Biblio

We report on the significant enhancement of perpendicular magnetic anisotropy of Ni/NiO multilayers after mild annealing up to 90 min at 250 °C. Transmission electron microscopy shows that after annealing, a partial crystallization of the initially amorphous NiO layers occurs. This turns out to be the source of the anisotropy enhancement. Magnetic measurements reveal that even multilayers with Ni layers as thick as 7 nm, which in the as-deposited state showed inplane anisotropy with square hysteresis loops, show reduced in-plane remanence after thermal treatment. Hysteresis loops recorded with the field in the normal-to-film-plane direction provide evidence for perpendicular magnetic anisotropy with up and down magnetic domains at remanence. A plot of effective uniaxial magnetic anisotropy constant times individual Ni layer thickness as a function of individual Ni layer thickness shows a large change in the slope of the data attributed to a drastic change of volume anisotropy. Surface anisotropy showed a small decrease because of some layer roughening introduced by annealing.

In this paper, we present a study about the remanence state and coercivity in 1-D chain of cobalt hollow nanospheres, by using micromagnetic simulation. The high coercivity values (Hc is determined in the range of 600-1800 Oe) and the monotonic decrease of remanence are attributed to the shape anisotropy effect due to an increase in the aspect ratio value. The configuration of magnetization in remanence showed the onion state for hollow spheres (HSs) with Re = 15 nm, whereas for Re = 30 nm, appear the curling-vortex (CV) state. Finally for a cluster of chains, constituted by cobalt HSs, with random orientations the CV state is preserved.

The discovery of the interstitial rare earth nitride Sm2Fe17N3 came about seven years after the discovery of the rare earth iron boride Nd2Fe [1],[2], and the nitride initially seemed to offer intrinsic magnetic properties that were superior (Curie temperature TC, magnetocrystalline anisotropy K1 or comparable (spontaneous magnetization Ms to those of its illustrious predecessor. However, the promise of the new material to seriously challenge Nd2Fe14B was not realized. The 2:17 nitride powder, prepared by a low-temperature gas-phase interstitial modification process proved difficult to orient and worse still, it lost its nitrogen at the temperatures needed to process dense sintered magnets [3]. Attempts at explosive compaction [4] or spark sintering [5] failed to yield material with good enough coercivity. Nevertheless, work continued in Japan and China to develop a coercive powder that could be used for bonded magnets. An early realization was zinc-bonded Sm2Fe17N3 [6] with an energy product of 84 kJm3 but a rather low coercivity of 480 kAm-1, less than 5 % of the anisotropy field (Ha = 2K1/Ms ≈ 11 MAm-1). The anisotropy field of Nd2Fe14B is significantly less (6 MAm-1) yet several decades of intensive development have led to higher values and continuous improvements of the coercivity, even in unsubstituted material. Historical experience with permanent magnets shows that a long period of materials development is needed to arrive at the best composition and processing conditions for a microstructure that allows the hard magnetism to be optimized. Coercivities of about 25% of the anisotropy field are ultimately achieved. Here we compare the magnetic properties of melt-spun material. Our Nitroquench powder, produced by Daido Steel, was in the form of flakes 10 μm thick and up to 100 μm in diameter. A crystal-lite size of approximately 15 nm deduced from Scherrer broadening of the X-ray reflections. Composition was checked by EDX microprobe analysis. Hysteresis loops have been measured in applied fields of up to 14 T, at room temperature and at 4 K.The material exhibits a room-temperature coercivity of 690 kAm-1 after saturation in 14 T, with a remanence of 700 kAm-1 in zero applied field and an extrapolated saturation magnetization of 1230 kAm-1. The remanence ratio Mr/Ms of 63% when the remanence is corrected to zero internal field, is reflected in a preferred orientation seen in the X-ray powder diffraction patterns and in 57Fe Mössbauer spectra of magnetized powder. Spectra obtained after saturation of an immobilized powder absorber either in-plane or perpendicular to the sample plane exhibit distinctly different relative intensities of the ΔM=0 absorption lines. The maximum energy product for the powder, assuming full density, is 162 kJm-3. The remanence enhancement is attributed to fact that the nanocrystallite size is not much greater than the exchange length. Melt-spun Sm-Fe-N powder has superior corrosion resistance and thermal stability compared to melt-spun Nd-Fe-B. The Nitroquench powder may be used to produce polymer-bonded magnets with an energy product in excess of 100 kJm-3.

One method to increase bit density in magnetic memory devices is to use multi-state structures, such as a ferromagnetic nanoring with multiple domain walls (DWs), to encode information. However, there is a competition between decreasing the ring size in order to more densely pack bits and increasing it to make multiple DWs stable. This paper examines the effects of ring geometry, specifically inner and outer diameters (ODs), on the formation of 360° DWs. By sequentially increasing the strength of an applied circular magnetic field, we examine how DWs form under the applied field and whether they remain when the field is returned to zero. We examine the relationships between field strength, number of walls initially formed, and the stability of these walls at zero field for different ring geometries. We demonstrate that there is a lower limit of 200 nm to the ring diameter for the formation of any 360° DWs under an applied field, and that a high number of 360° DWs are stable at remanence only for narrow rings with large ODs.

Micromagnetic simulations of coercivity as a function of external magnetic field direction were performed for a hexagonal array of hemispherical Permalloy nanocaps. The analysis was based on hysteresis loops for arrangements of nanocaps of variable thickness (5 nm and 10 nm). The angular dependence of coercivity had a maximum at about 80° with respect to the arrangement plane. An increase in coercivity with nanocap thickness is related to the magnetization reversal mechanism, where the dipole energy of individual caps generates an effective intermediate axis, locking the magnetic moments. The coercivity has maximum values of 109 Oe for 5 nm and 156 Oe for 10 nm thickness. The remanence decreases monotonically with angle. This is associated with the influence of shape anisotropy, where the demagnetizing field in the plane of the array is much smaller than the demagnetizing field perpendicular to the plane.

We demonstrate how a unique nanomodulation within a continuous ferromagnetic film can induce magnetic dipoles at predefined, submicrometer scale locations, which can tune the global magnetic properties of the film due to dipole-dipole interactions. Arrays of tunable magnetic dipoles are generated with in-plane and out-of-plane directions, which can be rotated in-plane within the three-dimensional (3-D) modulated structure of a continuous film. In-plane magnetic dipole rotation enables a methodology to control overall magnetic properties of a ferromagnetic thin film. Formation of magnetic dipoles and their tunability were studied in detail by magnetic force microscopy, high-resolution magnetic measurements, and micromagnetic simulation of a nanomodulated Ni45Fe55 alloy film. A pattern larger than a single magnetic domain would normally form a vortex in the remanent state. However, here the unique 3-D nanostructure prevents vortex formation due to the competition between in-plane and out-of-plane dipole-dipole interaction giving rise to a metastable state. Experimentally, at zero remanence, the magnetization goes through a transformation from a metastable to a stable state, where the dipole-dipole interaction depends on their geometrical arrangement. Thus, the magnetic properties of the continuous film can be varied by the proposed pattern geometry. A detail analytical study of the dipolar energy for the system agrees well with the experimental and simulated results.