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arXiv:2609.27601

Scalable integration of silicon carbide color centers into nanophotonic structures

Raphael Wörnle, Jonas Schmid, Dennis Grüner, Jonah Heiler, Flavie Davidson-Marquis, Georgy V. Astakhov, Vadim Vorobyov, Florian Kaiser, Jonathan Körber, Jörg Wrachtrup

quant-phSubmitted Sep 23, 2026• Announced Sep 24, 2026
arXivHTMLPDF

Abstract

Color centers in silicon carbide are a promising platform for quantum technologies, offering long-coherence electron and nuclear spins for storing and manipulating quantum information, as well as single-photon emission for quantum communication. Low photon collection efficiency is commonly addressed by integrating color centers into nanophotonic devices. Here, we report a scalable method for the deterministic integration of color centers into silicon carbide nanopillars, using the same nanoscale mask for both implantation of oxygen-related color centers (PL5, PL6) and subsequent nanopillar fabrication via dry etching. This approach solves the issue of low color center creation yield in nanostructures, with figures of merit comparable to bulk samples. We demonstrate count rate enhancements of up to one order of magnitude for PL5 and four times for PL6, while preserving spin coherence times. Our method is directly applicable to other solid-state platforms, offering a scalable route to efficiently integrate color centers into nanostructures.

AI Summary

The paper addresses how to integrate single spin-active color centers into SiC nanopillars without separate alignment of implantation sites and photonic structures. A single patterned PMMA mask defines both ion-implantation windows and, through nickel deposition and lift-off, the subsequent dry-etch mask. This registers implanted regions to pillars, but defect formation and lateral placement within each pillar remain probabilistic. PL5 and PL6 centers are characterized at room temperature in bulk SiC, conventional pillars, and pillars on 30–40 $\mu$m membranes with backside collection. Oxygen implantation gives pillar-site yields of 31.6% for PL5 and 22.7% for PL6, comparable to bulk-site yields of 19.2% and 28.5%, respectively, and substantially above carbon or nitrogen implantation. ODMR identifies defect types, while photon autocorrelation verifies single-emitter behavior with $g^{(2)}(0)<0.5$. Mean photon-count enhancements relative to bulk are $4.1\pm1.1$ and $2.1\pm0.7$ for PL5 and PL6 in conventional pillars, increasing to $6.0\pm2.0$ and $2.8\pm0.7$ in membrane pillars; individual enhancements exceed tenfold for PL5 and approach fourfold for PL6. Hahn-echo coherence times average $18.8\pm6.8\,\mu$s in conventional pillars and $12.2\pm5.6\,\mu$s in membrane pillars, compared with $21.5\pm5.7\,\mu$s for oxygen-implanted bulk defects. CW-ODMR parameters imply a best magnetic sensitivity of $140\,\mathrm{nT}/\sqrt{\mathrm{Hz}}$, approximately threefold better than bulk. Measured optical enhancements fall below FDTD predictions; the paper attributes this to averaging over pillar diameters, emitter-position variation, and fabrication inhomogeneity. Applicability to other hosts and photonic geometries is proposed rather than demonstrated.

Little sign of AI-generated textOverclaimsIncremental

Error found: The claim that nanopillar integration preserves spin coherence is not established by the reported comparisons: membrane-pillar emitters have a mean T2 of 12.2 microseconds versus 21.5 microseconds for oxygen-implanted bulk emitters, without a matched comparison or an analysis establishing equivalence.

Written by gpt-6.1-sol from the paper's full text. Automated: it can be wrong.

