arXiv subjects

Alexander Eisfeld

Publications and source records attributed to Alexander Eisfeld.

At least 37 records · Page 2Linked to original sources

arXiv2019

Excitonic Wave Function Reconstruction from Near-Field Spectra Using Machine Learning Techniques

A general problem in quantum mechanics is the reconstruction of eigenstate wave functions from measured data. In the case of molecular aggregates, information about excitonic eigenstates is vitally important to understand their optical and transport properties. Here we show that from spatially resolved near field spectra it is possible to reconstruct the underlying delocalized aggregate eigenfunctions. Although this high-dimensional nonlinear problem defies standard numerical or analytical approaches, we have found that it can be solved using a convolutional neural network. For both one-dimensional and two-dimensional aggregates we find that the reconstruction is robust to various types of disorder and noise.

quant-ph↗

arXiv2018

Cavity-free quantum optomechanical cooling by atom-modulated radiation

We theoretically study the radiation-induced interaction between the mechanical motion of an oscillating mirror and a remotely trapped atomic cloud. When illuminated by continuous-wave radiation, the mirror motion will induce red and blue sideband radiation, which respectively increases and reduces motional excitation. We find that by suitably driving $Λ$-level atoms, the mirror correlation with a specific radiation sideband could be converted from the outgoing to the incoming radiation. Such process allows us to manipulate the heating and cooling effects. Particularly, we develop an optomechanical cooling strategy that can mutually cancel the heating effect of the outgoing and incoming radiations, thus the motional ground state is attainable by net cooling. Without the necessity of cavity installation or perfect alignment, our proposal complements other efforts in quantum cooling of macroscopic objects.

quant-ph↗

arXiv2017

Hierarchy of equations to calculate the linear spectra of molecular aggregates - Time-dependent and frequency domain formulation

In a recent publication [J. Chem. Phys. 142, 034115 (2015)] we have derived a hierarchy of coupled differential equations in time domain to calculate the linear optical properties of molecular aggregates. Here we provide details about issues concerning the numerical implementation. In addition we present the corresponding hierarchy in frequency domain.

physics.chem-ph↗

arXiv2017

Probing weak dipole-dipole interaction using phase-modulated non-linear spectroscopy

Phase-modulated non-linear spectroscopy with higher harmonic demodulation has recently been suggested to provide information on many-body excitations. In the present work we theoretically investigate the application of this method to infer the interaction strength between two particles that interact via weak dipole-dipole interaction. To this end we use full numerical solution of the Schrödinger equation with time-dependent pulses. For interpretation purpose we also derive analytical expressions in perturbation theory. We find one can detect dipole-dipole interaction via peak intensities (in contrast to line-shifts which typically are used in conventional spectroscopy). We provide a detailed study on the dependence of these intensities on the parameters of the laser pulse and the dipole-dipole interaction strength. Interestingly, we find that there is a phase between the first and second harmonic demodulated signal, whose value depends on the sign of the dipole-dipole interaction.

quant-ph↗

arXiv2017

Reservoir engineering with ultracold Rydberg atoms

We apply reservoir engineering to construct a thermal environment with controllable temperature in an ultracold atomic Rydberg system. A Boltzmann distribution of the system's eigenstates is produced by optically driving a small environment of ultracold atoms, which is coupled to a photonic continuum through spontaneous emission. This technique provides a useful tool for quantum simulation of dynamics coupled to a thermal environment. Additionally, we demonstrate that pure eigenstates, such as Bell states, can be prepared in the Rydberg atomic system using this method.

quant-ph↗

arXiv2016

Optomechanical interactions in non-Hermitian photonic molecules

We study optomechanical interactions in non-Hermitian photonic molecules that support two photonic states and one acoustic mode. The nonlinear steady-state solutions and their linear stability landscapes are investigated as a function of the system's parameters and excitation power levels. We also examine the temporal evolution of the system and uncover different regimes of nonlinear dynamics. Our analysis reveals several important results: (1) Parity-time ($\mathcal{PT}$) symmetry is not necessarily the optimum choice for maximum optomechanical interaction. (2) Stable steady-state solutions are not always reached under continuous wave (CW) optical excitations. (3) Accounting for gain saturation effects can regulate the behavior of the otherwise unbounded oscillation amplitudes. Our study provides a deeper insight into the interplay between optical non-Hermiticity and optomechanical coupling and can thus pave the way for new device applications.

