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Using a high quality factor 3 GHz bulk acoustic wave resonator device, we demonstrate the acoustically driven single quantum spin transition ($left|m_{s}=0right>leftrightarrowleft|pm1right>$) for diamond NV centers and characterize the corresponding stress susceptibility. A key challenge is to disentangle the unintentional magnetic driving field generated by device current from the intentional stress driving within the device. We quantify these driving fields independently using Rabi spectroscopy before studying the more complicated case in which both are resonant with the single quantum spin transition. By building an equivalent circuit model to describe the devices current and mechanical dynamics, we quantitatively model the experiment to establish their relative contributions and compare with our results. We find that the stress susceptibility of the NV center spin single quantum transition is around $sqrt{2}(0.5pm0.2)$ times that for double quantum transition ($left|+1right>leftrightarrowleft|-1right>$). Although acoustic driving in the double quantum basis is valuable for quantum-enhanced sensing applications, double quantum driving lacks the ability to manipulate NV center spins out of the $left|m_{s}=0right>$ initialization state. Our results demonstrate that efficient all-acoustic quantum control over NV centers is possible, and is especially promising for sensing applications that benefit from the compact footprint and location selectivity of acoustic devices.
We demonstrate quantum interference between indistinguishable photons emitted by two nitrogen-vacancy (NV) centers in distinct diamond samples separated by two meters. Macroscopic solid immersion lenses are used to enhance photon collection efficienc
The neutral charge state plays an important role in quantum information and sensing applications based on nitrogen-vacancy centers. However, the orbital and spin dynamics remain unexplored. Here, we use resonant excitation of single centers to direct
We report electrical tuning by the Stark effect of the excited-state structure of single nitrogen-vacancy (NV) centers located less than ~100 nm from the diamond surface. The zero-phonon line (ZPL) emission frequency is controllably varied over a ran
We present systematic measurements of longitudinal relaxation rates ($1/T_1$) of spin polarization in the ground state of the nitrogen-vacancy (NV$^-$) color center in synthetic diamond as a function of NV$^-$ concentration and magnetic field $B$. NV
Hybrid quantum devices, in which disparate quantum elements are combined in order to achieve enhanced functionality, have received much attention in recent years due to their exciting potential to address key problems in quantum information processin