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The two-body density matrix of a system in thermodynamic equilibrium

Golli, B., Rosina, M., Milan Potokar

Published Jan 1, 1975• 0 citations
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The one-body density matrix has recently attracted considerable attention as a promising key quantity for the description of systems out of equilibrium. Its time evolution is given in terms of the two-body density matrix, and thus the central challenge is to find approximations to the latter. An extra layer of difficulty is added when dealing with strong electron correlations. In this work, we explore precisely this regime by looking at the two-site Anderson impurity model as a case study. To address the system's dynamics, we use an adiabatic approximation based on the exact ground-state two-body density matrix. We find that this adiabatic extension does not reproduce the exact results even for a slow switch-on of the external perturbation, and we trace back this behavior to the lack of an accurate imaginary part of the adiabatic approximation to the two-body density matrix. The attempt to restore an approximate imaginary part through a Hilbert transform of the real part works well only for very short times, but quickly deteriorates for longer times, with the one-body density matrix being pushed out of its N-representability domain. Our results thus pose an important constraint on practical prescriptions to perform the time evolution of the one-body density matrix.

Physical Chemistry Chemical Physics•Jan 1, 2021•9 citations
In a recent Letter [Phys. Rev. Lett. 88, 256403(2002), cond-mat/0109158] Cazalilla and Marston proposed a time-dependent density- matrix renormalization group (TdDMRG) algorithm for the accurate evaluation of out-of-equilibrium properties of quantum many-body systems. For a point contact junction between two Luttinger liquids, a current oscillation develops after initial transient in the insulating regime. Here we would like to point out that (a) the observed oscillation is an artifact of the method; (b) the TdDMRG can be significantly improved by incorporating the non-equilibrium evolution of the goundstate into the density matrix.
We investigate the open dynamics of a chain of interacting spins using the quantized version of the GENERIC equation from classical out-of-equilibrium thermodynamics. We focus on both equilibrium and nonequilibrium scenarios for chains of different sizes. While in the equilibrium case we demonstrate thermal equilibration to the correct many-body Gibbs density matrix, in the nonequilibrium dynamics we show a ballistic-to-diffusive transition in the steady-state energy current and a scaling that is consistent with Fourier's law of heat transfer.
The one-body density matrix has recently attracted considerable attention as a promising key quantity for the description of systems out of equilibrium. Its time evolution is given in terms of the two-body density matrix, and thus the central challenge is to find approximations to the latter. An extra layer of difficulty is added when dealing with strong electron correlations. In this work, we explore precisely this regime by looking at the two-site Anderson impurity model as a case study. To address the system's dynamics, we use an adiabatic approximation based on the exact ground-state two-body density matrix. We find that this adiabatic extension does not reproduce the exact results even for a slow switch-on of the external perturbation, and we trace back this behavior to the lack of an accurate imaginary part of the adiabatic approximation to the two-body density matrix. The attempt to restore an approximate imaginary part through a Hilbert transform of the real part works well only for very short times, but quickly deteriorates for longer times, with the one-body density matrix being pushed out of its N-representability domain. Our results thus pose an important constraint on practical prescriptions to perform the time evolution of the one-body density matrix.