arXiv subjects

J. Gemmer

Publications and source records attributed to J. Gemmer.

17 recordsLinked to original sources

arXiv2019

Dynamical typicality for initial states with a preset measurement statistics of several commuting observables

We consider all pure or mixed states of a quantum many-body system which exhibit the same, arbitrary but fixed measurement outcome statistics for several commuting observables. Taking those states as initial conditions, which are then propagated by the pertinent Schrödinger or von Neumann equation up to some later time point, and invoking a few additional, fairly weak and realistic assumptions, we show that most of them still entail very similar expectation values for any given observable. This so-called dynamical typicality property thus corroborates the widespread observation that a few macroscopic features are sufficient to ensure the reproducibility of experimental measurements despite many unknown and uncontrollable microscopic details of the system. We also discuss and exemplify the usefulness of our general analytical result as a powerful numerical tool.

cond-mat.stat-mech↗

arXiv2017

Charge diffusion in the one-dimensional Hubbard model

We study the real-time and real-space dynamics of charge in the one-dimensional Hubbard model in the limit of high temperatures. To this end, we prepare pure initial states with sharply peaked density profiles and calculate the time evolution of these nonequilibrium states, by using numerical forward-propagation approaches to chains as long as 20 sites. For a class of typical states, we find excellent agreement with linear-response theory and unveil the existence of remarkably clean charge diffusion in the regime of strong particle-particle interactions. Moreover, we demonstrate that this diffusive behavior does not depend on certain details of our initial conditions, i.e., it occurs for five different realizations with random and nonrandom internal degrees of freedom, single and double occupation of the central site, and displacement of spin-up and spin-down particles.

cond-mat.str-el↗

arXiv2017

Real-time broadening of non-equilibrium density profiles and the role of the specific initial-state realization

The real-time broadening of density profiles starting from non-equilibrium states is at the center of transport in condensed-matter systems and dynamics in ultracold atomic gases. Initial profiles close to equilibrium are expected to evolve according to linear response, e.g., as given by the current correlator evaluated exactly at equilibrium. Significantly off equilibrium, linear response is expected to break down and even a description in terms of canonical ensembles is questionable. We unveil that single pure states with density profiles of maximum amplitude yield a broadening in perfect agreement with linear response, if the structure of these states involves randomness in terms of decoherent off-diagonal density-matrix elements. While these states allow for spin diffusion in the XXZ spin-1/2 chain at large exchange anisotropies, coherences yield entirely different behavior.

cond-mat.str-el↗

arXiv2016

Eigenstate Thermalization Hypothesis and Quantum Jarzynski Relation for Pure Initial States

Since the first suggestion of the Jarzynski equality many derivations of this equality have been presented in both, the classical and the quantum context. While the approaches and settings greatly differ from one to another, they all appear to rely on the initial state being a thermal Gibbs state. Here, we present an investigation of work distributions in driven isolated quantum systems, starting off from pure states that are close to energy eigenstates of the initial Hamiltonian. We find that, for the nonintegrable system in quest, the Jarzynski equality is fulfilled to good accuracy.

quant-ph↗

arXiv2015

From single-shot towards general work extraction in a quantum thermodynamic framework

This paper considers work extraction from a quantum system to a work storage system (or weight) following reference [1]. An alternative approach is here developed that relies on the comparison of subspace dimensions without a need to introduce thermo-majorisation used previously. Optimal single shot work for processes where a weight transfers from (a) a single energy level to another single energy level is then re-derived. In addition we discuss the final state of the system after work extraction and show that the system typically ends in its thermal state, while there are cases where the system is only close to it. The work of formation in the single level transfer setting [1] is also re-derived. The approach presented now allows the extension of the single shot work concept to work extraction (b) involving multiple final levels of the weight. A key conclusion here is that the single shot work for case (a) is appropriate only when a \emph{resonance} of a particular energy is required. When wishing to identify "work extraction" with finding the weight in a specific available energy or any higher energy a broadening of the single shot work concept is required. As a final contribution we consider transformations of the system that (c) result in general weight state transfers. Introducing a transfer-quantity allows us to formulate minimum requirements for transformations to be at all possible in a thermodynamic framework. We show that choosing the free energy difference of the weight as the transfer-quantity one recovers various single shot results including single level transitions (a), multiple final level transitions (b), and recent results on restricted sets of multi-level to multi-level weight transfers.

