We have studied the magnetic properties of cobalt clusters in a beam as functions of cluster size (N=20–200), magnetic field, and cluster temperature. The measured magnetic moments per atom increase with applied magnetic field and cluster size but decrease with increasing temperature, consistent with superparamagnetic behavior. Rapid orientation fluctuations of the true magnetic moments of these isolated particles yield the smaller, time-averaged, observed values. The true magnetic moments are (2.08±0.20) per atom and exceed the bulk value. Magnetically resolved isomers are seen for N=55–66.
The basic magnetic properties of three-dimensional nanostructured materials can be drastically different from those of a continuous film. High-resolution magnetic force microscopy studies of magnetic submicrometer-sized cobalt dots with geometrical dimensions comparable to the width of magnetic domains reveal a variety of intricate domain patterns controlled by the details of the dot geometry. By changing the thickness of the dots, the width of the geometrically constrained magnetic domains can be tuned. Concentric rings and spirals with vortex configurations have been stabilized, with particular incidence in the magnetization reversal process as observed in the ensemble-averaged hysteresis loops.
Low-temperature spin-polarized scanning tunneling microscopy is employed to study spin transport across single cobalt-phthalocyanine molecules adsorbed on well-characterized magnetic nanoleads. A spin-polarized electronic resonance is identified over the center of the molecule and exploited to spatially resolve stationary spin states. These states reflect two molecular spin orientations and, as established by density functional calculations, originate from a ferromagnetic molecule-lead exchange interaction.
23 March 2007 in Angewandte Chemie International Edition