Abstract

We consider a system of single-domain magnetic nanoparticles placed along a linear chain and address the effect of the distance between them on the magnetic and thermal relaxation properties of the system. The nanoparticles interact with each other through the dipolar interaction and we introduce disorder into the system by allowing random sizes of the nanoparticles and random directions of their uniaxial anisotropy axes. In particular, the radius of the spherical nanoparticles are drawn from a log-normal distribution. The dynamical behavior of the magnetic moments of the system is studied through numerical simulations of the stochastic Landau-Lifshitz-Gilbert equation, taking into account explicit temperature dependence of the saturation magnetization and uniaxial anisotropy energy density to describe the magnetic properties of perovskite manganite oxide nanoparticles. Hysteresis, zero-field-cooled and field-cooled curves are measured, from which we can find the coercive field and the blocking temperature as a function of the magnitude of the dipolar coupling, controlled by the distance between the particles. We show that both the coercive field and blocking temperature decrease as a function of the separation between the nanoparticles. The magnetic relaxation is measured as a function of both temperature and time, from which we estimate the effective energy barrier distribution of the system. We show that the peak of the energy barrier distribution moves to lower energies as the separation between neighboring particles increases, or equivalently, as the dipolar interaction is reduced.

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