physics.optics↗

arXiv2015

Open quantum system parameters from molecular dynamics

We extract the site energies and spectral densities of the Fenna-Matthews-Olson (FMO) pigment protein complex of green sulphur bacteria from simulations of molecular dynamics combined with energy gap calculations. Comparing four different combinations of methods, we investigate the origin of quantitative differences regarding site energies and spectral densities obtained previously in the literature. We find that different forcefields for molecular dynamics and varying local energy minima found by the structure relaxation yield significantly different results. Nevertheless, a picture averaged over these variations is in good agreement with experiments and some other theory results. Throughout, we discuss how vibrations external- or internal to the pigment molecules enter the extracted quantities differently and can be distinguished. Our results offer some guidance to set up more computationally intensive calculations for a precise determination of spectral densities in the future. These are required to determine absorption spectra as well as transport properties of light-harvesting complexes.

physics.bio-ph↗

arXiv2015

Pseudomodes and the corresponding transformation of the temperature-dependent bath correlation function

In open system approaches with non-Markovian environments, the process of inserting an individual mode (denoted as "pseudomode") into the bath or extracting it from the bath is widely employed. This procedure, however, is typically performed on basis of the spectral density (SD) and does not incorporate temperature. Here, we show how the - temperature-dependent - bath correlation function (BCF) transforms in such a process. We present analytic formulae for the transformed BCF and numerically study the differences between factorizing initial state and global thermal (correlated) initial state of mode and bath, respectively. We find that in the regime of strong coupling of the mode to both system and bath, the differences in the BCFs give rise to pronounced differences in the dynamics of the system.

quant-ph↗

arXiv2015

Towards Outperforming Classical Algorithms with Analog Quantum Simulators

With quantum computers being out of reach for now, quantum simulators are the alternative devices for efficient and more exact simulation of problems that are challenging on conventional computers. Quantum simulators are classified into analog and digital, with the possibility of constructing "hybrid" simulators by combining both techniques. In this paper, we focus on analog quantum simulators of open quantum systems and address the limit that they can beat classical computers. In particular, as an example, we discuss simulation of the chlorosome light-harvesting antenna from green sulfur bacteria with over 250 phonon modes coupled to each electronic state. Furthermore, we propose physical setups that can be used to reproduce the quantum dynamics of a standard and multiple-mode Holstein model. The proposed scheme is based on currently available technology of superconducting circuits consist of flux qubits and quantum oscillators.

quant-ph↗

arXiv2014

Non-Markovian Quantum State Diffusion for Temperature-Dependent Linear Spectra of Light Harvesting Aggregates

Non-Markovian Quantum State Diffusion (NMQSD) has turned out to be an efficient method to calculate excitonic properties of aggregates composed of organic chromophores, taking into account the coupling of electronic transitions to vibrational modes of the chromophores. NMQSD is an open quantum system approach that incorporates environmental degrees of freedom (the vibrations in our case) in a stochastic way. We show in this paper that for linear optical spectra (absorption, circular dichroism) no stochastics is needed, even for finite temperatures. Thus, the spectra can be obtained by propagating a single trajectory. To this end we map a finite temperature environment to the zero temperature case using the so-called thermofield method. The resulting equations can then be solved efficiently by standard integrators.

physics.chem-ph↗

arXiv2014

Hierarchical equations for open system dynamics in fermionic and bosonic environments

We present novel approaches to the dynamics of an open quantum system coupled linearly to a non-Markovian fermionic or bosonic environment. In the first approach, we obtain a hierarchy of stochastic evolution equations of the diffusion type. For the bosonic case such a hierarchy has been derived and proven suitable for efficient numerical simulations recently [arXiv:1402.4647]. The stochastic fermionic hierarchy derived here contains Grassmannian noise, which makes it difficult to simulate numerically due to its anti-commutative multiplication. Therefore, in our second approach we eliminate the noise by deriving a related hierarchy of density matrices. A similar reformulation of the bosonic hierarchy of pure states to a master equation hierarchy is also presented.

quant-ph↗

arXiv2014

Analytic Representations of Bath Correlation Functions for Ohmic and Superohmic Spectral Densities Using Simple Poles

We present a scheme to express a bath correlation function (BCF) corresponding to a given spectral density (SD) as a sum of damped harmonic oscillations. Such a representation is needed, for example, in many open quantum system approaches. To this end we introduce a class of fit functions that enables us to model ohmic as well as superohmic behavior. We show that these functions allow for an analytic calculation of the BCF using pole expansions of the temperature dependent hyperbolic cotangent. We demonstrate how to use these functions to fit spectral densities exemplarily for cases encountered in the description of photosynthetic light harvesting complexes. Finally, we compare absorption spectra obtained for different fits with exact spectra and show that it is crucial to take properly into account the behavior at small frequencies when fitting a given SD.

quant-ph↗

arXiv2013

On-chip non-reciprocal optical devices based on quantum inspired photonic lattices