quant-ph↗

arXiv2014

Scaling of diffusion constants in the spin-1/2 XX ladder

We study the dynamics of spin currents in the XX spin-1/2 ladder at finite temperature. Within the framework of linear response theory, we numerically calculate autocorrelation functions for quantum systems larger than what is accessible with exact diagonalization using the concept of dynamical quantum typicality. We show that spin Drude weights vanish exponentially fast with increasing system size. As a main result, we unveil qualitatively different dependencies of the spin diffusion coefficient on the rung-interaction strength, resulting from a crossover from exponential to Gaussian dissipation as the rung coupling increases. This behavior is also derived analytically. We further discuss the relation of our results to experiments with cold atomic gases.

cond-mat.str-el↗

arXiv2013

Transport in topologically disordered one-particle, tight-binding models

We aim at quantitatively determining transport parameters like conductivity, mean free path, etc., for simple models of spatially completely disordered quantum systems, comparable to the systems which are sometimes referred to as Lifshitz models. While some low-energy eigenstates in such models always show Anderson localization, we focus on models for which most states of the full spectrum are delocalized, i.e., on the metallic regime. For the latter we determine transport parameters in the limit of high temperatures and low fillings using linear response theory. The Einstein relation (proportionality of conductivity and diffusion coefficient) is addressed numerically and analytically and found to hold. Furthermore, we find the transport behavior for some models to be in accord with a Boltzmann equation, i.e., rather long mean free paths, exponentially decaying currents, while this does not apply to other models even though they are also almost completely delocalized.

cond-mat.dis-nn↗

arXiv2012

Quantum thermal equilibration from equipartition

The problem of mutual equilibration between two finite, identical quantum systems, A and B, prepared initially at different temperatures is elucidated. We show that the process of energy exchange between the two systems leads to accurate equipartition within energy shells in the Hilbert space of the total non-interacting, composite system, A \otimes B. This scenario occurs under the general condition of a weak interaction between the systems. We predict that the sole hypothesis of such equipartition is sufficient to obtain a relaxation of the peers, A and B, towards a common thermal-like state. This conjecture is fully corroborated by an exact diagonalization of several quantum models.

cond-mat.stat-mech↗

arXiv2009

A real-time study of diffusive and ballistic transport in spin-1/2 chains using the adaptive time-dependent density matrix renormalization group method

Using the adaptive time-dependent density matrix renormalization group method, we numerically study the spin dynamics and transport in one-dimensional spin-1/2 systems at zero temperature. Instead of computing transport coefficients from linear response theory, we study the real-time evolution of the magnetization starting from spatially inhomogeneous initial states. In particular, we are able to analyze systems far away from equilibrium with this set-up. By computing the time-dependence of the variance of the magnetization, we can distinguish diffusive from ballistic regimes, depending on model parameters. For the example of the anisotropic spin-1/2 chain and at half filling, we find the expected ballistic behavior in the easy-plane phase, while in the massive regime the dynamics of the magnetization is diffusive. Our approach allows us to tune the deviation of the initial state from the ground state and the qualitative behavior of the dynamics turns out to be valid even for highly perturbed initial states in the case of easy-plane exchange anisotropies. We further cover two examples of nonintegrable models, the frustrated chain and the two-leg spin ladder, and we encounter diffusive transport in all massive phases. In the former system, our results indicate ballistic behavior in the critical phase. We discuss our findings in view of experiments on quasi-one dimensional quantum magnets and we propose that the study of the time-dependence of the spatial variance of particle densities could be instrumental in the characterization of the expansion of ultracold atoms in optical lattices as well.

cond-mat.str-el↗

arXiv2009

Projection operator approach to lifetimes of electrons in metals

We present an alternative approach to the calculation of the lifetime of a single excited electron (hole) which interacts with the Fermi sea of electrons in a metal. The metal is modelled on the level of a Hamilton operator comprising a pertinent dispersion relation and scattering term. To determine the full relaxation dynamics we employ an adequate implementation of the time-convolutionless projection operator method (TCL). This yields an analytic expression for the decay rate which allows for an intuitive interpretation in terms of scattering events. It may furthermore be efficiently evaluated by means of a Monte-Carlo integration scheme. As an example we investigate aluminium using, just for simplicity, a jellium-type model. This way we obtain data which are directly comparable to results from a self-energy formalism. Our approach applies to arbitrary temperatures.

