Victor Malyshev

Temperature dependent fluorescence in disordered Frenkel chains: Interplay of equilibration and local band-edge level structure

We model the optical dynamics in linear Frenkel exciton systems governed by scattering on static disorder and lattice vibrations, and calculate the temperature dependent fluorescence spectrum and lifetime. The fluorescence Stokes shift shows a nonmonotonic behavior with temperature, which derives from the interplay of the local band-edge level structure and thermal equilibration. The model yields excellent fits to experiments performed on linear dye aggregates.

Decoherence of excitons in multichromophore systems: Thermal line broadening and destruction of superradiant emission

We study the temperature-dependent dephasing rate of excitons in chains of chromophores, accounting for scattering on static disorder as well as acoustic phonons in the host matrix. From this we find a power-law temperature dependence of the absorption linewidth, in excellent quantitative agreement with experiments on dye aggregates. We also propose a relation between the linewidth and the exciton coherence length imposed by the phonons. The results indicate that the much debated steep rise of the fluorescence lifetime of pseudoisocyanine aggregates above 40 K results from the fact that this coherence length drops below the localization length imposed by static disorder.

Localization length of one-dimensional exciton and low-temperature behaviour of radiative lifetime of J-aggregated dye solutions

Abstract The relationship between the number of coherently bound molecules in a linear chain and the degree of diagonal disorder is obtained. An interpretation of the experimental low-temperature behaviour of the radiative lifetime of J-aggregated dye solutions is proposed. An estimate of the intermolecular dipole-dipole interaction is made that differs from the experimental value obtained by measuring the shift of the dimer absorption band maximum relative to that of monomer.

Optical bistability and hysteresis of a hybrid metal-semiconductor nanodimer

Optical response of an artificial composite nanodimer comprising a semiconductor quantum dot and a metal nanosphere is analyzed theoretically. We show that internal degrees of freedom of the system can manifest bistability and optical hysteresis as functions of the incident field intensity. We argue that these effects can be observed for real-world systems, such as a CdSe quantum dot and an Au nanoparticle hybrid. These properties can be revealed by measuring the optical hysteresis of Rayleigh scattering. We also show that the total dipole moment of the system can be switched abruptly between its two stable states by small changes in the excitation intensity. The latter promises various applications in the field of all-optical processing at the nanoscale, the most basic of them being the volatile optical memory.

Low-temperature dynamics of weakly localized Frenkel excitons in disordered linear chains

We calculate the temperature dependence of the fluorescence Stokes shift and the fluorescence decay time in linear Frenkel exciton systems resulting from the thermal redistribution of exciton population over the band states. The following factors, relevant to common experimental conditions, are accounted for in our kinetic model: (weak) localization of the exciton states by static disorder, coupling of the localized excitons to vibrations in the host medium, a possible non-equilibrium of the subsystem of localized Frenkel excitons on the time scale of the emission process, and different excitation conditions (resonant or non resonant). A Pauli master equation, with microscopically calculated transition rates, is used to describe the redistribution of the exciton population over the manifold of localized exciton states. We find a counterintuitive non-monotonic temperature dependence of the Stokes shift. In addition, we show that depending on experimental conditions, the observed fluorescence decay time may be determined by vibration-induced intra-band relaxation, rather than radiative relaxation to the ground state. The model considered has relevance to a wide variety of materials, such as linear molecular aggregates, conjugated polymers, and polysilanes.We calculate the temperature dependence of the fluorescence Stokes shift and the fluorescence decay time in linear Frenkel exciton systems resulting from the thermal redistribution of exciton population over the band states. The following factors, relevant to common experimental conditions, are accounted for in our kinetic model: (weak) localization of the exciton states by static disorder, coupling of the localized excitons to vibrations in the host medium, a possible nonequilibrium of the subsystem of localized Frenkel excitons on the time scale of the emission process, and different excitation conditions (resonant or nonresonant). A Pauli master equation, with microscopically calculated transition rates, is used to describe the redistribution of the exciton population over the manifold of localized exciton states. We find a counterintuitive nonmonotonic temperature dependence of the Stokes shift. In addition, we show that depending on experimental conditions, the observed fluorescence decay time may be determined by vibration-induced intraband relaxation, rather than radiative relaxation to the ground state. The model considered has relevance to a wide variety of materials, such as linear molecular aggregates, conjugated polymers, and polysilanes.

