Nitrogen-Vacancy (NV) centers in diamond are promising solid-state quantum emitters that can be utilized for photonic quantum applications. Various diamond nanophotonic devices have been fabricated for efficient extraction of single photons emitted from NV centers to a single guided mode. However, for constructing scalable quantum networks, further efficient coupling of single photons to a guided mode of a single-mode fiber (SMF) is indispensable and a difficult challenge. Here, we propose a novel efficient hybrid system between an optical nanofiber and a cylindrical-structured diamond nanowire. The maximum coupling efficiency as high as 75% for the sum of both fiber ends is obtained by numerical simulations. The proposed hybrid system will provide a simple and efficient interface between solid-state quantum emitters and a SMF suitable for constructing scalable quantum networks.
Nitrogen-Vacancy (NV) centers in diamond are promising solid-state quantum emitters that can be utilized for photonic quantum applications. Various diamond nanophotonic devices have been fabricated for efficient extraction of single photons emitted from NV centers to a single guided mode. However, for constructing scalable quantum networks, further efficient coupling of single photons to a guided mode of a single-mode fiber (SMF) is indispensable and a difficult challenge. Here, we propose a novel efficient hybrid system between an optical nanofiber and a cylindrical-structured diamond nanowire. The maximum coupling efficiency as high as 75% for the sum of both fiber ends is obtained by numerical simulations. The proposed hybrid system will provide a simple and efficient interface between solid-state quantum emitters and a SMF suitable for constructing scalable quantum networks.
A central goal in quantum information science is to efficiently interface photons with single optical modes for quantum networking and distributed quantum computing. Here, we introduce and experimentally demonstrate a compact and efficient method for the low-loss coupling of a solid-state qubit, the nitrogen vacancy (NV) center in diamond, with a single-mode optical fiber. In this approach, single-mode tapered diamond waveguides containing exactly one high quality NV memory are selected and integrated on tapered silica fibers. Numerical optimization of an adiabatic coupler indicates that near-unity-efficiency photon transfer is possible between the two modes. Experimentally, we find an overall collection efficiency between 16% and 37% and estimate a single photon count rate at saturation above 700 kHz. This integrated system enables robust, alignment-free, and efficient interfacing of single-mode optical fibers with single photon emitters and quantum memories in solids. A compact way to efficiently couple a solid-state qubit, the nitrogen vacancy center in diamond, with a single-mode optical fiber is shown. The ability to efficiently couple stationary quantum memories to a single spatial mode in a silica fiber is highly desired for various applications in quantum information processing. Now, Rishi Patel and co-workers, working in the group of Dirk Englund at the Massachusetts Institute of Technology have proposed and experimentally demonstrated an approach involving adiabatic power transfer between a tapered silica fiber and a single-mode micro-waveguide made from high-quality diamond. This integrated diamond–silica waveguide system enables optical collection from nitrogen vacancy centers with overall efficiencies in the range 16%–37%—a roughly four-fold improvement over previous approaches that employed diamond point emitters rather than waveguiding structures. Numerical optimization analysis suggests that near-unity efficiencies are theoretically feasible.
Tapered optical fibers are promising one-dimensional nanophotonic waveguides that can provide efficient coupling between their fundamental mode and quantum nanoemitters placed inside them. Here, we present numerical studies on the coupling of single nitrogen-vacancy (NV) centers (single point dipoles) in nanodiamonds with tapered fibers. Our results lead to two important conclusions: (1) A maximum coupling efficiency of 53.4% can be realized for the two fiber ends when the NV bare dipole is located at the center of the tapered fiber. (2) NV centers even in 100-nm-sized nanodiamonds where bulk-like optical properties were reported show a coupling efficiency of 22% at the taper surface, with the coupling efficiency monotonically decreasing as the nanodiamond size increases. These results will be helpful in guiding the development of hybrid quantum devices for applications in quantum information science.
A central goal in quantum information science is to efficiently interface photons with single optical modes for quantum networking and distributed quantum computing. Here, we introduce and experimentally demonstrate a compact and efficient method for the low-loss coupling of a solid-state qubit, the nitrogen vacancy (NV) center in diamond, with a single-mode optical fiber. In this approach, single-mode tapered diamond waveguides containing exactly one high quality NV memory are selected and integrated on tapered silica fibers. Numerical optimization of an adiabatic coupler indicates that near-unity-efficiency photon transfer is possible between the two modes. Experimentally, we find an overall collection efficiency between 16% and 37% and estimate a single photon count rate at saturation above 700 kHz. This integrated system enables robust, alignment-free, and efficient interfacing of single-mode optical fibers with single photon emitters and quantum memories in solids.
