Efficient collection of fluorescence light is essential for all optically adressable qubit platforms. For the nitrogen-vacancy (NV) center in diamond, the high refractive index of the host medium poses a major challenge as it limits the solid angle under which fluorescence light can leave the crystal. To enhance collection efficiency from single NV centers, we design and simulate micro-optical elements that shall be directly fabricated on the diamond surface using two-photon polymerization. Several optical designs and photoresists are evaluated for their expected coupling efficiency into single-mode fibers and their tolerance to fabrication errors. Additionally, an analytical solution for single lens collimation of the emission of a point source in diamond at a specific wavelength is presented, as well as considerations regarding the degradation of wavefront quality in multi-wavelength Fresnel designs.
Efficient collection of fluorescence light is essential for all optically adressable qubit platforms. For the nitrogen-vacancy (NV) center in diamond, the high refractive index of the host medium poses a major challenge as it limits the solid angle under which fluorescence light can leave the crystal. To enhance collection efficiency from single NV centers, we design and simulate micro-optical elements that shall be directly fabricated on the diamond surface using two-photon polymerization. Several optical designs and photoresists are evaluated for their expected coupling efficiency into single-mode fibers and their tolerance to fabrication errors. Additionally, an analytical solution for single lens collimation of the emission of a point source in diamond at a specific wavelength is presented, as well as considerations regarding the degradation of wavefront quality in multi-wavelength Fresnel designs.
Single Nitrogen-Vacancy centers (NV-centers) in diamond can be operated at ambient conditions as qubits in quantum memories and nanoscale quantum sensors. At TH Nürnberg, we plan to deterministically generate single NV-centers via femtosecond-laser pulses and integrate them into photonic platforms via 3D-printed microoptics and fs-written waveguides. This presentation gives a summary about our activites: The design and analysis of micro-lens systems to be manufactured via Two-Photon Polymerization on top of individual, self-written NV-centers for increased photon-collection efficiency, the programming of a spatial light modulator for wavefront optimization, the setup of a confocal scanning fluorescence microscope that addresses individual NV-Centers and laser material processing that allows to shape the diamond surface and to fabricate waveguides in the diamond for efficient optical coupling.
The nitrogen-vacancy (NV) center in diamond has an optically addressable, highly coherent spin. However, an NV center even in high quality single-crystalline material is a very poor source of single photons: extraction out of the high-index diamond is inefficient, the emission of coherent photons represents just a few per cent of the total emission, and the decay time is large. In principle, all three problems can be addressed with a resonant microcavity, which significantly boosts the emission rate of coherent photons into the cavity mode based on the Purcell effect. In practice though, it has proved difficult to implement this concept: photonic engineering hinges on nano-fabrication yet it is notoriously difficult to process diamond without degrading the NV centers. \nIn this thesis, we present a microcavity scheme which employs minimally processed diamond membranes, thereby preserving the high quality of the starting material. The miniaturized plano-concave Fabry-Perot microcavity platform features full in situ spatial and spectral tunability. We demonstrate a clear change in the lifetime for multiple individual NV centers on tuning both the cavity frequency and anti-node position. The overall Purcell factor for the zero-phonon line (ZPL) of ~30 translates to an increase in the ZPL emission probability from ~3% to ~46%. \nFurthermore, we report the creation of a low-loss, broadband optical antenna giving highly directed output from a coherent single spin in the solid state. The device, the first crystalline solid-state realization of a dielectric antenna, is engineered for individual NV electronic spins in diamond. The photonic structure preserves the high spin coherence of single-crystalline diamond (T2 ~100µs). We demonstrate a directionality of close to 10 and single photon count rates approaching one MHz. The analysis of the angular emission pattern of our device suggests that 95% of the broadband NV fluorescence is channeled into a solid angle corresponding to a numerical aperture of 0.8. \nThe abovementioned approaches feature complementary benefits. The narrowband enhancement of the ZPL emission rate provided by the microcavity benefits applications in quantum information processing relying on coherent photons. With the prospect of integrating lifetime-limited emitters and achieving a high ZPL collection efficiency our results pave the way for much enhanced spin-photon and spin-spin entanglement rates. On the other hand, by channeling the major fraction of the broadband NV fluorescence into a narrow solid angle the dielectric optical antenna facilitates efficient spin readout. Our approach enables a near-unity collection efficiency which, upon mitigation of the known photon losses, renders it a potential key technology for quantum sensing applications. \n
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.
