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 ($< 1\mu$m) cantilever structure, enable efficient light extraction from diamond in combination with a high magnetic field sensitivity ($\mathrm{\eta_{AC}}\approx50\pm20\,\mathrm{nT}/\sqrt{\mathrm{Hz}}$). 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

In several upcoming rheological approaches, including methods of micro- and nanorheology, the measurement geometry is of critical impact on the interpretation of the results. The relative size of the probe...

Inspired by chains of ferrimagnetic nanocrystals (NCs) in magnetotactic bacteria (MTB), the synthesis and detailed characterization of ferrimagnetic magnetite NC chain-like assemblies is reported. An easy green synthesis route in a thermoreversible gelatin hydrogel matrix is used. The structure of these magnetite chains prepared with and without gelatin is characterized by means of transmission electron microscopy, including electron tomography (ET). These structures indeed bear resemblance to the magnetite assemblies found in MTB, known for their mechanical flexibility and outstanding magnetic properties and known to crystallographically align their magnetite NCs along the strongest <111> magnetization easy axis. Using electron holography (EH) and angular dependent magnetic measurements, the magnetic interaction between the NCs and the generation of a magnetically anisotropic material can be shown. The electro-and magnetostatic modeling demonstrates that in order to precisely determine the magnetization (by means of EH) inside chain-like NCs assemblies, their exact shape, arrangement and stray-fields have to be considered (ideally obtained using ET).

The rotation of Ni nanorods, dispersed in dilute and semidilute poly­(ethylene oxide) solutions, is investigated. Ni nanorods with similar diameter but different lengths are synthesized using the anodic aluminum oxide template method and characterized by transmission electron microscopy and static magnetic field-dependent optical transmission (SFOT) of linearly polarized light. The rotational motion of nanorods, determined by oscillating magnetic field-dependent optical transmission (OFOT) measurements, is analyzed to retrieve the local dynamic modulus of the polymer solution. The effect of probe size relative to intrinsic length scales of the polymer solution is systematically investigated by variation of the nanorod size, polymer molar mass, and concentration. A significant decrease in the zero-shear rate viscosity is observed in the semidilute entangled regime, which depends on the hydrodynamic length of the nanorods, L h, and polymer radius of gyration, R g, but not on PEO concentration. The relative viscosity can be approximated by η 0 OFOT/η 0 macro = exp ( – 5.6R g/L h). The macroscopic dynamic modulus of the entangled polymer solutions is measured by small-amplitude oscillatory shear. The local dynamic modulus, obtained from nanorod oscillation measurements, exhibits systematic changes with decreasing size of the probe particles, which indicate entanglement reduction as the physical origin of the size effect in this particular particle/polymer system.

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