Sensing of single nuclear spins in random thermal motion with proximate nitrogen-vacancy centers
arXiv:1508.00905 · doi:10.1103/PhysRevB.93.115116
Abstract
Nitrogen-vacancy (NV) centers in diamond have emerged as valuable tools for sensing and polarizing spins. Motivated by potential applications in chemistry, biology, and medicine, we show that NV-based sensors are capable of detecting single spin targets even if they undergo diffusive motion in an ambient thermal environment. Focusing on experimentally relevant diffusion regimes, we derive an effective model for the NV-target interaction, where parameters entering the model are obtained from numerical simulations of the target motion. The practicality of our approach is demonstrated by analyzing two realistic experimental scenarios: (i) time-resolved sensing of a fluorine nuclear spin bound to an N-heterocyclic carbene-ruthenium (NHC-Ru) catalyst that is immobilized on the diamond surface and (ii) detection of an electron spin label by an NV center in a nanodiamond, both attached to a vibrating chemokine receptor in thermal motion. We find in particular that the detachment of a fluorine target from the NHC-Ru carrier molecule can be monitored with a time resolution of a few seconds.
14 pages, 8 figures, supplemental material
References in corpus (6)
- High-sensitivity diamond magnetometer with nanoscale resolution
- Dynamic polarization of single nuclear spins by optical pumping of NV color centers in diamond at room temperature
- Detection and control of individual nuclear spins using a weakly coupled electron spin
- Spectroscopy of Surface-Induced Noise Using Shallow Spins in Diamond
- Hyperpolarized Nanodiamond with Long Spin Relaxation Times
- Optical hyperpolarization of 13C nuclear spins in nanodiamond ensembles