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

Nitrogen-vacancy single-photon emission enhanced with nanophotonic structures (Presentation Recording)

Vladimir M. Shalaev, Mikhail Y. Shalaginov, Vadim Vorobyov, Simeon Bogdanov, Alexey V. Akimov, Alexei Lagutchev, Alexander V. Kildishev, Alexandra E. Boltasseva

Published Oct 5, 2015• 0 citations
Publisher

Abstract

Efficient generation of single photons is essential for the development of photonic quantum technologies. We have demonstrated that coupling a nanodiamond nitrogen-vacancy (NV) center to CMOS-compatible nanophotonic structures results in significant reduction of the excited state lifetime, increase in the collected single–photon emission, and modification of radiation pattern. In addition, we studied the effect of increased photonic density of states on spin dependent fluorescence contrast.

DOI
10.1117/12.2190251

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Efficient generation of single photons is essential for the development of photonic quantum technologies. We have demonstrated that coupling a nanodiamond nitrogen-vacancy (NV) center to CMOS-compatible nanophotonic structures results in significant reduction of the excited state lifetime, increase in the collected single–photon emission, and modification of radiation pattern. In addition, we studied the effect of increased photonic density of states on spin dependent fluorescence contrast.
Diamond based nitrogen-vacancy (NV) centers are promising solid state defects for applications in quantum information technologies. On the one hand, there is a growing interest in enhancing their single-photon emission by coupling them to plasmonic structures. On the other hand, the dependence of emission intensity on the electron spin state enables room temperature quantum information readout. We study the fluorescence contrast resulting from the spin resonance in the conditions of an increased photonic density of states. Fluorescence observations from NV center ensembles in diamond nanocrystals coupled to structures supporting plasmonic modes experimentally confirm the analytical results.
Single-photon sources are essential for quantum technologies, supporting secure communication, quantum computing, and integrated photonic systems. Nitrogen-vacancy (NV) centers in nanodiamonds are robust emitters that operate at room temperature and can be positioned on-chip, but efficient coupling to photonic modes remains challenging. We present the design, fabrication, and experimental characterization of a silicon nitride photonic structure engineered to enhance and extract emission from NV centers. The device features a subwavelength gap between waveguides, a Bragg reflector for emission redirection, and an output waveguide for collection. Simulations guided the optimization of the geometry to increase the spontaneous emission rate through photonic confinement. Nanodiamonds were deposited into the gap using lithographic patterning and drop-casting. Fluorescence lifetime measurements confirm that the structure modifies the emission dynamics of the NV centers. The approach is compatible with scalable fabrication techniques and offers a practical route toward integrated, chip-based single-photon sources.
Metamaterials and metasurfaces can be seen as a novel approach for constructing practical quantum photonic systems. In this talk, we present our recent advances in controlling single-photon emission from nitrogen-vacancy (NV) color centers in nanodiamonds using CMOS-compatible hyperbolic metamaterials. Further, we discuss how an increased photonic density of states affects the optical readout of the NV center spin-state. These results can be useful for engineering on-chip room-temperature quantum registers.
Spontaneous emission from crystal centers is influenced by both the photonic local density of states and non-radiative processes. Here, we monitor the spontaneous emission of single nitrogen vacancy (NV) centers as their host diamond is reduced in size from a large monolithic crystal to a nanocrystal by successive cycles of oxidation. The size reduction induces a quenching of the NV radiative emission. Additional non-radiative channels lead to a decrease of the fluorescence intensity and the excited state lifetime. In one case, we observe the onset of blinking which may provide a route to understand these additional non-radiative decay channels.
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.