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Register a new userMulti-Angle Reconstruction of Domain Morphology with All-Optical Diamond Magnetometry
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Scanning diamond magnetometers based on the optically detected magnetic resonance of the nitrogen-vacancy centre offer very high sensitivity and non-invasive imaging capabilities when the stray fields emanating from ultrathin magnetic materials are sufficiently low (< 10 mT). Beyond this low-field regime, the optical signal quenches and a quantitative measurement is challenging. While the field-dependent NV photoluminescence can still provide qualitative information on magnetic morphology, this operation regime remains unexplored particularly for surface magnetisation larger than $sim$ 3 mA. Here, we introduce a multi-angle reconstruction technique (MARe) that captures the full nanoscale domain morphology in all magnetic-field regimes leading to NV photoluminescence quench. To demonstrate this, we use [Ir/Co/Pt]$_{14}$ multilayer films with surface magnetisation an order of magnitude larger than previous reports. Our approach brings non-invasive nanoscale magnetic field imaging capability to the study of a wider pool of magnetic materials and phenomena.
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Detection of AC magnetic fields at the nanoscale is critical in applications ranging from fundamental physics to materials science. Isolated quantum spin defects, such as the nitrogen-vacancy center in diamond, can achieve the desired spatial resolution with high sensitivity. Still, vector AC magnetometry currently relies on using different orientations of an ensemble of sensors, with degraded spatial resolution, and a protocol based on a single NV is lacking. Here we propose and experimentally demonstrate a protocol that exploits a single NV to reconstruct the vectorial components of an AC magnetic field by tuning a continuous driving to distinct resonance conditions. We map the spatial distribution of an AC field generated by a copper wire on the surface of the diamond. The proposed protocol combines high sensitivity, broad dynamic range, and sensitivity to both coherent and stochastic signals, with broad applications in condensed matter physics, such as probing spin fluctuations.
The electronic spin of the nitrogen vacancy (NV) center in diamond forms an atomically sized, highly sensitive sensor for magnetic fields. To harness the full potential of individual NV centers for sensing with high sensitivity and nanoscale spatial resolution, NV centers have to be incorporated into scanning probe structures enabling controlled scanning in close proximity to the sample surface. Here, we present an optimized procedure to fabricate single-crystal, all-diamond scanning probes starting from commercially available diamond and show a highly efficient and robust approach for integrating these devices in a generic atomic force microscope. Our scanning probes consisting of a scanning nanopillar (200 nm diameter, $1-2,mu$m length) on a thin ($< 1mu$m) cantilever structure, enable efficient light extraction from diamond in combination with a high magnetic field sensitivity ($mathrm{eta_{AC}}approx50pm20,mathrm{nT}/sqrt{mathrm{Hz}}$). As a first application of our scanning probes, we image the magnetic stray field of a single Ni nanorod. We show that this stray field can be approximated by a single dipole and estimate the NV-to-sample distance to a few tens of nanometer, which sets the achievable resolution of our scanning probes.
Atomic comagnetometers, which measure the spin precession frequencies of overlapped species simultaneously, are widely applied to search for exotic spin-dependent interactions. Here we propose and implement an all-optical single-species Cs atomic comagnetometer based on the optical free induction decay (FID) signal of Cs atoms in hyperfine levels $F_g=3~&~4$ within the same atomic ensemble. We experimentally show that systematic errors induced by magnetic field gradients and laser fields are highly suppressed in the comagnetometer, but those induced by asynchronous optical pumping and drift of residual magnetic field in the shield dominate the uncertainty of the comagnetometer. With this comagnetometer system, we set the constraint on the strength of spin-gravity coupling of the proton at a level of $10^{-18}$ eV, comparable to the most stringent one. With further optimization in magnetic field stabilization and spin polarization, the systematic errors can be effectively suppressed, and signal-to-noise ratio (SNR) can be improved, promising to set more stringent constraints on spin-gravity interactions.
The sensing of magnetic fields has important applications in medicine, particularly to the sensing of signals in the heart and brain. The fields associated with biomagnetism are exceptionally weak, being many orders of magnitude smaller than the Earths magnetic field. To measure them requires that we use the most sensitive detection techniques, however, to be commercially viable this must be done at an affordable cost. The current state of the art uses costly SQUID magnetometers, although they will likely be superseded by less costly, but otherwise limited, alkali vapour magnetometers. Here, we discuss the application of diamond magnetometers to medical applications. Diamond magnetometers are robust, solid state devices that work in a broad range of environments, with the potential for sensitivity comparable to the leading technologies.
We experimentally demonstrate single-spin magnetometry with multi-pulse sensing sequences. The use of multi-pulse sequences can greatly increase the sensing time per measurement shot, resulting in enhanced ac magnetic field sensitivity. We theoretically derive and experimentally verify the optimal number of sensing cycles, for which the effects of decoherence and increased sensing time are balanced. We perform these experiments for oscillating magnetic fields with fixed phase as well as for fields with random phase. Finally, by varying the phase and frequency of the ac magnetic field, we measure the full frequency-filtering characteristics of different multi-pulse schemes and discuss their use in magnetometry applications.
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