Abstract: We study the electronic structure of the Sr2YRuO6 and Sr2YRu0.75Ir0.25O6 compounds using x-ray (resonant) photoemission and absorption spectroscopies. The experimental results are interpreted with first-principles calculations, which give a good agreement with all the spectra. These results show that, although the spin-orbit coupling does not induce orbital anisotropies in these systems, it is responsible for the reduction of magnetic moments within the the Ir5+ O-6 octahedra, weakening the magnetic ordering in the substituted system. Finally, our findings support the idea that the canting of Ru5+ magnetic moments actually plays an important role in the stabilization of the intriguing magnetic ordering in the Sr2YRuO6 compound.
Author(s): Guedes, E. B.; Abbate, M.; Abud, F.; et al.
O Laboratório Aberto de Interatividade para Disseminação do Conhecimento Científico e Tecnológico (LAbI), vinculado à Universidade Federal de São Carlos (UFSCar), é voltado à prática da divulgação científica pautada na interatividade; nas relações entre Ciência, Arte e Tecnologia.
Writers: Andrés Felipe Espinosa Pineda and Filiberto González Garcia and Alexandre Zirpoli Simões and Elson Longo da Silva Keywords: Epoxy adhesives; 316 L stainless steel; Lap shear; Cohesive fracture Abstract: In this study, the mechanical behaviors, adhesive properties […]
Synthesis, antifungal evaluation and optical properties of silver molybdate microcrystals in different solvents: a combined experimental and theoretical study Abstract: In this study, we investigate the structure, antifungal activity, and optical properties of beta-Ag2MoO4 using […]
Magnetocoupling and domain structure of BiFeO3/LaFeO3 heterostructures deposited on LaSrCoO3/Pt/TiO2/SiO2/Si (100) substrates by the soft chemical method Abstract: BiFeO3 (BFO) and LaFeO3 (LFO) heterostructures were obtained at room temperature on Pt/TiO2/SiO2/Si (100) substrates by chemical […]