Dispersible SmCo5 nanoparticles with huge coercivity.

It is difficult to obtain dispersed particles of SmCo5 by calciothermic reduction because of sintering during the high-temperature reaction. This study presents a new strategy to synthesize dispersible SmCo5 particles by co-precipitating a precursor containing amorphous Sm(OH)3 and coherent nanoscale Co(OH)2 and Ca(OH)2 crystallites. The Ca(OH)2 dehydrates into CaO which forms an isolation shell around the SmCo5 particles that prevents them sintering during the reaction at 860 °C. A magnetization of 90 Am2 kg-1, a remanence ratio of 0.96 and a huge coercivity of 6.6-7.2 T were achieved at room temperature after dissolving the CaO and orienting a dispersion of the particles in epoxy in a 0.8 T external field. Based on its scan-rate dependence in high quasi-static and pulsed magnetic fields, the coercivity mechanism is identified as nucleation and growth of 88 nm3 nucleation volumes in a low-anisotropy surface region about 15 nm thick. The coercivity is the highest yet reported for nanoparticles of any permanent magnet and it opens the prospect of new high-temperature magnet composites.

Fe-Doping-Induced Magnetism in Nano-Hydroxyapatites.

Doping of biocompatible nanomaterials with magnetic phases is currently one of the most promising strategies for the development of advanced magnetic biomaterials. However, especially in the case of iron-doped magnetic hydroxyapatites, it is not clear if the magnetic features come merely from the magnetic phases/ions used as dopants or from complex mechanisms involving interactions at the nanoscale. Here, we report an extensive chemical-physical and magnetic investigation of three hydroxyapatite nanocrystals doped with different iron species and containing small or no amounts of maghemite as a secondary phase. The association of several investigation techniques such as X-ray absorption spectroscopy, Mössbauer, magnetometry, and TEM allowed us to determine that the unusual magnetic properties of Fe2+/3+-doped hydroxyapatites (FeHA) occur by a synergy of two different phenomena: i.e., (i) interacting superparamagnetism due to the interplay between iron-doped apatite and iron oxide nanoparticles as well as to the occurrence of dipolar interactions and (ii) interacting paramagnetism due to Fe3+ ions present in the superficial hydrated layer of the apatite nanophase and, to a lesser extent, paramagnetism due to isolated Fe3+ ions in the apatite lattice. We also show that a major player in the activation of the above phenomena is the oxidation of Fe2+ into Fe3+, as induced by the synthesis process, and their consequent specific positioning in the FeHA structure.

Internalization of ferromagnetic nanowires by different living cells.

The ability of living cells, either adherent or suspended, to internalize nickel nanowires is demonstrated for MC3T3-E1, UMR106-tumour and Marrow-Stromal cells. Nanowires were produced by electrodeposition, 20 mum long and 200 nm in diameter. Cell separation and manipulation was achieved for the three cell types. Applied magnetic field successfully oriented the internalized nanowires but no clear anisotropy is induced on the adherent cells. Nanowires tend to bind to cytoplasm metalloproteins and trigger lysosome reorganization around the nucleus. This work demonstrates the applications of nanowires in adherent and suspended cells for cell separation and manipulation, and further explore into their role in nanobiotechnology.