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Scalable parallel measurement of individual nitrogen-vacancy centers
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The nitrogen-vacancy (NV) center in diamond is a solid-state spin defect that has been widely adopted for quantum sensing and quantum information processing applications. Typically, experiments are performed either with a single isolated NV center or with an unresolved ensemble of many NV centers, resulting in a trade-off between measurement speed and spatial resolution or control over individual defects. In this work, we introduce an experimental platform that bypasses this trade-off by addressing multiple optically resolved NV centers in parallel. We perform charge- and spin-state manipulations selectively on multiple NV centers from within a larger set, and we manipulate and measure the electronic spin states of over 100 NV centers in parallel. We show that the high signal-to-noise ratio of the measurements enables the detection of shot-to-shot pairwise correlations between the spin states of 108 NV centers, corresponding to the simultaneous measurement of 5,778 unique correlation coefficients. We discuss how our platform can be scaled to parallel experiments with thousands of individually resolved NV centers. These results enable parallelized high-throughput sensing experiments that retain the nanoscale spatial resolution of single defects, and will thereby help to unlock advances in applications such as single-molecule NMR and characterization of integrated circuits. In addition, our approach to multiplexing provides a natural platform for the application of recently developed correlated sensing techniques.
Forward citations
Cited by 2 Pith papers
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Hearing the light: stray-field noise from the emergent photon in quantum spin ice
Finite-size emergent-photon modes produce measurable, boundary-condition-dependent stray-field noise: superconducting boundaries give sharp NV-detected spectra, insulating boundaries give none.
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High-Efficiency, High-Fidelity Charge Initialization of Shallow Nitrogen Vacancy Centers in Diamond
A combined green and near-infrared laser protocol initializes the negative charge state of shallow nitrogen vacancy centers in diamond to 95% fidelity in 300 microseconds, and to 90% in 10 microseconds at higher power.
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