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Quantum 2.0 Conference and Exhibition

Optical and Spin Coherence of NV centers in Isotopically Purified Diamond for Quantum Networks

Hendrik Benjamin van Ommen, Kai-Niklas Schymik, T. Yamamoto, T. H. Taminiau

Published Jan 1, 2024• 0 citations
Publisher

Abstract

We discuss measurements on single NV centers in isotopically purified diamond and show coherent optical transitions combined with enhanced electron and carbon spin coherence. These results open avenues for new quantum network applications.
DOI
10.1364/quantum.2024.qth3a.39

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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.
We have studied optical and spin properties of near-surface nitrogen-vacancy (NV) centers incorporated during chemical vapor phase growth of isotopically purified (12)C single-crystal diamond layers. The spectral diffusion-limited line width of zero-phonon luminescence from the NV centers is 1.2 ± 0.5 GHz, a considerable improvement over that of NV centers formed by ion implantation and annealing. Enhanced spin dephasing times (T(2)* ≈ 90 μs, T(2) ≈ 1.7 ms) due to the reduction of (13)C nuclear spins persist even for NV centers placed within 100 nm of the surface.
Individual nuclear spins in diamond can be optically detected through hyperfine couplings with the electron spin of a single nitrogen-vacancy (NV) center; such nuclear spins have outstandingly long coherence times. Among the hyperfine couplings in the NV center, the nearest neighbor 13C nuclear spins have the largest coupling strength. Nearest neighbor 13C nuclear spins have the potential to perform fastest gate operations, providing highest fidelity in quantum computing. Herein, we report on the control of coherences in the NV center where all three nearest neighbor carbons are of the 13C isotope. Coherence among the three and four qubits are generated and analyzed at room temperature.
In recent years, nitrogen-vacancy (NV) color centers in diamond have become excellent solid-state quantum sensors due to their electronic spin properties. Especially for their easy optical initialization and detection, together with their very large spin coherence at room temperature. Many studies have reported their use for sensing temperature, strain, electric fields, and mainly magnetic fields. Here, we show how to build a two-dimensional map of the electronic spin coherence of an ensemble of NV centers in ultra-pure diamond, using an optical imaging protocol combined with microwave pulses relying simply on a regular CCD camera.
The complex environment of solid-state quantum bits is generally believed to pose a difficult challenge for solid state realizations of quantum information science. Close study of single electronic spins associated with the nitrogen-vacancy (NV) center in diamond has shown how a complex environment -- in this case a spin-bath formed by carbon-13 isotopic impurities -- may be understood and even controlled. Specifically, we show that optical and microwave excitation of the NV center can be used to perform robust initialization, manipulation, and measurement of the two-qubit register formed by the electronic spin and its nearest-neighbor carbon-13 nuclear spin. These few-qubit registers may be used as a basis for scalable quantum information systems provided that one can identify a means to connect different registers. For an optically active system such as the NV center, photons provide a natural medium for inter- register communication, and we discuss initial experiments studying the possibility of quantum optical interconnects. Such an optically-connected few-qubit register offers a flexible hardware for both quantum computation and long-distance quantum communication; in particular, it may allow realization of a solid-state quantum repeater.
Nitrogen-vacancy (NV) centers in diamond have recently emerged as a unique platform for fundamental studies in quantum information and nanoscience. The special properties of these impurity centers allow robust, room-temperature operation of solid-state qubits and have enabled several remarkable demonstrations in quantum information processing and precision nanoscale sensing. This article reviews the recent advances in magnetic and optical manipulation of the NV center’s quantum spin and their importance for prospective applications. We discuss how quantum control of individual centers can be harnessed for the protection of NV-center spin coherence, for multiqubit quantum operations in the presence of decoherence, and for high-fidelity initialization and readout. We also discuss the progress in resonant optical control, which has led to interfaces between spin and photonic qubits and may lead to spin networks based on diamond photonics. Many of these recently developed diamond-based technologies constitute critical components for the future leap toward practical multiqubit devices.