Microcavity quantum-dot systems for non-equilibrium Bose-Einstein condensation

We review the practical conditions required to achieve a non-equilibrium BEC driven by quantum dynamics in a system comprising a microcavity field mode and a distribution of localised two-level systems driven to a step-like population inversion profile. A candidate system based on eight 3.8nm layers of In(0.23)Ga(0.77)As in GaAs shows promising characteristics with regard to the total dipole strength which can be coupled to the field mode.Comment: 4 pages, 4 figures, to be published in J. Phys. Conf. Ser. for QD201

Quantum state preparation in semiconductor dots by adiabatic rapid passage

Preparation of a specific quantum state is a required step for a variety of proposed practical uses of quantum dynamics. We report an experimental demonstration of optical quantum state preparation in a semiconductor quantum dot with electrical readout, which contrasts with earlier work based on Rabi flopping in that the method is robust with respect to variation in the optical coupling. We use adiabatic rapid passage, which is capable of inverting single dots to a specified upper level. We demonstrate that when the pulse power exceeds a threshold for inversion, the final state is independent of power. This provides a new tool for preparing quantum states in semiconductor dots and has a wide range of potential uses.Comment: 4 pages, 4 figure

Dynamics of glass-forming liquids. XVI. Observation of ultrastable glass transformation via dielectric spectroscopy

The transformation of vapor-deposited ultrastable glasses of indomethacin (IMC) into the supercooled liquid state near Tg is monitored by means of dielectric spectroscopy. Films with thickness between 400 and 800 nm are deposited on differential interdigitated electrode cells and their loss profiles are measured during isothermal annealing using a dual-channel impedance technique for frequencies between 0.03 and 100 Hz. All dielectric loss spectra observed during the transformation process can be explained by a volume fraction of the supercooled liquid that increases linearly with time. From the early stages of the transformation to the liquid that is formed via complete annealing of the ultrastable glass, the average dielectric relaxation time as well as the distribution of relaxation times of the liquid component are identical to those of the conventional liquid obtained by cooling the melt. The dependence of the transformation rate on the film thickness is consistent with a growth front mechanism for the direct conversion from the ultrastable glass to the equilibrium supercooled liquid. We conclude that the IMC liquid recovered from the ultrastable glass is structurally and dynamically identical to the conventional supercooled state

Correlations of Structure and Dynamics in an Aging Colloidal Glass

We study concentrated colloidal suspensions, a model system which has a glass transition. Samples in the glassy state show aging, in that the motion of the colloidal particles slows as the sample ages from an initial state. We study the relationship between the static structure and the slowing dynamics, using confocal microscopy to follow the three-dimensional motion of the particles. The structure is quantified by considering tetrahedra formed by quadruplets of neighboring particles. We find that while the sample clearly slows down during aging, the static properties as measured by tetrahedral quantities do not vary. However, a weak correlation between tetrahedron shape and mobility is observed, suggesting that the structure facilitates the motion responsible for the sample aging.Comment: Submitted to Solid State Communication

Finite-temperature critical point of a glass transition

We generalize the simplest kinetically constrained model of a glass-forming liquid by softening kinetic constraints, allowing them to be violated with a small finite rate. We demonstrate that this model supports a first-order dynamical (space-time) phase transition, similar to those observed with hard constraints. In addition, we find that the first-order phase boundary in this softened model ends in a finite-temperature dynamical critical point, which we expect to be present in natural systems. We discuss links between this critical point and quantum phase transitions, showing that dynamical phase transitions in $d$ dimensions map to quantum transitions in the same dimension, and hence to classical thermodynamic phase transitions in $d+1$ dimensions. We make these links explicit through exact mappings between master operators, transfer matrices, and Hamiltonians for quantum spin chains.Comment: 10 pages, 5 figure

Reply to ``Comment on `Hole-burning experiments within glassy models with infinite range interactions' ''

This is a reply to the comments by Richter and Chamberlin, and Diezemann and Bohmer to our paper (Phys. Rev. Lett. 85, 3448 (2000)). As further evidence for the claims in this Letter, we here reproduce the nonlinear spectral hole-burning experimental protocol in an equilibrated fully connected spin-glass model and we exhibit frequency selectivity, together with a shift in the base of the spectral hole.Comment: 1 page, two figures, to appear in Phys. Rev. Let

Properties of cage rearrangements observed near the colloidal glass transition

We use confocal microscopy to study the motions of particles in concentrated colloidal systems. Near the glass transition, diffusive motion is inhibited, as particles spend time trapped in transient ``cages'' formed by neighboring particles. We measure the cage sizes and lifetimes, which respectively shrink and grow as the glass transition approaches. Cage rearrangements are more prevalent in regions with lower local concentrations and higher disorder. Neighboring rearranging particles typically move in parallel directions, although a nontrivial fraction move in anti-parallel directions, usually from pairs of particles with initial separations corresponding to the local maxima and minima of the pair correlation function $g(r)$, respectively.Comment: 5 pages, 4 figures; text & figures revised in v

Glassy freezing of orbital dynamics in FeCr2S4 and FeSc2S4

We report on a thorough dielectric investigation of the glass-like freezing of the orbital reorientation-dynamics, recently found for the crystalline sulpho-spinels FeCr2S4 and FeSc2S4. As the orbital reorientations are coupled to a rearrangement of the surrounding ionic lattice via the Jahn-Teller effect, the freezing of the orbital moments is revealed by a relaxational behaviour of the complex dielectric permittivity. Additional conductivity (both dc and ac) and contact contributions showing up in the spectra are taken into account by an equivalent circuit description. The orbital relaxation dynamics continuously slows down over six decades in time, before at the lowest temperatures the glass transition becomes suppressed by quantum tunnelling.Comment: J. Non-Cryst. Solids, in press. 6 pages, 4 figure

Subdiffusion and the cage effect studied near the colloidal glass transition

The dynamics of a glass-forming material slow greatly near the glass transition, and molecular motion becomes inhibited. We use confocal microscopy to investigate the motion of colloidal particles near the colloidal glass transition. As the concentration in a dense colloidal suspension is increased, particles become confined in transient cages formed by their neighbors. This prevents them from diffusing freely throughout the sample. We quantify the properties of these cages by measuring temporal anticorrelations of the particles' displacements. The local cage properties are related to the subdiffusive rise of the mean square displacement: over a broad range of time scales, the mean square displacement grows slower than linearly in time.Comment: submitted to Chemical Physics, special issue on "Strange Kinetics

Absorption and photoluminescence spectroscopy on a single self-assembled charge-tunable quantum dot

We have performed detailed photoluminescence (PL) and absorption spectroscopy on the same single self-assembled quantum dot in a charge-tunable device. The transition from neutral to charged exciton in the PL occurs at a more negative voltage than the corresponding transition in absorption. We have developed a model of the Coulomb blockade to account for this observation. At large negative bias, the absorption broadens as a result of electron and hole tunneling. We observe resonant features in this regime whenever the quantum dot hole level is resonant with two-dimensional hole states located at the capping layer-blocking barrier interface in our structure.Comment: 6 pages, 6 figure