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arXiv:0706.2536 · Journal of Physics B Atomic Molecular and Optical Physics

Exact wave packet decoherence dynamics in a discrete spectrum environment

Matisse Wei-Yuan Tu, Wei-Min Zhang

Published Dec 1, 2008• 0 citations
arXivHTMLPDF

Abstract

We find an exact analytical solution of the reduced density matrix from the Feynman-Vernon influence functional theory for a wave packet influenced by an environment containing a few discrete modes. We obtain two intrinsic energy scales relating to the time scales of the system and the environment. Different relationship between these two scales alters the overall form of the solution of the system. We also introduce a decoherence measure for a single wave packet which is defined as the ratio of Schrödinger uncertainty over the delocalization extension of the wave packet and characterizes the time-evolution behavior of the off-diagonal reduced density matrix element. We utilize the exact solution and the docherence measure to study the wave packet decoherence dynamics. We further demonstrate how the dynamical diffusion of the wave packet leads to non-Markovian decoherence in such a microscopic environment.

DOI
10.1088/0953-4075/41/24/245501

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We find an exact analytical solution of the reduced density matrix from the Feynman-Vernon influence functional theory for a wave packet influenced by an environment containing a few discrete modes. We obtain two intrinsic energy scales relating to the time scales of the system and the environment. Different relationship between these two scales alters the overall form of the solution of the system. We also introduce a decoherence measure for a single wave packet which is defined as the ratio of Schrödinger uncertainty over the delocalization extension of the wave packet and characterizes the time-evolution behavior of the off-diagonal reduced density matrix element. We utilize the exact solution and the docherence measure to study the wave packet decoherence dynamics. We further demonstrate how the dynamical diffusion of the wave packet leads to non-Markovian decoherence in such a microscopic environment.
Abstract The time evolution of wave packets in the Morse potential is investigated under the influence of the environment consisting of harmonic oscillators. We obtain a Markovian master equation that incorporates the fact that due to the nonequidistant spectrum, the relaxation rate of each energy eigenstate is different. The nonunitary time evolution is visualized by the aid of the Wigner function related to the reduced density operator of the Morse system. The time scale of decoherence is much shorter than that of dissipation, and gives rise to states which are mixtures of localized states along the phase space orbit of the corresponding classical particle. This behaviour is to a large extent independent of the coupling strength, the temperature of the environment and also of the initial state.
We microscopically model the decoherence dynamics of entangled coherent states under the influence of vacuum fluctuation. We derive an exact master equation with time-dependent coefficients reflecting the memory effect of the environment, by using the Feynman-Vernon influence functional theory in the coherent-state representation. Under the Markovian approximation, our master equation recovers the widely used Lindblad equation in quantum optics. We then investigate the non-Markovian entanglement dynamics of the quantum channel in terms of the entangled coherent states under noise. Compared with the results in Markovian limit, it shows that the non-Markovian effect enhances the disentanglement to the initially entangled coherent state. Our analysis also shows that the decoherence behaviors of the entangled coherent states depend sensitively on the symmetrical properties of the entangled coherent states as well as the interactions between the system and the environment.
The act of measurement on a quantum state is supposed to "dephase" (dephasing refers to the phenomenon that the states lose phase coherence; then the phases get randomized in interaction with a bath of other oscillators, which is referred to as "decoherence"), then "decohere" and "collapse" (or more precisely "register" and "reduce") the state into one of several eigenstates of the operator corresponding to the observable being measured. This measurement process is sometimes described as outside standard quantum-mechanical evolution and not calculable from Schrödinger's equation. Progress has, however, been made in studying this problem with two main calculation tools-one uses a time-independent Hamiltonian, while a rather more general approach proving that decoherence occurs under some generic conditions. The two general approaches to the study of wave-function collapse are as follows. The first approach, called the "consistent" or "decoherent"' histories approach, studies microscopic histories that diverge probabilistically and explains collapse as an event in our particular history. The other, referred to as the "environmental decoherence" approach studies the effect of the environment upon the quantum system, to explain wave-function decoherence which is produced by irreversible effects of various sorts. However, as we know, wave-function collapse is not related to thermal connection with