arXiv subjects

Aurélia Chenu

Publications and source records attributed to Aurélia Chenu.

31 records · Page 2Linked to original sources

arXiv2018

Quantum work statistics, Loschmidt echo and information scrambling

A universal relation is established between the quantum work probability distribution of an isolated driven quantum system and the Loschmidt echo dynamics of a two-mode squeezed state. When the initial density matrix is canonical, the Loschmidt echo of the purified double thermofield state provides a direct measure of information scrambling and can be related to the analytic continuation of the partition function. Information scrambling is then described by the quantum work statistics associated with the time-reversal operation on a single copy, associated with the sudden negation of the system Hamiltonian.

quant-ph↗

arXiv2018

Shortcuts to adiabaticity in Fermi gases

Shortcuts to adiabaticity (STA) provide an alternative to adiabatic protocols to guide the dynamics of the system of interest without the requirement of slow driving. We report the controlled speedup via STA of the nonadiabatic dynamics of a Fermi gas, both in the non-interacting and strongly coupled, unitary regimes. Friction-free superadiabatic expansion strokes, with no residual excitations in the final state, are demonstrated in the unitary regime by engineering the modulation of the frequencies and aspect ratio of the harmonic trap. STA are also analyzed and implemented in the high-temperature regime, where the shear viscosity plays a pivotal role and the Fermi gas is described by viscous hydrodynamics.

quant-ph↗

arXiv2018

Friction-free quantum machines

The operation of a quantum heat engine in finite time generally faces a trade-off between efficiency and power. Using shortcuts to adiabaticity (STA), this trade off can be avoided to engineer thermal machines that operate at maximum efficiency and tunable output power. We demonstrate the use of STA to engineer a scalable superadiabatic quantum Otto cycle and report recent experimental progress to tailor quantum friction in finite-time quantum thermodynamics. In the presence of quantum friction, it is also shown that the use of a many-particle working medium can boost the performance of the quantum machines with respect to an ensemble of single-particle thermal machines.

quant-ph↗

arXiv2017

Many-body formalism for thermally excited wave-packets: A way to connect the quantum regime to the classical regime

Free classical particles have well-defined momentum and position, while free quantum particles have well-defined momentum but a position fully delocalized over the sample volume. We develop a many-body formalism based on wave-packet operators that connects these two limits, the thermal energy being distributed between the state spatial extension and its thermal excitation. The corresponding `mixed quantum-classical' states, which render the Boltzmann operator diagonal, are the physically relevant states when the temperature is finite. The formulation of many-body Hamiltonians in terms of these thermally excited wave-packets and the resulting effective scatterings is provided.

quant-ph↗

arXiv2017

Superadiabatic quantum friction suppression in finite-time thermodynamics

Optimal performance of thermal machines is reached by suppressing friction. Friction in quantum thermodynamics results from fast driving schemes that generate nonadiabatic excitations. The far-from-equilibrium dynamics of quantum devices can be tailored by shortcuts to adiabaticity to suppress quantum friction. We experimentally demonstrate friction-free superadiabatic strokes with a trapped unitary Fermi gas as a working substance and establish the equivalence between the superadiabatic mean work and its adiabatic value.

cond-mat.quant-gas↗

arXiv2017

Light Adaptation in Phycobilisome antennas: Influence on the Rod Length and Structural Arrangement

Phycobilisomes, the light-harvesting antennas of cyanobacteria, can adapt to a wide range of environments thanks to a composition and function response to stress conditions. We study how structural changes influence excitation transfer in these super-complexes. Specifically, we show the influence of the rod length on the photon absorption and subsequent excitation transport to the core. Despite the fact that the efficiency of individual disks on the rod decreases with increasing rod length, we find an optimal length for which the average rod efficiency is maximal. Combining this study with experimental structural measurements, we propose models for the arrangement of the phycobiliproteins inside the thylakoid membranes, evaluate the importance of rod length, and predict the corresponding transport properties for different cyanobacterial species. This analysis, which links the functional and structural properties of full phycobilisome complexes, thus provides further rationals to help resolving their exact structure.

physics.chem-ph↗

arXiv2017

Quantum Simulation of Generic Many-Body Open System Dynamics Using Classical Noise

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.

quant-ph↗

arXiv2017

Construction of Multi-Chromophoric Spectra from Monomer Data: Applications to Resonant Energy Transfer

We develop a model that establishes a quantitative link between the physical properties of molecular aggregates and their constituent building blocks. The relation is built on the coherent potential approximation, calibrated against exact results, and proven reliable for a wide range of parameters. It provides a practical method to compute spectra and transfer rates in multi-chromophoric systems from experimentally accessible monomer data. Applications to Förster energy transfer reveal optimal transfer rates as functions of both the system-bath coupling and intra-aggregate coherence.

