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To take the energy loss of electrons during the step into
consideration, we have to replace
in the exponent
of Eq. (3) by
![\begin{displaymath}
G_l = 2 \pi N \int_0^t {\rm d}t^\prime\,\int_{-1}^1
{\rm d}...
...,\sigma(\cos \chi,t^\prime)
\Big[ 1 - P_l (\cos \chi) \Big]~.
\end{displaymath}](img171.gif) |
(39) |
Here,
is the number of atoms per unit volume and
the
path-length. The dependence of the single-scattering cross section
on the energy is expressed through the
dependence on the path-length
. Although in principle it is
possible to use
instead of
to calculate the
-surface, this approach would not be efficient on a
present-day computer due to the large increase of memory required to score the
pre-calculated data. In fact, when we take energy loss into account,
the dependence of the multiple-scattering distribution on the screening
parameter
alone is replaced by a dependence on the energy
and the material in which the transport takes place. Therefore, one
additional dimension will be needed to store the pre-calculated data.
We will therefore approximate
in such a way that the application
of the method presented in the last section becomes possible.
We rewrite Eq. (39)
Here,
and
are the initial and final kinetic
energies of the electron,
the restricted collision
stopping power4,
the total elastic cross section and
is again normalized to unity. To arrive at the second equation, we have
made use of the fact that
is proportional to
where
is the electron's velocity in units of the velocity of
light and introduced the short hand notation
for the product of
all constants in the total elastic cross section times
. If
we now neglect the very weak (logarithmic) energy dependence of
, Eq. (40) becomes
 |
(41) |
Here,
is the energy loss during the
step under consideration,
the
average energy of the electron and
the velocity
calculated from
. To carry out the
-integration we can
perform a power series expansion in
,
![\begin{displaymath}
\int_{E_{\rm f}}^{E_{\rm i}} {\rm d}E\,Q_l(E) \approx \Delta...
...\prime}(\tilde{E}) \over
Q_l(\tilde{E})} \pm \cdots \right]~,
\end{displaymath}](img198.gif) |
(42) |
where
is the second derivative of
with
respect to
. Using Eq. (18) for
and neglecting terms of
the order of
and terms small compared to
, we
arrive at the result
where
is the ratio of the average electron kinetic energy to
it's rest mass energy and
the energy loss
fraction. That means, when energy loss is taken into account, the
multiple-scattering distribution is to a good approximation equivalent
to the multiple-scattering distribution without energy loss resulting
from
elastic collisions of electrons with the
energy
. With this observation we can easily apply the
theory developed in the previous sections to realistic calculations
with electron energy loss taken into account.
Figure 4:
Ratio of the exact-MS distribution to the MS-distribution with
energy loss taken into account according to
Eq. (43) for 100 keV and 10 MeV electrons
in water and energy loss fractions
of 10, 25 and 33%.
For other energies and materials, similar
dependence on the energy-loss fraction
is observed.
 |
To test the accuracy of the approximations leading to Eq. (43),
we have calculated the multiple-scattering distribution resulting from
the exact GS-moments
and compared it to the distribution obtained with
the approximated
's given in Eq. (43) for various
energies, materials and energy-loss fractions. The energy integration
in (40) was done by a 32-point Gauss-Legendre quadrature.
The disagreement between the exact and approximated distributions
increases with increasing
. The maximum deviation found
for
% was of the order of 1%. For
%
the agreement was almost perfect. The ratio of the approximated
to the exact distribution for
, 25 and 33%
is shown for typical cases in
Fig. 4.
Next: Conclusions
Up: On the representation of
Previous: Numerical implementation
Iwan Kawrakow
2000-03-27