Hostname: page-component-848d4c4894-ndmmz Total loading time: 0 Render date: 2024-05-17T19:20:34.490Z Has data issue: false hasContentIssue false

High Temperature Gas Phases Reactions Of Trimethylgallium with Ammonia and Trimethylamine

Published online by Cambridge University Press:  15 February 2011

A. Thon
Affiliation:
Department of Chemical Engineering, University of Wisconsin, 1415 Engineering Drive, Madison, WI 53706.
S. A. Safvi
Affiliation:
Department of Chemical Engineering, University of Wisconsin, 1415 Engineering Drive, Madison, WI 53706.
T. F. Kuech
Affiliation:
Department of Chemical Engineering, University of Wisconsin, 1415 Engineering Drive, Madison, WI 53706.
Get access

Abstract

The use of trimethylgallium-trimethylamine (TMG:TMN) adduct as alternative cation precursor for MOVPE of GaN was studied by means of in-situ mass spectroscopy in an isothermal flow tube reactor. The temperature, pressure and reaction time were chosen to emulate the gas phase environment typical of the metal-organic vapor phase: epitaxy (MOVPE) of GaN. Dynamic changes in the mass spectra are reported for the gas phase reactions between trimethylgallium (TMG) and TMN in hydrogen (H2/D2) and ammonia (NH3/ND3) ambients. Evidence presented for the high temperature TMG:TMN adduct formation, followed by ethane elimination. The strength of the adduct bonding is comparable to that of TMG:NH3 and thus suppresses TMN displacement by ammonia. The thermal stability of TMG:TMN was found to be higher in ammonia ambient than it is in hydrogen. Kinetic parameters for some of the decomposition processes are given.

Type
Research Article
Copyright
Copyright © Materials Research Society 1996

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

1. Akasaki, I. and Amano, H., J. Crystal Growth. 146,455 (1995).Google Scholar
2. Neumayer, D. A. and Ekerdt, J. G., Chem. Mater. 8, 9 (1996).Google Scholar
3. Moss, R. H., J. Crystal Growth. 68, 78 (1984).Google Scholar
4. Sywe, B. S., Schlup, J. R. and Edgar, J. H., Chem. Mater. 3(4), 737 (1991).Google Scholar
5. Thon, A. and Kuech, T.F., to be published in APL.Google Scholar
6. Zaouk, A., Salvetat, E., Sakaya, J., Maury, F. and Constant, G., J. Crystal Growth. 55, 135 (1981).Google Scholar
7. DenBaars, S. P., Maa, B. Y., Dapkus, P.D., Danner, A. D. and Lee, H. C., J. Crystal Growth. 77, 188 (1986).Google Scholar
8. Chen, Q. and Dapkus, P.D., J. Electrochem. Soc. 138(9), 2821 (1991).Google Scholar
9. Dove, J. E. and Nip, U. S., Canadian Journal of Chemistry. 57, 689 (1979).Google Scholar
10. Durig, J. R., Bradly, C. B. and Odom, J. D., Inorg. Chem. 21, 1466 (1982).Google Scholar
11. Almond, M. J., Jenkins, C. E., Rice, D. A. and Hagen, K., J. Organomet. Chem. 439, 251 (1992).Google Scholar
12. Coates, G. E., J. Chem. Soc., 2003 (1951).Google Scholar
13. Redwing, J.M., Kuech, T.F., Saulys, D. and Gaines, D.F., J. Crystal Growth. 135, 423 (1994).Google Scholar