Room-temperature Single-photon Sources Research Articles

Nonclassical emission from single colloidal nanocrystals in a microcavity: a route towards room temperature single photon sources

Secure quantum communication systems (QCS) based on the transmission of crucial information through single photons are among the most appealing frontiers for telecommunications, though their development is still hindered by the lack of cheap and bright single photon sources (SPSs) operating at room temperature (RT). In this paper, we show the occurrence of photon antibunching at RT from single colloidal CdSe/ZnS nanocrystals (NCs) inserted in a vertical microcavity. Moreover, by using high-resolution lithographic techniques, we conceived a general route for positioning single colloidal quantum dots in the microcavity. The findings and the technique presented here can be considered a first step towards the development of SPS devices operating at RT.

Organic photonic bandgap microcavities doped with semiconductor nanocrystals for room-temperature on-demand single-photon sources

We report the first experimental observation of fluorescence from single semiconductor nanocrystals (colloidal quantum dots) in microcavities. In these room-temperature experiments we observed photon antibunching from single CdSe nanocrystals doped into a chiral one-dimensional photonic bandgap liquid-crystal microcavity. The chirality resulted in high-purity, circular polarization of definite handedness of the emitted single photons. We also report the fabrication of chiral microcavities for telecom wavelengths doped with PbSe nanocrystals as well as a solution-processed-polymer microcavity with a defect layer doped with CdSe nanocrystals between two distributed Bragg reflectors. These systems with their low host fluorescence background are attractive for on-demand single-photon sources for quantum information and communication.

Oriented semiconducting polymer nanostructures as on-demand room-temperature single-photon sources

We show that oriented nanostructures from single molecules of a conducting polymer act as highly robust room-temperature single-photon sources. Individual z-oriented polymer nanostructures show high-contrast photon antibunching with a modulation depth exceeding 90%. These results suggest the feasibility of a “push-button” technology for polymer-based single-photon sources in photonic-based quantum information processing applications.

Dye-doped cholesteric-liquid-crystal room-temperature single-photon source

Fluorescence antibunching from single terrylene molecules embedded in a cholesteric-liquid-crystal host is used to demonstrate operation of a room-temperature single-photon source. One-dimensional (1-D) photonic-band-gap microcavities in planar-aligned cholesteric liquid crystals with band gaps from visible to near-infrared spectral regions are fabricated. Liquid-crystal hosts (including liquid crystal oligomers and polymers) increase the source efficiency, firstly, by aligning the dye molecules along the direction preferable for maximum excitation efficiency (deterministic molecular alignment provides deterministically polarized output photons), secondly, by tuning the 1-D photonic-band-gap microcavity to the dye fluorescence band and thirdly, by protecting the dye molecules from quenchers, such as oxygen. In our present experiments, using oxygen-depleted liquid-crystal hosts, dye bleaching is avoided for periods exceeding one hour of continuous 532 nm excitation.

Room temperature single-photon source: single-dye molecule fluorescence in liquid crystal host

We report on new approaches toward an implementation of an efficient, room temperature, deterministically polarized, single-photon source (SPS) on demand-a key hardware element for quantum information and quantum communication. Operation of a room temperature SPS is demonstrated via photon antibunching in the fluorescence from single terrylene-dye molecules embedded in a cholesteric liquid crystal host. Using oxygen-depleted liquid crystal hosts, dye-bleaching was avoided over the course of more than 1 h of continuous 532-nm excitation. Liquid crystal hosts (including liquid crystal oligomers/polymers) permit further increase of the efficiency of the source: 1) by aligning the dye molecules along a direction preferable for maximum excitation efficiency; 2) by tuning a one-dimensional (1-D) photonic-band-gap microcavity of planar-aligned cholesteric (chiral nematic) liquid crystal layer to the dye fluorescence band.

Single Nanoobjects as Triggered Single Photons Sources

The generation of non-classical states of light [1] is an important scientific challenge with many potential applications. For example, squeezed states of light [2] have generated much interest in the past decade, because measurements can be performed with noise levels that are lower than those available with classical light. A particularly novel non-classical source of light is a triggered single-photon source: a source that has the property to emit with a high degree of certainty one (and only one) photon at a user-specified time. Such a deterministic source of single photons can be important for quantum information processing [3], quantum cryptography [4] and certain quantum computation problems [5]. A single quantum emitter such as a molecule or an atom is a good potential source because it can emit only one photon at a time. The emitted light is antibunched [6, 7] and consists of single photons separated by random time intervals, which depend on the excited state lifetime and on the pumping rate. Thus triggered emission of single photons can be obtained with controlled excitation of a single emitter. The first demonstration of a single photons source [8] using a single molecule in a solid is based on a rapid adiabatic passage method [9] to excite the molecule. In the effective spin picture, the Bloch vector follows the driving magnetic field adiabatically if the laser-molecule frequency detuning is swept slowly through the resonance. Since the passage inverts the field, the system goes from the ground to the excited state. From this fluorescent state the molecule can emit only a single photon. The molecular resonance is swept by Stark effect at fixed laser frequency. This is done easily by applying a radio frequency electric field to the molecule. The results showed photon states with statistics that differ radically from those of coherent states. But this method requires cryogenic temperatures (2K) since narrow zero phonon lines are needed for the adiabatic following. At room temperature a source of triggered single photons based on the concept of pulsed optical excitation of a single highly fluorescent molecule has been demonstrated [10]. A short pulse of green laser light pumps the molecule from the ground state to a vibronically excited level of the first electronic excited state. After fast (ps) relaxation to the lowest electronic excited state, the molecule subsequently emits a single photon. A frequency-doubled mode-locked Nd-YAG laser is used to pump highly stable single terrylene molecules contained in a p-terphenyl molecular crystal where they are protected from exposure to diffusing quenchers (such as oxygen). The result shows that the photons are emitted after the laser pulses at times separated by the laser repetition time within the lifetime of terrylene in p-terphenyl. Since the pump pulse width is very short compared to the fluorescence lifetime, the probability of two (or more) photon emission per pulse is always zero. At the maximum laser power, 90% of the laser pulses lead to a single photon emission. The parameters of this source (repetition rate and single photon generation probability) were limited only by the laser system used; nevertheless, this performance already surpasses that of previous work. The high performance combined with the vanishing two photon emission probability and the simplicity of this source suggests that it can be considered for a variety of quantum optical experiments and for secure quantum cryptography [11]. Semiconductor quantum dots (QD) are other potential systems for single photon generation [12]. QDs are often referred to as “artificial atoms” because many of their optical properties, such as ultranarrow transitions, arise from discrete, atomic-like energy levels [13, 14]. To reinforce this analogy a study of the photon antibunching in this system was needed. QDs differ from atoms and molecules since the creation of multiple excitons is possible in QDs. Consequently, if two electron-hole pairs can radiatively recombine, the simultaneous emission of two photons from a QD is then possible. Thus different regimes of photon statistics were expected because the probability of multiple exciton creation depends on excitation intensity. The fluorescence intensity correlation function of a single CdSe quantum dot has been investigated [15] using a coincidence setup (start-stop experiment). A strong photon antibunching has been observed over a large range of intensities (0.1-100 kW/cm2). The lack of coincidence at zero time delay indicates a highly efficient Auger ionization process [16], which suppresses multi-photon emission in these colloidal quantum dots. This result shows that room temperature single photon sources can be achieved with colloidal nanoparticles.