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中国物理B:英文版

Energy transfer and correlation dynamics in a three-quasi-spin-pigment system

张银苹, 李宏荣, 方爱萍, Chen Chun Hao, Li Fu Li

Published Jan 1, 2013• 0 citations
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Energy transfer and correlation dynamics in a three-quasi-spin-pigment system

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In this paper, the effects of quantum and classical correlations on the excitation energy transfer in a three-quasispin-pigment system are investigated. We first study the dependence of the energy transfer efficiency on various initial correlations of the donor pigments, and find that the initial concurrence is crucial to the efficiency no matter whether the initial states are pure or mixed. We then demonstrate the dynamics of correlations of the system and observe the appearance of sudden death of quantum correlations in the donor pigments. The relation between the energy transfer efficiency and the dynamics of correlations in the donor pigments is also discussed.

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Two chlorophylls of the FMO complex, the light-harvesting complex of the green sulfur bacteria, are modeled as two coupled qubits, each surrounded by one spin-bath simulating the environment. The dynamics of the system at a non-zero temperature provide exact analytical expressions for the transition probability and the coherence. It is shown that the decoherence-inducing interaction with the environment enhances the electronic energy transfer. Also the correlations in terms of entanglement and nonlocality are quantitatively studied, sensitively differing when introducing a decay term to resemble both chlorophylls being in their ground states. It is proved that nonlocality is a stronger form of correlation than entanglement.

•Jan 1, 2014•0 citations
In this paper, the effects of quantum and classical correlations on the excitation energy transfer in a three-quasispin-pigment system are investigated. We first study the dependence of the energy transfer efficiency on various initial correlations of the donor pigments, and find that the initial concurrence is crucial to the efficiency no matter whether the initial states are pure or mixed. We then demonstrate the dynamics of correlations of the system and observe the appearance of sudden death of quantum correlations in the donor pigments. The relation between the energy transfer efficiency and the dynamics of correlations in the donor pigments is also discussed.
Recently, long-lasting quantum effects in a number of photosynthetic complexes, which are pigment-protein molecular aggregates (PPMAs), were experimentally verified. These findings created an interest in trying to connect the known highly efficient excitation energy transfer (EET) in these systems to the existence of quantum effects such as quantum coherence and quantum correlations. It also raised the question of how these sensitive quantum effects can survive in such a macroscopic system. This thesis explores the existence and possible role of quantum effects in the EET in PPMAs. These systems can be modeled as non-Markovian open quantum systems and quantum effects can be investigated and quantified by methods developed in quantum information theory. Firstly, it is found that quantum nonlocal correlations in the EET in the Fenna-Matthews-Olson complex - a PPMA found in nature - are unlikely to exist when the initial excitation occurs in a natural manner. When the initial excitation occurs in an artificial manner by localization of the excitation on one pigment, nonlocal correlations exist on a short time scale. It is further found that in order for nonlocal correlations to be preserved in such a system, the excitation must be trapped on two pigments at the time and these pigments must not interact strongly with other pigments in the complex. Secondly, it is shown that quantum coherence is not in general a resource for efficient EET in model systems consisting of a network of pigments; systems optimized with respect to the amount of coherence do not coincide with systems with optimal EET efficiency between two end-site pigments. Thirdly, it is found that environmental effects and system-environment interactions can be tuned to optimize the EET efficiency in model PPMAs. The features of optimal environments highly depends on the structure of the pigment system and in particular, the relationship between the pigments excitation energies. It is further shown that a non-Markovian dynamics cannot be connected to an increased EET efficiency in these systems.
Two chlorophylls of the FMO complex, the light-harvesting complex of the green sulfur bacteria, are modeled as two coupled qubits, each surrounded by one spin-bath simulating the environment. The dynamics of the system at a non-zero temperature provide exact analytical expressions for the transition probability and the coherence. It is shown that the decoherence-inducing interaction with the environment enhances the electronic energy transfer. Also the correlations in terms of entanglement and nonlocality are quantitatively studied, sensitively differing when introducing a decay term to resemble both chlorophylls being in their ground states. It is proved that nonlocality is a stronger form of correlation than entanglement.