This paper focuses on the magnetic properties of CoFe 2 O 4 nanoparticles, discussing the influence of nanoparticles arrangements obtained by different synthesis methods. Using high thermal decomposition (HTD) and direct micellar (DM) routes, three samples of CoFe 2 O 4 nanoparticles with equal primary particle size (∼5 nm) were prepared. The HTD method allows one to obtain highly crystalline primary nanoparticles coated by oleic acid organized in a self-assembling arrangement (ACoFe HTD ). The DM method results to be appropriate to prepare either irregular arrangements (IACoFe DM ) or spherical iso-oriented nanoporous assemblies (SACoFe DM ) of primary CoFe 2 O 4 nanocrystals. Despite the same particle size, magnetization measurements of the HTD sample show a tendency toward cubic anisotropy (M r / M s ≈ 0.7), while in DM samples, a uniaxial anisotropy (M r /M s ≈ 0.4) is observed. The comparison between IACoFe DM and SACoFe DM samples indicates that the ordering of nanocrystals at the mesoscopic scale induces an increase of the coercive field (μ 0 H c ≈ 1.17 T → μ 0 H c ≈ 1.45 T) and of the reduced remanent magnetization (M r /M s ≈ 0.4 → M r /M s ≈ 0.5). The reason for these differences is discussed. In particular, a detailed study on interparticle interactions is carried out, highlighting the influence of the molecular coating and the formation of spherical iso-oriented assemblies.

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.

The complex interplay of individual particle anisotropy and interparticle interactions determines the overall magnetic behavior of dense nanoparticle ensembles.

This paper focuses on the study of the magnetic properties of 9 nm magnetite nanocrystals. XRD and TEM measurements indicate the presence of crystalline particles, with a fraction of them only partially crystallized or highly defective. The analysis of the temperature dependence of the zero-field-cooled/field-cooled magnetization and of the thermoremanent magnetization provides evidence of the existence of three magnetic regimes: a high temperature regime (300-100 K), an intermediate regime (100-20 K), and a low temperature regime (below 20 K). The characteristics of such regimes are discusse

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.

In Co/CoO nanostructures, of dimensions l×3l, at small Co thickness (≈6,10 nm), a strong increase in the bias field and the associated coercive field are found as the nanostructure size is reduced from l=120 nm to l=30 nm. This property indicates that the characteristic length D(AF) within the antiferromagnet which governs exchange-bias effects is the nanostructure size. By contrast, at larger Co thickness (≈23 nm), the exchange-bias field does not depend on the nanostructure size, implying that D(AF) is smaller than the nanostructure size. The results are discussed in the framework of the Malozemoff model, taking into account that the coupling between CoO grains is weak. Exchange bias is dominated either by coupling within the antiferromagnetic layer (6- and 10-nm-thick Co samples) or by ferromagnetic-antiferromagnetic interfacial coupling (23-nm-thick Co sample).

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

Carbonated hydroxyapatite (CHA)-coated titanium can find wide applications as bone substitute implant in bone and dental surgery and orthopedics, promoting osseointegration with a host bone and ensuring biocompatibility and bioactivity. In this work, carbonated hydroxyapatite films were prepared on titanium substrates by pulsed laser deposition at different substrate temperatures ranging from 30 to 750 degrees C. The properties of films were investigated by scanning electron microscopy, atomic force microscopy, energy-dispersive X-ray diffraction, and Fourier transform infrared spectroscopy. Vickers microhardness measurements of the composite film-substrate systems were performed, and the intrinsic hardness of films was separated from the composite hardness using a "law-of-mixtures" approach and taking into account the indentation size effect. The prepared CHA films are nearly stoichiometric with a Ca/P atomic ratio of 2.0-2.2. The films deposited in the 30-500 degrees C temperature range are about 9 microm thick, amorphous, having an average roughness of 60 nm. At higher temperature, 700-750 degrees C, the films are about 4 microm thick, show a finer surface morphology and an average roughness of 20 nm. At 750 degrees C the films are amorphous, whereas at 700 degrees C they are crystalline and textured along the (202) and (212) directions. The intrinsic hardness of the films increased with an increase in substrate temperature, being as low as 5 GPa at 30 degrees C and reaching a high value of 28 GPa at 700 degrees C. The rich information gained by the joint use of the mentioned techniques allowed a comprehensive characterization of this system.