Single-photon sources represent a key enabling technology in quantum optics, and single color centers in diamond are a promising platform to serve this purpose, due to their high quantum efficiency and photostability at room temperature. The widely studied nitrogen-vacancy (NV) centers are characterized by several limitations, thus other defects have recently been considered, with a specific focus of centers emitting in the near-infra red (NIR). In the present work, we report on the coupling of native NIR-emitting centers in high-quality single-crystal diamond with solid immersion lens (SIL) structures fabricated by focused ion beam (FIB) lithography. The reported improvements in terms of light collection efficiency make the proposed system an ideal platform for the development of single-photon emitters with appealing photophysical and spectral properties.
Luminescent lattice defects (so called “color centers”) in diamond provide a robust, solid-state architecture for exploring quantum optics, with many facilitating direct access to highly coherent electron and nuclear spins. The past two decades have seen tremendous advances in our ability to prepare and control the quantum states of these atom-like systems. For instance, demonstrations that leverage the diamond nitrogen vacancy (NV–) center as a spin-photon interface have included the generation of indistinguishable photons, a quantum bit memory exceeding 1 second, entanglement of two distance solid-state qubits, and deterministic long distance quantum teleportation. While diamond color centers are an attractive platform for scalable quantum information processing, the diamond solid-state matrix, by its very nature, inhibits efficient photon collection into either free-space or fiber-optical systems. Due to its large refractive index, emitted photons are inevitably trapped within the diamond crystal by total internal reflection, limiting count rates and overall scalability of information processing via quantum optical protocols. To this end, there has been significant progress towards integrating individual diamond color centers within well-defined radiation channels: namely, those provided by monolithic diamond nanophotonic networks. Currently, on-chip low loss (~ few db/cm) diamond waveguide networks are available, as well as key passive photonic elements like micron scale ring and disk resonators and photonic crystal cavities, with high optical quality (Q) factors. Specifically, we recently demonstrated a scalable ‘angled-etching’ nanofabrication method for realizing nanophotonic networks starting from bulk single-crystal diamond substrates (MJ Burek et al., Nano Letters 2012, MJ Burek et al., Nat Comm. 2014). Angled-etching employs anisotropic oxygen-based plasma etching at an oblique angle to the substrate surface, resulting in suspended optical structures with triangular cross-sections. Using this approach, we demonstrated high Q-factor (> 10^5) optical nanocavities fabricated in bulk single-crystal diamond, operating over a wide wavelength range (visible to telecom). Beyond isolated photonic devices, we have further developed free-standing angled-etched waveguides which efficiently route photons between diamond optical nanocavities, while maintaining physical support through attachment to the bulk substrate. Although on-chip diamond nanophotonics realized by angled-etching continue to mature, efficient off-chip optical coupling schemes which provide near seamless transition of photons on-chip into commercial optical fibers remain an outstanding challenge. This is especially pertinent in applications involving single photons, such as quantum optics with diamond color centers. Herein, we demonstrate a high efficiency fiber-optical interface with aforementioned on-chip diamond nanophotonic networks, achieving > 90% power coupling at both telecom and visible wavelengths. The coupling scheme utilizes a single mode optical fiber, with one end fabricated into a conical taper, to adiabatically transition guided light between on-chip tapered diamond waveguides and off-chip optical fiber networks. Additionally, we develop techniques to robustly pigtail single-mode fibers with diamond waveguide couplers, yielding a packaged technology that may potentially enable deployment in harsh environments, including vacuum, sub-Kelvin cryogenics, or even liquid/biological environments. With these newly developed optical integration schemes, single-crystal diamond is now a viable integrated nanophotonics platform, servicing a range of applications, from non-linear optics and chemical sensing, to quantum science and cavity optomechanics.
Diamond’s nitrogen-vacancy (NV) center has been shown as a promising candidate for sensing applications and quantum computing because of its long electron spin coherence time and its ability to be found, manipulated and read out optically. An integrated photonics platform in diamond would be useful for NV-based magnetometry and quantum computing, in which NV centers are optically linked for long-range quantum entanglement due to the integration and stability provided by monolithic optical waveguides. Surface microchannels in diamond would be a great benefit for sensing applications, where NV centers could be used to probe biomolecules. In this work, we applied femtosecond laser writing to form buried 3D optical waveguides in diamond. By engineering the geometry of the type II waveguide, we obtained single mode guiding from visible to the infrared wavelengths. Further, we demonstrate the first Bragg waveguide in bulk diamond with narrowband reflection. We show the formation of single, high quality NV centers on demand in ultrapure diamond using a single pulse from a femtosecond laser. With these building blocks in place, we fabricated an integrated quantum photonic circuit containing optical waveguides coupled to NV centers deterministically placed within the waveguide. The single NVs were excited and their emission collected by the optical waveguides, allowing easy interfacing to standard optical fibers. We also report high aspect ratio surface microchannels, which we will integrate with laser-written NVs and waveguides, paving the way for ultrasensitive, nanoscale resolution biosensors.