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Color centers in silicon carbide are a promising platform for quantum technologies, offering long-coherence electron and nuclear spins for storing and manipulating quantum information, as well as single-photon emission for quantum communication. Low photon collection efficiency is commonly addressed by integrating color centers into nanophotonic devices. Here, we report a scalable method for the deterministic integration of color centers into silicon carbide nanopillars, using the same nanoscale mask for both implantation of oxygen-related color centers (PL5, PL6) and subsequent nanopillar fabrication via dry etching. This approach solves the issue of low color center creation yield in nanostructures, with figures of merit comparable to bulk samples. We demonstrate count rate enhancements of up to one order of magnitude for PL5 and four times for PL6, while preserving spin coherence times. Our method is directly applicable to other solid-state platforms, offering a scalable route to efficiently integrate color centers into nanostructures.
The paper addresses how to integrate single spin-active color centers into SiC nanopillars without separate alignment of implantation sites and photonic structures. A single patterned PMMA mask defines both ion-implantation windows and, through nickel deposition and lift-off, the subsequent dry-etch mask. This registers implanted regions to pillars, but defect formation and lateral placement within each pillar remain probabilistic.
PL5 and PL6 centers are characterized at room temperature in bulk SiC, conventional pillars, and pillars on 30–40 μ\muμm membranes with backside collection. Oxygen implantation gives pillar-site yields of 31.6% for PL5 and 22.7% for PL6, comparable to bulk-site yields of 19.2% and 28.5%, respectively, and substantially above carbon or nitrogen implantation. ODMR identifies defect types, while photon autocorrelation verifies single-emitter behavior with g(2)(0)<0.5g^{(2)}(0)<0.5g(2)(0)<0.5. Mean photon-count enhancements relative to bulk are 4.1±1.14.1\pm1.14.1±1.1 and 2.1±0.72.1\pm0.72.1±0.7 for PL5 and PL6 in conventional pillars, increasing to 6.0±2.06.0\pm2.06.0±2.0 and 2.8±0.72.8\pm0.72.8±0.7 in membrane pillars; individual enhancements exceed tenfold for PL5 and approach fourfold for PL6.
Hahn-echo coherence times average 18.8±6.8 μ18.8\pm6.8\,\mu18.8±6.8μs in conventional pillars and 12.2±5.6 μ12.2\pm5.6\,\mu12.2±5.6μs in membrane pillars, compared with 21.5±5.7 μ21.5\pm5.7\,\mu21.5±5.7μs for oxygen-implanted bulk defects. CW-ODMR parameters imply a best magnetic sensitivity of 140 nT/Hz140\,\mathrm{nT}/\sqrt{\mathrm{Hz}}140nT/Hz​, approximately threefold better than bulk. Measured optical enhancements fall below FDTD predictions; the paper attributes this to averaging over pillar diameters, emitter-position variation, and fabrication inhomogeneity. Applicability to other hosts and photonic geometries is proposed rather than demonstrated.
Spin-active optical emitters in silicon carbide are excellent candidates toward the development of scalable quantum technologies. However, efficient photon collection is challenged by undirected emission patterns from optical dipoles, as well as low total internal reflection angles due to the high refractive index of silicon carbide. Based on recent advances with emitters in silicon carbide waveguides, we now demonstrate a comprehensive study of nanophotonic waveguide-to-fiber interfaces in silicon carbide. We find that across a large range of fabrication parameters, our experimental collection efficiencies remain above 90%. Further, by integrating silicon vacancy color centers into these waveguides, we demonstrate an overall photon count rate of 181 kilo-counts per second, which is an order of magnitude higher compared to standard setups. We also quantify the shift of the ground state spin states due to strain fields, which can be introduced by waveguide fabrication techniques. Finally, we show coherent electron spin manipulation with waveguide-integrated emitters with state-of-the-art coherence times of T 2 ∼ 42 μs. The robustness of our methods is very promising for quantum networks based on multiple orchestrated emitters.
Color centers are optically active point defects in semiconductor materials, many of them carrying a spin degree of freedom that couples coherently to emitted photons. This makes them a leading candidate for building quantum computers, networks, and sensors, but realizing that promise depends on the interface between the emitter and light. Color centers must be integrated into nanophotonic structures, such as nanopillars that collect their emission efficiently and optical cavities that couple them to a single mode. This dissertation studies the physics of quantum emitters inside such structures along two complementary threads: the direct cryogenic spectroscopy of color centers integrated into silicon carbide nanostructures, and the study of the physics of many-body cavity quantum electrodynamics (CQED) through simulation on superconducting and trapped-ion quantum hardware. The first thread concerns the nitrogen-vacancy (NV) center in 4H silicon carbide integrated into nanopillars. We show that the sub-wavelength geometry of a nanopillar reshapes the local