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Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE

A novel concept to generate single photons: incoherent conversion from the visible into the infrared spectrum

Tim Schröder, Ping Jiang, Friedemann Gädeke, Michael Barth, Vladimir Lesnyak, Nikolai P. Gaponik, Alexander Eychmüller, Oliver J. Benson

Published Apr 1, 2013• 0 citations
Publisher

Abstract

Further improvement of infrared single photon sources is a major challenge for future implementations of quantum information and quantum communication applications. In this paper, we give further insight into a recently presented, conceptually novel method for the generation of single photons.1 The method is of particular interest for spectral domains where stable room temperature single photon sources are not available. For example, this is the presently the case for the near-infrared. This wavelength regime is important for data transfer over long distances where optical losses in fibers are minimal. The presented method is based on the following idea. The fundamental key requirement for single photon generation is the generation of a single excitation in an optically active system. It is not the presence of a single quantum system. The presented method is applied to realize a stable, non-blinking, room temperature infrared single photon source by converting visible single photons from a defect center in diamond to the near infrared. For the presented implementation, the theoretical conversion efficiency was estimated to be 26 %. In a first prove of principle experiment, a conversion efficiency of 0.1 % was achieved.

DOI
10.1117/12.2008382

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Further improvement of infrared single photon sources is a major challenge for future implementations of quantum information and quantum communication applications. In this paper, we give further insight into a recently presented, conceptually novel method for the generation of single photons.1 The method is of particular interest for spectral domains where stable room temperature single photon sources are not available. For example, this is the presently the case for the near-infrared. This wavelength regime is important for data transfer over long distances where optical losses in fibers are minimal. The presented method is based on the following idea. The fundamental key requirement for single photon generation is the generation of a single excitation in an optically active system. It is not the presence of a single quantum system. The presented method is applied to realize a stable, non-blinking, room temperature infrared single photon source by converting visible single photons from a defect center in diamond to the near infrared. For the presented implementation, the theoretical conversion efficiency was estimated to be 26 %. In a first prove of principle experiment, a conversion efficiency of 0.1 % was achieved.
At present, there exist a number of on-demand single photon sources with high emission rates and stability even at room temperature. However, their emission wavelength is restricted to specific transitions in single quantum emitters. Single photon generation in the near infrared, possibly within the telecom band, though most urgently needed, is particularly crucial. In this paper, we suggest an experimental method to convert visible single photons from a defect center in diamond to the near infrared. The conversion relies on efficient absorption by colloidal quantum dots and subsequent Stokes-shifted emission. The desired target wavelength can be chosen almost arbitrarily by selecting quantum dots with a suitable emission spectrum. A hollow core photonic crystal fiber selectively filled with a solution of quantum dots was used to achieve at the same time a single photon absorption probability of near unity and a very high re-collection efficiency of Stokes-shifted fluorescence (theoretically estimated to be 26%). A total conversion efficiency of light of 0.1% is achieved. Experimental strategies to significantly enhance this number are presented.
Quantum communication and quantum metrology established a demand for an accessible solid state systems which can generate a stream of single photons on demand [1]. Although single photon emission has been demonstrated from quantum dots (QD)[1,2], single molecules [3] and nanowires [4], their practical operation is limited by the temperature or photostability. Diamond crystals, however, are the most promising platform for generation of robust, photo-stable, single photons at room temperature [5,6]. Nevertheless, out of more than 500 existing optical centers in diamond only three known centers demonstrated a clear single photon emission: the nitrogen-vacancy complex [6,7], the silicon-vacancy complex [8] and the nickel-nitrogen complex [9,10]. Recent progress in materials science and fabrication techniques of diamond color centers unveiled novel quantum emitters with photo-physical properties surpassing the current mainstream [11,12,13]. Consequently, the versatility of the diamond lattice to host various impurities which give luminescence signals lead to a dramatic discovery of ultra bright single photon emitters operating in the MHz regime [14]. These new centers, comparable with QD in terms of brightness [1], but have the tremendous advantage of their room temperature operation and photo-stability. Furthermore, it opened a new avenue to investigate essentially an unknown group of single photon emitters. A brief description of the fabrication methods and a detailed quantum optical characterization of this class of diamond emitters is the subject of this presentation. In particular we will present the photo-physical properties of a novel family of single photon emitters, most likely originated from Cr impurities within the chemical vapor deposition grown nano-diamond crystals. We concentrate on the typical emission lines in the range of 740 - 790 nm, which exhibit single photon emission with count rate in the range of 0.8-3.2 106 counts/s at the limit of infinite optical excitation power, and life time as short as 1 ns. Even more, some of the emitters exhibit a photon statistics without any photon bunching, indicating a two-level system with unitary quantum efficiency. We will also show preliminary results of a resonant excitation at 4 K. We will highlight future directions to optimize these sources and avenues to investigate the fundamental properties of these centers.
The development of reliable devices to generate single photons is crucial for applications in quantum cryptography, as well as for fundamental quantum optics experiments. Due to their extremely high photostability at room temperature, optically active defects in solids, the so called color centers, are among the most promising candidates. Single NV (nitrogen-vacancy) centers in diamond have been demonstrated to be able to generate single photons and have already shown advantages compared to attenuated laser pulses in a quantum cryptography experiment. The nitrogen-vacancy center (NV center) in diamond consists of a substitutional nitrogen atom and an adjacent vacancy. This complex exhibits an optical transition with a fluorescence lifetime of 11.6 ns. The room temperature spectrum of the NV center consists of the zero-phonon line at 637 nm and broad phononic sidebands with a FWHM of more than 100 nm. Due to the existence of a shelving level the efficiency of the NV center as a single photon source is limited. Additionally, the high diffraction index of bulk diamond restricts the efficiency to collect the fluorescence light.
Owing to their unsurpassed photostability, defects in solids may be ideal candidates for single-photon sources. Here we report on generation of single photons by optical excitation of a yet unexplored defect in diamond, the nickel–nitrogen complex (NE8) centre. The most striking feature of the defect is its emission bandwidth of 1.2 nm at room temperature. The emission wavelength of the defect is around 800 nm, which is suitable for telecom fibres. In addition, in this spectral region little background light from the diamond bulk material is detected. Consequently, a high contrast in antibunching measurements is achieved.
We report the realization of a solid-state triggered single-photon source with narrow emission in the near infrared at room temperature. It is based on the photoluminescence of a single nickel–nitrogen NE8 colour centre in a chemical vapour deposited diamond nanocrystal. Stable single-photon emission has been observed in the photoluminescence under both continuous-wave and pulsed excitations. The realization of this source represents a step forward in the application of diamond-based single-photon sources to quantum key distribution (QKD) under practical operating conditions.
Quantum measurements using single-photon detectors are opening interesting new perspectives in diverse fields such as remote sensing, quantum cryptography and quantum computing. A particularly demanding class of applications relies on the simultaneous detection of correlated single photons. In the visible and near infrared wavelength ranges suitable single-photon detectors do exist. However, low detector quantum efficiency or excessive noise has hampered their mid-infrared (MIR) counterpart. Fast and highly efficient single-photon detectors are thus highly sought after for MIR applications. Here we pave the way to quantum measurements in the MIR by the demonstration of a room temperature coincidence measurement with non-degenerate twin photons at about 3.1 μm. The experiment is based on the spectral translation of MIR radiation into the visible region, by means of efficient up-converter modules. The up-converted pairs are then detected with low-noise silicon avalanche photodiodes without the need for cryogenic cooling.