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Physical Principles of Electron Microscopy: An Introduction to TEM ...

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The Transmission <strong>Electron</strong> Microscope 73<br />

increase in the beam angle � at the electron-source image plane. In this<br />

context, it should be noted that the convergence angle <strong>of</strong> the illumination is<br />

always defined in terms <strong>of</strong> the variation in angle <strong>of</strong> the electrons that arrive<br />

at a single point in the specimen.<br />

u<br />

v 0<br />

d 1<br />

D<br />

d 0<br />

demagnified source<br />

� �<br />

C2<br />

aperture<br />

specimen<br />

image plane<br />

d 1<br />

(a) (b) (c)<br />

�<br />

v'<br />

d d<br />

�<br />

u<br />

u<br />

v'<br />

d 1<br />

�<br />

�<br />

image<br />

plane<br />

Figure 3-8. Operation <strong>of</strong> the second condenser (C2) lens; solid rays represent electrons<br />

emitted from the center <strong>of</strong> the C1-demagnified source. (a) Fully-focused illumination whose<br />

diameter d0 is comparable <strong>to</strong> the diameter d1 <strong>of</strong> the demagnified source (see dashed rays) and<br />

whose convergence angle (2�0) depends on the diameter <strong>of</strong> the C2 aperture. (b) Underfocused<br />

illumination whose diameter d depends on the image distance v and whose convergence angle<br />

� depends on v and on d1. (c) Overfocused illumination, also providing large d and small � .<br />

Figure 3-9. (a) Current density at the specimen as a function <strong>of</strong> distance from the optic axis,<br />

for illumination fully focused and for defocused (underfocused or overfocused) illumination.<br />

(b) Convergence semi-angle <strong>of</strong> the specimen illumination, as a function <strong>of</strong> C2-lens excitation.

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