electromagnetic environment, granting optical access to transitions that selection rules forbid in bulk material: emission from the PL3 divacancy, nearly absent in planar devices, becomes pronounced in nanopillars through a polarization transformation of the excitation field, and the orientation-dependent collection of the pillar resolves the previously ambiguous NV4′ line, establishing nanophotonic integration as a symmetry-sensitive probe of defect structure. We then take up the complementary problem of quantifying how many emitters a device contains, adapting the number-and-brightness technique from fluorescence microscopy to solid-state emitters. This calibration-free method counts dense NV ensembles in silicon carbide nanopillars, a regime beyond the reach of existing optical techniques, and extracts their areal density and formation yield. The second thread turns to many-body cavity QED, in which placing N emitters in a common cavity enhances the light-matter coupling by √N and gives rise to collective effects that are central to strong-coupling applications yet difficult to achieve in solid-state devices based on defects. We realize one such effect on a superconducting circuit, demonstrating photon blockade, the conversion of a coherent drive into a stream of single photons, in a Tavis–Cummings system of N = 1, 2, 3 transmon qubits coupled to a common resonator. To study the open-system dynamics that govern these systems, we digitally simulate the dissipative Tavis–Cummings model on both a superconducting and a trapped-ion processor. Platform-specific compilation and error mitigation yield population dynamics in close agreement with exact solutions, providing a recipe for simulating cavity-emitter systems on contemporary quantum computers. Together, the two threads connect the fabrication and characterization of color-center devices to the many-body cavity-QED physics that will ultimately govern their performance.
Silicon carbide (SiC) is a promising platform for scalable quantum technologies owing to its well-established, wafer-scale industrial processing. SiC also hosts a variety of optically active color centres including the nitrogen vacancy defect that has a spin-triplet ground state. However, strong phonon coupling in the infrared range limits photon extraction from these defects. Here, we use nanophotonic structures, specifically micro-pillar and micro-disk resonators, to enhance optical collection and spin-readout. The micro-pillar geometry yields a 4-fold increase in photon collection, accompanied by a 2.4-fold reduction in spectral noise in optically detected magnetic resonance measurements. Consequently, the magnetic field sensitivity is improved by 24%. The large mode volume of the micro-disk supports resonances spanning 1150-1250 nm, enabling broadband coupling to nitrogen vacancy emission lines. Our results demonstrate that fabrication of scalable photonic structures efficiently improves performance of silicon carbide color centers for integrated quantum light generation and sensing.
Color centers in wide bandgap semiconductors are prominent candidates for solid-state quantum technologies due to their attractive properties including optical interfacing, long coherence times, and spin–photon and spin–spin entanglement, as well as the potential for scalability. Silicon carbide color centers integrated into photonic devices span a wide range of applications in quantum information processing in a material platform with quantum-grade wafer availability and advanced processing capabilities. Recent progress in emitter generation and characterization, nanofabrication, device design, and quantum optical studies has amplified the scientific interest in this platform. We provide a conceptual and quantitative analysis of the role of silicon carbide integrated photonics in three key application areas: quantum networking, simulation, and computing.
Abstract Nanophotonic devices in color center-containing hosts provide efficient readout, control, and entanglement of the embedded emitters. Yet control over color center formation – in number, position, and coherence – in nanophotonic devices remains a challenge to scalability. Here, we report a controlled creation of highly coherent diamond nitrogen-vacancy (NV) centers with nanoscale three-dimensional localization in prefabricated nanostructures with high yield. Combining nitrogen δ -doping during chemical vapor deposition diamond growth and localized electron irradiation, we form shallow NVs registered to the center of diamond nanopillars with wide tunability over NV number. We report a positioning precision of ~ 4 nm in depth and 46(1) nm laterally in 280 nm-diameter pillars (102(2) nm in bulk diamond). We reliably form single NV centers with long spin coherence times (average T2Hahn=98 μs{T}_{2}^{Hahn}=98\, \mu {{{\rm{s}}}}T2Hahn​=98μs T 2 H a h n = 98 μ s ) and higher average photoluminescence compared to NV centers randomly positioned in pillars. Our method can improve the performance of various NV-based devices. In the realm of magnetic sensing, we achieve a 3 × improved yield of NV centers with single electron-spin sensitivity over conventional implantation-based methods. Our high-yield defect creation method will enable scalable production of solid-state defect sensors and processors.