196 The transmission electron microscope
far greater than that of the older machines. The easiest way to understand why there
are so many lenses is to analyze what each lens does in relation to its neighbors.
It is instructive to start with a microscope without lenses and to add lenses, one
at a time. We will divide the microscope column into prespecimen, specimen, and
post-specimen regions, and describe the functionality of the main lenses in each of
those regions. While the actual number of lenses for any particular microscope may
vary, we will focus in the next sections on those lenses that are present in nearly
every recent microscope model.
The illumination system of a TEM serves one important purpose: to create a beam
of electrons in a well-defined reference state (either a plane wave or a converged
fine probe). Only if we know what the reference state is can we hope to extract
information concerning the sample by analyzing the modified signal R
(recall the
discussion on page 106). It is thus important for the microscope operator to under-
stand the purpose of each of the lenses in the illumination system. This situation is
somewhat similar to that encountered when one tries to solve a differential equation:
the equation can only be completely solved if the initial conditions are specified,
and solutions may depend in a rather sensitive way on those initial conditions. We
have already seen that, in the case of the TEM, the relevant differential equation is
the stationary Schr¨odinger equation. If we wish to compare theoretical solutions to
this equation with experimental observations, we must from the beginning ensure
that both have the same initial conditions. The illumination system is, hence, of cru-
cial importance for the interpretation of experimental images based on a theoretical
description of the image formation mechanism.
Let us consider the configuration shown in Fig. 3.26(a): an electron gun directly
illuminates a specimen, without any magnetic lenses present. This configuration
offers only limited control over the electron beam: the Wehnelt voltage or gun bias
combined with the geometry of the entire assembly determine the location and size
of the cross-over. The total number of electrons that reach any specific area on the
specimen is rather small and can be changed somewhat by adjusting the gun bias.
Since this changes the area on the filament from which electrons are emitted, the
beam brightness would also change. This is clearly an undesirable configuration
since we would like to be able to form a very fine probe on the sample surface or use
a parallel incident beam. So we decide to add a single magnetic lens, the condensor
lens C
1
, positioned close to the anode, as shown in Fig. 3.26(b).
If this lens C
1
is excited such that the image of the gun cross-over (with a
diameter of s = 10–100
µm) is formed on the specimen surface, then the size of
the smallest illuminated area (the spot size) equals sv/u, generally of the same order
of magnitude as the cross-over diameter itself. This is again undesirable because
we may wish to investigate details on a length scale of nanometers, not microns,
and this will require nanometer-sized probes.