arXiv subjects

Erik Schroedter

Publications and source records attributed to Erik Schroedter.

7 recordsLinked to original sources

arXiv2026

Real-time Dyson expansion for the nonequilibrium $GW$ approximation: Correlated spectra and dependence on the reference propagator

Electronic spectra provide direct insight into the excitations and correlations of condensed matter systems. Their description requires electron correlations beyond mean field. In equilibrium, the $GW$ approximation has become the method of choice for many materials. Extending this approximation to nonequilibrium, however, is challenging. Full two-time $GW$ simulations within the nonequilibrium Green's functions approach scale at least cubically with propagation time, whereas improved scaling schemes such as time-local (adiabatic) approximations or the generalized Kadanoff--Baym ansatz usually retain only mean-field character in the spectra. The recently introduced real-time Dyson expansion recovers dynamical correlations in the spectrum at time-linear cost, but has so far been restricted to the second-order Born approximation with mean-field reference propagators. Here we formulate and implement the RT-DE for the nonequilibrium $GW$ self-energy with reference propagators of general form whose off-diagonal evolution is time local. In particular, we assess Hartree--Fock propagators, propagators with statically screened exchange with nonequilibrium screening, and a correlated propagator based on the Hartree--Fock GKBA. Benchmarks against exact diagonalization for a driven two-band lattice model with long-range interactions show that the mean-field and statically screened references yield the most accurate spectra, including satellite structures absent at mean-field level, whereas the GKBA-based approach best captures scattering-induced occupation dynamics, but artificially broadens and splits spectral peaks. When applied to large systems that are beyond the reach of exact methods, the scheme resolves the excitonic replica of the valence band and satellites identified as exciton shake-up, as well as their reshaping with increasing excitation density.

cond-mat.str-el↗

arXiv2026

Nonequilibrium Green Functions Simulations for Large Correlated Systems

Correlated real-time dynamics in large, spatially inhomogeneous quantum systems remain difficult to access with nonequilibrium many-body methods. Two-time nonequilibrium Green functions (NEGF) retain dynamical correlations but their computational runtime grows cubically with the number of time steps $N_\mathrm{t}$. This scaling bottleneck could recently be overcome by introducing the G1--G2 scheme that is linear in $N_\mathrm{t}$, but requires propagation of a two-particle correlation function and may suffer from numerical instabilities. This has restricted simulations to small systems with $N_\mathrm{b} \sim 10^2$ basis states. Here we introduce a quantum-fluctuation formulation of nonequilibrium Green functions, denoted $δ$NEGF, that represents dynamical two-particle correlations through fluctuations of field-operator products, $δ\hat G$. This guarantees stable dynamics by preserving the positivity of the reduced density matrices, avoids the explicit storage of the two-particle Green function, and reduces the propagation to a finite ensemble of Hartree-Fock-like trajectories. Combined with a stochastic low-rank decomposition of the correlation functions, the method retains time-linear scaling while extending dynamical $GW$ and particle-particle and particle-hole $T$-matrix simulations to basis sizes of order $N_\mathrm{b}\sim 10^4$. We benchmark $δ$NEGF against exact and HF-GKBA results for lattice systems, finding stable correlated dynamics also at strong coupling. We further demonstrate large-scale simulations of diffusion in two-dimensional Hubbard lattices and ultrafast relaxation in graphene nanoribbon heterostructures with long-range Coulomb interactions. These results establish $δ$NEGF as a scalable route to dynamical self-energy simulations of large, spatially inhomogeneous correlated quantum systems beyond the reach of existing NEGF implementations.

cond-mat.str-el↗

arXiv2024

Accelerating Nonequilibrium Green functions simulations: the G1-G2 scheme and beyond

The theory of Nonequilibrium Green functions (NEGF) has seen a rapid development over the recent three decades. Applications include diverse correlated many-body systems in and out of equilibrium. Very good agreement with experiments and available exact theoretical results could be demonstrated if the proper selfenergy approximations were used. However, full two-time NEGF simulations are computationally costly, as they suffer from a cubic scaling of the computation time with the simulation duration. Recently we have introduced the G1-G2 scheme that exactly reformulates the Kadanoff-Baym ansatz with Hartree-Fock propagators (HF-GKBA) into time-local equations, allowing for a dramatic reduction of the scaling to time-linear scaling [Schluenzen et al., Phys. Rev. Lett. \textbf{124}, 076601 (2020)]. Remarkably, this scaling is achieved quickly, and also for high-level selfenergies, including the nonequilibrium $GW$ and $T$-matrix approximations [Joost et al., Phys. Rev. B \textbf{101}, 245101 (2020)]. Even the dynamically screened ladder approximation is now feasible [Joost et al., Phys. Rev. B \textbf{105}, 165155 (2022)], and also applications to electron-boson systems were demonstrated. Here we present an overview on recent results that were achieved with the G1--G2 scheme. We discuss problems and open questions and present further ideas how to overcome the current limitations of the scheme.We illustrate the G1--G2 scheme by presenting applying it to the excitation dynamics of Hubbard clusters, to optical excitation of graphene, and to charge transfer during stopping of ions by correlated materials.

cond-mat.str-el↗

arXiv2024

Classical and Quantum Theory of Fluctuations for Many-Particle Systems out of Equilibrium

