ﻻ يوجد ملخص باللغة العربية
The theoretical description of modern nanoelectronic devices requires a quantum mechanical treatment and often involves disorder, e.g. form alloys. Therefore, the ab initio theory of transport using non-equilibrium Greens functions is extended to the case of disorder described by the coherent potential approximation. This requires the calculation of non-equilibrium vertex corrections. We implement the vertex corrections in a Korringa-Kohn-Rostoker multiple scattering scheme. In order to verify our implementation and to demonstrate the accuracy and applicability we investigate a system of an iron-cobalt alloy layer embedded in copper. The results obtained with the coherent potential approximation are compared to supercell calculations. It turns out that vertex corrections play an important role for this system.
We investigate the non-equilibrium transport properties of a disordered molecular nanowire. The nanowire is regarded as a quasi-one-dimensional organic crystal composed of self-assembled molecules. One orbital and a single random energy are assigned
The resonant-level model represents a paradigmatic quantum system which serves as a basis for many other quantum impurity models. We provide a comprehensive analysis of the non-equilibrium transport near a quantum phase transition in a spinless dissi
As a strongly spin-orbit coupled metallic model with ferromagnetism, we have considered an extended Stoner model to the relativistic regime, named Dirac ferromagnet in three dimensions. In the previous paper~[Phys. Rev. B 90, 214418 (2014)], we stu
Scaling laws and universality play an important role in our understanding of critical phenomena and the Kondo effect. Here we present measurements of non-equilibrium transport through a single-channel Kondo quantum dot at low temperature and bias. We
We analyze charge-$e/4$ quasiparticle tunneling between the edges of a point contact in a non-Abelian model of the $ u=5/2$ quantum Hall state. We map this problem to resonant tunneling between attractive Luttinger liquids and use the time-dependent