Quantum interference between two single photons emitted by independently trapped atoms.

When two indistinguishable single photons are fed into the two input ports of a beam splitter, the photons will coalesce and leave together from the same output port. This is a quantum interference effect, which occurs because two possible paths-in which the photons leave by different output ports-interfere destructively. This effect was first observed in parametric downconversion (in which a nonlinear crystal splits a single photon into two photons of lower energy), then from two separate downconversion crystals, as well as with single photons produced one after the other by the same quantum emitter. With the recent developments in quantum information research, much attention has been devoted to this interference effect as a resource for quantum data processing using linear optics techniques. To ensure the scalability of schemes based on these ideas, it is crucial that indistinguishable photons are emitted by a collection of synchronized, but otherwise independent sources. Here we demonstrate the quantum interference of two single photons emitted by two independently trapped single atoms, bridging the gap towards the simultaneous emission of many indistinguishable single photons by different emitters. Our data analysis shows that the observed coalescence is mainly limited by wavefront matching of the light emitted by the two atoms, and to a lesser extent by the motion of each atom in its own trap.

Controlled single-photon emission from a single trapped two-level atom.

By illuminating an individual rubidium atom stored in a tight optical tweezer with short resonant light pulses, we created an efficient triggered source of single photons with a well-defined polarization. The measured intensity correlation of the emitted light pulses exhibits almost perfect antibunching. Such a source of high-rate, fully controlled single-photon pulses has many potential applications for quantum information processing.

Statistical aging and nonergodicity in the fluorescence of single nanocrystals.

The relation between single particle and ensemble measurements is addressed for semiconductor CdSe nanocrystals. We record their fluorescence at the single molecule level and analyze their emission intermittency, which is governed by unusual random processes known as Lévy statistics. We report the observation of statistical aging and ergodicity breaking, both related to the occurrence of Lévy statistics. Our results show that the behavior of ensemble quantities, such as the total fluorescence of an ensemble of nanocrystals, can differ from the time-averaged individual quantities, and must be interpreted with care.

Bunching and antibunching in the fluorescence of semiconductor nanocrystals.

The fluorescence of single-colloidal CdSe quantum dots is investigated at room temperature by means of the autocorrelation function over a time scale of almost 12 orders of magnitude. Over a short time scale, the autocorrelation function shows complete antibunching, indicating single-photon emission and atomiclike behavior. Over longer time scales (up to tens of seconds), we measure a bunching effect that is due to fluorescence intermittency and that cannot be described by fluctuations between two states with constant rates. The autocorrelation function also exhibits nonstationary behavior related to power-law distributions of On and Off times.

Parametric polariton amplification in semiconductor microcavities.

We present novel experimental results demonstrating the coherence properties of the nonlinear emission from semiconductor microcavities in the strong coupling regime, recently interpreted by parametric polariton four-wave mixing. We use a geometry corresponding to degenerate four-wave mixing. In addition to the predicted threshold dependence of the emission on the pump power and spectral blueshift, we observe a phase dependence of the amplification which is a signature of a coherent polariton wave mixing process.