Correlated classical and quantum many-particle systems out of equilibrium are of high interest in many fields, including dense plasmas, correlated solids, and ultracold atoms. Accurate theoretical description of these systems is challenging both, conceptionally and with respect to computational resources. While for classical systems, in principle, exact simulations are possible via molecular dynamics, this is not the case for quantum systems. Alternatively, one can use many-particle approaches such as hydrodynamics, kinetic theory or nonequilibrium Green functions (NEGF). However, NEGF exhibit a very unfavorable cubic scaling of the CPU time with the number of time steps. An alternative is the G1--G2 scheme [N. Schlünzen et al., Phys. Rev. Lett. \textbf{124}, 076601 (2020)] which allows for NEGF simulations with time linear scaling, however, at the cost of large memory consumption. The reason is the need to store the two-particle correlation function. This problem can be overcome for a number of approximations by reformulating the kinetic equations in terms of fluctuations -- an approach that was developed, for classical systems, by Yu.L. Klimontovich [JETP \textbf{33}, 982 (1957)]. Here we present an overview of his ideas and extend them to quantum systems. In particular, we demonstrate that this quantum fluctuations approach can reproduce the nonequilibrium $GW$ approximation [E. Schroedter \textit{et al.}, Cond. Matt. Phys. \textbf{25}, 23401 (2022)] promising high accuracy at low computational cost which arises from an effective semiclassical stochastic sampling procedure. We also demonstrate how to extend the approach to the two-time exchange-correlation functions and the density response properties. [E. Schroedter \textit{et al.}, Phys. Rev. B \textbf{108}, 205109 (2023)].

cond-mat.stat-mech↗

arXiv2024

Two-Time Quantum Fluctuations Approach and its Relation to the Bethe--Salpeter Equation

Correlated quantum many-particle systems out of equilibrium are of high interest in many fields, including correlated solids, ultracold atoms or dense plasmas. Accurate theoretical description of these systems is challenging both, conceptionally and with respect to computational resources. We have recently presented a quantum fluctuations approach which is equivalent to the nonequilibrium $GW$ approximation [E. Schroedter \textit{et al.}, Cond. Matt. Phys. \textbf{25}, 23401 (2022)] that promises high accuracy at low computational cost. In a second publication [E. Schroedter \textit{et al.}, Phys. Rev. B \textbf{108}, 205109 (2023)], this approach was extended to the two-time exchange-correlation functions and the density response properties. Here, we analyze the properties of this approach in more detail. We demonstrate that the method is equivalent to the Bethe--Salpeter equation for the two-time exchange-correlation function when the generalized Kadanoff-Baym ansatz with Hartree-Fock propagators is applied.

cond-mat.str-el↗

arXiv2023

Quantum Fluctuations Approach to the Nonequilibrium $GW$-Approximation II: Density Correlations and Dynamic Structure Factor

The quantum dynamics of correlated fermionic or bosonic many-body systems following external excitation can be successfully studied using nonequilibrium Green functions (NEGF) or reduced density matrix methods. Approximations are introduced via a proper choice of the many-particle selfenergy or decoupling of the BBGKY-hierarchy, respectively. These approximations are based on Feynman's diagram approaches or on cluster expansions into single-particle and correlation operators. In a recent paper [E. Schroedter, J.-P. Joost, and M. Bonitz, Cond. Matt. Phys. \textbf{25}, 23401 (2022)] we have presented a different approach where, instead of equations of motion for the many-particle NEGF (or density operators), equations for the correlation functions of fluctuations are analyzed. In particular, we derived the stochastic GW and polarization approximations that are closely related to the nonequilibrium GW approximation. Here, we extend this approach to the computation of two-time observables depending on the specific ordering of the underlying operators. In particular, we apply this extension to the calculation of the density correlation function and dynamic structure factor of correlated Hubbard clusters in and out of equilbrium.

cond-mat.str-el↗

arXiv2022

Quantum fluctuations approach to the nonequilibrium $GW$ approximation

The quantum dynamics of fermionic or bosonic many-body systems following external excitation can be successfully studied using two-time nonequilibrium Green's functions (NEGF) or single-time reduced density matrix methods. Approximations are introduced via a proper choice of the many-particle self-energy or decoupling of the BBGKY hierarchy. These approximations are based on Feynman's diagram approaches or on cluster expansions into single-particle and correlation operators. Here, we develop a different approach where, instead of equations of motion for the many-particle NEGF (or density operators), single-time equations for the correlation functions of fluctuations are analyzed. We present a derivation of the first two equations of the alternative hierarchy of fluctuations and discuss possible decoupling approximations. In particular, we derive the polarization approximation (PA) which is shown to be equivalent to the single-time version [following by applying the generalized Kadanoff-Baym ansatz (GKBA)] of the nonequilibrium $GW$ approximation with exchange effects of NEGF theory, for weak coupling. The main advantage of the quantum fluctuations approach is that the standard ensemble average can be replaced by a semiclassical average over different initial realizations, as was demonstrated before by Lacroix and co-workers [see e.g. D. Lacroix et al., Phys. Rev. B, 2014, 90, 125112]. Here, we introduce the stochastic $GW$ (SGW) approximation and the stochastic polarization approximation (SPA) which are demonstrated to be equivalent to the single-time $GW$ approximation without and with exchange, respectively, in the weak coupling limit. Our numerical tests confirm that our approach has the same favorable linear scaling with the computation time as the recently developed G1-G2 scheme [Schluenzen et al., Phys. Rev. Lett., 2020, 124, 076601].

cond-mat.str-el↗