Soft and anisotropic local moments in 4d and 5d mixed-valence M2O9 dimers
Abstract
We investigate via exact diagonalization of finite clusters the electronic structure and magnetism of M2O9 dimers in the mixed-valence hexagonal perovskites A3B'M2O9 for various different fillings of 4d and 5d transition-metal M ions. We find that the magnetic moments of such dimers are determined by a subtle interplay of spin-orbit coupling, Hund's coupling, and Coulomb repulsion, as well as the electron filling of the M ions. Most importantly, the magnetic moments are anisotropic and temperature-dependent. This behavior is a result of spin-orbit coupling, magnetic field effects, and the existence of several nearly-degenerate electronic configurations whose proximity allows occupation of excited states already at room temperature. This analysis is consistent with experimental susceptibility measurements for a variety of dimer-based materials. Furthermore, we perform a survey of A3B'M2O9 materials and propose ground-state phase diagrams for the experimentally relevant M fillings of d4.5, d3.5 and d2.5. Finally, our results show that the usually applied Curie-Weiss law with a constant magnetic moment cannot be used in these spin-orbit-coupled materials.