A highly efficient single photon-single quantum dot interface

Semiconductor quantum dots are a promising system to build a solid state quantum network. A critical step in this area is to build an efficient interface between a stationary quantum bit and a flying one. In this chapter, we show how cavity quantum electrodynamics allows us to efficiently interface a single quantum dot with a propagating electromagnetic field. Beyond the well known Purcell factor, we discuss the various parameters that need to be optimized to build such an interface. We then review our recent progresses in terms of fabrication of bright sources of indistinguishable single photons, where a record brightness of 79% is obtained as well as a high degree of indistinguishability of the emitted photons. Symmetrically, optical nonlinearities at the very few photon level are demonstrated, by sending few photon pulses at a quantum dot-cavity device operating in the strong coupling regime. Perspectives and future challenges are briefly discussed.Comment: to appear as a book chapter in a compilation "Engineering the Atom-Photon Interaction" published by Springer in 2015, edited by A. Predojevic and M. W. Mitchel

Dynamic percolation theory for particle diffusion in a polymer network

Tracer-diffusion of small molecules through dense systems of chain polymers is studied within an athermal lattice model, where hard core interactions are taken into account by means of the site exclusion principle. An approximate mapping of this problem onto dynamic percolation theory is proposed. This method is shown to yield quantitative results for the tracer correlation factor of the molecules as a function of density and chain length provided the non-Poisson character of temporal renewals in the disorder configurations is properly taken into account

Collisional decay of 87Rb Feshbach molecules at 1005.8 G

We present measurements of the loss-rate coefficients K_am and K_mm caused by inelastic atom-molecule and molecule-molecule collisions. A thermal cloud of atomic 87Rb is prepared in an optical dipole trap. A magnetic field is ramped across the Feshbach resonance at 1007.4 G. This associates atom pairs to molecules. A measurement of the molecule loss at 1005.8 G yields K_am=2 10^-10 cm^3/s. Additionally, the atoms can be removed with blast light. In this case, the measured molecule loss yields K_mm=3 10^-10 cm^3/s

Dynamic Variation in Sexual Contact Rates in a Cohort of HIV-Negative Gay Men

Human immunodeficiency virus (HIV) transmission models that include variability in sexual behavior over time have shown increased incidence, prevalence, and acute-state transmission rates for a given population risk profile. This raises the question of whether dynamic variation in individual sexual behavior is a real phenomenon that can be observed and measured. To study this dynamic variation, we developed a model incorporating heterogeneity in both between-person and within-person sexual contact patterns. Using novel methodology that we call iterated filtering for longitudinal data, we fitted this model by maximum likelihood to longitudinal survey data from the Centers for Disease Control and Prevention's Collaborative HIV Seroincidence Study (1992–1995). We found evidence for individual heterogeneity in sexual behavior over time. We simulated an epidemic process and found that inclusion of empirically measured levels of dynamic variation in individual-level sexual behavior brought the theoretical predictions of HIV incidence into closer alignment with reality given the measured per-act probabilities of transmission. The methods developed here provide a framework for quantifying variation in sexual behaviors that helps in understanding the HIV epidemic among gay men

A Mott-like State of Molecules

We prepare a quantum state where each site of an optical lattice is occupied by exactly one molecule. This is the same quantum state as in a Mott insulator of molecules in the limit of negligible tunneling. Unlike previous Mott insulators, our system consists of molecules which can collide inelastically. In the absence of the optical lattice these collisions would lead to fast loss of the molecules from the sample. To prepare the state, we start from a Mott insulator of atomic 87Rb with a central region, where each lattice site is occupied by exactly two atoms. We then associate molecules using a Feshbach resonance. Remaining atoms can be removed using blast light. Our method does not rely on the molecule-molecule interaction properties and is therefore applicable to many systems.Comment: Proceedings of the 20th International Conference on Atomic Physics (ICAP 2006), edited by C. Roos, H. Haffner, and R. Blatt, AIP Conference Proceedings, Melville, 2006, Vol. 869, pp. 278-28

Feshbach blockade: single-photon nonlinear optics using resonantly enhanced cavity-polariton scattering from biexciton states

We theoretically demonstrate how the resonant coupling between a pair of cavity-polaritons and a biexciton state can lead to a large single-photon Kerr nonlinearity in a semiconductor solid-state system. A fully analytical model of the scattering process between a pair of cavity-polaritons is developed, which explicitly includes the biexcitonic intermediate state. A dramatic enhancement of the polariton-polariton interactions is predicted in the vicinity of the biexciton Feshbach resonance. Application to the generation of non-classical light from polariton dots is discussed

Atom-molecule Rabi oscillations in a Mott insulator

We observe large-amplitude Rabi oscillations between an atomic and a molecular state near a Feshbach resonance. The experiment uses 87Rb in an optical lattice and a Feshbach resonance near 414 G. The frequency and amplitude of the oscillations depend on magnetic field in a way that is well described by a two-level model. The observed density dependence of the oscillation frequency agrees with the theoretical expectation. We confirmed that the state produced after a half-cycle contains exactly one molecule at each lattice site. In addition, we show that for energies in a gap of the lattice band structure, the molecules cannot dissociate