Physical Principles of Electron Microscopy: An Introduction to TEM ...
Physical Principles of Electron Microscopy: An Introduction to TEM ...
Physical Principles of Electron Microscopy: An Introduction to TEM ...
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The Transmission <strong>Electron</strong> Microscope 83<br />
<strong>of</strong> amplitude and orientation, as discussed in Section 2.6. One way <strong>of</strong> setting<br />
these controls is <strong>to</strong> insert an amorphous specimen, whose image contains<br />
small point-like features. With astigmatism present, there is a “streaking<br />
effect” (preferred direction) visible in the image, which changes in direction<br />
through 90 degrees when the objective is adjusted from underfocus <strong>to</strong><br />
overfocus <strong>of</strong> the specimen image (similar <strong>to</strong> Fig. 5.17). The stigma<strong>to</strong>r<br />
controls are adjusted <strong>to</strong> minimize this streaking effect.<br />
Selected-area aperture<br />
As indicated in Fig. 3-12c and Fig. 3-14, a diaphragm can be inserted in the<br />
plane that contains the first magnified (real) image <strong>of</strong> the specimen, the<br />
image plane <strong>of</strong> the objective lens. This selected-area diffraction (SAD)<br />
diaphragm is used <strong>to</strong> limit the region <strong>of</strong> specimen from which an electron<br />
diffraction pattern is recorded. <strong>Electron</strong>s are transmitted through the aperture<br />
only if they fall within its diameter D, which corresponds <strong>to</strong> a diameter <strong>of</strong><br />
D/M at the specimen plane. In this way, diffraction information can be<br />
obtained from specimen regions whose diameter can be as small as 0.2 �m<br />
(taking D � 20 �m and an objective-lens magnification M � 100).<br />
As seen from Fig. 3-12c, sharp diffraction spots are formed at the<br />
objective back-focal plane (for electrons scattered at a particular angle) only<br />
if the electron beam incident on the specimen is almost parallel. This<br />
condition is usually achieved by defocusing the second condenser lens,<br />
giving a low convergence angle but a large irradiation area at the specimen<br />
(Fig. 3-9). The purpose <strong>of</strong> the SAD aperture is therefore <strong>to</strong> provide<br />
diffraction information with good angular resolution, combined with good<br />
spatial resolution.<br />
Intermediate lens<br />
A modern <strong>TEM</strong> contains several lenses between the objective and the final<br />
(projec<strong>to</strong>r) lens. At least one <strong>of</strong> these lenses is referred <strong>to</strong> as the intermediate,<br />
and the combined function <strong>of</strong> all <strong>of</strong> them can be described in terms <strong>of</strong> the<br />
action <strong>of</strong> a single intermediate lens, as shown in Fig. 3-14. The intermediate<br />
serves two purposes. First <strong>of</strong> all, by changing its focal length in small steps,<br />
its image magnification can be changed, allowing the overall magnification<br />
<strong>of</strong> the <strong>TEM</strong> <strong>to</strong> be varied over a large range, typically 10 3 <strong>to</strong> 10 6 .<br />
Second, by making a larger change <strong>to</strong> the intermediate lens excitation, an<br />
electron diffraction pattern can be produced on the <strong>TEM</strong> viewing screen. As<br />
depicted in Fig. 3-14, this is achieved by reducing the current in the<br />
intermediate so that this lens produces, at the projec<strong>to</strong>r object plane, a