No Arabic abstract
We apply the Nonequilibrium Greens Function (NEGF) formalism to the problem of a multi-terminal nanojunction subject to an arbitrary time-dependent bias. In particular, we show that taking a generic one-particle system Hamiltonian within the wide band limit approximation (WBLA), it is possible to obtain a closed analytical expression for the current in each lead. Our formula reduces to the well-known result of Jauho et. al. [doi:10.1103/PhysRevB.50.5528] in the limit where the switch-on time is taken to the remote past, and to the result of Tuovinen et. al. [doi:10.1088/1742-6596/427/1/012014] when the bias is maintained at a constant value after the switch-on. As we use a partition-free approach, our formula contains both the long-time current and transient effects due to the sudden switch-on of the bias. Numerical calculations performed for the simple case of a single-level quantum dot coupled to two leads are performed for a sinusoidally-varying bias. At certain frequencies of the driving bias, we observe `ringing oscillations of the current, whose dependence on the dot level, level width, oscillation amplitude and temperature is also investigated.
We study the differential conductance in the Kondo regime of a quantum dot coupled to multiple leads. When the bias is applied symmetrically on two of the leads ($V$ and $-V$, as usual in experiments), while the others are grounded, the conductance through the biased leads always shows the expected enhancement at {it zero} bias. However, under asymmetrically applied bias ($V$ and $lambda V$, with $lambda>0$), a suppression - dip - appears in the differential conductance if the asymmetry coefficient $lambda$ is beyond a given threshold $lambda_0= sqrt[3]{1+r}$ determined by the ratio $r$ of the dot-leads couplings. This is a recipe to determine experimentally this ratio which is important for the quantum-dot devices. This finding is a direct result of the Keldysh transport formalism. For the illustration we use a many-lead Anderson Hamiltonian, the Green functions being calculated in the Lacroix approximation, which is generalized to the case of nonequilibrium.
Working within the Nonequilibrium Greens Function (NEGF) formalism, a formula for the two-time current correlation function is derived for the case of transport through a nanojunction in response to an arbitrary time-dependent bias. The one-particle Hamiltonian and the Wide Band Limit Approximation (WBLA) are assumed, enabling us to extract all necessary Greens functions and self energies for the system, extending the analytic work presented previously [Ridley et al. Phys. Rev. B (2015)]. We show that our new expression for the two-time correlation function generalises the Buttiker theory of shot and thermal noise on the current through a nanojunction to the time-dependent bias case including the transient regime following the switch-on. Transient terms in the correlation function arise from an initial state that does not assume (as is usually done) that the system is initially uncoupled, i.e. our approach is partition-free. We show that when the bias loses its time-dependence, the long time-limit of the current correlation function depends on the time difference only, as in this case an ideal steady state is reached. This enables derivation of known results for the single frequency power spectrum and for the zero frequency limit of this power spectrum. In addition, we present a technique which for the first time facilitates fast calculations of the transient quantum noise, valid for arbitrary temperature, time and voltage scales. We apply this to the quantum dot and molecular wire systems for both DC and AC biases, and find a novel signature of the traversal time for electrons crossing the wire in the time-dependent cross-lead current correlations.
Recently [Phys. Rev. B 91, 125433 (2015)] we derived a general formula for the time-dependent quantum electron current through a molecular junction subject to an arbitrary time-dependent bias within the Wide Band Limit Approximation (WBLA) and assuming a single particle Hamiltonian. Here we present an efficient numerical scheme for calculating the current and particle number. Using the Pade expansion of the Fermi function, it is shown that all frequency integrals occurring in the general formula for the current can be removed analytically. Furthermore, when the bias in the reservoirs is assumed to be sinusoidal it is possible to manipulate the general formula into a form containing only summations over special functions. To illustrate the method, we consider electron transport through a one-dimensional molecular wire coupled to two leads subject to out-of-phase biases. We also investigate finite size effects in the current response and particle number that results from the switch-on of such a bias.
We show that smooth variations, delta n({bf r}), of the local electron concentration in a clean 2D electron gas give rise to a zero-bias anomaly in the tunnel density of states, u(omega), even in the absence of scatterers, and thus, without the Friedel oscillations. The energy width, omega_0, of the anomaly scales with the magnitude, delta n, and characteristic spatial extent, D, of the fluctuations as (delta n/D)^{2/3}, while the relative magnitude delta u/ u scales as (delta n/D). With increasing omega, the averaged delta u oscillates with omega. We demonstrate that the origin of the anomaly is a weak curving of the classical electron trajectories due to the smooth inhomogeneity of the gas. This curving suppresses the corrections to the electron self-energy which come from the virtual processes involving two electron-hole pairs
In recent years there has been an increasing interest in nanomachines. Among them, current-driven ones deserve special attention as quantum effects can play a significant role there. Examples of the latter are the so-called adiabatic quantum motors. In this work, we propose using Andersons localization to induce nonequilibrium forces in adiabatic quantum motors. We study the nonequilibrium current-induced forces and the maximum efficiency of these nanomotors in terms of their respective probability distribution functions. Expressions for these distribution functions are obtained in two characteristic regimes: the steady-state and the short-time regimes. Even though both regimes have distinctive expressions for their efficiencies, we find that, under certain conditions, the probability distribution functions of their maximum efficiency are approximately the same. Finally, we provide a simple relation to estimate the minimal disorder strength that should ensure efficient nanomotors.