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Register a new userInterplay between surface anisotropy and dipolar interactions in an assembly of nanomagnets
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We study the interplay between the effects of surface anisotropy and dipolar interactions in monodisperse assemblies of nanomagnets with oriented anisotropy. We derive asymptotic formulas for the assembly magnetization taking account of temperature, applied field, core and surface anisotropy, and dipolar inter-particle interactions. We find that the interplay between surface anisotropy and dipolar interactions is well described by the analytical expression of the assembly magnetization derived here: the overall sign of the product of the two parameters governing the surface and the dipolar contributions determines whether intrinsic and collective terms compete or have synergistic effects on the magnetization. This is illustrated by the magnetization curves of $gamma-Fe_{2}O_{3}$ nanoparticles assemblies in the low concentration limit.
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We compute the AC susceptibility of a weakly dipolar-interacting monodisperse assembly of magnetic nanoclusters with oriented anisotropy. For this purpose we first compute the relaxation rate in a longitudinal magnetic field of a single nanomagnet taking account of both dipolar interactions in the case of dilute assemblies and surface anisotropy. We then study the behavior of the real and imaginary components of the AC susceptibility as functions of temperature, frequency, surface anisotropy and inter-particle interactions. We find that the surface anisotropy induces an upward shift of the temperature at the maximum of the AC susceptibility components and that its effects may be tuned so as to screen out the effects of interactions. The phenomenological Vogel-Fulcher law for the effect of dipolar interaction on the relaxation rate is revisited within our formalism and a semi-analytical expression is given for the effective temperature is given in terms of inter alia the applied field, surface anisotropy and dipolar interaction.
We develop an analytical approach for studying the FMR frequency shift due to dipolar interactions and surface effects in two-dimensional arrays of nanomagnets with (effective) uniaxial anisotropy along the magnetic field. For this we build a general formalism on the basis of perturbation theory that applies to dilute assemblies but which goes beyond the point-dipole approximation as it takes account of the size and shape of the nano-elements, in addition to their separation and spatial arrangement. The contribution to the frequency shift due to the shape and size of the nano-elements has been obtained in terms of their aspect ratio, their separation and the lattice geometry. We have also varied the size of the array itself and compared the results with a semi-analytical model and reached an agreement that improves as the size of the array increases. We find that the red-shift of the ferromagnetic resonance due to dipolar interactions decreases for smaller arrays. Surface effects may induce either a blue-shift or a red-shift of the FMR frequency, depending on the crystal and magnetic properties of the nano-elements themselves. In particular, some configurations of the nano-elements assemblies may lead to a full compensation between surface effects and dipole interactions.
Controlled assembly of single-crystal, colloidal maghemite nanoparticles is facilitated via a high-temperature polyol-based pathway. Structural characterization shows that size-tunable nanoclusters of 50 and 86 nm diameters (D), with high dispersibility in aqueous media, are composed of $sim$ 13 nm (d) crystallographically oriented nanoparticles. The interaction effects are examined against the increasing volume fraction, $phi$, of the inorganic magnetic phase that goes from individual colloidal nanoparticles ($phi$= 0.47) to clusters ($phi$= 0.72). The frozen-liquid dispersions of the latter exhibit weak ferrimagnetic behavior at 300 K. Comparative Mossbauer spectroscopic studies imply that intra-cluster interactions come into play. A new insight emerges from the clusters temperature-dependent ac susceptibility that displays two maxima in $chi$(T), with strong frequency dispersion. Scaling-law analysis, together with the observed memory effects suggest that a superspin glass state settles-in at T$_{B}$ $sim$ 160-200 K, while at lower-temperatures, surface spin-glass freezing is established at T$_{f}$ $sim$40- 70 K. In such nanoparticle-assembled systems, with increased $phi$, Monte Carlo simulations corroborate the role of the inter-particle dipolar interactions and that of the constituent nanoparticles surface spin disorder in the emerging spin-glass dynamics.
We study the dynamical behavior of a square lattice Ising model with exchange and dipolar interactions by means of Monte Carlo simulations. After a sudden quench to low temperatures we find that the system may undergo a coarsening process where stripe phases with different orientations compete or alternatively it can relax initially to a metastable nematic phase and then decay to the equilibrium stripe phase through nucleation. We measure the distribution of equilibration times for both processes and compute their relative probability of occurrence as a function of temperature and system size. This peculiar relaxation mechanism is due to the strong metastability of the nematic phase, which goes deep in the low temperature stripe phase. We also measure quasi-equilibrium autocorrelations in a wide range of temperatures. They show a distinct decay to a plateau that we identify as due to a finite fraction of frozen spins in the nematic phase. We find indications that the plateau is a finite size effect. Relaxation times as a function of temperature in the metastable region show super-Arrhenius behavior, suggesting a possible glassy behavior of the system at low temperatures.
We study the competition of magneto-dipole, anisotropy and exchange interactions in composite three dimensional multiferroics. Using Monte Carlo simulations we show that magneto-dipole interaction does not suppress the ferromagnetic state caused by the interaction of the ferroelectric matrix and magnetic subsystem. However, the presence of magneto-dipole interaction influences the order-disorder transition: depending on the strength of magneto-dipole interaction the transition from the ferromagnetic to the superparamagnetic state is accompanied either by creation of vortices or domains of opposite magnetization. We show that the temperature hysteresis loop occurs due to non-monotonic behavior of exchange interaction versus temperature. The origin of this hysteresis is related to the presence of stable magnetic domains which are robust against thermal fluctuations.
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