Fast, high efficiency and low error single-photon sources are required for the implementation of a number of quantum information processing applications. The fastest triggered single-photon sources to date have been demonstrated using epitaxially grown semiconductor quantum dots (QDs), which can be conveniently integrated with optical microcavities. Recent advances in QD technology, including demonstrations of high temperature and telecommunications wavelength single-photon emission, have made QD single-photon sources more practical. Here we discuss the applications of single-photon sources and their various requirements, before reviewing the progress made on a QD platform in meeting these requirements.

We describe and experimentally demonstrate a technique for deterministic, large coupling between a photonic crystal (PC) nanocavity and single photon emitters. The technique is based on in situ scanning of a PC cavity over a sample and allows the precise positioning of the cavity over a desired emitter with nanoscale resolution. The power of the technique is demonstrated by coupling the PC nanocavity to a single nitrogen vacancy (NV) center in diamond, an emitter system that provides optically accessible electron and nuclear spin qubits.

We demonstrate second harmonic generation in photonic crystal nanocavities fabricated in the semiconductor gallium phosphide. We observe second harmonic radiation at 750 nm with input powers of only nanowatts coupled to the cavity and conversion effciency P(out)/P(2)(in,coupled)=430%/W. The large electronic band gap of GaP minimizes absorption loss, allowing effcient conversion. Our results are promising for integrated, low-power light sources and on-chip reduction of input power in other nonlinear processes.

Organic light-emitting devices (OLEDs) are a promising technology for flat-panel displays and solid-state lighting. While OLED efficiencies have increased dramatically in recent years, further progress is complicated by the fact that the vast majority of organic materials are fluorescent and therefore emit only from molecular excited states ('excitons') with spin 0, or 'singlet' spin symmetry. Here, we demonstrate the ability to manipulate the fraction of excitons which form as singlets in fluorescent materials by altering the OLED structure. We insert a mixing layer that affects only charge-transfer (CT) states, which are the precursors to excitons. As a result, we triple the singlet fraction and the efficiency of the red fluorophore DCM2. We term fluorescence enhanced by CT spin mixing 'extrafluorescence', and show that its origin is in part an inversion of the usual energetic ordering of the singlet and triplet CT states.

We describe a photonic crystal nanocavity with multiple spatially overlapping resonances that can serve as a platform for nonlinear frequency conversion. We show nonlinear characterization of structures with two resonances nearly degenerate in frequency. We also demonstrate structures with resonances separated by up to 523 nm.