Ambient Nanoscale Sensing with Single Spins Using Quantum Decoherence
L. P. McGuinness, L. T. Hall, A. Stacey, D. A. Simpson, C. D. Hill, J., H. Cole, K. Ganesan, B. C.Gibson, S. Prawer, P. Mulvaney, F. Jelezko, J., Wrachtrup, R. E. Scholten, and L. C. L. Hollenberg

TL;DR
This paper demonstrates ambient nanoscale magnetic sensing using single NV spins in nanodiamonds, detecting fluctuations from small ensembles of Mn ions with high spatial resolution and sensitivity, significantly surpassing traditional ESR methods.
Contribution
The study introduces a method for detecting nanoscale spin ensembles at ambient conditions via quantum decoherence of single NV spins, achieving higher resolution and sensitivity than existing techniques.
Findings
Detected ~2,500 Mn spins in (16 nm)^3 volume within 4.2 seconds
Achieved spatial resolution at the nanometer scale
Reduced target ensemble size and acquisition time by orders of magnitude
Abstract
Magnetic resonance detection is one of the most important tools used in life-sciences today. However, as the technique detects the magnetization of large ensembles of spins it is fundamentally limited in spatial resolution to mesoscopic scales. Here we detect the natural fluctuations of nanoscale spin ensembles at ambient temperatures by measuring the decoherence rate of a single quantum spin in response to introduced extrinsic target spins. In our experiments 45 nm nanodiamonds with single nitrogen-vacancy (NV) spins were immersed in solution containing spin 5/2 Mn^2+ ions and the NV decoherence rate measured though optically detected magnetic resonance. The presence of both freely moving and accreted Mn spins in solution were detected via significant changes in measured NV decoherence rates. Analysis of the data using a quantum cluster expansion treatment of the NV-target system found…
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