K. Elst et W. Vandervorst, THE INFLUENCE OF OXYGEN ON THE ANALYSIS OF A PT SI STRUCTURE WITH SECONDARY-ION MASS-SPECTROMETRY/, Journal of applied physics, 73(9), 1993, pp. 4649-4659
The introduction of oxygen during analysis with secondary ion mass spe
ctrometry (SIMS) is an important tool to reduce ion beam induced topog
raphy, to enhance positive ion yields, and to remove transient effects
during shallow and multilayer profiling. Its main drawback, however,
is that due to the tendency of some elements to segregate towards the
internal SiO2/Si interface (formed by an oxygen primary beam), large p
rofile distortions can occur. In this work, the influence of oxygen pr
essure on the measurement of the Pt/Si structure is investigated and i
ts relation to the observed SIMS depth profile is established. In the
low pressure regime (leading to incomplete oxidation of Si), the profi
le disturbances occur in the interface region and are totally the resu
lt of ionization variations. The depth at which these disturbances are
seen, as well as as the magnitude of the variations, are strongly dep
endent on the oxygen pressure in relation to the primary current densi
ty. The latter can be explained by the competition for the Si atoms be
tween the formation of a Pt-Si alloy and an oxide. For high pressures
where Si is completely oxidized, two regimes are observed. In the firs
t regime, when the sample still contains a large amount of Pt, a large
decay length is observed, representative of the strong segregation to
ward the SiO2/Si interface. In a later stage, when the amount of Pt ha
s been reduced, the decay length decreases significantly suggesting th
at the segregation disappears. Internal depth profiling has shown that
the two decay lengths can be correlated with two different internal P
t distributions, whereby the longest decay length corresponds to a Pt
accumulation in the interface region. This correlation is in agreement
with theoretical predictions about the role of the internal distribut
ion on the SIMS decay length. The work also revealed that the polarity
of the detected ions has a pronounced influence on the segregation ca
used by field-induced migration. This segregation depended strongly on
the oxidizing conditions, suggesting the formation of higher quality
oxides under higher oxygen pressures.