Stability of α''-Fe16N2 in hydrogenous atmospheres.

We revealed the inherent instability of α''-Fe16N2 in hydrogenous atmospheres due to the denitrification toward α-Fe by forming NH3 at the particle surface. Coating the particle surface with SiO2 to suppress the formation of NH3 has proven to be a simple yet powerful method to enhance the stability of α''-Fe16N2 in hydrogenous atmospheres.

Magnetic ordered states induced by interparticle magnetostatic interaction in α-Fe/Au mixed nanoparticle assembly.

The magnetic behavior of α-Fe/Au nanoparticle (NP) assemblies is studied over a very wide range of dipolar interactions among α-Fe NPs, by changing the volume density of the α-Fe NP. The assembly whose α-Fe NP density is lower than 0.1% exhibits typical superparamagnetic behavior. When Fe NP density exceeds 8.6% the magnetic dynamics changes to that resembling superspin glass. Moreover, NP assembly with highest Fe concentration (43%), whose dipolar interaction is enormously strong compared with previous studies, exhibits a two-stage magnetic transition, i.e., ferromagnetic and spin glass-like transitions at 385 K and around 150 K, respectively. Therefore, we first observed the reentrant spin glass-like magnetism at the limit of strong interaction in a close-packed NP assembly. Based on these observations, the magnetic phase diagram of the interacting α-Fe NP assembly is determined over a very wide range of interaction.

Quantitative understanding of thermal stability of α''-Fe16N2.

The thermal stability of α''-Fe16N2, which attracts much interest because of its superior magnetic properties featuring a large magnetocrystalline anisotropy (Ku ~ 1 × 10(7) erg cm(-3)) and a large saturation magnetization (Ms ~ 234 emu g(-1)), though unfortunately thermally unstable, has been quantitatively studied.

Oblique-incidence sputtering of Ru intermediate layer for decoupling of intergranular exchange in perpendicular recording media.

During the Ru deposition process for granular type perpendicular magnetic recording media, both a reduction in the Ru intermediate layer thickness and lowering of sputtering gas pressure were successfully achieved by focusing on a self-shadowing effect. Oblique-incidence sputtering with a 60° incident angle under an Ar gas pressure of 0.6 Pa yielded (1) columnar Ru grains with a growth direction of 30° from the film normal, (2) c-plane sheet texture by epitaxial growth on the Pt underlayer, and (3) a flat envelope of the surface and a deep gap at grain boundaries. This change in the Ru structure significantly contributes to reducing exchange coupling among magnetic grains, especially in the initial growth region in an overlying granular medium.

Translocation of bio-functionalized magnetic beads using smart magnetophoresis.

We demonstrate real time on-chip translocation of bio-functionalized superparamagnetic beads on a silicon surface in a solution using a magnetophoresis technique. The superparamagnetic beads act as biomolecule carriers. Fluorescent-labeled Atto-520 biotin was loaded to streptavidin-coated magnetic beads (Dynabead(®) M-280) by means of ligand-receptor interactions. The magnetic pathways were patterned lithographically such that semi-elliptical Ni(80)Fe(20) elements were arranged sequentially for a few hundred micrometers in length. An external rotating magnetic field was used to drive translational forces on the magnetic beads that were proportional to the product of the field strength and its gradient. The translational force at the curving edge of the pathway element of 6 µm diameter was calculated to be ∼1.2 pN for an applied field of 7.9 kA m(-1). However, the force at the flat edge was calculated to be ∼0.16 pN. The translational force was larger than the drag force and thus allowed the magnetic beads to move in a directional way along the curving edge of the pathway. However, the force was not sufficient to move the beads along the flat edge. The top and bottom curving edge semi-elliptical NiFe pathways were obliquely-arranged on the left and right sides of the converging site, respectively. This caused a central translational force that allowed the converging and diverging of the Atto-520 biotin loaded streptavidin magnetic beads at a particular site.

Size control and characterization of wustite (core)/spinel (shell) nanocubes obtained by decomposition of iron oleate complex.

Monodisperse wustite (core)/spinel (shell) nanocubes with controllable size from 9 to 22 nm were synthesized by the decomposition of iron oleate complex at high temperature. The composition of the nanocubes was confirmed by X-ray diffraction and magnetic analysis, meanwhile the distributions of wustite and spinel phases within the nanocubes were directly observed by high resolution transmission electron microscopy using the dark-field image technique. The core/shell structure is quite unique, in which spinel phase is distributed not only preferentially on the surface, but also in the interior, while almost all of the wustite phase is located in the core of the nanocubes. The formation of wustite is inherent in the decomposition of the iron oleate complex, as indirectly inferred through the detection of a huge quantity of carbon monoxide generated from the reactor.

Facile synthesis of Fe3O4 nanoparticles by reduction phase transformation from gamma-Fe2O3 nanoparticles in organic solvent.

A phase transformation induced by the reduction of as-synthesized gamma-maghemite (gamma-Fe(2)O(3)) nanoparticles was performed in solution by exploiting the reservoir of reduction gas (CO) generated from the incomplete combustion reaction of organic substances in the reactor. Results from X-ray diffraction, color indicator, and magnetic analysis using a SQUID strongly support this phase transformation. Based on this route, monodisperse magnetite (Fe(3)O(4)) nanoparticles were simply produced in the range from 260 to 300 degrees C. Almost all aspects of the original gamma-Fe(2)O(3) nanoparticles, such as shape, size, and monodispersity, were maintained in the produced Fe(3)O(4) nanoparticles.

Magnetic characterization of Fe-nanoparticles encapsulated single-walled carbonnanotubes.

Magnetic Fe nanoparticles less than 1 nm have been successfully filled in single-walled carbon nanotubes (SWNTs), and their magnetic properties are characterized by means of SQUID measurements in the temperature range of 5-300 K.

Fabrication of Fe(3)O(4) nanoparticle arrays via patterned template assisted self-assembly.

Magnetic nanoparticle arrays have been fabricated by combining chemically synthesized Fe(3)O(4) nanoparticles with a diblock copolymer template substrate consisting of self-assembled polystyrene (PS) dots in a polymethylmethacrylate (PMMA) matrix. The influence of the volume fraction of the Fe(3)O(4) suspending solution and the withdrawal speed of the template on the formation of array structures was investigated. A small volume fraction of the nanoparticles and low withdrawal speed play an important role in the fabrication of the patterned arrays of nanoparticles via template assisted self-assembly. Below a withdrawal speed of 0.5 mm s(-1) and a nanoparticle volume fraction below 0.05 vol% (in particular, at extremely high dilutions of less than 0.01 vol%), the selective deposition of one to several nanoparticles on every single PS dot becomes possible.