The
passivation of n-type InP (100) using sulfur in combination
with a gadolinium aluminate (GAO) dielectric layer has been studied.
Photoluminescence, minority-carrier lifetime, and capacitance–voltage
measurements indicate that a (NH4)2S vapor passivation
step prior to atomic layer deposition of the oxide effectively lowers
the interface state density. Surface and interface chemistry were
studied by synchrotron radiation photoemission spectroscopy (SRPES).
The effect of ex situ surface passivation after native
oxide removal in HCl solution was examined. It was observed that surface
reoxidation occurred during (NH4)2S vapor exposure,
leading to the formation of In
x
(HPO4)
y
. S was present on the surface
as a sulfide in both surface and subsurface sites. After atomic layer
deposition of GAO, sulfates were detected in addition to In
x
(HPO4)
y
, which
was confirmed by near-edge X-ray absorption fine structure analysis.
The S in the stack was quantified using reference-free grazing incidence
X-ray fluorescence analysis. X-ray absorption spectroscopy showed
that Gd was oxidized and present in the 3+ oxidation state, most likely
as a phosphate close to the InP interface and possibly mixed with
sulfates. Energy-dependent SRPES measurements of Al 2p and Gd 4d core
levels, complemented by transmission electron microscopy, further
suggest that the dielectric layer was segregated. Valence band measurements
confirm the effective passivation of InP, indicating unpinning of
the surface Fermi level.