M. Dalcolle et al., QUANTITATIVE ARXPS DEPTH PROFILING CHARACTERIZATION OF NATIVE OXIDES GROWN ON IN0.53GA0.47AS(100) SINGLE-CRYSTALS, Journal of electron spectroscopy and related phenomena, 70(2), 1994, pp. 129-143
We report the results of an angle-resolved X-ray photoelectron spectro
scopy (ARXPS) quantitative study of room-temperature native oxides on
LPE grown In0.53Ga0.47As(100). ARXPS is a powerful non-destructive exp
erimental technique for identifying chemical species and following com
positional variations close to the surface (less than 100 angstrom of
thickness). Such investigations can be of relevance for understanding
the growth mechanism, competition between different cations with respe
ct to oxidation, and surface damage due to the degradation process. In
this approach a model of photoemission from a planar InGaAs bulk cove
red with two homogeneous overlayers (representing an oxide and a degra
dation region) constitutes the basis of the computer-aided ARXPS analy
sis. The thickness and the composition of the two overlayers are the p
arameters of a curve fitting, based on the Laplace transform of step-l
ike profile functions, of the experimental data taken at different pho
toelectron escape angles. Our results indicate the presence of non-sto
ichiometric oxides lacking oxygen with respect to In(OH)3, Ga2O3 and A
s2O3, respectively. An oxide layer about 9 angstrom thick is detected
on the top of the original surface and is composed of 66% indium hydro
xide, 31% arsenic oxide and 3% elemental arsenic. The following inner
region corresponds to a diffuse interface oxide/substrate about 12 ang
strom thick, containing 41% GaAs, 28% gallium oxide, 28% indium hydrox
ide and 3% InAs. Finally, the composition of the substrate agrees with
the nominal composition of the epitaxially grown crystal. These resul
ts indicate a preferential oxidation of InAs with respect to GaAs and
suggests that the driving force of the oxidation process is the bindin
g energy difference of the two binary compounds constituting the cryst
al.