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arXiv:2103.14771 · Physical review. B./Physical review. B

Exact solution of two simple non-equilibrium electron-phonon and electron-electron coupled systems: The atomic limit of the Holstein-Hubbard model and the generalized Hatsugai-Komoto model

R. D. Nesselrodt, J. K. Freericks

Published Oct 4, 2021• 7 citations
arXivHTMLPDF

Abstract

One of the challenges in many-body physics is determining the effects of phonons on strongly correlated electrons. The difficulty arises from strong correlations at differing energy scales---for band metals, Migdal-Eliashberg theory accurately determines electron-phonon coupling effects due to the absence of vertex corrections, but strongly correlated electrons require a more complex description, and the standard Migdal-Eliashberg approach does not necessarily apply. In this work, we solve for the atomic limit Green's function of the Holstein-Hubbard model with both time-dependent electron-electron and electron-phonon couplings. We then examine the photoemission spectra of this model in and out of equilibrium. Next, we use similar methods to exactly solve an extended version of the Hatsugai-Komoto model and examine its behavior in and out of equilibrium. These calculations lead us to propose using the first moment of the photoemission spectra to signal non-equilibrium changes in electron-electron and electron-phonon couplings.

DOI
10.1103/physrevb.104.155104

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One of the challenges in many-body physics is determining the effects of phonons on strongly correlated electrons. The difficulty arises from strong correlations at differing energy scales---for band metals, Migdal-Eliashberg theory accurately determines electron-phonon coupling effects due to the absence of vertex corrections, but strongly correlated electrons require a more complex description, and the standard Migdal-Eliashberg approach does not necessarily apply. In this work, we solve for the atomic limit Green's function of the Holstein-Hubbard model with both time-dependent electron-electron and electron-phonon couplings. We then examine the photoemission spectra of this model in and out of equilibrium. Next, we use similar methods to exactly solve an extended version of the Hatsugai-Komoto model and examine its behavior in and out of equilibrium. These calculations lead us to propose using the first moment of the photoemission spectra to signal non-equilibrium changes in electron-electron and electron-phonon couplings.
One of the challenges in many-body physics is determining the effects of phonons on strongly correlated electrons. The difficulty arises from strong correlations at differing energy scales -- for band metals, Migdal-Eliashberg theory accurately determines electron-phonon coupling effects due to the absence of vertex corrections -- but strongly correlated electrons require a more complex description and the standard Migdal-Eliashberg approach does not necessarily apply. In this work, we solve for the atomic limit Green's function of the Holstein-Hubbard model with both time-dependent electron-electron and electron-phonon couplings. We derive nonequilibrium spectral moment sum rules for the first four moments of the single-particle Green's function. We then analytically confirm that this Green's function exactly satisfies the zeroth, first, and second moment sum rules, and provide numerical evidence that the third spectral moment sum rule also holds. Finally we calculate the two-particle Green's function in the atomic limit. These two functions are required inputs to create a self-consistent strong-coupling expansion for the lattice Green's functions of the Hubbard-Holstein model.
The interplay of electron-phonon coupling and strong electronic correlations is studied in the frame of the two-dimensional Hubbard-Holstein model. Static and dynamic properties are determined by quantum Monte Carlo simulations and by Migdal-Eliashberg theory. The comparison allows us to assess the diagrammatic approach. The competition between the phonon-mediated electron-electron attraction and the local Coulomb repulsion leads to a rich phase diagram, which we study in detail for a wide range of parameters. We address the question, to which extent the systems can be described by an effective negative-U Hubbard model.
We investigate the effect of electronic correlations on the coupling of electrons to Holstein phonons in the one-band Hubbard model. We calculate the static electron-phonon vertex within the linear response of Kotliar-Ruckenstein slave bosons in the paramagnetic saddle-point approximation. Within this approach the on-site Coulomb interaction UUU strongly suppresses the coupling to Holstein phonons at low temperatures. Moreover, the vertex function does not show particularly strong forward scattering. Going to larger temperatures $kT\ensuremath{\sim}t$ we find that after an initial decrease with UUU, the electron-phonon coupling starts to increase with UUU, confirming a recent result of Cerruti, Cappelluti, and Pietronero. We show that this behavior is related to an unusual reentrant behavior from a phase separated to a paramagnetic state upon decreasing the temperature.
