Magnetization Reversal in Two-dimensional Ensemble of Nanoparticles with Positional Defects

Abstract

We study relaxation behaviour in the two-dimensional assembly of magnetic nanoparticles (MNPs) with aligned anisotropy axes and positional defects. The anisotropy axes orientation and disorder strength is changed by varying α and , respectively. The magnetization decay does not depend on the aspect ratio Ar of the system and for small dipolar interaction strength hd=0.2. Remarkably, the magnetization decays rapidly for considerable hd with negligible and Ar=1.0. The dipolar interaction of enough strength promotes antiferromagnetic coupling in square ensembles of MNPs. There is a prolonged magnetization decay for large because of enhancement in ferromagnetic coupling. Notably, magnetization relaxes slowly for α<α even with moderate hd and a significant Ar. Interestingly, the slowing down of the magnetic relaxation shifts to a lower α with hd=1.0. The magnetization ceases to relax for α≤60 and hd≤0.6 due to large shape anisotropy with Ar=400.0. Remarkably, a majority of the magnetic moment reverses its direction by 180 for α>60 and large hd, resulting in the negative magnetization. The effective N\'eel relaxation time τN also depends strongly on these parameters. τN depends weakly on α and for hd≤0.2, irrespective of Ar. On the other hand, τN decreases with α for significant hd provided α is greater than 45 because of antiferromagnetic coupling dominance. In a highly anisotropic system, there is an enhancement in τN with α (≤30) even with moderate hd. While for α>30, τN decreases with α. These observations are useful in novel materials, spintronics based applications, etc.

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