Magnetic interactions in silica coated spherical nanoporous assemblies of CoFe(2)O(4) nanoparticles have been investigated by low temperature field dependent remanent magnetization (M(DCD) and M(IRM)) and magnetization relaxation measurements. The synthesis procedure leads to the formation of spherical aggregates of about 50-60 nm in diameter composed of hexagonal shaped nanocrystals with shared edges. The negative deviation from the non-interacting case in the Henkel plot indicates the predominance of dipole-dipole interactions favouring the demagnetized state, although the presence of exchange interactions in the porous system cannot be excluded. The activation volume, derived from time dependent magnetization measurements, turns out to be comparable with the particle physical volume, thus indicating, in agreement with static and dynamic irreversible magnetization measurements, that the magnetization reversal actually involves individual crystals.

Artificial magnetoception is a new and yet to be explored path for humans to interact with the surroundings. This technology is enabled by thin film magnetic field sensors embedded in a soft and flexible format to constitute magnetosensitive electronic skins (e-skins). Being limited by the sensitivity to in-plane magnetic fields, magnetosensitive e-skins are restricted to basic proximity and angle sensing and are not used as switches or logic elements of interactive wearable electronics. Here, a novel magnetoreceptive platform for on-skin touchless interactive electronics based on flexible spin valve switches with sensitivity to out-of-plane magnetic fields is demonstrated. The technology relies on all-metal Co/Pd-based spin valves with a synthetic antiferromagnet possessing perpendicular magnetic anisotropy. The flexible magnetoreceptors act as logic elements, namely momentary and permanent (latching) switches. The switches maintain their performance even upon bending to a radius of less than 3.5 mm and withstand repetitive bending for hundreds of cycles. Here, flexible switches are integrated in on-skin interactive electronics and their performance as touchless human-machine interfaces is demonstrated, which are intuitive to use, energy efficient, and insensitive to external magnetic disturbances. This technology offers qualitatively new functionalities for electronic skins and paves the way towards full-fledged on-skin touchless interactive electronics.

Two kinds of nanocomposites of transition metal oxides were synthesized and investigated. Each nanocomposite comprises nanoparticles of La0.67Ca0.33MnO3 and CoFe2O4 in similar volume fractions, however arranged with different morphologies. The temperature-dependent magnetic and electrical properties of the two systems are found to greatly differ, suggesting different degrees of interaction and coupling of their constituents. This is confirmed by magnetic field-dependent experiments, which reveal contrasted magnetization reversal and magnetoresistance in the systems. We discuss this morphology-physical property relationship, and the possibility to further tune the magnetism and magneto-transport in such nanocomposites.

Sol–gel synthesis was used in order to obtain nanocrystallites of the SrFe12O19 (SFO) hexaferrite in an efficient and reliable way. By optimizing the initial synthetic conditions, we were able to control the size of the nanoparticles (NPs), at lower annealing temperature. The x-ray powder diffraction, transmission electron microscopy (TEM), and magnetic measurements have demonstrated a significant relation between the morphology, size, and magnetic properties of the nanoscale SFO, revealing a definite dependence on the crystallite size along the c-axis. The obtained NPs appear almost isotropic, in the form of platelets and exhibit similar magnetic performance, in terms of the energy product (BH)MAX, thus, demonstrating the suitability of reducing the annealing temperature without any deterioration in the magnetic properties. Additionally, this work illustrates the feasibility of the sol–gel bottom-up approach to employ magnetic NPs as building-blocks for designing hard/soft exchange-coupled bi-magnetic nanocomposites, combining the high coercivity of a hard phase (SFO) and the high saturation magnetization of a soft phase (CoFe2O4); in this regard, we discuss the tunability of the magnetic anisotropy by symbiotically restricting the growth of both phases.

The prepared bioactive Si-HAp coatings could be considered for applications in orthopedics and dentistry to improve the osteointegration of bone implants.

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Magnetic nanocomposites (NCs) are extremely appealing for a wide range of energy-related technological applications, specifically as building blocks for next-generation permanent magnets. The design of such nanostructures requires precise chemical synthesis methods, which will permit the fine-tuning of the magnetic properties. Here we present an in-depth structural, morphological and magnetic characterization of ferrite-based nanostructures obtained through a bottom-up sol−gel approach. The combination of the high coercivity of a hard phase SrFe 12 O 19 (SFO) and the high saturation magnetization of a soft phase, CoFe 2 O 4 (CFO), allowed us to develop exchange-coupled bimagnetic NCs. A symbiotic effect is observed in a SFO/CFO nanocomposite, as the unique oriented growth of SFO prevents grain growth of the CFO, thus restricting the crystallite size of both. Through X-ray powder diffraction (XRPD), transmission electron microscopy (TEM), and magnetic measurements we clarify the relationship between the distribution and size of hard/soft particles, the optimization of interfaces and the obtained uniform magnetic response. This study allowed us to establish the potentiality of hard/soft SFO/CFO nanostructures in current permanent magnet technology.

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