The nitrogen vacancy centre in diamond is a leading platform for nanoscale sensing and imaging, as well as quantum information processing in the solid state. To date, individual control of two nitrogen vacancy electronic spins at the nanoscale has been demonstrated. However, a key challenge is to scale up such control to arrays of nitrogen vacancy spins. Here, we apply nanoscale magnetic resonance frequency encoding to realize site-selective addressing and coherent control of a four-site array of nitrogen vacancy spins. Sites in the array are separated by 100 nm, with each site containing multiple nitrogen vacancies separated by~15 nm. Microcoils fabricated on the diamond chip provide electrically tuneable magnetic field gradients~0.1 G/nm. Tailored application of gradient fields and resonant microwaves allow site-selective nitrogen vacancy spin manipulation and sensing applications, including Rabi oscillations, imaging, and nuclear magnetic resonance spectroscopy with nanoscale resolution. Microcoil-based magnetic resonance of solid-state spins provides a practical platform for quantum-assisted sensing, quantum information processing, and the study of nanoscale spin networks.

We locally probe the magnetic fields generated by a spin-torque oscillator (STO) in a microbar of ferrimagnetic insulator yttrium-iron-garnet using the spin of a single nitrogen-vacancy (NV) center in diamond. The combined spectral resolution and sensitivity of the NV sensor allows us to resolve multiple spin-wave modes and characterize their damping. When damping is decreased sufficiently via spin injection, the modes auto-oscillate, as indicated by a strongly reduced linewidth, a diverging magnetic power spectral density, and synchronization of the STO frequency to an external microwave source. These results open the way for quantitative, nanoscale mapping of the microwave signals generated by STOs, as well as harnessing STOs as local probes of mesoscopic spin systems.