Electron Spin Resonance (ESR) describes a suite of techniques for characterising electronic systems, with applications in physics, materials science, chemistry, and biology. However, the requirement for large electron spin ensembles in conventional ESR techniques limits their spatial resolution. Here we present a method for measuring the ESR spectrum of nanoscale electronic environments by measuring the relaxation time (T1) of an optically addressed single-spin probe as it is systematically tuned into resonance with the target electronic system. As a proof of concept we extract the spectral distribution for the P1 electronic spin bath in diamond using an ensemble of nitrogen-vacancy centres, and demonstrate excellent agreement with theoretical expectations. As the response of each NV spin in this experiment is dominated by a single P1 spin at a mean distance of 2.7\,nm, the extension of this all-optical technique to the single NV case will enable nanoscale ESR spectroscopy of atomic and molecular spin systems.
@article{arxiv.1503.00830,
title = {Electron Spin Resonance Spectroscopy via Relaxation of Solid-State Spin Probes at the Nanoscale},
author = {L. T. Hall and P. Kehayias and D. A. Simpson and A. Jarmola and A. Stacey and D. Budker and L. C. L. Hollenberg},
journal= {arXiv preprint arXiv:1503.00830},
year = {2015}
}
Comments
fourteen pages (seven pages associated with main body of work, and seven pages of supplementary information), five figures (four figures associated with main body of work, and one supplementary figure)