The nanodiamond technology has developed the first packaged, single-photon source that operates at room temperature and in well-lit environments, where an ideal single-photon source produces one photon per pulse. These sources are key components for building quantum information systems that can implement quantum-key distribution (QKD) for ultrasecure communications. The optically active color centers in diamond have been found to exhibit attractive optical properties through the nitrogen-vacancy (N-V) center emission ranging 600 to 750 nm, and that have realized the practical sources of single-photon emission. Photo statistics has to be determined to measure the performance of a single-photon source, which can be measured by the autocorrelation function g2 (0) using Hanbury-Brown and Twiss interferometer. The results showed that the SPS 1.01 demonstrates stable single-photon performance without requirement of recalibration.
The nanodiamond technology has developed the first packaged, single-photon source that operates at room temperature and in well-lit environments, where an ideal single-photon source produces one photon per pulse. These sources are key components for building quantum information systems that can implement quantum-key distribution (QKD) for ultrasecure communications. The optically active color centers in diamond have been found to exhibit attractive optical properties through the nitrogen-vacancy (N-V) center emission ranging 600 to 750 nm, and that have realized the practical sources of single-photon emission. Photo statistics has to be determined to measure the performance of a single-photon source, which can be measured by the autocorrelation function g2 (0) using Hanbury-Brown and Twiss interferometer. The results showed that the SPS 1.01 demonstrates stable single-photon performance without requirement of recalibration.
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 a robust light source that emits one photon at a time is an outstanding challenge in quantum science and technology. Here, at the transition from many to single photon optical communication systems, fully quantum mechanical effects may be utilized to achieve new capabilities, most notably perfectly secure communication via quantum cryptography. Practical implementations place stringent requirements on the device properties, including stable photon generation, room temperature operation, and efficient extraction of many photons. Single photon light emitting devices based on fluorescent dye molecules, quantum dots, and carbon nanotube material systems have all been explored, but none have simultaneously demonstrated all criteria. Here, we describe the design, fabrication, and characterization of a bright source of single photons consisting of an individual Nitrogen-vacancy color center (NV center) in a diamond nanowire operating in ambient conditions. The nanowire plays a positive role in increasing the number of single photons collected from the NV center by an order of magnitude over devices based on bulk diamond crystals, and allows operation at an order of magnitude lower power levels. This result enables a new class of nanostructured diamond devices for room temperature photonic and quantum information processing applications, and will also impact fields as diverse as biological and chemical sensing, opto-mechanics, and scanning-probe microscopy.
Single-photon sources (SPS) play a key-role in many applications, spanning from quantum metrology, to quantum information and to the foundations of quantum mechanics. Even if an ideal SPS (i. e. emitting indistinguishable, ”on-demand” single photons, at an arbitrarily fast repetition rate) is far to be realized due to real-world deviations from the ideality, much effort is currently devoted to improving the performance of real sources. With regards to the emission probability, it appears natural to employ sources that are in principle deterministic in the single- photon emission (single quantum emitters such as single atoms, ions, molecules, quantum dots, or color centers in diamond) as opposed to probabilistic ones (usually heralded SPS based on parametric down-conversion). We present an overview of our latest results concerning a work-in-progress NIR pulsed single photon source based on single quantum emitters (color centers in diamond) exploiting recently reported centers. They are particularly interesting because of the narrow emission line (tipically less than 5 nm), the shorter excited state lifetime with respect to NV centres (1 - 2 ns compared to 12 ns, allowing a ten-fold photon emission rate upon saturation) and the polarized emission.
Color centres in diamond represent a very interesting system for realizing single photon emitters, even at room temperature, in particular are attracting an ever-growing interest in quantum optics, quantum information and quantum sensing, due to their appealing photo-physical properties combined with ease of access and manipulation in a solid state system characterized by high transparency and structural stability. Literally hundreds of optically active color centers can be created and controlled in the diamond matrix, to be employed either as bright and stable single-photon sources or individual spin systems with optical readout, with record performances even at room temperature. In concurrence with the remarkable results obtained at the state of the art on the exploitation of the unique properties of the negatively-charged nitrogen-vacancy complex (NV), new and appealing color centers are continuously being discovered and characterized. In the present contribution, the most recent results obtained by a collaboration among the Italian National Institutes of Metrologic Research (INRiM), the University of Torino and the Italian National Institutes of Nuclear Physics (INFN) will be overviewed and critically assessed in their future perspectives.
For applications in Quantum Information and Quantum Key Distribution an on-demand source of single photons is desirable because absolute security is of utmost importance. Photons are quantum systems; hence encoding information onto them offers a secure alternative to classical cryptography as a measurement cannot be performed on photons without altering their properties. The Nitrogen Vacancy (NV) centre in diamond is a good source of such photons. It is photo-stable and its location in diamond offers robustness. It has zero phonon line at 637 nm and its relative short luminescence life-time of about 12 ns makes it suitable for generating single photons. This thesis covers two aspects: Firstly the characterization of defects in diamonds and subsequent selection of diamonds suitable for use in the single photon setup and secondly, the development of the experimental setup for single photon generation. This thesis sets out to describe the development of a laboratory based single photon source using the NV centre in diamond. For this purpose a suite of diamond samples were selected and subjected to various spectroscopic tests in order to characterize and classify the samples, especially the presence of the NV centres and their concentrations. The characterization of the defects was done through the use of the following spectroscopic techniques: UltravioletVisible-Near infrared spectroscopy, Infrared spectroscopy, Electron Spin Resonance and Photoluminescence. These techniques enabled us to understand the types and origins of crystal defects that were present in the diamond samples used in this study and to use this to select diamonds that are most suitable for use in generation of single photons. The experimental setup for single photon generation using the NV centre is based on a confocal microscope arrangement. Single NV centres were identified by measuring the second order autocorrelation function of the fluorescence light emitted by the sample when illuminated with a laser. This measurement was done using a Hanbury-Brown Twiss (HBT) interferometer.
Abstract Single photon sources (SPSs) are one of the key components in quantum communication technology. Here we report on the development of a new approach to the controlled formation of SPSs in nanodiamonds synthesized from hydrocarbons at high pressure and high temperature (HPHT). The conditions of HPHT synthesis were determined, allowing for the highly efficient production of scalable single-photon emitters based on single silicon-vacancy (SiV) centers in individual diamond particles of 250-300 nm in size. A new type of SPSs, emitting in a wide spectral range (500-800 nm) at room temperature, was found in hydrogen-terminated nanodiamonds. The recorded rate of the SPS emission exceeds 1 million photons per second. The HPHT nanodiamonds containing both SiV and the new emitters are a promising material for quantum photonics applications.