the environment, rather, it is inherent to how measurements are performed by macroscopic apparata. In the "environmental decoherence" approach, one studies decoherence using a Markovian-approximated Master equation to study the time-evolution of the reduced density matrix (post dephasing) and obtains the long-time dependence of the off-diagonal elements of this matrix. The calculation in this paper studies the evolution of a quantum system starting with "dephasing" followed by the effects of the environment with some differences from prior analyses. We start from the Schrödinger equation for the state of the system, with a time-dependent Hamiltonian that reflects the actual microscopic interactions that are occurring. Then we systematically solve (exactly) for the time-evolved state, without invoking a Markovian approximation when writing out the effective time-evolution equation, i.e., keeping the evolution unitary until the end. This approach is useful, and it shows that the system wave-function will explicitly "un-collapse" if the measurement apparatus is sufficiently small. However, in the limit of a macroscopic system, this "dephasing" quickly leads to "decoherence"-collapse is a temporary state that will simply take extremely long (of the order of multiple universe lifetimes) to reverse. This has been attempted previously and our calculation is particularly simple and calculable. We make some connections to the work by Linden et al. while doing so. The calculation in this paper has interesting implications for the interpretation of the Wigner's friend experiment, as well as the Mott experiment, which is explored in "Connection to some general theoretical results" and "Recurrence times" (especially the enumerated points in "Recurrence times"). The upshot is that as long as Wigner's friend is macroscopically large (or uses a macroscopically large measuring instrument), no one needs to worry that Wigner would see something different from his friend. Indeed, Wigner's friend does not even need to be conscious during the measurement that she conducts. It also allows one to reasonably interpret some of the more recent thought experiments proposed. In particular, as a result of the mathematical analysis, the short-time behavior of a collapsing system, at least the one considered in this paper, is not exponential. Instead, it is the usual Fermi-golden rule result. The long-term behavior is, of course, still exponential. This is a second novel feature of the paper-we connect the short-term Fermi-golden rule (quadratic-in-time behavior) transition probability to the exponential long-time behavior of a collapsing wave-function in one continuous mathematical formulation.
The time evolution of wave packets in the Morse potential is investigated under the influence of the environment consisting of harmonic oscillators. These oscillators represent photon or phonon modes and are assumed to be in thermal equilibrium. Our model explicitly incorporates the fact that in the case of a nonequidistant spectrum the rates of the environment induced transitions are different for each transition. The nonunitary time evolution is visualized by the aid of the corresponding Wigner function. The time scale of decoherence is much shorter than that of dissipation, and gives rise to states that are mixtures of localized states along the phase-space orbit of the corresponding classical particle. This behavior is to a large extent independent of the coupling strength, the temperature of the environment, and also the initial state.
We investigate the entanglement dynamics of continuous-variable quantum channels in terms of an entangled squeezed state of two cavity fields in a general non-Markovian environment. Using the Feynman-Vernon influence functional theory in the coherent-state representation, we derive an exact master equation with time-dependent coefficients reflecting the non-Markovian influence of the environment. The influence of environments with different spectral densities, e.g., Ohmic, sub-Ohmic, and super-Ohmic, is numerically studied. The non-Markovian process shows its remarkable influence on the entanglement dynamics due to the sensitive time dependence of the dissipation and noise functions within the typical time scale of the environment. The Ohmic environment shows a weak dissipation-noise effect on the entanglement dynamics, while the sub-Ohmic and super-Ohmic environments induce much more severe noise. In particular, the memory of the system interacting with the environment contributes a strong decoherence effect to the entanglement dynamics in the super-Ohmic case.
We study a model of dephasing (decoherence) in a two-state quantum system (qubit) coupled to a bath of harmonic oscillators. An exact analytic solution for the reduced dynamics of a two-state system in this model has been obtained previously for factorizing initial states of the combined system. We show that the model admits exact solutions for a large class of correlated initial states which are typical in the theory of quantum measurements. We derive exact expressions for the off-diagonal elements of the qubit density matrix, which hold for an arbitrary strength of coupling between the qubit and the bath. The influence of initial correlations on decoherence is considered for different bath spectral densities. Time behavior of the qubit entropy in the decoherence process is discussed.