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Artificial spin ices are periodic arrangements of interacting nanomagnets which allow investigating emergent phenomena in the presence of geometric frustration. Recently, it has been shown that artificial spin ices can be used as building blocks for creating functional materials, such as magnonic crystals. We investigate the magnetization dynamics in a system exhibiting anisotropic magnetostatic interactions owing to locally broken structural inversion symmetry. We find a rich spin-wave spectrum and investigate its evolution in an external magnetic field. We determine the evolution of individual modes, from building blocks up to larger arrays, highlighting the role of symmetry breaking in defining the mode profiles. Moreover, we demonstrate that the mode spectra exhibit signatures of long-range interactions in the system. These results contribute to the understanding of magnetization dynamics in spin ices beyond the kagome and square ice geometries and are relevant for the realization of reconfigurable magnonic crystals based on spin ices.

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.