A Simple Analytical Model for Magnetization and Coercivity of Hard/Soft Nanocomposite Magnets.

We present a simple analytical model to estimate the magnetization (σ s) and intrinsic coercivity (H ci) of a hard/soft nanocomposite magnet using the mass fraction. Previously proposed models are based on the volume fraction of the hard phase of the composite. However, it is difficult to measure the volume of the hard or soft phase material of a composite. We synthesized Sm2Co7/Fe-Co, MnAl/Fe-Co, MnBi/Fe-Co, and BaFe12O19/Fe-Co composites for characterization of their σ s and H ci. The experimental results are in good agreement with the present model. Therefore, this analytical model can be extended to predict the maximum energy product (BH)max of hard/soft composite.

Synthesis and characterization of FeCo nanowires with high coercivity.

Ferromagnetic FeCo nanocrystals with high coercivity have been synthesized using a reductive decomposition method. The sizes and shapes of the nanocrystals were found to be dependent on reaction parameters such as the surfactant ratio, the precursor concentration and the heating rate. Synthesized nanocrystals have a body-centered cubic crystal structure for both particles and nanowires and the (110) crystalline direction is along the long axis of the nanowires. The coercivity and magnetization of the FeCo nanocrystals are found to be dependent on morphology. Nanowires of Fe60Co40 with saturation magnetization of 92 emu g(-1) and coercive force of 1.2 kOe have been obtained in this study.

High energy product developed from cobalt nanowires.

Cobalt nanowires with high aspect ratio have been synthesized via a solvothermal chemical process. Based on the shape anisotropy and orientation of the nanowire assemblies, a record high room-temperature coercivity of 10.6 kOe has been measured in Co nanowires with a diameter of about 15 nm and a mean length of 200 nm. As a result, energy product of the wires reaches 44 MGOe. It is discovered that the morphology uniformity of the nanowires is the key to achieving the high coercivity and high energy density. Nanowires of this type are ideal building blocks for future bonded, consolidated and thin film magnets with high energy density and high thermal stability.

Synthesis of monodisperse FeCo nanoparticles by reductive salt-matrix annealing.

We report here a novel synthetic method to prepare monodisperse air-stable FeCo nanoparticles with average sizes of 8, 12 and 20 nm. CoFe2O4 nanoparticles of different sizes were first synthesized by a chemical solution method. The as-synthesized CoFe2O4 nanoparticles were then mixed with ball-milled NaCl powders and heated to 400-500 ° C in forming gas (Ar 93%+H2 7%). The salt powder worked as a separating medium that prevents the CoFe2O4 nanoparticles from agglomerating during the heat treatment while the forming gas reduces the CoFe2O4 nanoparticles to FeCo nanoparticles. Monodisperse FeCo nanoparticles were recovered by dissolving the NaCl in water and subsequently washing with ethanol and acetone. Structural analyses confirmed that FeCo nanoparticles retained the same size as their oxide precursors. The size of the FeCo nanoparticles can be well tuned by controlling the size of the CoFe2O4 nanoparticles. The saturation magnetization of FeCo nanoparticles is size dependent and increases with size.

Synthesis of FePt nanorods and nanowires by a facile method.

FePt nanorods and nanowires have been synthesized by the reduction of Pt(acac)(2) and the thermal decomposition of Fe(CO)(5) in the presence of solvents/surfactants by simply controlling the sequence of addition of surfactants. The as-synthesized FePt nanorods and nanowires have a face centered cubic structure with average diameter of 3 nm. Length of nanorods and nanowires can be adjusted in the range of 15-150 nm by varying reaction parameters. Nanocrystalline L1(0) FePt phase with coercivity up to 24 kOe was obtained after heat treatments.

Magnetic Nanoparticles to Enhance Cell Seeding and Distribution in Tissue Engineering Scaffolds.

The success of tissue engineering scaffolds is intimately linked with the ability of the seeded cells to adequately distribute and proliferate within the scaffold matrix. In tissue engineering scaffolds, it is difficult to achieve adequate distribution due to the hydrophobic nature of most scaffold materials and poor initial distribution following scaffold seeding. In this study, we investigated the distribution of cells in PLGA salt-leached scaffolds after seeding with magnetic nanoparticle loaded cells with a neodymium magnet placed below. The combined use of magnetic nanoparticle seeded cells and magnetic force was able to not only increase the total number of scaffold adherent cells, but also increase the infiltration and distribution compared with controls. This method to control the distribution of cells may provide a method to increase the functionality of tissue engineering scaffolds.