It has been shown that the reaction-diffusion theory is not able to predict the different observed recovery characteristics following from different stress conditions. Therefore scaling and normalization routines are empirically used to characterize the recovery traces [14, 33, 82, 61].
In Fig. 4.1 the normalization routine is depicted step by step. First, the relative
recovery2
after different is normalized to the last corresponding stress value.
Furthermore, all relaxation times are divided by the last stress times,
yielding
. The normalized data now lie on top of each other
and feature the same “universal” behavior. Based on [61], this universal
behavior can be described by the universal relaxation function
which
reads
![]() | (4.1) |
Here denotes the relaxation depending on the total stress time
and the relaxation time
,
the total degradation observed right at
,
the permanent component, which only depends on the total stress
time, and
stands for the total amount the device is going to recover
from
. As such the term universality in NBTI was not a new finding in
2007, but was already reported by Denais et al., who claimed that the relative
recovery follows the same pattern when plotted over the stress time
[82, 61].
Unfortunately yet no generally accepted and valid theory exists for BTI,
which means that the exact form of remains speculative. Empirically
derived expressions have therefore been presented so far: Kakalios et al. for
example used a stretched-exponential of the form
to describe
“relaxation in disordered systems” [83]. Other empirical “log-like” expressions are
[82] or
[84]. Also a generalized
power-law-like expression after [61]
![]() | (4.2) |
amongst many others [85, 17, 86, 87], can be used. Whereas equation (4.2) can
be used to fit the OTF-data from [82], the first recovery point of the
MSM-data, depicted in Fig. 4.2, is unknown due to the instant recovery. The
first MSM point is obtained with a delay time
and according to [61, 11] even
a
is still too slow. Thus back-extrapolation to reconstruct the
“true” initial degradation has been suggested. With
we
get
![]() | (4.3) |
Provided that there is a set of relaxation data with different stress
times, and
can be determined, as shown in Fig. 4.2 taken from
[11, 61]3 .
The slight deviation for
is due to the existence of a non-negligible
permanent component
, which is additionally present here and
consequently has to be considered too.