The development of integrated quantum technologies relies on efficient single-photon sources and deterministic quantum operations. Solid-state quantum emitters coupled to nanophotonic structures present a promising solution. This work investigates color centers in nanodiamonds,particularly Germanium Vacancy (GeV) [1], Silicon Vacancy (SiV), and Magnesium Vacancy (MgV) centers, a novel, understudied emitter [2], at both room and cryogenic temperatures. These nanodiamonds are chosen for their stability and superior coherence properties at cryogenic conditions. To collect their emission we have successfully deposited a single GeV- nanodiamond on tapered optical nanofibers by gently contacting a diluted droplet to the nanofiber [3], demonstrating an average coupling of 15% into a conventional optical fiber through the confined evanescent field of the nanofiber mode and single photon emission. Building on this achievement, we aim to study the system at cryogenic temperatures, which should enable the demonstration of efficient and indistinguishable single photons coupling to conventional optical fibers.Current collection efficiencies are intrinsically limited to 30% with the nanofiber[4], and improving light-matter coupling efficiency remains a key goal for high-performance single-photon sources and more advanced applications.To achieve this, we are investigating a newly developed technique [5]: the deterministic fabrication of dielectric and plasmonic nanostructures directly on the nanofiber surface using an “electron beam induced deposition” (EBID). The precision and versatility of this technique openthe way to different applications: Purcell enhancement of the quantum emitter emission using metallic nanoantennas and efficient light-matter coupling using dielectric structures. Our first calculation shown that optimizing the composition, geometry, and placement of these nanostructures a simple pattern of carbon pillars around the emitter should increase coupling efficiency up to 69% while maintaining high transmission in the nanofiber. We also demonstratethe fabrication of those nanostructures on top of the nanofiber.This work advances integrated nanophotonic devices for single-photon sources.[1] M. Nahra et al.,Single germanium vacancy centers in nanodia-monds with bulk-like spectral stability, AVS Quantum Science3(1), (2021).[2] E. Corte et al, Magnesium-Vacancy Optical Centers in Diamond, ACS Photonics, 10(1), p101-110, (2023)[3] Pierini et al. Highly Photostable Perovskite Nanocubes : TowardIntegrated Single Photon Sources Based on Tapered Nanofibers.ACS Photonics, 7(8), p.2265-2272, (2020).[4] Fujiwara et al., Highly efficient coupling of photons from na-noemitters into single-mode optical fibers, Nano Letters, 11(10),4362–4365, (2011).[5] A.Balena et al, Deterministic Bottom-Up Fabrication of Plasmonic Nanostructures on OpticalNanofibers via Blurred Electron Beam Deposition (soon to be published in Advance Material).
The authors demonstrate on-chip diamond nanophotonics with a high-efficiency fiber-optic interface, achieving >90% power coupling at visible wavelengths. They use this approach to create a bright source of narrowband single photons, based on a silicon-vacancy color center embedded in a waveguide-coupled diamond photonic-crystal cavity. Their quantum nanophotonic interface yields a high flux of coherent single photons into a single-mode fiber, enabling possibilities for quantum networks that couple multiple emitters, either on the same chip or separated by long distances.
We report the direct integration and efficient coupling of nitrogen vacancy (NV) color centers in diamond nanophotonic structures into a fiber-based photonic architecture at cryogenic temperatures. NV centers are embedded in diamond micro-waveguides (μWGs), which are coupled to fiber tapers. Fiber tapers have low-loss connection to single-mode optical fibers and hence enable efficient integration of NV centers into optical fiber networks. We numerically optimize the parameters of the μWG-fiber-taper devices designed particularly for use in cryogenic experiments, resulting in 35.6% coupling efficiency, and experimentally demonstrate cooling of these devices to the liquid helium temperature of 4.2 K without loss of the fiber transmission. We observe sharp zero-phonon lines in the fluorescence of NV centers through the pigtailed fibers at 100 K. The optimized devices with high photon coupling efficiency and the demonstration of cooling to cryogenic temperatures are an important step to realize fiber-based quantum nanophotonic interfaces using diamond spin defect centers.