ImprovementoftheAccuracyoftheIn-situEllipsometricMeasurementsofTemperature
and Alloy Composition for MBE Grown HgCdTe LWIR/MWIR Structures
641
rotation j was found to be 8.88∞. Every time the
detector is reinstalled on the reactor this parameter
mustberecalculatedforabettercalibrationaccuracy.
The parameter F in the AOI representation is of
special concern. Representing the undisturbed angle
ofincidence,thisparameterprimarilydeterminesthe
run-to-runreproducibilityofthecalibrationandmust
be optimized specifically for the in-situ configuration.
We propose two means of F parameter determina-
tion with sufficient accuracy. One is based on its
direct single time in-situ determination by fitting the
AOI for a perfectly aligned system using any reliable
material system such as a SiO2/Si sample. The
obtained F parameter can be fixed for all successive
growth runs together with the detector unit align-
ment. The alignment for any new sample in this case
should be limited only by the manipulator position
adjustments, leaving the detector and polarizer un-
touched. However, a better accuracy can be achieved
using an alternative approach, which involves the
alignment of the sample and detector before the
growth run and fitting for the AOI using the current
substrate. Nevertheless, great care must be taken in
the interpretation of the fit results for over-etched
CdTe or CdZnTe substrates.
Usually MBE-ready CdTe substrates have signifi-
cant scatter in the overlayer thickness (from 10 Å to
70 Å depending on sample preparation details). This
is especially true for composite CdTe/Si(211) and
CdZnTe/Si(211) substrates, the etching rate of which
also depends on material quality and surface mor-
phology. Inaccuracies in the model representation of
theCdTeandCZToxidesandlargevariationsintheir
thickness result in a large scatter in the fitted AOI
parameter. However, a precise determination of the
AOI still can be performed for such substrates at the
expense of reduced accuracy at the initial stages of
the growth run, if the analysis is done after the
Te desorption is completed. The successful Te re-
moval process leaves less than a few Å of overlayer,
which is well represented by surface roughness in a
two-layer optical model.
CALIBRATION OF THE ANGLE
OF INCIDENCE
It has already been mentioned that significantly
higheraccuracyincompositionandtemperaturecould
be achieved if the AOI were excluded as a free fit
parameter. On the other hand, keeping it fixed is not
justified for our setup. Under the conditions when the
polarizer and analyzer units are maintained at fixed
orientations, any deflections in the light beam enter-
ing the detector result only from changes in sample
surface orientation. We were able to relate the varia-
tions in the measured alignment parameters AlignX
andAlignYtovariationsintheAOIandtoparameter-
ize this relation using a calibration process quite
similartotheoneforwavelength, exceptthatonlythe
sample position would be changed, leaving all other
components fixed.
Because the control on the sample alignment is
very limited in the in-situ configuration, we have
performed our calibration on the ex-situ stage. The
arm length and the angle of incidence were chosen to
beclosetothoseforthein-situconfigurationtoensure
nearly the same degree of beam defocus and spatial
intensity distribution. The detector unit azimuth was
alsochosentobeclosetotheoneforreactormounting.
The same type of thick thermal SiO2/Si sample was
used for our calibrations because the SE data from
this specimen shows the highest sensitivity to the
AOI, due to the relatively high thickness and low
refractive index of the SiO2 film.
The alignment parameters were scanned in a
zigzag pattern by adjusting the sample tilt while the
angle of incidence was fitted for every sample surface
position. A wavelength correction also was applied to
the raw SE data before processing. The AOI was
parameterized as a function of the alignment param-
eters using of a formula similar to Eq. 1. As in the
wavelength calibration case, the coefficients A to F
were obtained using a regression analysis and are
presented in Table III. In both the ex-situ and in-situ
configurations, thedetectorunitwasmountedsothat
its X-axis is almost parallel to the system p-plane.
Therefore, as expected, the Y-sensitivity of the AOI is
significantly smaller than the X-sensitivity.
It is important to note here that the AOI obtained
inthecalibrationisexpressedasafunctionofthelocal
detectorcoordinates. Relocationofthedetectoronthe
MBE reactor generally involves changing of its azi-
muth.Thusinordertomaintainabettertransferabil-
ity of our ex-situ results to the in-situ configuration
we introduced an extra parameter, j, defining the
degree of rotation of the detector coordinate system
around the beam axis. The parameter, j, allows the
conversion of the actual alignment parameters of
real-time experiments to the x and y parameters used
in Eq. 1. It can be found as the difference between the
ex-situ and in-situ analyzer offset parameters As
produced by the ellipsometer regression calibration
procedure12 and accessible within the WVASE soft-
ware. For our experiment, the coordinate system
Theangleofincidencealignmentdependentcorrec-
tion procedure complements the wavelength shift
correction and is handled in real time by the above-
mentioned extension of the original WVASE soft-
ware. This extension communicates with the original
software through the TCPIP link and uses the elec-
tronic position indicator (EPI) command interface
implemented in WVASE.
SUMMARY AND CONCLUSIONS
We quantitatively studied the degree of error sup-
pression in the determined temperature and alloy
composition parameters by wavelength and AOI cor-
rection procedures.
Two sets of CdTe SE data were obtained during
two independent in-situ experiments in which after
Te desorption both samples were held at T = 200∞C
while their alignment was changing. The wavelength
and AOI corrections were applied only during one of