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arXiv:2604.07439 · npj Quantum Information

Ten-Second Electron-Spin Coherence in Isotopically Engineered Diamond

Takashi Yamamoto, H. Benjamin van Ommen, Kai-Niklas Schymik, Beer de Zoeten, Shinobu Onoda, Seiichi Saiki, Takeshi Ohshima, Hadi Arjmandi-Tash, René Vollmer, Tim H. Taminiau

quant-phSubmitted Apr 8, 2026• Announced Apr 10, 2026• 1 citation
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Abstract

Solid-state spin defects are a promising platform for quantum networks. A key requirement is to combine long ground-state spin-coherence times with a coherent optical transition for spin-photon entanglement. Here, we investigate the spin and optical coherence of single nitrogen-vacancy (NV) centres in (111)-grown isotopically engineered diamond. Our diamond-growth process yields a precisely controlled $^{13}\mathrm{C}$ concentration and low-ppb nitrogen concentrations. Combined with the mitigation of 50 Hz noise using a real-time feedforward scheme and tailored decoupling sequences, this enables record defect-electron-spin coherence times of $T_2 = 6.8(1)$ ms for a Hahn echo and of $T_2^{DD} = 11.2(8)$ s under dynamical decoupling. In addition, we observe coherent optical transitions with a near-lifetime-limited homogeneous linewidth of 16.9(4) MHz and characterize the spectral diffusion dynamics. These results provide new avenues to investigate the incorporation of impurities in diamond and new opportunities for improved spin-qubit control for quantum networks and other quantum technologies.

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Controlling the quantum dynamics of a mesoscopic spin bath in diamond

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Understanding and mitigating decoherence is a key challenge for quantum science and technology. The main source of decoherence for solid-state spin systems is the uncontrolled spin bath environment. Here, we demonstrate quantum control of a mesoscopic spin bath in diamond at room temperature that is composed of electron spins of substitutional nitrogen impurities. The resulting spin bath dynamics are probed using a single nitrogen-vacancy (NV) centre electron spin as a magnetic field sensor. We exploit the spin bath control to dynamically suppress dephasing of the NV spin by the spin bath. Furthermore, by combining spin bath control with dynamical decoupling, we directly measure the coherence and temporal correlations of different groups of bath spins. These results uncover a new arena for fundamental studies on decoherence and enable novel avenues for spin-based magnetometry and quantum information processing.

