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Investigation of low- and high-resistance Ni–Ge–Au ohmic contacts to n+ GaAs using electron microbeam and surface analytical techniques

Published online by Cambridge University Press:  31 January 2011

Nancy E. Lumpkin
Affiliation:
Division of Radiophysics, CSIRO, P.O. Box 77, Epping, New South Wales, 2121, Australia
Gregory R. Lumpkin
Affiliation:
Advanced Materials Program, Australian Nuclear Science and Technology Organisation, Private Mail Bag 1, Menai, New South Wales, Australia
K. S. A. Butcher
Affiliation:
Department of Physics, Semiconductor Science and Technology Laboratories, Macquarie University, New South Wales, 2109, Australia
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Abstract

A process for the formation of low-resistance Ni–Ge–Au ohmic contacts to n+ GaAs has been refined using multivariable screening and response surface experiments. Samples from the refined, low-resistance process (which measure 0.05 ± 0.02 Ω · mm) and the unrefined, higher resistance process (0.17 ± 0.02 Ω · mm) were characterized using analytical electron microscopy (AEM), transmission electron microscopy (TEM), scanning electron microscopy-energy dispersive spectroscopy (SEM-EDS), and x-ray photoemission spectroscopy (XPS) depth profiling methods. This approach was used to identify microstructural differences and compare them with electrical resistance measurements. Analytical results of the unrefined ohmic process sample reveal a heterogeneous, multiphase microstructure with a rough alloy-GaAs interface. The sample from the refined ohmic process exhibits an alloy which is homogeneous, smooth, and has a fine-grained microstructure with two uniformly distributed phases. XPS analysis for the refined ohmic process sample indicates that the Ge content is relatively depleted in the alloy (relative to the deposited Ge amount) and enriched in the GaAs. This is not evidenced in the unrefined ohmic process sample. Our data lead us to conclude that a smooth, uniform, two-phase microstructure, coupled with a shift in Ge content from the post-alloy metal to the GaAs, is important in forming low-resistance ohmic contacts.

Type
Articles
Copyright
Copyright © Materials Research Society 1996

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References

REFERENCES

1.Piotrowska, A., Electron Technol. 24, 3 (1991).Google Scholar
2.Sharma, B. L., Semiconductors and Semimetals 15, (1981).Google Scholar
3.Rideout, V. L., Solid State Electron. 18, 541 (1975).Google Scholar
4.Myers, R. H., Khuri, A. I., and Cater, W. Jr., Technometrics 31, 137 (1989).Google Scholar
5.Herr, D.J.C., SPIE Advances in Resist Technology and Processing IV 771, 290 (1987).Google Scholar
6.May, G. S., Huang, J., and Spanos, C. J., IEEE Trans. Semicon. Manufact. 4, 83 (1991).CrossRefGoogle Scholar
7.Montgomery, D. C., Design and Analysis of Experiments, 2nd ed. (John Wiley & Sons, New York, 1984), 538 pp.Google Scholar
8.Box, G. E. P. and Draper, N. R., Empirical Model Building and Response Surfaces (John Wiley and Sons, New York, 1987), 669 pp.Google Scholar
9.Lumpkin, N. E., King, W. D., and Tansley, T. L., J. Mater. Res. 11, 1238 (1996).Google Scholar
10.Iliadis, A. and Singer, K. E., Solid State Electron. 26, 7 (1983).Google Scholar
11.Buhlmann, H. J. and Ilegems, M., J. Electrochem. Soc. 138, 9 (1991).CrossRefGoogle Scholar
12.Grovenor, C. R. M., Properties of Gallium Arsenide (The Institution of Electrical Engineers, New York, 1986), 17.4.Google Scholar
13.Ren, F., Emerson, A. B., Pearton, S.J., Fullowan, T. R., and Brown, J.M., Appl. Phys. Lett. 58, 1040 (1991).Google Scholar
14.Christou, A., Solid State Electron. 22, 141 (1979).CrossRefGoogle Scholar
15.Kuan, T. S., Batson, P. E., Jackson, T. N., Rupprecht, H., and Wilkie, E. L., J. Appl. Phys. 54, 6952 (1983).CrossRefGoogle Scholar
16.Cliff, G. and Lorimer, G. W., J. Microscopy 103, 203 (1975).CrossRefGoogle Scholar
17.Hofmann, S., in Practical Surface Analysis, Volume 1, Auger and X-ray Photoelectron Spectroscopy, 2nd ed., edited by Briggs, D. and Seah, M. P. (John Wiley and Sons, Chichester, 1990), p. 105.Google Scholar
18.Wittmaack, K., in Practical Surface Analysis, Volume 2, Ion and Neutral Spectroscopy, 2nd ed., edited by Briggs, D. and Seah, M. P. (John Wiley and Sons, Chichester, 1990), p. 161.Google Scholar
19.Epp, J. M., Dillard, J.G., Siochi, A., Zallen, R., Sen, S., and Burton, L. C., Chem. Mater. 2, 173 (1990).CrossRefGoogle Scholar
20.Chambers, P. and Fine, J., in Practical Surface Analysis, Volume 2, Ion and Neutral Spectroscopy, 2nd ed., edited by Briggs, D. and Seah, M. P. (John Wiley and Sons, Chicester, 1990), p. 717.Google Scholar
21.Reid, M. J., Gancarz, A. J., and Albee, A. L., Earth Planetary Sci. Lett. 17, 433 (1973).CrossRefGoogle Scholar
22.Christou, A. and Papanicolaou, N., Solid State Electron. 29, 2 (1986).CrossRefGoogle Scholar