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 ...
Create successful ePaper yourself
Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.
Recent Developments 189<br />
holder containing an environmental cell. To allow adequate gas pressure<br />
inside, the latter employs small differential-pumping apertures or very thin<br />
carbon-film “windows” above and below the specimen.<br />
Recent efforts have shortened the time resolution <strong>to</strong> the sub-picosecond<br />
region. One example (Lobas<strong>to</strong>v et al., 2005) is a 120-keV <strong>TEM</strong> fitted with a<br />
lanthanum hexaboride cathode from which electrons are released, not by<br />
thermionic emission but via the pho<strong>to</strong>electric effect. The LaB6 is illuminated<br />
by the focused beam from an ultrafast laser that produces short pulses <strong>of</strong> UV<br />
light, repeated at intervals <strong>of</strong> 13 ns and each less than 100 fem<strong>to</strong>seconds long<br />
(1 fs = 10 -15 s). The result is a pulsed electron beam, similar <strong>to</strong> that used for<br />
stroboscopic imaging in the SEM (see page 141) but with much shorter<br />
pulses. As the electron is a charged particle, incorporating many <strong>of</strong> them in<strong>to</strong><br />
the same pulse would result in significant Coulomb repulsion between the<br />
electrons so that they no longer travel independently, as needed <strong>to</strong> focus<br />
them with electromagnetic lenses. This problem is circumvented by reducing<br />
the laser-light intensity, so that each pulse generates (on average) only one<br />
electron. Although the laser pulses themselves can be used for ultrafast<br />
imaging, the image resolution is then limited by the pho<strong>to</strong>n wavelength.<br />
One goal <strong>of</strong> such ultrafast microscopy is <strong>to</strong> study the a<strong>to</strong>mic-scale<br />
dynamics <strong>of</strong> chemical reactions; it is known that the motion <strong>of</strong> individual<br />
a<strong>to</strong>ms in a molecular structure occurs on a fem<strong>to</strong>second time scale. <strong>An</strong>other<br />
aim is <strong>to</strong> obtain structural information from beam-sensitive (e.g., biological)<br />
specimens before they become damaged by the electron beam (Neutze et al.,<br />
2000).