Temporal response of nonequilibrium correlated electrons

In this work we examine the time-resolved, instantaneous current response for the spinless FalicovKimball model at half-filling, on both sides of the Mott-Hubbard metal-insulator transition, driven by a strong electric field pump pulse. The results are obtained using an exact, nonequilibrium, many-body impurity solution specifically designed to treat the out-of-equilibrium evolution of electrons in timedependent fields. We provide a brief introduction to the method and its computational details. We find that the current develops Bloch oscillations, similar to the case of DC driving fields, with an additional amplitude modulation, characterized by beats and induced by correlation effects. Correlations primarily manifest themselves through an overall reduction in magnitude and shift in the onset time of the current response with increasing interaction strength

Time-resolved photoemission of correlated electrons driven out of equilibrium

We describe the temporal evolution of the time-resolved photoemission response of the spinless Falicov-Kimball model driven out of equilibrium by strong applied fields. The model is one of the few possessing a metal-insulator transition and admitting an exact solution in the time domain. The nonequilibrium dynamics, evaluated using an extension of dynamical mean-field theory, show how the driven system differs from two common viewpoints - a quasiequilibrium system at an elevated effective temperature (the "hot" electron model) or a rapid interaction quench ("melting" of the Mott gap) - due to the rearrangement of electronic states and redistribution of spectral weight. The results demonstrate the inherent trade-off between energy and time resolution accompanying the finite width probe pulses, characteristic of those employed in pump-probe time-domain experiments, which can be used to focus attention on different aspects of the dynamics near the transition.Comment: Original: 5 pages, 3 figures; Replaced: updated text and figures, 5 pages, 4 figure

Strong Electronic Correlation Effects in Coherent Multidimensional Nonlinear Optical Spectroscopy

We discuss a many−body theory of the coherent ultrafast nonlinear optical response of systems with a strongly correlated electronic ground state that responds unadiabatically to photoexcitation. We introduce a truncation of quantum kinetic density matrix equations of motion that does not rely on an expansion in terms of the interactions and thus applies to strongly correlated systems. For this we expand in terms of the optical field, separate out contributions to the time−evolved many−body state due to correlated and uncorrelated multiple optical transitions, and use “Hubbard operator” density matrices to describe the exact dynamics of the individual contributions within a subspace of strongly coupled states, including “pure dephasing”. Our purpose is to develop a quantum mechanical tool capable of exploring how, by coherently photoexciting selected modes, one can trigger nonlinear dynamics of strongly coupled degrees of freedom. Such dynamics could lead to photoinduced phase transitions. We apply our theory to the nonlinear response of a two−dimensional electron gas (2DEG) in a magnetic field. We coherently photoexcite the two lowest Landau level (LL) excitations using three time−delayed optical pulses. We identify some striking temporal and spectral features due to dynamical coupling of the two LLs facilitated by inter−Landau−level magnetoplasmon and magnetoroton excitations and compare to three−pulse four−wave−mixing (FWM) experiments. We show that these features depend sensitively on the dynamics of four−particle correlations between an electron−hole pair and a magnetoplasmon/magnetoroton, reminiscent of exciton−exciton correlations in undoped semiconductors. Our results shed light into unexplored coherent dynamics and relaxation of the quantum Hall system (QHS) and can provide new insight into non−equilibrium co−operative phenomena in strongly correlated systems

Examining electron-boson coupling using time-resolved spectroscopy

Nonequilibrium pump-probe time domain spectroscopies can become an important tool to disentangle degrees of freedom whose coupling leads to broad structures in the frequency domain. Here, using the time-resolved solution of a model photoexcited electron-phonon system we show that the relaxational dynamics are directly governed by the equilibrium self-energy so that the phonon frequency sets a window for "slow" versus "fast" recovery. The overall temporal structure of this relaxation spectroscopy allows for a reliable and quantitative extraction of the electron-phonon coupling strength without requiring an effective temperature model or making strong assumptions about the underlying bare electronic band dispersion.Comment: 23 pages, 4 figures + Supplementary Material and movies, to appear in PR

Nonequilibrium perturbation theory of the spinless Falicov-Kimball model

We perform a perturbative analysis for the nonequilibrium Green functions of the spinless Falicov-Kimball model in the presence of an arbitrary external time-dependent but spatially uniform electric field. The conduction electron self-energy is found from a strictly truncated second-order perturbative expansion in the local electron-electron repulsion U. We examine the current at half-filling, and compare to both the semiclassical Boltzmann equation and exact numerical solutions for the contour-ordered Green functions from a transient-response formalism (in infinite dimensions) on the Kadanoff-Baym-Keldysh contour. We find a strictly truncated perturbation theory in the two-time formalism cannot reach the long-time limit of the steady state; instead it illustrates pathological behavior for times larger than approximately 2/U