Using half-metallic manganite interfaces to reveal insights into spintronics.

A half-metal has been defined as a material with propagating electron states at the Fermi energy only for one of the two possible spin projections, and as such has been promoted as an interesting research direction for spin electronics. This review details recent advances on manganite thin film research within the field of spintronics, before presenting the structural, electronic and spin-polarized solid-state tunnelling transport studies that we have performed on heterostructures involving La(2/3)Sr(1/3)MnO(3) thin films separated by SrTiO(3) barriers. These experiments demonstrate that, with a polarization of spin [Formula: see text] electrons at the Fermi level that can reach 99%, the La(2/3)Sr(1/3)MnO(3)/SrTiO(3) interface for all practical purposes exhibits half-metallic behaviour. We offer insight into the electronic structure of the interface, including the electronic symmetry of any remaining spin [Formula: see text] states at the Fermi level. Finally, we present experiments that use the experimental half-metallic property of manganites as tools to reveal novel features of spintronics.

Magnetic relaxation of interacting co clusters: crossover from two- to three-dimensional lattices.

The influence that dipole-dipole interactions exert on the dynamics of the magnetization of nanometer-sized Co clusters has been studied by means of ac and dc susceptibility experiments. These clusters grow in a quasiordered layered structure, where all relevant parameters can be tailored and measured independently. Our data show without ambiguity that the magnetic relaxation becomes slower as the degree of interaction increases. The effective activation energy increases linearly with the number of nearest neighbor clusters, evolving from the value for a 2D layer to the fully 3D behavior, which is nearly reached for five layers. The experimental results agree quantitatively with the predictions of a simple model.

Growth of Au clusters on amorphous Al2O3: evidence of cluster mobility above a critical size.

We study the 3D growth of clusters during the deposition of Au atoms on amorphous Al2O3. By comparing transmission electron microscopy images of the growth with Monte Carlo simulations, we show that nucleation takes place on substrate defects, but that further stages of growth imply that clusters leave the defects after they have reached a given critical size, and diffuse. An interesting consequence of this property is that, in contrast to intuition, and in a certain range of size, larger clusters are more mobile than smaller ones in this system.