The techniques (temperature range of study) of in situ thermal desorption (
500-1100 degrees C) and chemical vapor cleaning (CVC) via exposure to SiH4
and/or C2H4 (750-1100 degrees C) have been investigated for preparing 6H Si
C [(0001)(Si), (000 (1) over bar)(C), (11 (2) over bar 0), and (10 (1) over
bar 0)] surfaces suitable for epitaxial growth of SiC and III-nitride film
s, and are compared with regard to surface purity, stoichiometry, and struc
tural order. Oxide removal below the detection limits of Auger electron spe
ctroscopy was achieved for all orientations via annealing in 200 L SiH4 at
850-900 degrees C or approximate to 200 degrees lower than necessary by the
rmal desorption. No non-SiC carbon was detected on the surface by X-ray pho
toelectron spectroscopy. An approximately one-tenth of a monolayer of oxyge
n coverage and significant quantities of non-SiC carbon were detected for a
ll 6H SiC surfaces prepared by thermal desorption. In contrast to the predo
minantly non-SiC carbon-rich surfaces prepared by thermal desorption, the s
toichiometry of the SiC surfaces prepared by CVC could be manipulated from
Si-rich to C-rich without non-SiC carbon formation by either extending the
SiH4 exposures or by following with C2H4 exposure. The latter surfaces also
had lower concentrations of both oxygen and non-SiC carbon and increased s
urface order. (C) 1999 The Electrochemical Society. S0013-4651(98)11-055-8.
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