A precise control and understanding of the magnetization dynamics of nanostructures is an important topic in applied nanosciences. Herein, we perform such control by annealing crystalline (Co/core)-(Pt/shell) nanoparticles. Using electron tomography, temperature dependent electron microscopy and time-resolved magneto-optics, we establish a clear correlation between the magnetization dynamics and the crystalline structure of the nanoparticles. For a mild laser annealing (370 K) the Co-Pt nanoparticles keep their core-shell structure and remain superparamagnetic with a blocking temperature T(B) = 66 K. Their time-resolved reflectivity shows that they are locally organized into a supra-crystalline ordered layer in the region of the laser spot. In contrast, a thermal annealing at higher temperatures (up to 700 K) modifies the structure of the individual nanoparticles into a CoPt crystalline ferromagnetic phase, with T(B,anneal) = 347 K. Correspondingly, the magneto-crystalline anisotropy of the annealed CoPt nanoparticles increases and their magnetization dynamics displays a motion of precession, characteristic of ferromagnetic nanostructures and which is absent in the superparamagnetic Co-Pt core-shells.

Computational and experimental results on the thermally-induced magnetization reversal in single-domain magnetic nanoparticles are reported. The simulations are based on the direct integration of the Fokker-Planck equation that governs the dynamics of the magnetic moment associated with the nanoparticles. A mean field approximation is used to account for the influence of the dipolar interaction between nanoparticles. It is shown that the interactions can either speed up or slow down the reversal process, depending on the angle between the external magnetic field and the axis of easy magnetization. The numerical results are in good agreement with experimental measurements on cobalt-platinum nanoparticles.