Magnetic Anisotropy


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magnetic anisotropy

[mag′ned·ik ‚an·ə′sä·trə·pē]
(electromagnetism)
The dependence of the magnetic properties of some materials on direction.

Magnetic Anisotropy

 

the nonidentical nature of the magnetic properties of bodies in different directions. It is caused by the anisotropic character of the magnetic interaction between atomic carriers of magnetic moment in substances.

Magnetic anisotropy is not manifested on a macroscopic scale in isotropic gases and liquids or in polycrystalline solids. On the other hand, in single crystals it leads to major observable effects, such as the difference in the value of magnetic susceptibility of paramagnetic crystals along different directions. Magnetic anisotropy is particularly great in ferromagnetic single crystals, where it is manifested in the presence of directions of easy magnetization, along which the vectors of spontaneous magnetization Jj of ferromagnetic domains are directed. The energy of magnetization of an external magnetic field that is necessary to rotate the vector Js from its position along the direction of easiest magnetization to a new position along the external field is a measure of magnetic anisotropy for a given direction in a crystal. At constant temperature the energy determines the free energy of magnetic anisotropy Fan for a given direction. The dependence of Fan on the orientation of Js in a crystal is determined on the basis of symmetry considerations. For example, for cubic crystals

Fan, cubc = K112α22 + α22α23 + α32α12)

where a1, a2, and a3 are the direction cosines of Js with respect to the axes of the crystal [100], and K1 is the first constant of natural crystallographic magnetic anisotropy (see Figure 1). Its value and sign are determined by the atomic structure of the substance and also depend on the temperature and pressure. For example, at room temperature K1 is of the order of 105 ergs/ cm3, or 104 joules per cu m (J/m3), in iron and of the order of —104 ergs/cm3 (—103 J/m3) in nickel. As the temperature in-creases these quantities decrease, tending toward zero at the Curie point. In antiferromagnets, which contain at least two magnetic sublattices (J1 and J2, there are at least two constants of magnetic anisotropy. For a uniaxial antiferromagnetic crystal, Fan may be written in the form (a/2) (J1z2 + J2z) + bJ1zJ2Z (where z is the direction of the axis of magnetic anisotropy). The values of the constants a and b are of the same order as in ferromagnets. Considerable anisotropy of the magnetic susceptibility K is observed in antiferromagnets; along the direction of easy magnetization K tends toward zero with a drop in temperature, but in the direction perpendicular to the axis (below the Neel temperature) K is independent of temperature.

Figure 1. Magnetic anisotropy of cubic single crystals of iron. The magnetization curves-for the three main crystallographic axes [100], [110], and [111] of a cell of an iron crystal are shown; (J) magnetization, (H) strength of magnetizing field

The constants of magnetic anisotropy may be determined experimentally by comparing the values of the energy of magnetic anisotropy for different crystallographic directions. Another method of determining the constants of magnetic anisotropy consists in the measurement of the torque moments acting on disks of ferromagnetic single crystals in an external field, since they are proportional to the constants of magnetic anisotropy. Finally, the constants may be determined graphically from the area bounded by the magnetization curves of ferromagnetic crystals and the axis along which the magnetization is plotted, for this area is also proportional to the constants of magnetic anisotropy. The values of the constants of magnetic anisotropy also can be determined from data on electron paramagnetic resonance (for paramagnets), ferromagnetic resonance (for ferromagnets), and antiferromagnetic resonance (for antiferromagnets). In addition to natural crystallographic magnetic anisotropy, magnetoelastic anisotropy, which occurs when external unilateral stresses are applied to a specimen, is also observed in magnets as a result of magnetostriction. Magnetic anisotropy is also manifested in polycrystals when a magnetic or crystallographic structure is present.

REFERENCES

Akulov, N. S. Ferromagnetizm. Moscow-Leningrad, 1939.
Bozorth, R. Ferromagnetizm. Moscow, 1956. (Translated from English.)
Vonsovskii, S. V., and Ia. S. Shur. Ferromagnetizm. Moscow-Leningrad, 1948.
Vonsovskii, S. V. Magnetizm. Moscow, 1971.
S. V. VONSOVSKII
References in periodicals archive ?
Perzynski, Dynamic optical probing of the magnetic anisotropy of nickel-ferrite nanoparticles, J.
Samples will be rotated by rotors at different positions to the magnetic field, which is suitable for the study of magnetic anisotropy of nanostructured materials.
In this paper, we report the motion of magnetic skyrmions driven by propagating SWs in a nanostrip with perpendicular magnetic anisotropy (PMA) by means of micromagnetic simulations.
Mill et al., "Influence of nanoparticular impurities on the magnetic anisotropy of self-assembled magnetic Co-nanoparticles," Journal of Magnetism and Magnetic Materials, vol.
We installed a sample heating system with a maximum temperature of 500[degrees]C in our spin SEM [15] to investigate the temperature dependence of the magnetic properties such as magnetic anisotropy and saturated magnetization.
The magnetic anisotropy appears while the analysis of the magnetization curves shapes--a steeper curves obtained for the samples measured in magnetic field oriented parallel confirm magnetic domain theory of the filler particles in the elastomer.
After reaching the maximum value of [chi] and below the magnetite Curie temperature, the [chi] as a temperature function follows the relationship: [chi](T) [varies] [M.sub.S](T)/K(T), where MS is the spontaneous magnetization and K the magnetic anisotropy. Both MS and K(T) decreased as the temperature increased, so when T approaches to [T.sub.C] both of these factors tend to go to 0 (Harrison & Putnis, 1996).
The magnetic anisotropy of the sample was determined by the sample rotation relative to a normal to the surface.
In the second case if rapidly quenched ribbon sensitive element is employed the advantage of natural nonuniform magnetic anisotropy was taken [5].
However, there is very little agreement with respect to the effective origin of magnetic anisotropy even for iron oxide nanoparticles that are widely used for over half a century, not to mention the recently developed core-shell nanoparticles.
They reported that the most important factors for heat are particle size, solvent viscosity, magnetic anisotropy, and the AMF frequency and amplitude.
The value of [T.sub.B] can be used to estimate the cluster size using the relationship [T.sub.B] = [K.sub.Co]V/[k.sub.B] ln([[tau].sub.m]/[[tau].sub.0]), where [K.sub.Co] is the magnetic anisotropy energy density for Co (4.9 x [10.sup.5] J [m.sup.-3]), V is the volume of the nanoparticle, [k.sub.B] is the Boltzmann constant, rm is the experimental measurement time (taken to be 10 s), and [[tau].sub.0] is the attempt period (1 x [10.sup.-10] s).