59,174 research outputs found

    Exact closed master equation for Gaussian non-Markovian dynamics

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    Non-Markovian master equations describe general open quantum systems when no approximation is made. We provide the exact closed master equation for the class of Gaussian, completely positive, trace preserving, non-Markovian dynamics. This very general result allows to investigate a vast variety of physical systems. We show that the master equation for non-Markovian quantum Brownian motion is a particular case of our general result. Furthermore, we derive the master equation unraveled by a non-Markovian, dissipative stochastic Schr\"odinger equation, paving the way for the analysis of dissipative non-Markovian collapse models

    A class of commutative dynamics of open quantum systems

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    We analyze a class of dynamics of open quantum systems which is governed by the dynamical map mutually commuting at different times. Such evolution may be effectively described via spectral analysis of the corresponding time dependent generators. We consider both Markovian and non-Markovian cases.Comment: 22 page

    Post-Markovian quantum master equations from classical environment fluctuations

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    In this paper we demonstrate that two commonly used phenomenological post-Markovian quantum master equations can be derived without using any perturbative approximation. A system coupled to an environment characterized by self-classical configurational fluctuations, the latter obeying a Markovian dynamics, defines the underlying physical model. Both Shabani-Lidar equation [A. Shabani and D. A. Lidar, Phys. Rev. A 71, 020101(R) (2005)] and its associated approximated integro-differential kernel master equation are obtained by tracing out two different bipartite Markovian Lindblad dynamics where the environment fluctuations are taken into account by an ancilla system. Furthermore, conditions under which the non-Markovian system dynamics can be unravelled in terms of an ensemble of measurement trajectories are found. In addition, a non-Markovian quantum jump approach is formulated. Contrary to recent analysis [L. Mazzola, E. M. Laine, H. P. Breuer, S. Maniscalco, and J. Piilo, Phys. Rev. A 81, 062120 (2010)], we also demonstrate that these master equations, even with exponential memory functions, may lead to non-Markovian effects such as an environment-to-system backflow of information if the Hamiltonian system does not commutate with the dissipative dynamics.Comment: 13 pages, 4 figure

    Reactive conformations and non-Markovian reaction kinetics of a Rouse polymer searching for a target in confinement

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    We investigate theoretically a diffusion-limited reaction between a reactant attached to a Rouse polymer and an external fixed reactive site in confinement. The present work completes and goes beyond a previous study [T. Gu\'erin, O. B\'enichou and R. Voituriez, Nat. Chem., 4, 268 (2012)] that showed that the distribution of the polymer conformations at the very instant of reaction plays a key role in the reaction kinetics, and that its determination enables the inclusion of non-Markovian effects in the theory. Here, we describe in detail this non-Markovian theory and we compare it with numerical stochastic simulations and with a Markovian approach, in which the reactive conformations are approximated by equilibrium ones. We establish the following new results. Our analysis reveals a strongly non-Markovian regime in 1D, where the Markovian and non-Markovian dependance of the relation time on the initial distance are different. In this regime, the reactive conformations are so different from equilibrium conformations that the Markovian expressions of the reaction time can be overestimated by several orders of magnitudes for long chains. We also show how to derive qualitative scaling laws for the reaction time in a systematic way that takes into account the different behaviors of monomer motion at all time and length scales. Finally, we also give an analytical description of the average elongated shape of the polymer at the instant of the reaction and we show that its spectrum behaves a a slow power-law for large wave numbers
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