S. Iwata et A. Ishizaka, ELECTRON SPECTROSCOPIC ANALYSIS OF THE SIO2 SI SYSTEM AND CORRELATIONWITH METAL-OXIDE-SEMICONDUCTOR DEVICE CHARACTERISTICS/, Journal of applied physics, 79(9), 1996, pp. 6653-6713
ESCA (electron spectroscopy for chemical analysis) measurement results
on thin SiO2/Si samples are examined comprehensively, critically, and
in detail to show that it is possible to correlate these results with
MOS (metal-oxide-semiconductor) device characteristics such as flatba
nd (threshold) voltage, oxide breakdown field, mobile-ion density, hol
e and electron trap density, and hot-carrier lifetime. Up to now, much
effort has been made to detect SiO2 phases at SiO2/Si interfaces sinc
e they are thought to have a significant effect on MOS device characte
ristics. However, correlating the SiO2 phases with device characterist
ics is difficult and involves overcoming two problems. First, the chem
ical state is difficult to determine exactly due to x-ray-irradiation
effects. Second, the amount of defects and impurities which influence
device characteristics is usually below the ESCA detection limit (10(1
2)-10(13) cm(-2)) in device-quality SiO2/Si samples. Investigation of
the first problem led to the conclusion that it is possible to correct
for these effects from the x-ray intensity or oxide thickness depende
nce of the chemical shift. However, accurate (better than +/-0.2 eV) c
hemical state determination is not easy. It is therefore necessary to
approach this detection problem from a different viewpoint. Our first
attempt involves measuring the ESCA thickness, which decreases when ox
ide defects like unoxidized Si or uneven thickness (or pinholes) are p
resent, resulting in breakdown field degradation. Our second attempt s
tarted while we were studying how to interpret the measured chemical s
hift. The photoelectron peaks of the SiO2 and the Si can be observed t
o shift due to small amounts of charged defects and impurities; althou
gh they cannot be detected as peaks. This method is considered to be e
specially useful for characterizing ultrathin (a few mn thick) SiO2/Si
samples which are difficult to characterize using conventional C-V (c
apacitance-voltage) measurements because of tunneling currents. Accord
ingly, we discuss the data obtained in steady-state and transient peak
position measurements of SiO2/Si samples containing 10(10)-10(12) cm(
-2) of Na (sodium) ions, 10(12)-10(13) cm(-2) of hole and electron tra
ps, and 10(14)-10(21) cm(-3) of impurities such as P (phosphorus) (in
the Si). It is shown that a correlation with MOS characteristics is po
ssible. A close scrutiny of various results concerning x-ray irradiati
on time, intensity, and oxide thickness dependence of the above peak p
ositions indicates that electric charging during ESCA measurements is
correlated to the trap-capturing process. As MOS characteristics are a
lso related to this process, more studies in this direction are needed
and will certainly yield more information on the defects influencing
the MOS characteristics and the trap-capturing mechanism. (C) 1996 Ame
rican Institute of Physics.