In this thesis the electron transport through interacting quantum wires is studied.The time-dependent properties of the system are investigated by using the non-equilibrium Green function technique.This technique provides a way to include ultra-fast timedependent processes, arbitrary strong external fields and also brings forward an effective treatment of electron-electron and electron-phonon interactions.The electronelectron interactions are included via various self-energy approximations at Hartree-Fock, second-order Born and GW levels.These approximations are called conserving since they fulfill the physical conservation laws like the charge conservation law.The interacting central system is coupled to one-dimensional tight-binding leads, which are considered effectively as noninteracting.The system is perturbed by a bias voltage after which the time-evolution of the system is followed by Kadanoff-Baym equations.The non-equilibrium steady-state value of the current depends on the used self-energy approximation, which indicates the importance of the history-dependence in the calculation of current.This is an important observation in the aspect of time-dependent density functional theory, since it is one indication for the need of functionals with memory.The steady-state current is independent of the initial state, which is in accordance with the memory-loss theorem.The transient current shows small oscillations, which are consequence of the density oscillations especially in the first and last site.The density oscillations in the sites are effect of the electron transition from the lead to the central system and vice versa.
We propose a time-dependent many-body approach to study the short-time dynamics of correlated electrons in quantum transport through nanoscale systems contacted to metallic leads. This approach is based on the time propagation of the Kadanoff-Baym equations for the nonequilibrium many-body Green's function of open and interacting systems out of equilibrium. An important feature of the method is that it takes full account of electronic correlations and embedding effects in the presence of time-dependent external fields, while at the same time satisfying the charge conservation law. The method further extends the Meir-Wingreen formula to the time domain for initially correlated states. We study the electron dynamics of a correlated quantum wire attached to two-dimensional leads exposed to a sudden switch on of a bias voltage using conserving many-body approximations at Hartree-Fock, second Born and GW level. We obtain detailed results for the transient currents, dipole moments, spectral functions, charging times, and the many-body screening of the quantum wire as well as for the time-dependent density pattern in the leads, and we show how the time dependence of these observables provides a wealth of information on the energy level structure of the quantum wire out of equilibrium. For moderate interaction strengths the second Born and GW results are in excellent agreement at all times. We find that many-body effects beyond the Hartree-Fock approximation have a large effect on the qualitative behavior of the system and lead to a bias-dependent gap closing and quasiparticle broadening, shortening of the transient times and washing out of the step features in the current-voltage curves.
We develop a detailed theory for spin transport in a one-dimensional quantum wire described by Luttinger-liquid theory. A hydrodynamic description of the quantum wire is supplemented by boundary conditions, taking into account the exchange coupling between the magnetization of ferromagnetic reservoirs and the boundary magnetization in the wire. Spin-charge separation is shown to imply drastic and qualitative consequences for spin-dependent transport. In particular, the spin accumulation effect is quenched except for fine-tuned parameter regimes. We propose several feasible setups involving an external magnetic field to detect this phenomenon in transport experiments on single-wall carbon nanotubes. In addition, electron-electron backscattering processes, which do not have an important effect on thermodynamic properties or charge transport, are shown to modify spin-dependent transport through long quantum wires in a crucial way.
We study charge and spin transport through an interacting quantum wire, caused by backscattering of electrons off an effective impurity potential with a periodic time dependence. The adiabatic regime of this pump for charge and spin is shown to depend on the presence of interactions in the wire. For the noninteracting case, the transported quantities in a period are calculated and found to be adiabatic (independent of the pumping frequency) for all frequencies $\ensuremath{\Omega}\ensuremath{\ll}{v}_{F}/\mathcal{l},$ where
l is the range of the scattering potential and
vF is the Fermi velocity; this result is along the lines of adiabatic pumping in mesoscopic systems. On the other hand, we show that for a wire with repulsive electron-electron interactions, the adiabatic regime is confined to $\ensuremath{\Elzxh}\ensuremath{\Omega}\ensuremath{\ll}{\ensuremath{\omega}}_{\ensuremath{\Gamma}},$ where ${\ensuremath{\omega}}_{\ensuremath{\Gamma}}$ is an energy scale set by the backscattering potential. Using symmetry and scaling properties of the quantum wire Hamiltonian, we relate the charge Q and spin S transported through the wire in a period $2\ensuremath{\pi}/\ensuremath{\Omega}$ to an integral involving quasistatic backscattering conductances. We also show that the pumped charge Q (or the spin
S) is quantized in the adiabatic limit if the conductance of the system is zero at the stable fixed point of the renormalization-group (RG) transformations. The quanta transported are given by the winding number of a complex coupling $\ensuremath{\Gamma}(\ensuremath{\Omega}t)$ as it traverses a closed path
C enclosing the origin $\ensuremath{\Gamma}=0.$ No adiabatic charge or spin is transported when the RG fixed point corresponds to a perfectly conducting wire, or if the path
C does not enclose the point $\ensuremath{\Gamma}=0.$ By contrast, for a RG marginal conductance---which is the case for noninteracting electrons---the charge transported in a cycle is not quantized, rather it is proportional to the area enclosed by the path or circuit
C, in agreement with previous studies of noninteracting mesoscopic systems. Finite size, temperature, and frequency effects on the transported quantities follow from the relation between adiabatic transport coefficients (backscattering conductances) and the quasistatic conductance of the system.
We formulate a quantum theory of electron waiting time distributions for charge transport in nanostructures described by non-Markovian generalized master equations. We illustrate our method by calculating the waiting time distribution of electron transport through a dissipative double quantum dot, where memory effects are present due to a strongly coupled heat bath. We consider the influence of non-Markovian dephasing on the distribution of electron waiting times and discuss how spectral properties of the heat bath may be detected through measurements of the electron waiting time.
We describe microscopic theory for the quantum transport through finite interacting systems connected to noninteracting leads. It can be applied to small systems such as quantum dots, quantum wires, atomic chain, molecule, and so forth. The Keldysh formalism is introduced to study the nonlinear current-voltage characteristics, and general properties of the nonequilibrium Green's functions are provided. We apply the formulated to an out-of-equilibrium Anderson model that has been used widely for the Kondo effect in quantum dots. In the linear-response regime the Kubo formalism still has an advantage, because it relates the transport coefficients directly to the correlation functions defined with respect to the thermal equilibrium, and it has no ambiguities about a profile of the inner electric field. We introduce a many-body transmission coefficient, by which the dc conductance can be expressed in a Landauer-type form, quite generally. We also discuss transport properties of the Tomonaga-Luttinger liquid, which has also been an active field of research in this decade.