Ultrafast energy transfer is used to transmit electronic excitation among the many molecules in photosynthetic antenna complexes. Recent experiments and theories have highlighted the role of coherent transfer in femtosecond studies of these proteins, suggesting the need for accurate dynamical models to capture the subtle characteristics of energy transfer mechanisms. Here we discuss how to think about coherence in light harvesting and electronic energy transfer. We review the various fundamental concepts of coherence, spanning from classical phenomena to the quantum superposition, and define coherence in electronic energy transfer. We describe the current status of experimental studies on light-harvesting complexes. Insights into the microscopic process are presented to highlight how and why this is a challenging problem to elucidate. We present an overview of the applicable dynamical theories to model energy transfer in the intermediate coupling regime.

We introduce a scheme for the quantum simulation of many-body decoherence based on the unitary evolution of a stochastic Hamiltonian. Modulating the strength of the interactions with stochastic processes, we show that the noise-averaged density matrix simulates an effectively open dynamics governed by $k$-body Lindblad operators. Markovian dynamics can be accessed with white-noise fluctuations; non-Markovian dynamics requires colored noise. The time scale governing the fidelity decay under many-body decoherence is shown to scale as $N^{-2k}$ with the system size $N$. Our proposal can be readily implemented in a variety of quantum platforms including optical lattices, superconducting circuits, and trapped ions.

A vibronic-exciton model is applied to investigate the recently proposed mechanism of enhancement of coherent oscillations due to mixing of electronic and nuclear degrees of freedom. We study a dimer system to elucidate the role of resonance coupling, site energies, vibrational frequency and energy disorder in the enhancement of vibronic-exciton and ground-state vibrational coherences and to identify regimes where this enhancement is significant. For a heterodimer representing two coupled bachteriochloropylls of the FMO complex, long-lived vibronic coherences are found to be generated only when the frequency of the mode is in the vicinity of the electronic energy difference. Although the vibronic-exciton coherences exhibit a larger initial amplitude compared to the ground-state vibrational coherences, we conclude that, due to the dephasing of the former, both type of coherences have a similar magnitude at longer population time.

Friction in quantum thermodynamics results from fast driving schemes that generate nonadiabatic excitations.

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.

We study the ultimate limits to the decoherence rate associated with dephasing processes. Fluctuating chaotic quantum systems are shown to exhibit extreme decoherence, with a rate that scales exponentially with the particle number, thus exceeding the polynomial dependence of systems with fluctuating $k$-body interactions. Our findings suggest the use of quantum chaotic systems as a natural test bed for spontaneous wave function collapse models. We further discuss the implications on the decoherence of AdS/CFT black holes resulting from the unitarity loss associated with energy dephasing.