Monte Carlo investigation of the magnetic anisotropy in Fe/Dy multilayers

By Monte Carlo simulations in the canonical ensemble, we have studied the magnetic anisotropy in Fe/Dy amorphous multilayers. This work has been motivated by experimental results which show a clear correlation between the magnetic perpendicular anisotropy and the substrate temperature during elaboration of the samples. Our aim is to relate macroscopic magnetic properties of the multilayers to their structure, more precisely their concentration profile. Our model is based on concentration dependent exchange interactions and spin values, on random magnetic anisotropy and on the existence of locally ordered clusters that leads to a perpendicular magnetisation. Our results evidence that a compensation point occurs in the case of an abrupt concentration profile. Moreover, an increase of the non-collinearity of the atomic moments has been evidenced when the Dy anisotropy constant value grows. We have also shown the existence of inhomogeneous magnetisation profiles along the samples which are related to the concentration profiles.     

Fitting the flow curve of a plastically deformed silicon steel for the prediction of magnetic properties

We report measurements and modelling of magnetic effects due to plastic deformation in 2.2% Si steel, emphasizing new tensile deformation data. The modelling approach is to take the Ludwik law for the strain-hardening stress and use it to compute the dislocation density, which is then used in the computation of magnetic hysteresis. A nonlinear extrapolation is used across the discontinuous yield region to obtain the value of stress at the yield point that is used in fitting Ludwik's law to the mechanical data. The computed magnetic hysteresis exhibits sharp shearing of the loops at small deformation, in agreement with experimental behavior. Magnetic hysteresis loss is shown to follow a Ludwik-like dependence on the residual strain, but with a smaller Ludwik exponent than applies for the mechanical behavior.     

Ferrimagnetic properties of Co/(Gd–Co) multilayers

Co/(Gd–Co) multilayers have been prepared by rf-sputtering and investigated by means of Transverse Magnetooptic Kerr Effect (TMOKE), SQUID and VSM magnetometry. The composition of amorphous _Gd0.36Co0.64${\mathrm{Gd}}_{0.36}{\mathrm{Co}}_{0.64}$ layers was chosen so that their saturation magnetization was dominated by Gd moments in all the temperature range. Co and Gd–Co layers formed a macroscopic ferrimagnetically coupled system displaying a compensation temperature. Complete magnetic moment compensation was found at such point. An inversion of TMOKE hysteresis loops and a divergent behaviour of coercivity were also observed. By changing the layers thickness it has been possible to control the magnetic characteristics of the Co/(Gd–Co) structures, in particular the compensation takes place at different temperatures.     

Cosmology with inhomogeneous magnetic fields

We review spacetime dynamics in the presence of large-scale electromagnetic fields and then consider the effects of the magnetic component on perturbations to a spatially homogeneous and isotropic universe. Using covariant techniques, we refine and extend earlier work and provide the magnetohydrodynamic equations that describe inhomogeneous magnetic cosmologies in full general relativity. Specialising this system to perturbed Friedmann–Robertson–Walker models, we examine the effects of the field on the expansion dynamics and on the growth of density inhomogeneities, including non-adiabatic modes. We look at scalar perturbations and obtain analytic solutions for their linear evolution in the radiation, dust and inflationary eras. In the dust case we also calculate the magnetic analogue of the Jeans length. We then consider the evolution of vector perturbations and find that the magnetic presence generally reduces the decay rate of these distortions. Finally, we examine the implications of magnetic fields for the evolution of cosmological gravitational waves.     

Monte Carlo study of half-magnetization plateau and magnetic phase diagram in pyrochlore antiferromagnetic Heisenberg model

The antiferromagnetic Heisenberg model on a pyrochlore lattice under external magnetic field is studied by classical Monte Carlo simulation. The model includes bilinear and biquadratic interactions; the latter effectively describes the coupling to lattice distortions. The magnetization process shows a half-magnetization plateau at low temperatures, accompanied with strong suppression of the magnetic susceptibility. Temperature dependence of the plateau behavior is clarified. Finite-temperature phase diagram under the magnetic field is determined. The results are compared with recent experimental results in chromium spinel oxides.     

Explicit solutions to phenomenological models of magnetization reversal of thin ferromagnetic films in the presence of a sawtooth magnetic field

Explicit solutions are derived for several phenomenological models of magnetization reversal in thin ferromagnetic films driven by a sawtooth magnetic field. For a domain wall velocity that is linear in the magnetic field, it is found that the dynamic coercive field follows a square-root power-law in the slope of the magnetic field, shifted by the depinning field. For a more general domain wall velocity different power-law exponents are found, yet the overall form for the scaling of the area of the hysteresis loop remains a power-law shifted by the depinning field. This shifted power-law could be interpreted to be a crossover between adiabatic and dynamic regimes.     

Peculiar magnetic aftereffect of highly diluted frozen magnetic fluids

A very stably dispersed magnetic fluid (mother MF) and its 1000-times diluted solution were independently zero-field-cooled from room temperature to 5 K followed by application of a magnetic field of 2.86 MA/m for 300 s. After the field was removed (t=0)$(t=0)$, its residual magnetization M was measured as a function of time t for 80 000 s. After measurement, the MF sample was heated to room temperature, and the experiment was repeated after cooling to 5 K and again applying and removing the 2.86 MA/m field. We performed the same experiment several times, and obtained a different M vs t curve each time. With each cycle, the average M increased and the M vs t curve converged to a universal curve. In the initial few cycles, the value of M is very small, fluctuates and surprisingly increases with t in some time region. These characteristics are common in both the mother MF and diluted MF. We consequently propose the following physical model. When the MF is cooled, the isolated surfactant molecules in the solvent trigger the generation of magnetic colloid micelles. In other words, there occurs a phase transition from the magnetic colloids’ monodispersed phase to a micelle phase. The magnetic dipoles of the micelle's colloids make a closed magnetic flux loop. That is the origin of the anomalously small value of the residual magnetization in the early cycles. After a certain time elapses the micelles spontaneously break due to their residual stress, and a finite magnetic moment of the individual micelle develops. Consequently, M increases with t during this period.     

