Diploma - Max Planck Institute for Solid State Research
Diploma - Max Planck Institute for Solid State Research
Diploma - Max Planck Institute for Solid State Research
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12 2 Theoretical foundation<br />
Figure 2.4: photoemission models – left: three-step model, dividing the photoemission process<br />
into (1) excitation, (2) transport and (3) transmission to the vacuum; right: one-step model,<br />
quantum mechanical description of the excitation process by calculating the transition propability<br />
between the bound state and the unbound free state whose tail decays into the solid [28,<br />
p. 245]<br />
routine methods to obtain ultra-high vacuum (UHV) have been developed to establish<br />
the precondition <strong>for</strong> analyzing clean surfaces [28, p. 8] which enabled the community<br />
<strong>for</strong> the first time to distinguish surface and bulk originated spectral features. Since the<br />
discovery of the high-T c compounds and the development of devices capable of angular<br />
resolved photoemission spectroscopy (ARPES) , the interest in PES is regrowing.<br />
Photoemission (PE) is basically a “photon in – electron out” process granting access<br />
to the electronic structure of solids. Measuring the emission angle and the energy of the<br />
electron one is able to analyze the manybody transition. Initial states will be marked<br />
by the index i, final states correspondingly by f. In the following the two major models<br />
are sketched (a detailed description is given in [28]).<br />
2.2.1 Three-step model<br />
The originally single-step quantum mechanical PE process is devided into three steps,<br />
which will be discussed below. Nevertheless, this approximation is purely phenomenological<br />
and has been described in detail in [29, 30].<br />
(i) Optical excitation<br />
The incoming photon (excited electron) is characterized by the energy E ph (E e )<br />
and the momentum p ph (p e ), respectively. Neglecting the photon’s momentum<br />
(since p ph ≪ p e ≈ 100p ph , this is only valid <strong>for</strong> ω ≪ 500 eV) and respecting<br />
momentum conservation allows only “vertical” transitions – where the electron’s<br />
momentum changes by plus / minus a reciprocal lattice vector. In principle, one<br />
should deal with the extended zone scheme because elsewise one is not able to