Solid-state spin defects are promising qubits for quantum network nodes. A key challenge toward larger networks is creating defects with high yield into nanophotonic devices while maintaining good optical and spin properties. Here, we demonstrate the creation of single V2 centers in nanopillars fabricated from commercial bulk-grown 4H-silicon carbide using a pulsed above-bandgap (UV) laser. We observe an 11-fold increase in the V2 center occurrence after UV laser illumination. These laser-induced V2 centers exhibit narrow optical line widths and spectral diffusion rates comparable to naturally occurring V2 centers in nanopillars of the same material. Furthermore, we measure a spin coherence time of (Formula presented) under dynamical decoupling, consistent with dephasing by the nuclear-spin bath. This demonstration of the in situ, postfabrication generation of coherent V2 centers in nanostructures in widely available bulk-grown 4H-SiC shows the potential for above-bandgap laser illumination for scalable defect creation in integrated photonic devices.

Spins associated to optically accessible solid-state defects have emerged as a versatile platform for exploring quantum simulation, quantum sensing and quantum communication. Pioneering experiments have shown the sensing, imaging, and control of multiple nuclear spins surrounding a single electron spin defect. However, the accessible size of these spin networks has been constrained by the spectral resolution of current methods. Here, we map a network of 50 coupled spins through high-resolution correlated sensing schemes, using a single nitrogen-vacancy center in diamond. We develop concatenated double-resonance sequences that identify spin-chains through the network. These chains reveal the characteristic spin frequencies and their interconnections with high spectral resolution, and can be fused together to map out the network. Our results provide new opportunities for quantum simulations by increasing the number of available spin qubits. Additionally, our methods might find applications in nano-scale imaging of complex spin systems external to the host crystal.

Efficient hyperpolarization of nuclear spins via optically active defect centers, such as the nitrogen vacancy (NV) center in diamond, has great potential for enhancing NMR-based quantum information processing and nanoscale magnetic resonance imaging. Recently, pulse-based protocols have been shown to efficiently transfer optically induced polarization of the electron defect spin to surrounding nuclear spins - at particular resonant pulse intervals. In this work, we investigate the performance of these protocols, both analytically and experimentally, with the electronic spin of a single NV defect. We find that whenever polarization resonances of nuclear spins are near degenerate with a "blocking"spin, which is single spin with stronger off-diagonal coupling to the electronic central spin, they are displaced out of the central resonant region - without, in general, significant weakening in the rate of polarization. We analyze the underlying physical mechanism and obtain a closed-form expression for the displacement. We propose that spin blocking represents a common but overlooked effect in hyperpolarization of nuclear spins and suggest solutions for improved protocol performance in the presence of (naturally occurring) blocking nuclear spins.