The problem of quantum dynamics in open systems has gained attention in recent decades and not the least due to the advances made in quantum transport in molecular systems. The main motivation behind quantum transport and molecular electronics is the futuristic goal to be able at some point to replace, or to complement, the silicon-based technology and to make the electronic devices faster. On a fundamental level, one has to deal with time-dependent processes where electron-electron or electron- phonon interactions are of great importance, and they can cause profound quantitative and qualitative changes on the physical and dynamical properties of electronic systems compared to the non-interacting case. Most of the studies of quantum transport have been focused on the steady-state description while neglecting the short-time dynamics. However, the dynamical effects are of great importance since fast- switching processes play a pivotal role in the operation of future devices. We studied the problem of time-dependent electron transport through the Anderson impurity model by using many-body perturbation theory (MBPT) together with Keldysh Green’s functions as well as with time-dependent density functional theory (TDDFT). These methods were compared with numerically exact time-dependent density-matrix renormalization group (tDMRG) method. We found that the many-body perturbation theory results beyond Hartree-Fock approximation were in close agreement with tDMRG results. In addition we studied the possibility of multistablity in the density and current of an interacting nanoscale junction as well as how to reversibly switch between the multiple solutions in time domain. An accurate theoretical treatment of electron correlation even in as simple model as an interacting electron gas at metallic densities still continues to be a challenge; especially description of features in the photoemission spectra due to electron correlations provides a theoretical challenge. The many-body perturbation theory yields a systematic way to study electron-electron (electron-phonon) correlations in various systems. One of the widely used approximations in MBPT is the GW approximation in which the bare interaction line is replaced with screened interaction line in the first order exchange diagram. The GW approximation gives good estimates for the band gap values close to experimental ones but especially the self-consistent GW approximation has a number of deficiencies like washing out of plasmon features and overestimation of bandwidths compared to experiment. One way to improve GW calculations is to include vertex corrections. Unfortunately, the straightforward inclusion of vertex corrections yields negative spectra in some frequency regions. We developed a diagrammatic approach to construct self-energy approximations with positive spectral properties. Our approach consists of expressing a self-energy of response diagram as a product of half-diagrams after which a minimal set of additional diagrams is identified to construct a perfect square. We applied this method to study vertex corrections in a homogeneous electron gas. In addition we analyzed the diagrammatic content of photocurrent with density functional theory. The expression for the photocurrent was obtained as an integral over the Kohn-Sham spectral function renormalized by effective potentials that depend on the exchange correlation kernel of current density functional theory. The expression for the photocurrent gives us the angular dependence of the photocurrent but it does not provide a direct access to the kinetic energy distribution of the photoelectrons.
This work contains a computationally efficient Green's function scheme for treating correlated electron-boson systems out of equilibrium. The numerical effort scales linearly with the simulation time, thus competing with that of the fastest quantum methods available. On a more fundamental level the proposed scheme fulfills energy balance as well as other fundamental conservation laws, and it can be systematically improved using standard many-body perturbation theory. We demonstrate its accuracy and stability through benchmarks against exact results in the Holstein model. However, our formulation equally applies to molecules and solids for first-principles transient calculations with quantum bosons, such as photons and phonons.
The many-body Green functions for the three-dimensional electron–phonon Holstein model are calculated via the Feynman diagram technique. The lowest-order contributions to the one-electron self-energy are considered (the Hartree–Fock approximation). The chemical potential is adjusted to yield the desired band-filling. The temperature dependence of the chemical potential has the correct asymptotic form in the non-interacting limit. The behavior of the one-electron occupancy factor is examined for various parameter values of the model. Tian's theorem is satisfied at half-filling. Luttinger liquid behavior is observed in the strong electron–phonon coupling regime.