Spins in solids are cornerstone elements of quantum spintronics. Leading contenders such as defects in diamond or individual phosphorus dopants in silicon have shown spectacular progress, but either lack established nanotechnology or an efficient spin/photon interface. Silicon carbide (SiC) combines the strength of both systems: it has a large bandgap with deep defects and benefits from mature fabrication techniques. Here, we report the characterization of photoluminescence and optical spin polarization from single silicon vacancies in SiC, and demonstrate that single spins can be addressed at room temperature. We show coherent control of a single defect spin and find long spin coherence times under ambient conditions. Our study provides evidence that SiC is a promising system for atomic-scale spintronics and quantum technology.

and macroscopic diamond 10 . Here we experimentally demonstrate entanglement between two engineered single solid-state spin quantum bits (qubits) at ambient conditions. Photon emission of defect pairs reveals ground-state spin correlation. Entanglement (fidelity = 0.67 ± 0.04) is proved by quantum state tomography. Moreover, the lifetime of electron spin entanglement is extended to milliseconds by entanglement swapping to nuclear spins. The experiments mark an important step towards a scalable room-temperature quantum device being of potential use in quantum information processing as well as metrology.Engineering entangled quantum states is a decisive step in quantum technology. Although entanglement among weakly interacting systems such as photons has been demonstrated already in the early stages of quantum optics, deterministic generation of entanglement in more complex systems such atoms or ions, not to mention solids, is a relatively recent achievement 11 . Usually in solid-state systems rapid dephasing ceases any useful degree of quantum correlations. Either decoupling must be used to protect quantum states or careful materials engineering is required to prolong coherence. Most often however, and this is especially important for solid-state systems, one needs to resort to low (milliKelvin) temperatures to achieve sufficiently robust and longlasting quantum coherence. Spins are sufficiently weakly coupled to their environment to allow for the observation of coherence at room temperatures.Diamond defect spins are particularly interesting solid-state spin qubit systems. A number of hallmark demonstrations such as single-, two-and three-qubit operations, high-fidelity single-shot readout 12 , one-and two-qubit algorithms 13 , and entanglement between nuclear and electron and nuclear spin qubits have been achieved 6,14 . Different schemes to scale the system to a larger number of entangled electron spins have been proposed [15][16][17] . A path towards room-temperature entanglement is strong coupling among the ground-state spin magnetic dipole moment of adjacent defects centres. This mutual dipolar interaction scales as distance d −3 and should be larger than the interaction of each electron spin with the residual paramagnetic impurities or nuclear spin moments in the lattice (Fig. 1d). Typical cutoff distances for strong interaction are thus limited by the electron spin dephasing time (milliseconds) to be around 30 nm. Here we demonstrate entanglement between two electron and nuclear spins at a distance of approximately 25 nm. At these distances magnetic dipole coupling is strong enough to attain high-fidelity entanglement while being able to address the spins individually by super-resolution optical microscopy 18 . The optical as well as spin physics of nitrogen vacancy (NV) defects in diamond has been subject to numerous investigations 11,19 . The fluorescence intensity of the strongly allowed optical transition between ground and excited spin triplet states depends on the magnetic quantum number of the groun...

To exploit the quantum coherence of electron spins in solids in future technologies such as quantum computing, it is first vital to overcome the problem of spin decoherence due to their coupling to the noisy environment. Dynamical decoupling, which uses stroboscopic spin flips to give an average coupling to the environment that is effectively zero, is a particularly promising strategy for combating decoherence because it can be naturally integrated with other desired functionalities, such as quantum gates. Errors are inevitably introduced in each spin flip, so it is desirable to minimize the number of control pulses used to realize dynamical decoupling having a given level of precision. Such optimal dynamical decoupling sequences have recently been explored. The experimental realization of optimal dynamical decoupling in solid-state systems, however, remains elusive. Here we use pulsed electron paramagnetic resonance to demonstrate experimentally optimal dynamical decoupling for preserving electron spin coherence in irradiated malonic acid crystals at temperatures from 50 K to room temperature. Using a seven-pulse optimal dynamical decoupling sequence, we prolonged the spin coherence time to about 30 mus; it would otherwise be about 0.04 mus without control or 6.2 mus under one-pulse control. By comparing experiments with microscopic theories, we have identified the relevant electron spin decoherence mechanisms in the solid. Optimal dynamical decoupling may be applied to other solid-state systems, such as diamonds with nitrogen-vacancy centres, and so lay the foundation for quantum coherence control of spins in solids at room temperature.

The detection of single nuclear spins would be useful for fields ranging from basic science to quantum information technology. However, although sensing based on diamond defects and other methods have shown high sensitivity, they have not been capable of detecting single nuclear spins, and defect-based techniques further require strong defect-spin coupling. Here, we present the detection and identification of single and remote (13)C nuclear spins embedded in nuclear spin baths surrounding a single electron spin of a nitrogen-vacancy centre in diamond. We are able to amplify and detect the weak magnetic field noise (∼10 nT) from a single nuclear spin located ∼3 nm from the centre using dynamical decoupling control, and achieve a detectable hyperfine coupling strength as weak as ∼300 Hz. We also confirm the quantum nature of the coupling, and measure the spin-defect distance and the vector components of the nuclear field. The technique marks a step towards imaging, detecting and controlling nuclear spins in single molecules.

The detection of single nuclear spins is an important goal in magnetic resonance spectroscopy. Optically detected magnetic resonance can detect single nuclear spins that are strongly coupled to an electron spin, but the detection of distant nuclear spins that are only weakly coupled to the electron spin has not been considered feasible. Here, using the nitrogen-vacancy centre in diamond as a model system, we numerically demonstrate that it is possible to detect two or more distant nuclear spins that are weakly coupled to a centre electron spin if these nuclear spins are strongly bonded to each other in a cluster. This cluster will stand out from other nuclear spins by virtue of characteristic oscillations imprinted onto the electron spin decoherence profile, which become pronounced under dynamical decoupling control. Under many-pulse dynamical decoupling, the centre electron spin coherence can be used to measure nuclear magnetic resonances of single molecules. This atomic-scale magnetometry should improve the performance of magnetic resonance spectroscopy for applications in chemical, biological, medical and materials research, and could also have applications in solid-state quantum computing.