Bloch-Like Oscillations in a One-Dimensional Lattice with Long-Range Correlated Disorder

We study the dynamics of an electron subjected to a uniform electric field within a tight-binding model with long-range-correlated diagonal disorder. The random distribution of site energies is assumed to have a power spectrum S(k) approximately 1/k(alpha) with alpha>0. de Moura and Lyra [Phys. Rev. Lett. 81, 3735 (1998)]] predicted that this model supports a phase of delocalized states at the band center, separated from localized states by two mobility edges, provided alpha>2. We find clear signatures of Bloch-like oscillations of an initial Gaussian wave packet between the two mobility edges and determine the bandwidth of extended states, in perfect agreement with the zero-field prediction.

Intraband relaxation and temperature dependence of the fluorescence decay time of one-dimensional Frenkel excitons : The Pauli master equation approach

In molecular J-aggregates one often observes an increase of the fluorescence decay time when increasing the temperature from 0 K. This phenomenon is usually attributed to the thermal population of the dark Frenkel exciton states that lie above the superradiant bottom state of the exciton band. In this paper, we study this effect for a homogeneous one-dimensional aggregate in a host medium and we model the scattering between different exciton states as arising from their coupling to the host vibrations. A Pauli master equation is used to describe the redistribution of excitons over the band. The rates entering this equation are calculated within the framework of first-order perturbation theory, assuming a linear on-site interaction between excitons and acoustic phonons. Solving the master equation numerically for aggregates of up to 100 molecules, we calculate the temperature dependence of the fluorescence kinetics in general and the decay time scale in particular. The proper definition of the fluorescence decay time is discussed in detail. We demonstrate that, even at a quantum yield of unity, the possibility to directly interpret fluorescence experiments in terms of a simple radiative time scale depends crucially on the initial excitation conditions in combination with the competition between spontaneous emission and intraband phonon-assisted relaxation.

Statistics of low energy levels of a one-dimensional weakly localized Frenkel exciton: A numerical study

Numerical study of the one-dimensional Frenkel Hamiltonian with on-site randomness is carried out. We focus on the statistics of the energy levels near the lower exciton band edge, i.e., those determining optical response. We found that the distribution of the energy spacing between the states that are well localized at the same segment is characterized by a nonzero mean, i.e. these states undergo repulsion. This repulsion results in a local discrete energy structure of a localized Frenkel exciton. On the contrary, the energy spacing distribution for weakly overlapping local ground states (the states with no nodes within their localization segments) that are localized at different segments has zero mean and shows almost no repulsion. The typical width of the latter distribution is of the same order of magnitude as the typical spacing in the local discrete energy structure so that this local structure is hidden: it does not reveal itself either in the density of states or in the linear absorption spectra. However. this structure affects the two-exciton transitions involving the states of the same segment and can be observed by the pump-probe spectroscopy. We analyze also the disorder degree scaling of the first and second momenta of the distributions.

Frequency-controlled localization of optical signals in graded plasmonic chains

We study theoretically the optical response of graded linear arrays of noble metal nanospheres in which the center-to-center distances and/or the radii of the spheres change linearly along the chain. A strong asymmetry of the system response with respect to the direction of incidence of the incoming light is revealed. We show that for light propagating from smaller to larger spheres the optical signal can be localized in a controlled way at an arbitrary subset of a few neighboring spheres by adjusting the wavelength of the incoming field. This opens new opportunities to control the flow of electromagnetic energy at the nanometer scale.

Thermal broadening of the J-band in disordered linear molecular aggregates : A theoretical study

We theoretically study the temperature dependence of the J-band width in disordered linear molecular aggregates, caused by dephasing of the exciton states due to scattering on vibrations of the host matrix. In particular, we consider inelastic one- and two-phonon scatterings between different exciton states (energy-relaxation-induced dephasing), as well as the elastic two-phonon scattering of the excitons (pure dephasing). The exciton states follow from numerical diagonalization of a Frenkel exciton Hamiltonian with diagonal disorder; the scattering rates between them are obtained using the Fermi golden rule. A Debye-type model for the one- and two-phonon spectral densities is used in the calculations. We find that, owing to the disorder, the dephasing rates of the individual exciton states are distributed over a wide range of values. We also demonstrate that the dominant channel of two-phonon scattering is not the elastic one, as is often tacitly assumed, but rather comes from a similar two-phonon inelastic scattering process. In order to study the temperature dependence of the J-band width, we simulate the absorption spectrum, accounting for the dephasing-induced broadening of the exciton states. We find a power-law (T(p)) temperature scaling of the effective homogeneous width, with an exponent p that depends on the shape of the spectral density of the host vibrations. In particular, for a Debye model of vibrations, we find p approximately 4, which is in good agreement with the experimental data on J aggregates of pseudoisocyanine [I. Renge and U. P. Wild, J. Phys. Chem. A, 101, 7977 (1997)].