Room-temperature ferromagnetic Mn-alloyed ZnO films obtained by pulsed laser deposition

Ferromagnetic, semi-insulating Mn-alloyed ZnO films with a Curie temperature above 375 K have been grown by pulsed laser deposition on c-plane sapphire substrates. Antiferromagnetic coupling is revealed by temperature-dependent magnetization measurements. The antiferromagnetic coupling would be compatible with the observed weak ferromagnetism by assuming that the magnetic moments order antiferromagnetically but nonparallel (canted). We find a clear correlation between coercivity and mosaicity of the ferromagnetic Mn-alloyed ZnO films and explain it on the basis of a coercivity mechanism known from soft magnetic materials.     

Anisotropy and magnetization process in soft magnets: Principles,experiments, applications

Understanding and controlling the anisotropy energy and its effects has proved vital to the development of soft magnetic materials and their applications. Indeed, acting on composition and structure and working out specific annealing treatments, a large variety of anisotropy-governed behaviors under DC and AC excitation can be obtained. These are discussed in the present paper, together with special problems arising in the characterization of anisotropic soft magnets and a few significant applications. It is stressed how features like J$J$–H$H$ loop shape, energy losses, and magnetoresistance effects can be controlled, in crystalline and amorphous materials, by the methods of induced anisotropy. The high-frequency behavior of these materials can be strongly affected by the anisotropy field via resonant absorption of energy. This calls for tradeoff between the values of permeability and resonance frequency.     

Needle-like domain structure in Co films deposited on Mo (1 1 0)

Magnetization reversal processes and domain structures have been studied in Mo(1 1 0)/Co(0 0 0 1)/Au(1 1 1) structures grown by molecular beam epitaxy on monocrystalline (11–20) sapphire substrates. Wedge-shaped samples with different Co thickness gradients relative to the Mo [0 0 1] direction were fabricated. Observation of the domain structure was performed at room temperature using Kerr microscopy in a Co thickness range varying from 5 to 50 nm, where the magnetization is oriented in the plane of the sample. A Co thickness-dependent coercivity field was determined through analysis of the domain wall position during the reversal process. A preferential orientation of magnetic domain walls was found, with the domains being needle-like. The orientation, as well as the size of the needles, depends on the Co thickness and the orientation of the magnetic field applied in the sample plane.     

Synthesis,assembly and physical properties of magnetic nanoparticles

Compared with the top-down lithographic techniques, bottom-up chemical synthesis and self-assembly approaches offer much more flexibilities in creating magnetic nanostructures with controlled size, shape, composition and physical properties. This review summarizes some of the latest developments in this field, with emphasis mainly on transition metals, their alloys and metal oxide nanoparticles. The focus is directed towards the conditions of individual particles as well as large assemblies of particles through colloidal chemistry. Furthermore, some of the future directions in nanomagnetism from the perspective of physical chemists is also presented.     

Vibrational and rotational bound states in floppy triatomic systems: The distributed Gaussian functions approach

A variational method based on the use of bond coordinates and of a basis set expansion described by distributed Gaussian functions (DGF) is reviewed for its applications to the study of weakly bound triatomic clusters. This approach will be shown to be particularly well suited to treat very diffuse states as those presented by Noble gas (Ng) containing systems like the Ng₃, and Ng₂X, with X being also a very weakly bound atomic impurity. Several statistical properties such as radial distributions, sizes and dominance of triangular configurations for the corresponding bound states are shown to be directly obtained with this method over the whole spectrum of the floppy cluster bound states, in both the rotationless case and also when special care is taken to define rotational constants to yield rovibrational states and their energy levels.     

The method of increments—a wavefunction-based ab initio correlation method for solids

An overview of wavefunction-based correlation methods generalised for the application to solids is presented. Those methods based on a preceding Hartree–Fock treatment explicitly calculate the many-body wavefunction in contrast to the density-functional theory which relies on the ground-state density of the system. This review focus on the so-called method of increments where the correlation energy of the solid is expanded in terms of localised orbitals or of a group of localised orbitals. The method of increments is applied to a great variety of materials, from covalent semiconductors to ionic insulators, from large band-gap materials like diamond to the half-metal α$\alpha$-tin, from large molecules like fullerenes over polymers, graphite to three-dimensional solids. Rare-gas crystals where the binding is van der Waals like are treated as well as solid mercury, where the metallic binding is entirely due to correlation. Strongly correlated systems are examined and the correlation driven metal–insulator transition is described at an ab initio level.     

Coverage-dependent spin reorientation transition temperature of the Fe double-layer on W(1 1 0) observed by scanning tunneling microscopy

The magnetic domain structure of the Fe double-layer on W(1 1 0) is investigated using a variable-temperature scanning tunneling microscope. At low temperature the well-known periodic magnetic stripe domain structure is identified via the observation of domain walls. This is done with a non-spin-polarized tip by taking advantage of a spin–orbit coupling effect. At higher temperature a reorientation to an in-plane easy axis is observed. The spin reorientation temperature is found to be coverage-dependent and it is determined for samples with a coverage of 1.5–2.2 atomic layers of Fe on W(1 1 0).