We show that quantum coherence of biomolecular excitons is maintained over exceedingly long times due to the constructive role of their non-Markovian protein-solvent environment. Using a numerically exact approach, we demonstrate that a slow quantum bath helps to sustain quantum entanglement of two pairs of Förster coupled excitons, in contrast to a Markovian environment. We consider the crossover from a fast to a slow bath and from weak to strong dissipation and show that a slow bath can generate robust entanglement. This persists to surprisingly high temperatures, even higher than the excitonic gap and is absent for a Markovian bath.
We present numerically exact results for the quantum coherent energy transfer in the Fenna-Matthews-Olson molecular aggregate under realistic physiological conditions, including vibrational fluctuations of the protein and the pigments for an experimentally determined fluctuation spectrum. We find coherence times shorter than observed experimentally. Furthermore, we determine the energy transfer current and quantify its "quantumness" as the distance of the density matrix to the classical pointer states for the energy current operator. Most importantly, we find that the energy transfer happens through a "Schrödinger-cat-like" superposition of energy current pointer states.
We show that the quantum coherent transfer of excitations between biomolecular chromophores is strongly influenced by spatial correlations of the environmental fluctuations. The latter are due either to propagating environmental modes or to local fluctuations with a finite localization length. A simple toy model of a single donor-acceptor pair with spatially separated chromophore sites allows to investigate the influence of these spatial correlations on the quantum coherent excitation transfer. The sound velocity of the solvent determines the wave lengths of the environmental modes, which, in turn, has to be compared to the spatial distance of the chromophore sites. When the wave length exceeds the distance between donor and acceptor site, we find strong suppression of decoherence. In addition, we consider two spatially separated donor-acceptor pairs under the influence of propagating environmental modes. Depending on their wave lengths fixed by the sound velocity of the solvent material, the spatial range of correlations may extend over typical interpair distances, which can lead to an increase of the decohering influence of the solvent. Surprisingly, this effect is counteracted by increasing temperature.
We study Landau-Zener transitions in a dissipative environment by means of the numerically exact quasiadiabatic propagator path integral. It allows to cover the full range of the involved parameters. We discover a nonmonotonic dependence of the transition probability on the sweep velocity which is explained in terms of a simple phenomenological model. This feature, not captured by perturbative approaches, results from a nontrivial competition between relaxation and the external sweep.
We show that the low-frequency modes of a sub-Ohmic bosonic heat bath generate an effective dynamical asymmetry for an intrinsically symmetric quantum spin−1/2. An initially fully polarized spin first decays towards a quasiequilibrium determined by the dynamical asymmetry, thereby showing coherent damped oscillations on the (fast) time scale of the spin splitting. On top of this, the dynamical asymmetry itself decays on an ultraslow time scale and vanishes asymptotically since the global equilibrium phase is symmetric. We quantitatively study the nature of the initial fast decay to the quasiequilibrium and discuss the features of ultraslow dynamics of the quasiequilibrium itself. The dynamical asymmetry is more pronounced for smaller values of the sub-Ohmic exponent and for lower temperatures, which emphasizes the quantum many-body nature of the effect. The symmetry breaking is related to the dynamic crossover between coherent and overdamped relaxation of the spin polarization and is not connected to the localization quantum phase transition. In addition to this delocalized phase, we identify a novel phase which is characterized by damped coherent oscillations in the localized phase. This allows for a sketch of the zero-temperature phase diagram of the sub-Ohmic spin-boson model with four distinct phases.
We have performed broad-band two-dimensional (2D) electronic spectroscopy of light-harvesting complex II (LHCII) at ambient temperature. We found that electronic dephasing occurs within ∼60 fs and inhomogeneous broadening is approximately 120 cm(-1). A three-dimensional global fit analysis allows us to identify several time scales in the dynamics of the 2D spectra ranging from 100 fs to ∼10 ps and to uncover the energy-transfer pathways in LHCII. In particular, the energy transfer between the chlorophyll b and chlorophyll a pools occurs within ∼1.1 ps. Retrieved 2D decay-associated spectra also uncover the spectral positions of corresponding diagonal peaks in the 2D spectra. Residuals in the decay traces exhibit periodic modulations with different oscillation periods. However, only one of them can be associated with the excitonic cross-peaks in the 2D spectrum, while the remaining ones are presumably of vibrational origin. For the interpretation of the spectroscopic data, we have applied a refined exciton model for LHCII. It reproduces the linear absorption, circular dichroism, and 2D spectra at different waiting times. Several components of the energy transport are revealed from theoretical simulations that agree well with the experimental observations.
We investigate an artificial molecular dimer made of two dipole coupled cyanine dye monomers in which a strong coherent coupling between electronic and vibrational degrees of freedom arises. Clear signatures of this coupling are reflected in an oscillatory time evolution of the off-diagonal vibronic cross peaks in the two-dimensional optical photon echo spectrum. We find a strong coherence component damped by fast electronic dephasing ( 50 ≈ fs) accompanied by a much weaker component which decays on the longer time scales (ps) associated to vibrational dephasing. We find that vibronic coupling does not cause longer dephasing times of the dominant photo echo component but additional weak but long-lived components emerge.
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