293 research outputs found
Tailoring optical response of a hybrid comprising a quantum dimer emitter strongly coupled to a metal nanoparticle
We study theoretically the optical response of a nanohybrid comprising a
symmetric quantum dimer emitter coupled to a metal nanoparticle (MNP). The
interactions between the exitonic transitions in the dimer and the plasmons in
the MNP lead to novel effects in the composite's input-output characteristics
for the light intensity and the absorption spectrum, which we study in the
linear and nonlinear regimes. We fnd that the exciton-plasmon hybridization
leads to optical bistability and hysteresis for the one-exciton transition and
enhancement of excitation for the two-exciton transition. The latter leads to a
signifcant decrease of the field strength needed to saturate the system. In the
linear regime, the absortion spectrum has a dispersive (Fano-like) line shape.
The spectral position and shape of this spectrum depend on the detuning of the
dimer's one-exciton resonance relative to the plasmon resonance. Upon
increasing the applied field intensity to the nonlinear regime, the Fano-like
singularities in the absorption spectra are smeared and they disappear due to
the saturation of the dimer, which leads to the MNP dominating the spectrum.
The above effects, for which we provide physical explanations, allow one to
tailor the Fano-like shape of the absorption spectrum, by changing either the
detuning or the input power
Trapping time statistics and efficiency of transport of optical excitations in dendrimers
We theoretically study the trapping time distribution and the efficiency of
the excitation energy transport in dendritic systems. Trapping of excitations,
created at the periphery of the dendrimer, on a trap located at its core, is
used as a probe of the efficiency of the energy transport across the dendrimer.
The transport process is treated as incoherent hopping of excitations between
nearest-neighbor dendrimer units and is described using a rate equation. We
account for radiative and non-radiative decay of the excitations while
diffusing across the dendrimer. We derive exact expressions for the Laplace
transform of the trapping time distribution and the efficiency of trapping and
analyze those for various realizations of the energy bias, number of dendrimer
generations, and relative rates for decay and hopping. We show that the
essential parameter that governs the trapping efficiency, is the product of the
on-site excitation decay rate and the trapping time (mean first passage time)
in the absence of decay.Comment: 26 pages, 6 figure
Plasmon-assisted two-photon Rabi oscillations in a semiconductor quantum dot -- metal nanoparticle heterodimer
Tho-photon Rabi oscillations hold potential for quantum computing and quantum
information processing, because during a Rabi cycle a pair of entangled photons
may be created. We theoretically investigate the onset of this phenomenon in a
heterodimer comprising a semiconductor quantum dot strongly coupled to a metal
nanoparticle. Two-photon Rabi oscillations in this system occur due to a
coherent two-photon process involving the ground-to-biexciton transition in the
quantum dot. The presence of a metal nanoparticle nearby the quantum dot
results in a self-action of the quantum dot via the metal nanoparticle, because
the polatization state of the latter depends on the quantum state of the
former. The interparticle interaction gives rise to two principal effects: (i)
- enhancement of the external field amplitude and (ii) - renormalization of the
quantum dot's resonance frequencies and relaxation rates of the off-diagonal
density matrix elements, both depending on the populations of the quantum dot's
levels. Here, we focus on the first effect, which results in interesting new
features, in particular, in an increased number of Rabi cycles per pulse as
compared to an isolated quantum dot and subsequent growth of the number of
entangled photon pairs per pulse. We also discuss the destructive role of
radiative decay of the excitonic states on two-photon Rabi oscillations for
both an isolated quantum dot and a heterodimer.Comment: 11 pages, 19 figure
Nonlinear optical dynamics of 2D super-crystals of quantum Λ-emitters
We study theoretically the optical response of a 2D super-crystal of quantum Λ-emitters which are coupled by their secondary dipole field. The latter introduces a feedback into the system, the interplay of which with the intrinsic nonlinearity of emitters results in an exotic behavior of the system's optical response, such as periodic or quasi-periodic self-oscillations and chaotic dynamics. We argue therefore that these predicted features can be promising for various nanophotonic applications
