Spin-orbit coupling and electron-phonon scattering - Fachbereich ...
Spin-orbit coupling and electron-phonon scattering - Fachbereich ...
Spin-orbit coupling and electron-phonon scattering - Fachbereich ...
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4 Introduction<br />
(<strong>phonon</strong>s). Therefore, the <strong>electron</strong>-<strong>electron</strong> (e-e) <strong>and</strong> <strong>electron</strong>-<strong>phonon</strong> (e-p) interactions<br />
set the limit for the observation of coherent phenomena in nanostructures<br />
at low temperatures. On the other h<strong>and</strong>, the e-e interaction itself causes profound<br />
effects like collective excitations of <strong>electron</strong>s, which in the parlance of many body<br />
physics are called plasmons. The importance of e-e interaction is determined by<br />
the <strong>electron</strong> density. In nanostructures the latter can be tuned by means of gates<br />
voltages which may draw <strong>electron</strong>s from or to the system. With increasing <strong>electron</strong><br />
concentration the average kinetic energy is expected to become larger than<br />
the average interaction energy. In this regime, many body effects can be neglected<br />
<strong>and</strong> the <strong>electron</strong> is approximately a freely moving particle in an averaged background<br />
potential caused by the other <strong>electron</strong>s. It is this approximation that we<br />
shall apply throughout this work.<br />
Similar to the phase information of a particle, the nature of its spin degree of<br />
freedom is purely quantum mechanical. The fundamental issue of the influence<br />
of the spin in <strong>electron</strong> transport has been a driving force in the field of magneto<strong>electron</strong>ics<br />
in the last decades [8]. The quantum nature of spin makes it inaccessible<br />
to many of the dominating forces in a solid. Recently, this non-volatility<br />
of spin has considerably sparked interest in the emerging field of spintronics [9],<br />
which is an amalgamation of different areas in physics (<strong>electron</strong>ics, photonics,<br />
<strong>and</strong> magnetics). Being motivated by fundamental <strong>and</strong> applicational interests, the<br />
paradigm of spintronics is either to add the spin degree of freedom to conventional<br />
charge-based <strong>electron</strong>ic devices, or to use the spin alone, aiming at the advantages<br />
of its non-volatility. Such devices are expected to have an increased data processing<br />
speed <strong>and</strong> integration density, <strong>and</strong> a decreased power consumption compared<br />
to conventional semiconductor devices. From a very basic point of view, manipulating<br />
the spin requires it to be distinguishable. This implies that the spin<br />
degeneracy has to be lifted. Simple reasoning shows that single-particle states<br />
of <strong>electron</strong>s in a solid are two-fold spin degenerate if time-reversal <strong>and</strong> spaceinversion<br />
symmetry are simultaneously present. Thus, there are two generic ways<br />
to address the spin: (i) Lift spin degeneracy by breaking time-reversal symmetry<br />
by e.g. magnetic fields (external or internal as in the case of ferromagnets).<br />
This corresponds to the magneto-<strong>electron</strong>ic aspect of spintronics which has led to<br />
e.g. the discovery of the giant magnetoresistance (GMR) effect in 1988 [10] that<br />
is already employed in present-day hard disk drives. (ii) Lift spin degeneracy by<br />
breaking space-inversion symmetry. In semiconductor nanostructures this leads<br />
to the issue of spin-<strong>orbit</strong> <strong>coupling</strong>.<br />
The relativistic <strong>coupling</strong> of spin <strong>and</strong> <strong>orbit</strong>al motion is well known from atomic<br />
physics in the context of fine-structure corrections to the spectrum of the hydrogen<br />
atom. There, the effect of spin-<strong>orbit</strong> <strong>coupling</strong> can be estimated by the Sommerfeld<br />
fine-structure constant α FS ≈ 1/137 as H SO /H 0 ≈ α 2 FS , being clearly a small<br />
perturbation. On the contrary, in semiconductor nanostructures, the strength of