Magnetometry of random AC magnetic fields using a single Nitrogen-Vacancy center

We report on the use of a single NV center to probe fluctuating AC magnetic fields. Using engineered currents to induce random changes in the field amplitude and phase, we show that stochastic fluctuations reduce the NV center sensitivity and, in general, make the NV response field-dependent. We also introduce two modalities to determine the field spectral composition, unknown a priori in a practical application. One strategy capitalizes on the generation of AC-field-induced coherence 'revivals', while the other approach uses the time-tagged fluorescence intensity record from successive NV observations to reconstruct the AC field spectral density. These studies are relevant for magnetic sensing in scenarios where the field of interest has a non-trivial, stochastic behavior, such as sensing unpolarized nuclear spin ensembles at low static magnetic fields.Comment: 11 pages, 3 figure

METHOD FOR HYPER-POLARIZING NUCLEAR SPNS AT ARBTRARY MAGNETIC FELDS

A method of dynamically polarizing the nuclear spin host of nitrogen-vacancy (NV) centers in diamond is provided. The method uses optical, microwave and radio-frequency pulses to recursively transfer spin polarization from the NV electronic spin. Nitrogen nuclear spin initialization approaching 80% at room temperature is demonstrated both in ensemble and single NV centers without relying on level anti-crossings. This makes the method applicable at arbitrary magnetic fields

Optical patterning of trapped charge in nitrogen-doped diamond

The nitrogen-vacancy (NV) centre in diamond is emerging as a promising platform for solid-state quantum information processing and nanoscale metrology. Of interest in these applications is the manipulation of the NV charge, which can be attained by optical excitation. Here we use two-color optical microscopy to investigate the dynamics of NV photo-ionization, charge diffusion, and trapping in type-1b diamond. We combine fixed-point laser excitation and scanning fluorescence imaging to locally alter the concentration of negatively charged NVs, and to subsequently probe the corresponding redistribution of charge. We uncover the formation of spatial patterns of trapped charge, which we qualitatively reproduce via a model of the interplay between photo-excited carriers and atomic defects. Further, by using the NV as a probe, we map the relative fraction of positively charged nitrogen upon localized optical excitation. These observations may prove important to transporting quantum information between NVs or to developing three-dimensional, charge-based memories

Direct current control of three magnon scattering processes in spin-valve nanocontacts

We have investigated the generation of spin waves in the free layer of an extended spin-valve structure with a nano-scaled point contact driven by both microwave and direct electric current using Brillouin light scattering microscopy. Simultaneously with the directly excited spin waves, strong nonlinear effects are observed, namely the generation of eigenmodes with integer multiple frequencies (2 \emph{f}, 3 \emph{f}, 4 \emph{f}) and modes with non-integer factors (0.5 \emph{f}, 1.5 \emph{f}) with respect to the excitation frequency \emph{f}. The origin of these nonlinear modes is traced back to three magnon scattering processes. The direct current influence on the generation of the fundamental mode at frequency \emph{f} can be related to the spin-transfer torque, while the efficiency of three-magnon-scattering processes is controlled by the Oersted field as an additional effect of the direct current

High-resolution correlation spectroscopy of 13C spins near a nitrogen-vacancy centre in diamond

Spin complexes comprising the nitrogen-vacancy centre and neighbouring spins are being considered as a building block for a new generation of spintronic and quantum information processing devices. As assembling identical spin clusters is difficult, new strategies are being developed to determine individual node structures with the highest precision. Here we use a pulse protocol to monitor the time evolution of the 13C ensemble in the vicinity of a nitrogenvacancy centre. We observe long-lived time correlations in the nuclear spin dynamics, limited by nitrogen-vacancy spin–lattice relaxation. We use the host 14N spin as a quantum register and demonstrate that hyperfine-shifted resonances can be separated upon proper nitrogenvacancy initialization. Intriguingly, we find that the amplitude of the correlation signal exhibits a sharp dependence on the applied magnetic field.We discuss this observation in the context of the quantum-to-classical transition proposed recently to explain the field dependence of the spin cluster dynamics

Imaging thermal conductivity with nanoscale resolution using a scanning spin probe

The ability to probe nanoscale heat flow in a material is often limited by lack of spatial resolution. Here, we use a diamond-nanocrystal-hosted nitrogen-vacancy centre attached to the apex of a silicon thermal tip as a local temperature sensor. We apply an electrical current to heat up the tip and rely on the nitrogen vacancy to monitor the thermal changes the tip experiences as it is brought into contact with surfaces of varying thermal conductivity. By combining atomic force and confocal microscopy, we image phantom microstructures with nanoscale resolution, and attain excellent agreement between the thermal conductivity and topographic maps. The small mass and high thermal conductivity of the diamond host make the time response of our technique short, which we demonstrate by monitoring the tip temperature upon application of a heat pulse. Our approach promises multiple applications, from the investigation of phonon dynamics in nanostructures to the characterization of heterogeneous phase transitions and chemical reactions in various solid-state systems

Nitrogen-vacancy magnetometry of individual Fe-triazole spin crossover nanorods

[Fe(Htrz)2(trz)](BF4) (Fe-triazole) spin crossover molecules show thermal, electrical, and optical switching between high spin (HS) and low spin (LS) states, making them promising candidates for molecular spintronics. The LS and HS transitions originate from the electronic configurations of Fe(II) and are considered to be diamagnetic and paramagnetic respectively. The Fe(II) LS state has six paired electrons in the ground states with no interaction with the magnetic field and a diamagnetic behavior is usually observed. While the bulk magnetic properties of Fe-triazole compounds are widely studied by standard magnetometry techniques their magnetic properties at the individual level are missing. Here we use nitrogen vacancy (NV) based magnetometry to study the magnetic properties of the Fe-triazole LS state of nanoparticle clusters and individual nanorods of size varying from 20 to 1000 nm. Scanning electron microscopy (SEM) and Raman spectroscopy are performed to determine the size of the nanoparticles/nanorods and to confirm their respective spin states. The magnetic field patterns produced by the nanoparticles/nanorods are imaged by NV magnetic microscopy as a function of applied magnetic field (up to 350 mT) and correlated with SEM and Raman. We found that in most of the nanorods the LS state is slightly paramagnetic, possibly originating from the surface oxidation and/or the greater Fe(III) presence along the nanorods’ edges. NV measurements on the Fe-triazole LS state nanoparticle clusters revealed both diamagnetic and paramagnetic behavior. Our results highlight the potential of NV quantum sensors to study the magnetic properties of spin crossover molecules and molecular magnets