We present a theoretical framework for biexciton dynamics in molecular aggregates that explicitly treats populations and coherences across excitation manifolds within a reduced density-matrix formalism. By extending kinetic descriptions beyond the weak-coupling limit, the approach captures the influence of exciton delocalization and exciton-exciton annihilation while remaining computationally tractable within a Markovian description of environmental relaxation. Using this framework, we investigate how the spatial profile and momentum composition of the initial biexciton state govern fluorescence decay and transport. Incoherent initial conditions lead to strongly non-exponential relaxation and time-dependent diffusion driven by nonlinear population kinetics. In contrast, coherently prepared biexciton states exhibit pronounced early-time coherent transport, whose character depends sensitively on whether the initial state is prepared as a standing-wave or traveling-wave superposition of single-exciton modes. Despite nearly identical emission dynamics for J and H aggregate, biexciton transport properties differ markedly due to band structure-dependent interference effect. Our results demonstrate that biexciton dynamics remains strongly influenced by initial-state coherence and momentum composition. Besides initial-state preparation, the coherent-to-incoherent crossover and the diffusive spreading of the exciton density are sensitive to internal conversion processes such as exciton fusion and the decay to the first excited state. The present work establishes initial-state preparation as a key control parameter for many-exciton transport in excitonic systems and provides a general framework for interpreting nonlinear optical experiments beyond population-based descriptions.
We present a theoretical framework for biexciton dynamics in molecular aggregates that explicitly treats populations and coherences across excitation manifolds within a reduced density-matrix formalism. By extending kinetic descriptions beyond the weak-coupling limit, the approach captures the influence of exciton delocalization and exciton-exciton annihilation while remaining computationally tractable within a Markovian description of environmental relaxation. Using this framework, we investigate how the spatial profile and momentum composition of the initial biexciton state govern fluorescence decay and transport. Incoherent initial conditions lead to strongly non-exponential relaxation and time-dependent diffusion driven by nonlinear population kinetics. In contrast, coherently prepared biexciton states exhibit pronounced early-time coherent transport, whose character depends sensitively on whether the initial state is prepared as a standing-wave or traveling-wave superposition of single-exciton modes. Despite nearly identical emission dynamics for J and H aggregate, biexciton transport properties differ markedly due to band structure-dependent interference effect. Our results demonstrate that biexciton dynamics remains strongly influenced by initial-state coherence and momentum composition. Besides initial-state preparation, the coherent-to-incoherent crossover and the diffusive spreading of the exciton density are sensitive to internal conversion processes such as exciton fusion and the decay to the first excited state. The present work establishes initial-state preparation as a key control parameter for many-exciton transport in excitonic systems and provides a general framework for interpreting nonlinear optical experiments beyond population-based descriptions.
We study excitation transfer dynamics in a lattice of two level systems characterized by dynamic disorder. The diagonal and off-diagonal energy disorders arise from the coupling of system and bath. We consider both the same and the independent bath limits. In case of independent bath all diagonal and off-diagonal bath coupling elements fluctuate independently of each other and the dynamics is complicated. We obtain the time dependent population distribution by solving quantum stochastic Liouville equation (QSLE) derived by Kubo. The main result of our study is both the population transfer dynamics and the mean square displacement of the exciton behave the similar way in the same and independent bath cases in the Markovian limit. However, these two baths can give rise to markedly different behavior in the non-Markovian limit where coherent transport becomes important. There are also several additional new results as follows. (i) Exciton migration remains coherent all the time for an average, non-zero off-diagonal coupling value J for the same bath case while it becomes incoherent for independent bath case in the Markovian limit. (ii) An oscillatory behavior of the population transfer dynamics supports the coherent mode of transfer of exciton. (iii) Agreement with available analytical expression of mean squared displacement is good in the Markovian limit for independent bath case with off-diagonal fluctuation but only qualitative in the non-Markovian limit for which no complete analytical solution is available. (iv) Transition from coherent to incoherent transport is observed in the independent bath case with diagonal fluctuation when the bath is made progressively more Markovian. (v) The correlation time of the bath plays a unique role in dictating the diffusive spread that is not anticipated in a Markovian treatment.
