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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.
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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

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