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Register a new userGain and loss in open quantum systems
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Photosynthesis is the basic process used by plants to convert light energy in reaction centers into chemical energy. The high efficiency of this process is not yet understood today. Using the formalism for the description of open quantum systems by means of a non-Hermitian Hamilton operator, we consider initially the interplay of gain (acceptor) and loss (donor). Near singular points it causes fluctuations of the cross section which appear without any excitation of internal degrees of freedom of the system. This process occurs therefore very quickly and with high efficiency. We then consider the excitation of resonance states of the system by means of these fluctuations. This second step of the whole process takes place much slower than the first one, because it involves the excitation of internal degrees of freedom of the system. The two-step process as a whole is highly efficient and the decay is bi-exponential. We provide, if possible, the results of analytical studies, otherwise characteristic numerical results. The similarities of the obtained results to light harvesting in photosynthetic organisms are discussed.
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We consider different properties of small open quantum systems coupled to an environment and described by a non-Hermitian Hamilton operator. Of special interest is the non-analytical behavior of the eigenvalues in the vicinity of singular points, the so-called exceptional points (EPs), at which the eigenvalues of two states coalesce and the corresponding eigenfunctions are linearly dependent from one another. The phases of the eigenfunctions are not rigid in approaching an EP and providing therewith the possibility to put information from the environment into the system. All characteristic properties of non-Hermitian quantum systems hold true not only for natural open quantum systems that suffer loss due to their embedding into the continuum of scattering wavefunctions. They appear also in systems coupled to different layers some of which provide gain to the system. Thereby gain and loss, respectively, may be fixed inside every layer, i.e. characteristic of it.
We present the novel approach to mathematical modeling of information processes in biosystems. It explores the mathematical formalism and methodology of quantum theory, especially quantum measurement theory. This approach is known as {it quantum-like} and it should be distinguished from study of genuine quantum physical processes in biosystems (quantum biophysics, quantum cognition). It is based on quantum information representation of biosystems state and modeling its dynamics in the framework of theory of open quantum systems. This paper starts with the non-physicist friendly presentation of quantum measurement theory, from the original von Neumann formulation to modern theory of quantum instruments. Then, latter is applied to model combinations of cognitive effects and gene regulation of glucose/lactose metabolism in Escherichia coli bacterium. The most general construction of quantum instruments is based on the scheme of indirect measurement, in that measurement apparatus plays the role of the environment for a biosystem. The biological essence of this scheme is illustrated by quantum formalization of Helmholtz sensation-perception theory. Then we move to open systems dynamics and consider quantum master equation, with concentrating on quantum Markov processes. In this framework, we model functioning of biological functions such as psychological functions and epigenetic mutation.
A generic and intuitive model for coherent energy transport in multiple minima systems coupled to a quantum mechanical bath is shown. Using a simple spin-boson system, we illustrate how a generic donor-acceptor system can be brought into resonance using a narrow band of vibrational modes, such that the transfer efficiency of an electron-hole pair (exciton) is made arbitrarily high. Coherent transport phenomena in nature are of renewed interest since the discovery that a photon captured by the light-harvesting complex (LHC) in photosynthetic organisms can be conveyed to a chemical reaction centre with near-perfect efficiency. Classical explanations of the transfer use stochastic diffusion to model the hopping motion of a photo-excited exciton. This accounts inadequately for the speed and efficiency of the energy transfer measured in a series of recent landmark experiments. Taking a quantum mechanical perspective can help capture the salient features of the efficient part of that transfer. To show the versatility of the model, we extend it to a multiple minima system comprising seven-sites, reminiscent of the widely studied Fenna-Matthews-Olson (FMO) light-harvesting complex. We show that an idealised transport model for multiple minima coupled to a narrow-band phonon can transport energy with arbitrarily high efficiency.
In 2D electronic spectroscopy studies, long-lived quantum beats have recently been observed in photosynthetic systems, and it has been suggested that the beats are produced by quantum mechanically mixed electronic and vibrational states. Concerning the electronic-vibrational quantum mixtures, the impact of protein-induced fluctuations was examined by calculating the 2D electronic spectra of a weakly coupled dimer with vibrational modes in the resonant condition [J. Chem. Phys. 142, 212403 (2015)]. This analysis demonstrated that quantum mixtures of the vibronic resonance are rather robust under the influence of the fluctuations at cryogenic temperatures, whereas the mixtures are eradicated by the fluctuations at physiological temperatures. However, this conclusion cannot be generalized because the magnitude of the coupling inducing the quantum mixtures is proportional to the inter-pigment coupling. In this study, we explore the impact of the fluctuations on electronic-vibrational quantum mixtures in a strongly coupled dimer. with an off-resonant vibrational mode. Toward this end, we calculate electronic energy transfer (EET) dynamics and 2D electronic spectra of a dimer that corresponds to the most strongly coupled bacteriochlorophyll molecules in the Fenna-Matthews-Olson complex in a numerically accurate manner. The quantum mixtures are found to be robust under the exposure of protein-induced fluctuations at cryogenic temperatures, irrespective of the resonance. At 300 K, however, the quantum mixing is disturbed more strongly by the fluctuations, and therefore, the beats in the 2D spectra become obscure even in a strongly coupled dimer with a resonant vibrational mode. Further, the overall behaviors of the EET dynamics are demonstrated to be dominated by the environment and coupling between the 0-0 vibronic transitions as long as the Huang-Rhys factor of the vibrational mode is small.
A universal scheme is introduced to speed up the dynamics of a driven open quantum system along a prescribed trajectory of interest. This framework generalizes counterdiabatic driving to open quantum processes. Shortcuts to adiabaticity designed in this fashion can be implemented in two alternative physical scenarios: one characterized by the presence of balanced gain and loss, the other involves non-Markovian dynamics with time-dependent Lindblad operators. As an illustration, we engineer superadiabatic cooling, heating, and isothermal strokes for a two-level system, and provide a protocol for the fast thermalization of a quantum oscillator.
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