This dissertation addresses both fundamental aspects of the coherent exciton kinetics in single semiconductor quantum wells and more application-oriented aspects of the collective excitonic optical properties in quantum well Bragg structures. We use a bosonic theory to investigate the ultrafast coherent exciton dynamics after an optical excitation in a single semiconductor quantum well. It is shown that, on intermediate time scales, nonlinear mean-field interactions between excitons lead to a coherent, wave-like evolution in the momentum distribution of optically inactive excitons, which can survive for some time before dephasing sets in. Driven by two-exciton correlations, this coherent quantum kinetic effect bridges the well-known kinetics associated with optical excitation on the one hand and incoherent relaxation on the other. We also study more general dynamical properties of bosonic mean field systems with N-species of excitons (in a single semiconductor quantum well). We find that the momentum-conserving exciton mean field equations, including the coupling to external fields and fermionic corrections, have the dynamical structure su(N,N). We show that one can define a non-real generalized "Bloch vector" and a non-hermitian "density matrix" description, which allow us to explicitly obtain all the constants of motion associated with the su(N,N) symmetry. The many-body effects and correlations of excitons in a single quantum well are mainly induced by the Coulomb interactions. In the case of a semiconductor quantum well Bragg structure, the light induced coupling between different quantum wells also dramatically affects the excitons' behavior, especially through the collective excitations of excitons in the whole structure. We investigate the linear excitonic optical properties of the quantum well Bragg structure induced by the collective excitations using the transfer matrix approach. We show that the so called "intermediate band" (IB) created by the exciton resonance, which does not exist in conventional photonic crystals, can be used for the stopping, storing and releasing of light, which is important in information processing devices. We also discuss the compensation of the dispersive distortion in the light delay process through reversing the IB band structure. Other conceptual and practical issues such as the decay rate of the IB modes and the generalized anti-reflection coating are also investigated.
One of the most pertinent problems in the debate on non-trivial quantum effects in biology concerns natural photosynthesis. Since sunlight is composed of thermal photons, it was argued to be unable to induce quantum coherence in matter, and that quantum mechanics is therefore irrelevant for the dynamical processes following photoabsorption. Our present analysis of a toy 'molecular aggregate'—composed of two dipole–dipole interacting two-level atoms treated as an open quantum system—however shows that incoherent excitations indeed can trigger persistent, coherent dynamics in both the site and the exciton bases: we demonstrate that collective decay processes induced by the dipole–dipole interactions create coherent intermolecular transport—regardless of the coherence properties of the incoming radiation. Our analysis shows that the steady state coherence is mediated by the population imbalance between the molecules and, therefore, increases with the energy difference between the two-level atoms. Our results establish the importance of collective decay processes in the study of ultrafast photophysics, and especially their potential role to generate stationary coherence in incoherently driven quantum transport.
This work presents new results of experimental studies of exciton relaxation in GaAs/AlGaAs multiple quantum well materials, using transient nonlinear laser spectroscopy techniques. In the low excitation regime, effective optical Bloch equations similar to the density matrix formalism of a two-level system describe the response. Solutions of these equations appropriate for three-pulse scattering studies are presented, along with a discussion of new experimental techniques used in this work. Non-ideal conditions present in the molecular beam epitaxy growth process introduce monolayer fluctuations in the quantum well thickness, leading to inhomogeneous broadening and exciton localization at sites of minimum energy. Localized excitons are separated in energy from extended, quasi-delocalized states by the mobility edge. Studies of localized exciton relaxation indicate that these excitons relax on a much slower timescale than delocalized excitons. The temperature dependence of the localized exciton relaxation rate shows that above 15K, the excitons are thermally activated to extended states above the mobility edge. Below 15K the excitons relax by phonon assisted migration between localization sites. For temperatures above 5K, and for exciton energies greater than 1 meV below line center, an extra dephasing mechanism characterizes the exciton relaxation. The inhomogeneous broadening of the exciton leads to the emission of stimulated photon echoes in the experimental geometry used in this work. The time-resolved emission demonstrates the stimulated photon echo nature at low excitation densities. At higher excitation densities, the decay dynamics is more complex. The time-resolved emission shows the presence of a stimulated photon echo and a free polarization decay. This unusual result suggests that both a homogeneous and an inhomogeneous exciton distribution comprise the exciton resonance. Exciton relaxation at low excitation densities represents the interaction of the exciton with the lattice. At higher excitation densities, exciton-exciton and exciton-free carrier interactions modify the relaxation rates. The dependence of the exciton relaxation rate on excitation density shows that many-body effects play an important role in the exciton physics. Free carrier interactions are more efficient at increasing the exciton relaxation rate; both types of interactions are more important in quantum well systems than in bulk materials.
Exciton transport in molecular aggregates is a fundamental process governing the performance of organic optoelectronics and light-harvesting systems. While most theoretical studies have emphasized long-time transport behavior, recent advances in ultrafast spectroscopy have brought into focus the short-time regime, in which exciton motion remains ballistic on femtosecond-to-picosecond timescales. In this work, we develop an analytical framework for short-time exciton dynamics in a one-dimensional lattice subject to both on-site energetic (diagonal) disorder and intermolecular coupling (off-diagonal) fluctuations. Utilizing the reciprocal-space analysis, we derive closed-form expressions for the first and second spatial moments considering both localized excitation and moving Gaussian initial conditions. Our analytical and numerical results show that, while the long-time dynamics are influenced by diagonal disorder, the short-time ballistic expansion is governed primarily by off-diagonal disorder. Crucially, we reveal a synergistic interplay between the average intermolecular coupling and the off-diagonal coupling disorder strength, demonstrating that they contribute equivalently to short-time exciton transport. Moreover, we integrate this generic disorder model with a realistic molecular system within the framework of macroscopic quantum electrodynamics, thereby providing a theoretical foundation for characterizing and optimizing ultrafast energy flow of disordered molecular aggregates in complex dielectric media.