| Literature DB >> 31853078 |
M H Abobeih1,2, J Randall1,2, C E Bradley1,2, H P Bartling1,2, M A Bakker1,2, M J Degen1,2, M Markham3, D J Twitchen3, T H Taminiau4,5.
Abstract
Nuclear magnetic resonance (NMR) is a powerful method for determining the structure of molecules and proteins1. Whereas conventional NMR requires averaging over large ensembles, recent progress with single-spin quantum sensors2-9 has created the prospect of magnetic imaging of individual molecules10-13. As an initial step towards this goal, isolated nuclear spins and spin pairs have been mapped14-21. However, large clusters of interacting spins-such as those found in molecules-result in highly complex spectra. Imaging these complex systems is challenging because it requires high spectral resolution and efficient spatial reconstruction with sub-ångström precision. Here we realize such atomic-scale imaging using a single nitrogen vacancy centre as a quantum sensor, and demonstrate it on a model system of 27 coupled 13C nuclear spins in diamond. We present a multidimensional spectroscopy method that isolates individual nuclear-nuclear spin interactions with high spectral resolution (less than 80 millihertz) and high accuracy (2 millihertz). We show that these interactions encode the composition and inter-connectivity of the cluster, and develop methods to extract the three-dimensional structure of the cluster with sub-ångström resolution. Our results demonstrate a key capability towards magnetic imaging of individual molecules and other complex spin systems9-13.Entities:
Year: 2019 PMID: 31853078 DOI: 10.1038/s41586-019-1834-7
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962