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The design of future spintronic devices requires a quantitative understanding of the microscopic linear and nonlinear spin relaxation processes governing the magnetization reversal in nanometer-scale ferromagnetic systems. Ferromagnetic resonance is the method of choice for a quantitative analysis of relaxation rates, magnetic anisotropy and susceptibility in a single experiment. The approach offers the possibility of coherent control and manipulation of nanoscaled structures by microwave irradiation. Here, we analyze the different excitation modes in a single nanometer-sized ferromagnetic stripe. Measurements are performed using a microresonator set-up which offers a sensitivity to quantitatively analyze the dynamic and static magnetic properties of single nanomagnets with volumes of (100 nm)(3). Uniform as well as non-uniform volume modes of the spin wave excitation spectrum are identified and found to be in excellent agreement with the results of micromagnetic simulations which allow the visualization of the spatial distribution of these modes in the nanostructures.

Correlating the electronic structure and magnetic response with the morphology and crystal structure of the same single ferromagnetic nanoparticle has been up to now an unresolved challenge. Here, we present measurements of the element-specific electronic structure and magnetic response as a function of magnetic field amplitude and orientation for chemically synthesized single Fe nanocubes with 18 nm edge length. Magnetic states and interactions of monomers, dimers, and trimers are analyzed by X-ray photoemission electron microscopy for different particle arrangements. The element-specific electronic structure can be probed and correlated with the changes of magnetic properties. This approach opens new possibilities for a deeper understanding of the collective response of magnetic nanohybrids in multifunctional materials and in nanomagnetic colloidal suspensions used in biomedical and engineering technologies.

The magnetization reversal process of single Co nanowires is investigated experimentally by magnetoresistance measurements at low temperatures. The results are compared to magnetic force micrographs of the remanent domain configuration. The theoretical expectation for the reversal process is obtained from Monte Carlo simulations. We find that both the width and the thickness of the wires as well as surface scattering play a significant role for the magnetization reversal processes. While thick ͑t Ͼ 15 nm͒ and narrow nanowires ͑w Ͻ 800 nm͒ switch by domain wall nucleation at the wire ends followed by wall motion, the magnetization reversal process in wide and/or thin nanowires is achieved by the generation of a multidomain state of the magnetization. It is shown both experimentally as well as theoretically that the wire width dependence of the coercive field can be used to pin a domain wall between two wire parts of different widths.