We propose a novel geometry for integrated photonic devices that can be used as isolators and polarization splitters based on engineered photonic lattices. Starting from optical waveguide arrays that mimic Fock space representation of a non-interacting two-site Bose Hubbard Hamiltonian, we show that introducing magneto-optic nonreciprocity to these structures leads to a superior optical isolation performance. In the forward propagation direction, an input TM polarized beam experiences a perfect state transfer between the input and output waveguide channels while surface Bloch oscillations block the backward transmission between the same ports. Our analysis indicates a large isolation ratio of 75 dB after a propagation distance of 8 mm inside seven coupled waveguides. Moreover, we demonstrate that, a judicious choice of the nonreciprocity in this same geometry can lead to perfect polarization splitting.

physics.optics↗

arXiv2013

Nonclassical light in coupled optical systems: anomalous power distribution, Fock space dynamics and supersymmetry

We investigate the dynamics of nonclassical states of light in coupled optical structures and we demonstrate a number of intriguing features associated with such arrangements. By diagonalizing the system's Hamiltonian, we show that these geometries can support eigenstates having anomalous optical intensity distribution with no classical counterpart. These features may provide new avenues towards manipulating light flow at the quantum level. By projecting the Hamiltonian operator on Hilbert subspaces spanning different numbers of photon excitations, we demonstrate that processes such as coherent transport, state localization and surface Bloch oscillations can take place in Fock space. Furthermore, we show that Hamiltonian representations of Fock space manifolds differing by one photon obey a discrete supersymmetry relation

physics.optics↗

arXiv2013

Break-up of Rydberg superatoms via dipole-dipole interactions

We investigate resonant dipole-dipole interactions between two "superatoms" of different angular momentum, consisting of two Rydberg-blockaded atom clouds where each of them carries initially a coherently shared single excitation. We demonstrate that the dipole-dipole interaction breaks up the superatoms by removing the excitations from the clouds. The dynamics is akin to an ensemble average over systems where only one atom per cloud participates in entangled motion and excitation transfer. Our findings should thus facilitate the experimental realization of adiabatic exciton transport in Rydberg systems by replacing single sites with atom clouds.

physics.atom-ph↗

arXiv2013

Photonics meets excitonics: natural and artificial molecular aggregates

Organic molecules store the energy of absorbed light in the form of charge-neutral molecular excitations -- Frenkel excitons. Usually, in amorphous organic materials, excitons are viewed as quasiparticles, localized on single molecules, which diffuse randomly through the structure. However, the picture of incoherent hopping is not applicable to some classes of molecular aggregates -- assemblies of molecules that have strong near field interaction between electronic excitations in the individual subunits. Molecular aggregates can be found in nature, in photosynthetic complexes of plants and bacteria, and they can also be produced artificially in various forms including quasi-one dimensional chains, two-dimensional films, tubes, etc. In these structures light is absorbed collectively by many molecules and the following dynamics of molecular excitation possesses coherent properties. This energy transfer mechanism, mediated by the coherent exciton dynamics, resembles the propagation of electromagnetic waves through a structured medium on the nanometer scale. The absorbed energy can be transferred resonantly over distances of hundreds of nanometers before exciton relaxation occurs. Furthermore, the spatial and energetic landscape of molecular aggregates can enable the funneling of the exciton energy to a small number of molecules either within or outside the aggregate. In this review we establish a bridge between the fields of photonics and excitonics by describing the present understanding of exciton dynamics in molecular aggregates.

cond-mat.mes-hall↗

arXiv2012

Quantum simulator of an open quantum system using superconducting qubits: exciton transport in photosynthetic complexes

Open quantum system approaches are widely used in the description of physical, chemical and biological systems. A famous example is electronic excitation transfer in the initial stage of photosynthesis, where harvested energy is transferred with remarkably high efficiency to a reaction center. This transport is affected by the motion of a structured vibrational environment, which makes simulations on a classical computer very demanding. Here we propose an analog quantum simulator of complex open system dynamics with a precisely engineered quantum environment. Our setup is based on superconducting circuits, a well established technology. As an example, we demonstrate that it is feasible to simulate exciton transport in the Fenna-Matthews-Olson photosynthetic complex. Our approach allows for a controllable single-molecule simulation and the investigation of energy transfer pathways as well as non-Markovian noise-correlation effects.

quant-ph↗

arXiv2011

Robustness of spatial Penning trap modes against environment-assisted entanglement

The separability of the spatial modes of a charged particle in a Penning trap in the presence of an environment is studied by means of the positive partial transpose (PPT) criterion. Assuming a weak Markovian environment, described by linear Lindblad operators, our results strongly suggest that the environmental coupling of the axial and cyclotron degrees of freedom does not lead to entanglement at experimentally realistic temperatures. We therefore argue that, apart from unavoidable decoherence, the presence of such an environment does not alter the effectiveness of recently suggested quantum information protocols in Penning traps, which are based on the combination of a spatial mode with the spin of the particle.

quant-ph↗