physics.chem-ph↗

arXiv2016

Thermal light cannot be represented as a statistical mixture of single pulses

We ask whether or not thermal light can be represented as a mixture of single broadband coherent pulses. We find that it cannot. Such a mixture is simply not rich enough to mimic thermal light; indeed, it cannot even reproduce the first-order correlation function. We show that it is possible to construct a modified mixture of single coherent pulses that does yield the correct first-order correlation function at equal space points. However, as we then demonstrate, such a mixture cannot reproduce the second-order correlation function.

quant-ph↗

arXiv2015

Transform-Limited-Pulse Representation of Excitation with Natural Incoherent Light

We study the natural excitation of molecular systems, applicable to, for example, photosynthetic light-harvesting complexes, by natural incoherent light. In contrast with the conventional classical models, we show that the light need not have random character to properly represent the resultant linear excitation. Rather, thermal excitation can be interpreted as a collection of individual events resulting from the system's interaction with individual, deterministic pulsed realizations that constitute the field. The derived expressions for the individual field realizations and excitation events allow for a wave function formalism, and therefore constitute a useful calculational tool to study dynamics following thermal-light excitation. Further, they provide a route to the experimental determination of natural incoherent excitation using pulsed laser techniques.

physics.chem-ph↗

arXiv2014

First-order decomposition of thermal light in terms of a statistical mixture of pulses

We investigate the connection between thermal light and coherent pulses, constructing mixtures of single pulses that yield the same first-order, equal-space-point correlation function as thermal light. We present mixtures involving (i) pulses with a Gaussian lineshape and narrow bandwidths, and (ii) pulses with a coherence time that matches that of thermal light. We characterize the properties of the mixtures and pulses. Our results introduce an alternative description of thermal light in terms of multi-frequency coherent states, valid for the description of broadband linear light-matter interactions. We anticipate our results will be relevant to time-resolved measurements that aim to probe the dynamics of systems as if they were excited by natural thermal light.

quant-ph↗

arXiv2013

Dynamic Coherence in Excitonic Molecular Complexes under Various Excitation Conditions

We investigate the relevance of dynamic quantum coherence in the energy transfer efficiency of molecular aggregates. We contrast the dynamics after excitation of a quantum mechanical system with that of a classical system. We demonstrate how a classical description of an ensemble average can be satisfactorily interpreted either as a single system driven by a continuous force or as an ensemble of systems each driven by an impulsive force. We derive the time evolution of the density matrix for an open quantum system excited by light or by a neighboring antenna. We argue that unlike in the classical case, the quantum description does not allow for a formal decomposition of the dynamics into sudden jumps in the quantum mechanical state. Rather, there is a natural finite time-scale associated with the excitation process. We propose a simple experiment how to test the influence of this time scale on the yield of photosynthesis. Because photosynthesis is intrinsically an average process, the efficiency of photosynthesis can be assessed from the quantum mechanical expectation value calculated from the second-order response theory, which has the same validity as the perturbative description of ultrafast experiments. We demonstrate using typical parameters of the currently most studied photosynthetic antenna, the Fenna-Matthews-Olson (FMO) complex, and a typical energy transfer rate from the chlorosome baseplate, that dynamic coherences are averaged out in the complex despite excitation proceeding through a coherent superposition of its eigenstates. The dynamic coherence averages out even when the FMO model is completely free of all dissipation and dephasing. We conclude that under natural excitation conditions coherent dynamics cannot be responsible for the remarkable efficiency of the photosynthesis even when considering the dynamics at a single molecular level.

physics.bio-ph↗

arXiv2012

Enhancement of Vibronic and Ground-State Vibrational Coherences in 2D Spectra of Photosynthetic Complexes

A vibronic-exciton model is applied to investigate the mechanism of enhancement of coherent oscillations due to mixing of electronic and nuclear degrees of freedom recently proposed as the origin of the long-lived oscillations in 2D spectra of the FMO complex [Christensson et al. J. Phys. Chem. B 116 (2012) 7449]. We reduce the problem to a model BChl dimer to elucidate the role of resonance coupling, site energies, nuclear mode 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 the two coupled BChls 3 and 4 of the FMO complex, the initial amplitude of the vibronic-exciton and vibrational coherences are enhanced by up to 15 and 5 times, respectively, compared to the vibrational coherences in the isolated monomer. This maximum initial amplitude enhancement occurs when there is a resonance between the electronic energy gap and the frequency of the vibrational mode. The bandwidth of this enhancement is about 100 cm-1 for both mechanisms. The excitonic mixing of electronic and vibrational DOF leads to additional dephasing relative to the vibrational coherences. We evaluate the dephasing dynamics by solving the quantum master equation in Markovian approximation and observe a strong dependence of the life-time enhancement on the mode frequency. Long-lived vibronic-exciton coherences are found to be generated only when the frequency of the mode is in the vicinity of the electronic resonance. Although the vibronic-exciton coherences exhibit a larger initial amplitude compared to the ground-state vibrational coherences, we conclude that both type have a similar magnitude at long time for the present model. The ability to distinguish between vibronic-exciton and ground-state vibrational coherences in the general case of molecular aggregate is discussed.

physics.chem-ph↗