Research Society 1991

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. Kisker, D.W., Miller, J.N., and Stringfellow, G.B., Appl. Phys. Lett., 40 615 (1982).Google Scholar
2. Kuech, T.F., Veuhoff, E., Kuan, T.S., Deline, V., and Potemski, R., J. Crystal Growth 77 252 (1986).Google Scholar
3. Tsai, M.J., Tashima, M.M., and Moon, R.L., J. Electron. Mater. 13 437 (1984).Google Scholar
4. Wallis, R.H., Poisson, M.-A. Forte, Bonnet, M., Beachet, G., and Duchemin, J.-P., Inst. Phys. Conf. Ser. 56 73 (1981).Google Scholar
5. Bhattacharya, P.K., Matsumoto, T., and Subramanian, S., J. Crystal Growth 68 301 (1978).Google Scholar
6. Tsai, M.J., Tashima, M.M., Twu, B.L., and Noon, R.L., Inst. Phys. Conf. Ser. 65 85 (1983).Google Scholar
7. Smith, F.W., Calwa, A.R., Chen, C.-L., Manfar, M.J., and Mahoney, L.J., IEEE Electron Dev. Lett. EDL 9 77 (1988).Google Scholar
8. Davidson, N. and Brown, H.C., J. Amer. Chem. Soc. 64 316 (1942).Google Scholar
9. Goorsky, M.S., Kuech, T.F., Cardone, F., Mooney, P., Scilla, G.J., and Potemski, R.M., submitted for publication.Google Scholar
10. Kuech, T.F., Goorsky, M.S., Cardone, F.C, Scilla, G.J., and Potemski, R.M., unpublished.Google Scholar
11. Terao, H. and Sunakawa, H. J. Crystal Growth 68 157 (1984).Google Scholar
12. See, for example, “Oxygen, Carbon, Hydrogen, and Nitrogen in Crystalline Silicon”, Mikkelsen, J.C. Jr., Pearton, S.J., Corbett, J.W., and Pennycook, S.J., eds. Materials Reserach Society (1986).Google Scholar
13. Yu, P.W. and Walters, D.C., Appl. Phys. Lett. 41 863 (1982).Google Scholar