Quantum metasurfaces of arrays of Λ-emitters for photonic nano-devices
We address exotic optical response of a planar metasurface comprising a monolayer of regularly spaced quantum three-level emitters with a doublet in the ground state (the so-called Λ-emitters). All emitters are coupled by the retarded dipole field which depends on the current state of all emitters. This coupling introduces a feedback into the system. Complex interplay of the latter with the intrinsic nonlinearity of a three-level system results in several remarkable effects in the monolayer's optical response, such as multistability, self-oscillations, and chaos. The peculiarity of the considered system is that some of the predicted nonlinear effects manifest themselves at very low excitation field intensities (on the order of 1 W/cm2), which is advantageous for possible applications: the monolayer can operate as a perfect reflector, a bistable mirror, and a THz or noise generator. It is argued therefore that the proposed system is a promising candidate for a building block for various photonic nano-devices
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 non-zero 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 as the typical spacing in the local
discrete energy structure, so that this local structure is hidden; it does not
reveal itself neither in the density of states nor 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.Comment: 10 pages, 6 figure
Intrinsic optical bistability of thin films of linear molecular aggregates: The two-exciton approximation
We generalize our recent work on the optical bistability of thin films of
molecular aggregates [J. Chem. Phys. 127, 164705 (2007); arXiv:0707.1264v1
[cond-mat.dis-nn]] by accounting for the optical transitions from the
one-exciton manifold to the two-exciton manifold as well as the exciton-exciton
annihilation of the two-exciton states via a high-lying molecular vibronic
term. We also include the relaxation from the vibronic level back to both the
one-exciton manifold and the ground state. By selecting the dominant optical
transitions between the ground state, the one-exciton manifold, and the
two-exciton manifold, we reduce the problem to four levels, enabling us to
describe the nonlinear optical response of the film. The one- and two-exciton
states are obtained by diagonalizing a Frenkel Hamiltonian with an uncorrelated
on-site (diagonal) disorder. The optical dynamics is described by means of the
density matrix equations coupled to the electromagnetic field in the film. We
show that the one-to-two exciton transitions followed by a fast exciton-exciton
annihilation promote the occurrence of bistability and reduce the switching
intensity. We provide estimates of pertinent parameters for actual materials
and conclude that the effect can be realized.Comment: 11 two-column pages, 6 figures, to appear in the Journal of Chemical
Physic
Plasmon-assisted two-photon absorption in a semiconductor quantum dot -- metallic nanoshell composite
Tho-photon absorption holds potential for many practical applications. We
theoretically investigate the onset of this phenomenon in a semiconductor
quantum dot -- metallic nanoshell composite subjected to a resonant CW
excitation. Two-photon absorption in this system may occur in two ways:
incoherent -- due to a consecutive ground-to-one-exciton-to-biexciton
transition and coherent -- due to a coherent two-photon process, involving the
direct ground-to-biexciton transition in the quantum dot. The presence of the
nanoshell nearby the quantum dot gives rise to two principal effects: (i) --
renormalization of the applied field amplitude and (ii) -- renormalization of
the resonance frequencies and radiation relaxation rates of the quantum dot,
both depending on the the quantum dot level populations. We show that in the
perturbation regime, when the excitonic levels are only slightly populated,
each of these factors may give rise to either suppression or enhancement of the
two-photon absorption. The complicated interplay of the two determines the
final effect. Beyond the perturbation regime, it is found that the two-photon
absorption experiences a drastic enhancement, which occurs independently of the
type of excitation, either into the one-exciton resonance or into the
two-photon resonance. Other characteristic features of the two-photon
absorption of the composite, emerging from the coupling between both
nanoparticles, are bistability and self-oscillations.Comment: 10 two-column pages, 7 figure
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