Abstract

Ni Nanoparticle assembled thin films were prepared using an unconventional approach based on the use of a secondary nanosecond (ns) ultraviolet (UV) laser irradiation interacting with the plume of ablated nanoparticles (NPs) during the femtosecond pulsed laser deposition (fs-PLD). The secondary laser beam determines the reduction of the NPs size and their dispersion by partial vaporization of the NPs during their flight from the target to the substrate. The proper selection of the time delay between fs and ns laser pulses allows the latter to interact selectively with different parts of the NPs plume, controlling, to a certain degree, the reduction of the NPs size and dispersion. Another original effect of the UV laser irradiation is the change in the deposited films topology, due to a reduction of the NP-aggregates density and size, fostering non-uniform dense assemblies of NPs with concentration well above the percolation threshold, with the consequent reduction of the influence of the exchange interactions on the macroscopic magnetic properties. The magnetic behavior of the films prepared using two laser beams with respect to that obtained in the case of fs-PLD only is characterized by higher H(c) values (up to approximately 70%) and a good compromise between the hysteresis loops squareness and moderate exchange interactions, strongly correlated with the NPs topology.

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