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Nanodiamond Emitters of Single Photons

Igor I. Vlasov, Svetlana G. Lukishova, В. И. Конов

Published Jan 1, 2015• 1 citation
Publisher

Abstract

Luminescence properties of single color centers were studied in nanodiamonds of different origin. It was found that single photon emitters could be realized even in molecularsized diamond (less than 2 nm) capable of housing stable luminescent center “silicon-vacancy.” First results on incorporation of single-photon emitters based on luminescent nanodiamonds in plasmonic nanoantennas to enhance the photon count rate and directionality, diminish the fluorescence decay time, and provide polarization selectivity are presented.

DOI
10.1051/epjconf/201510301013

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Luminescence properties of single color centers were studied in nanodiamonds of different origin. It was found that single photon emitters could be realized even in molecularsized diamond (less than 2 nm) capable of housing stable luminescent center “silicon-vacancy.” First results on incorporation of single-photon emitters based on luminescent nanodiamonds in plasmonic nanoantennas to enhance the photon count rate and directionality, diminish the fluorescence decay time, and provide polarization selectivity are presented.
The prospects of using individual nanodiamond particles as a source of single photons were studied for diamonds of various origin. It was shown that the single photon emitters could be produced on a base of "nitrogen-vacancy" centers in detonation nanodiamond synthesized from graphite-hexogen mixture. Studying meteoritic NDs we have found that single photon emitters based on "silicon-vacancy" centers could be realized even in molecular-sized diamond (less than 2 nm). Currently we are developing a new class of diamond materials, nanodiamonds synthesized from organic compounds at high pressure. In particular, we have demonstrated the possibility of synthesis of nanodiamond from its molecular analogue adamantane, controlling the size of crystallites in a wide range by changing synthesis temperature. A minimum size of obtained diamond particles about 3 nm was reached. Crystal structure of such diamonds is the most perfect in comparison with other classes of diamond materials, therefore they are the most promising material platform for production of single photon emitters.
We demonstrate the coupling of single color centers in diamond to plasmonic and dielectric photonic structures to realize novel nanophotonic devices. Nanometer spatial control in the creation of single color centers in diamond is achieved by implantation of nitrogen atoms through high-aspect-ratio channels in a mica mask. Enhanced broadband single-photon emission is demonstrated by coupling nitrogen-vacancy centers to plasmonic resonators, such as metallic nanoantennas. Improved photon-collection efficiency and directed emission is demonstrated by solid immersion lenses and micropillar cavities. Thereafter, the coupling of diamond nanocrystals to the guided modes of micropillar resonators is discussed along with experimental results. Finally, we present a gas-phase-doping approach to incorporate color centers based on nickel and tungsten, in situ into diamond using microwave-plasma-enhanced chemical vapor deposition. The fabrication of silicon-vacancy centers in nanodiamonds by microwave-plasma-enhanced chemical vapor deposition is discussed in addition.
Engineering the photo-emission characteristics of single-photon emitters is crucial for the growing field of quantum technologies. We show that the photoluminescence of a single nitrogen-vacancy color center in nanodiamond could be significantly enhanced when attached to a gold film of 50 nm with preserving photophysical properties as a single photon source. The nitrogen-vacancy center on the gold film showed a decreased excited-state lifetime and a modified saturation characteristic. The photoluminescence enhancement was due to the enhanced electric field by the surface plasmon and the energy transfer from the excited state of nitrogen-vacancy centers to the surface plasmon.
Unlocking the quantum potential of nitrogen-vacancy (NV) centers in diamonds has led to innovative advancements in sensing applications. By coupling NV centers with plasmonic nanostructures, ultrasensitive biolabels are envisioned. To this end, we exploit DNA self-assembly to create hybrid plasmonic nanodiamonds, featuring a closed nanocavity encapsulating a single nanodiamond. Correlated spectroscopy reveals enhanced brightness and emission rates, crucial for quantum sensing. This synergy between plasmonics and diamond fluorescence augments photon emission intensity and accelerates emission rates, enabling improved temporal resolution. These nanodiamonds hold promise as stable single-photon sources and versatile platforms for probing quantum effects in biology. This talk highlights the development, properties, and potential applications of these nanodiamonds, bridging quantum sensing and biomedicine, and fostering transformative changes in biophotonics.
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.
Color centers in nanodiamonds are promising candidates to realize high-bandwidth quantum optical devices integrated on mature photonic platforms. However, both the optical properties of these emitters and the geometries of host nanoparticles are highly heterogenous. The interfacing of nanodiamond-based color centers with the on-chip photonic circuitry requires their careful pre-selection and deterministic manipulation with nanoscale precision. We present a suite of recently developed techniques for rapid emitter selection and nanofabrication aimed at realizing deterministically assembled plasmon-enhanced single-photon sources. These techniques include optical nanoparticle metrology, machine learning for quantum optical measurements, probe-assisted nanoantenna assembly and the control of plasmonic cavity volume through photomodification.