Single-photon sources have a variety of applications. One of these is quantum radiometry, which is reported on in this paper in the form of an overview, specifically of the current state of the art in the application of deterministic single photon sources to the calibration of single photon detectors. To optimize single-photon sources for this purpose, extensive research is currently carried out at the European National Metrology Institutes (NMIs), in collaboration with partners from universities. Single-photon sources of different types are currently under investigation, including sources based on defect centres in (nano-)diamonds, on molecules and on semiconductor quantum dots. We will present, summarise, and compare the current results obtained at European NMIs for single-photon sources in terms of photon flux, single-photon purity, and spectral power distribution as well as the results of single-photon detector calibrations carried out with this type of light sources.

Stefan Kück, Marco López, Pietro Lombardi, Constanza Toninelli, Marco Trapuzzano, Maja Colautti, Giancarlo Margheri, Ivo P. Degiovanni Physikalisch-Technische Bundesanstalt (PTB), Braunschweig, Germany, Istituto Nazionale di Ottica (CNR-INO), Florence, Italy, Università degli Studi di Firenze, Florence, Italy, LENS, Università degli Studi di Firenze, Florence, Italy, Istituto dei Sistemi Complessi (CNR-ISC), Florence, Italy, Istituto Nazionale di Ricerca Metrologica (INRiM), Torino, Italy Corresponding e-mail address: stefan.kueck@ptb.de

Single photon sources (SPSs) based on quantum emitters hold promise in quantum radiometry as metrology standard for photon fluxes at the low light level. Ideally this requires control over the photon flux in a wide dynamic range, sub-Poissonian photon statistics and narrow-band emission spectrum. In this work, a monochromatic single-photon source based on an organic dye molecule is presented, whose photon flux is traceably measured to be adjustable between 144 000 and 1320 000 photons per second at a wavelength of (785.6 +/- 0.1) nm, corresponding to an optical radiant flux between 36.5 fW and 334 fW. The high purity of the single-photon stream is verified, with a second-order autocorrelation function at zero time delay below 0.1 throughout the whole range. Featuring an appropriate combination of emission properties, the molecular SPS shows here application in the calibration of a silicon Single-Photon Avalanche Detector (SPAD) against a low-noise analog silicon photodiode traceable to the primary standard for optical radiant flux (i.e. the cryogenic radiometer). Due to the narrow bandwidth of the source, corrections to the SPAD detection efficiency arising from the spectral power distribution are negligible. With this major advantage, the developed device may finally realize a low-photon-flux standard source for quantum radiometry.

The successful development of future photonic quantum technologies will much depend on the possibility of realizing robust and scalable nanophotonic devices. These should include quantum emitters like on‐demand single‐photon sources and non‐linear elements, provided their transition linewidth is broadened only by spontaneous emission. However, conventional strategies to on‐chip integration, based on lithographic processes in semiconductors, are typically detrimental to the coherence properties of the emitter. Moreover, such approaches are difficult to scale and bear limitations in terms of geometries. Here an alternative platform is discussed, based on molecules that preserve near‐Fourier‐limited fluorescence even when embedded in polymeric photonic structures. 3D patterns are achieved via direct laser writing around selected molecular emitters, with a fast, inexpensive, and scalable fabrication process. By using an integrated polymeric design, detected photon counts of about 2.4 Mcps from a single cold molecule are reported. The proposed technology will allow for competitive organic quantum devices, including integrated multi‐photon interferometers, arrays of indistinguishable single‐photon sources, and hybrid electro‐optical nanophotonic chips.

A major challenge in quantum technologies is the on-chip integration of quantum emitters in a way that can be scaled up and preserves the emitter coherence properties. In the unconventional platform presented by Costanza Toninelli and co-workers in article number 2000004, molecular single-photon sources are embedded in three-dimensional polymeric structures, obtained by direct laser writing. Anthracene nanocrystals doped with dibenzoterrylene chromophores (chemical structure in the zoom) are previously selected and integrated in a scalable way, without perturbing the emitter optical features. In particular, suspended waveguides are designed to route the emitted fluorescence towards convenient output modes while micro-dome solid immersion lenses efficiently redirect the emission enabling unprecedented collected single-photon rates from a cold molecule.

The successful development of future photonic quantum technologies heavily depends on the possibility of realizing robust, reliable and, crucially, scalable nanophotonic devices. In integrated networks, quantum emitters can be deployed as single-photon sources or non-linear optical elements, provided their transition linewidth is broadened only by spontaneous emission. However, conventional fabrication approaches are hardly scalable, typically detrimental for the emitter coherence properties and bear limitations in terms of geometries and materials. Here we introduce an alternative platform, based on molecules embedded in polymeric photonic structures. Three-dimensional patterns are achieved via direct laser writing around selected molecular emitters, which preserve near-Fourier-limited fluorescence. By using an integrated polymeric design, record-high photon fluxes from a single cold molecule are reported. The proposed technology allows to conceive a novel class of quantum devices, including integrated multi-photon interferometers, arrays of indistinguishable single photon sources and hybrid electro-optical nanophotonic devices.