cond-mat.mes-hall↗

arXiv2009

Generalizations of the Brachistochrone Problem

Consider a frictionless surface S in a gravitational field that need not be uniform. Given two points A and B on S, what curve is traced out by a particle that starts at A and reaches B in the shortest time? This paper considers this problem on simple surfaces such as surfaces of revolution and solves the problem two ways: First, we use conservation of mechanical energy and the Euler-Lagange equation; second, we use geometrical optics and the eikonal equation. We conclude with a discussion of the relativistic effects at relativistic velocities.

math-ph↗

arXiv2003

Scaling behavior of interactions in a modular quantum system and the existence of local temperature

We consider a quantum system of fixed size consisting of a regular chain of $n$-level subsystems, where $n$ is finite. Forming groups of $N$ subsystems each, we show that the strength of interaction between the groups scales with $N^{- 1/2}$. As a consequence, if the total system is in a thermal state with inverse temperature $β$, a sufficient condition for subgroups of size $N$ to be approximately in a thermal state with the same temperature is $\sqrt{N} \gg β\bar{δE}$, where $\bar{δE}$ is the width of the occupied level spectrum of the total system. These scaling properties indicate on what scale local temperatures may be meaningfully defined as intensive variables. This question is particularly relevant for non-equilibrium scenarios such as heat conduction etc.

quant-ph↗

arXiv2003

Relaxation into equilibrium under pure Schrödinger dynamics

We consider bipartite quantum systems that are described completely by a state vector $|Ψ(t)>$ and the fully deterministic Schrödinger equation. Under weak constraints and without any artificially introduced decoherence or irreversibility, the smaller of the two subsystems shows thermodynamic behaviour like relaxation into an equilibrium, maximization of entropy and the emergence of the Boltzmann energy distribution. This generic behaviour results from entanglement.

quant-ph↗

arXiv2003

On the concept of pressure in quantum mechanics

Heat and work are fundamental concepts for thermodynamical systems. When these are scaled down to the quantum level they require appropriate embeddings. Here we show that the dependence of the particle spectrum on system size giving rise to a formal definition of pressure can, indeed, be correlated with an external mechanical degree of freedom, modelled as a spatial coordinate of a quantum oscillator. Under specific conditions this correlation is reminiscent of that occurring in the classical manometer.

quant-ph↗

arXiv2002

Distribution of local entropy in the Hilbert space of bi-partite quantum systems: Origin of Jaynes' principle

For a closed bi-partite quantum system partitioned into system proper and environment we interprete the microcanonical and the canonical condition as constraints for the interaction between those two subsystems. In both cases the possible pure-state trajectories are confined to certain regions in Hilbert space. We show that in a properly defined thermodynamical limit almost all states within those accessible regions represent states of some maximum local entropy. For the microcanonical condition this dominant state still depends on the initial state; for the canonical condition it coincides with that defined by Jaynes' principle. It is these states which thermodynamical systems should generically evolve into.

quant-ph↗

arXiv2002

Failure of Effective Potential Approach: Nucleus-Electron Entanglement in the He-Ion

Entanglement may be considered a resource for quantum-information processing, as the origin of robust and universal equilibrium behaviour, but also as a limit to the validity of an effective potential approach, in which the influence of certain interacting subsystems is treated as a potential. Here we show that a closed three particle (two protons, one electron) model of a He-ion featuring realistic size, interactions and energy scales of electron and nucleus, respectively, exhibits different types of dynamics depending on the initial state: For some cases the traditional approach, in which the nucleus only appears as the center of a Coulomb potential, is valid, in others this approach fails due to entanglement arising on a short time-scale. Eventually the system can even show signatures of thermodynamical behaviour, i.e. the electron may relax to a maximum local entropy state which is, to some extent, independent of the details of the initial state.

quant-ph↗

arXiv2001

Entanglement and the factorization-approximation

For a bi-partite quantum system defined in a finite dimensional Hilbert space we investigate in what sense entanglement change and interactions imply each other. For this purpose we introduce an entanglement operator, which is then shown to represent a non-conserved property for any bi-partite system and any type of interaction. This general relation does not exclude the existence of special initial product states, for which the entanglement remains small over some period of time, despite interactions. For this case we derive an approximation to the full Schroedinger equation, which allows the treatment of the composite systems in terms of product states. The induced error is estimated. In this factorization-approximation one subsystem appears as an effective potential for the other. A pertinent example is the Jaynes-Cummings model, which then reduces to the semi-classical rotating wave approximation.

quant-ph↗