How systems of single-molecule magnets magnetize at low temperatures
J.F.Fernandez (1), J.J.Alonso (2), ((1) CSIC, Universidad de, Zaragoza, Spain, (2) Universidad de Malaga, Spain)

TL;DR
This paper models the low-temperature magnetization of single-molecule magnets through tunneling, revealing lattice-dependent behaviors and the influence of initial correlations, with results supported by Monte Carlo simulations.
Contribution
It introduces a stochastic model for dipole field diffusion and demonstrates how initial correlations influence magnetization dynamics in different lattice structures.
Findings
In simple cubic lattices, magnetization follows a sqrt(t) law for certain time scales.
In BCC and FCC lattices, magnetization scales as t^p with p approximately 0.7.
Magnetization eventually saturates at a constant value after initial growth.
Abstract
We model magnetization processes that take place through tunneling in crystals of single-molecule magnets, such as Mn_12 and Fe_8. These processes take place when a field H is applied after quenching to very low temperatures. Magnetic dipolar interactions and spin flipping rules are essential ingredients of the model. The results obtained follow from Monte Carlo simulations and from the stochastic model we propose for dipole field diffusion. Correlations established before quenching are shown to later drive the magnetization process. We also show that in simple cubic lattices, m \propto sqrt(t) at time t after H is applied, as observed in Fe_8, but only for 1+2\log_10(h_d/h_w) time decades, where h_d is some near-neighbor magnetic dipolar field and a spin reversal can occur only if the magnetic field acting on it is within some field window (-h_w,h_w). However, the sqrt(t) behavior is…
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