arXiv:1104.4648•Scientific Reports•Apr 25, 2012•142 citations
Solid-state spin defects are a promising platform for quantum networks. A key requirement is to combine long ground-state spin-coherence times with a coherent optical transition for spin-photon entanglement. Here, we investigate the spin and optical coherence of single nitrogen-vacancy (NV) centres in (111)-grown isotopically engineered diamond. Our diamond-growth process yields a precisely controlled 13C^{13}\mathrm{C}13C concentration and low-ppb nitrogen concentrations. Combined with the mitigation of 50 Hz noise using a real-time feedforward scheme and tailored decoupling sequences, this enables record defect-electron-spin coherence times of T2=6.8(1)T_2 = 6.8(1)T2​=6.8(1) ms for a Hahn echo and of T2DD=11.2(8)T_2^{DD} = 11.2(8)T2DD​=11.2(8) s under dynamical decoupling. In addition, we observe coherent optical transitions with a near-lifetime-limited homogeneous linewidth of 16.9(4) MHz and characterize the spectral diffusion dynamics. These results provide new avenues to investigate the incorporation of impurities in diamond and new opportunities for improved spin-qubit control for quantum networks and other quantum technologies.
Quantum networks require qubits that combine efficient optical access, coherent control, and long-lived quantum memory, but realizing all three in one scalable platform remains a central bottleneck. Diamond color centers are leading candidates, yet widely studied defects retain tradeoffs among these capabilities. Here, we show that transition-metal defects in diamond provide a distinct route beyond these platforms by combining spin-orbit protected ground-state coherence, all-optical control, and near-infrared emission. Using a single nickel-vacancy (NiV−^-−), we demonstrate an all-optically controlled diamond spin qubit with coherence exceeding one millisecond at 1.65 K, compatible with compact closed-cycle cryogenics. We implement Raman Rabi oscillations and Ramsey interferometry and use all-optical dynamical decoupling to extend coherence from T2∗T_2^*T2∗​ = 371 ns to T2CPMG−4T_2^{CPMG-4}T2CPMG−4​ = 1.27 ms, establishing NiV−^-− as a deployable diamond spin-photon interface.
Abstract Nitrogen-vacancy (NV) centers in diamond have been developed into essential hardware units for a wide range of solid-state-based quantum technology applications. While such applications require the long spin coherence times of the NV centers, they are often limited due to decoherence. In this study, we theoretically investigate the decoherence of NV-spin ensembles induced by nitrogen impurities (P1 centers), which are one of the most dominant and inevitable magnetic field noise sources in diamond. We combined cluster correlation expansion and density functional theory to compute the Hahn-echo spin-coherence time of the NV centers for a broad range of P1 concentrations. Results indicate a clear linear dependence of T2 on P1 concentrations on a log scale with a slope of −1.06, which is in excellent agreement with previous experimental results. The interplay between the Jahn–Teller effect and the hyperfine interaction in the P1 center plays a critical role in determining the bath dynamics and the resulting NV decoherence. Our results provide a theoretical upper bound for the NV-spin T2 over a wide range of P1 densities, serving as a key reference for materials optimization and spin bath characterization to develop highly coherent NV-based devices for quantum information technology.
Ensembles of nitrogen-vacancy (NV) centers in diamond are versatile quantum sensors with broad applications in the physical and life sciences. The concentration of neutral substitutional nitrogen ( [ N s 0 ]) strongly influences NV electronic spin coherence times, sensitivity, and optimal sensing strategies. Diamonds with [ N s 0 ] ∼ 1–10 ppm are a focus of recent material engineering efforts, with higher concentrations being favorable for continuous-wave optically detected magnetic resonance (CW-ODMR) and lower concentrations expected to benefit pulsed magnetometry techniques through extended NV spin coherence times and improved sensing duty cycles. In this work, we synthesize and characterize low- [ N s 0 ] ( ∼ 0.8 ppm), NV-enriched diamond material, engineered through low-strain chemical vapor deposition (CVD) growth on high-quality substrates, 12 C isotopic purification, and controlled electron irradiation and annealing. Our results demonstrate good strain homogeneity in diamonds grown on CVD substrates and spin-bath-limited NV dephasing times. By measuring NV spin and charge properties across a wide range of optical NV excitation intensity, we provide direct comparisons of photon-shot-noise-limited magnetic field sensitivity between the current low- [ N s 0 ] and previously studied higher- [ N s 0 ] ( ∼ 14 ppm) NV-diamond sensors. We show that low- [ N s 0 ] diamond can outperform higher- [ N s 0 ] diamond at moderate and low optical NV excitation intensity. Our results provide practical benchmarks and guidance for selecting NV-diamond sensors tailored to specific experimental constraints and sensing requirements.
Nitrogen impurities help to stabilize the negatively-charged-state of ${\mathrm{NV}}^{\ensuremath{-}}$ in diamond, whereas magnetic fluctuations from nitrogen spins lead to decoherence of ${\mathrm{NV}}^{\ensuremath{-}}$ qubits. It is not known what donor concentration optimizes these conflicting requirements. Here we used 10-MeV 15N3+{}^{15}{\mathrm{N}}^{3+}15N3+ ion implantation to create ${\mathrm{NV}}^{\ensuremath{-}}$ in ultrapure diamond. Optically detected magnetic resonance of single centers revealed a high creation yield of $40\ifmmode\pm\else\textpm\fi{}3%$ from 15N3+{}^{15}{\mathrm{N}}^{3+}15N3+ ions and an additional yield of $56\ifmmode\pm\else\textpm\fi{}3%$ from 14N^{14}\mathrm{N}14N impurities. High-temperature anneal was used to reduce residual defects, and charge stable ${\mathrm{NV}}^{\ensuremath{-}}$, even in a dilute 14N^{14}\mathrm{N}14N impurity concentration of 0.06 ppb were created with long coherence times.
Abstract Quantum networks can enable quantum communication and modular quantum computation. A powerful approach is to use multi-qubit nodes that provide quantum memory and computational power. Nuclear spins associated with defects in diamond are promising qubits for this role. However, dephasing during optical entanglement distribution hinders scaling to larger systems. Here, we show that a 13C-spin quantum memory in isotopically engineered diamond is robust to the optical link operation of a nitrogen-vacancy centre. The memory lifetime is improved by two orders-of-magnitude upon the state-of-the-art, surpassing reported times for entanglement distribution. Additionally, we demonstrate that the nuclear-spin state can survive ionisation and recapture of the nitrogen-vacancy electron. Finally, we use simulations to show that combining this memory with previously demonstrated entanglement links and gates can enable key network primitives, such as deterministic non-local two-qubit gates, paving the way for test-bed quantum networks capable of investigating complex algorithms and error correction.
Understanding and mitigating decoherence is a key challenge for quantum science and technology. The main source of decoherence for solid-state spin systems is the uncontrolled spin bath environment. Here, we demonstrate quantum control of a mesoscopic spin bath in diamond at room temperature that is composed of electron spins of substitutional nitrogen impurities. The resulting spin bath dynamics are probed using a single nitrogen-vacancy (NV) centre electron spin as a magnetic field sensor. We exploit the spin bath control to dynamically suppress dephasing of the NV spin by the spin bath. Furthermore, by combining spin bath control with dynamical decoupling, we directly measure the coherence and temporal correlations of different groups of bath spins. These results uncover a new arena for fundamental studies on decoherence and enable novel avenues for spin-based magnetometry and quantum information processing.