Orbital selective coupling in CeRh3B2: co-existence of high Curie and high Kondo temperature
Abstract
We investigated the electronic structure of the enigmatic CeRh3B2 using resonant inelastic scattering and x-ray absorption spectroscopy in combination with ab initio density functional calculations. We find that the Rh 4d states are irrelevant for the high-temperature ferromagnetism and the Kondo effect. We also find that the Ce 4f crystal-field strength is too small to explain the strong reduction of the Ce magnetic moment. The data reveal instead the presence of two different active Ce 4f orbitals, with each coupling selectively to different bands in CeRh3B2. The inter-site hybridization of the |J=5/2,Jz=+/-1/2> crystal-field state and Ce 5d band combined with the intra-site Ce 4f-5d exchange creates the strong ferromagnetism, while hybridization between the |J=5/2,Jz=+/-5/2> and the B sp in the ab-plane contributes to the Kondo interaction which causes the moment reduction. This orbital selective coupling explains the unique and seemingly contradictory properties of CeRh3B2.
Turn this paper into a full lesson
ArcXiv compiles a staged curriculum from this paper: 8-12 lessons across beginner → advanced, synthesised section guides, visuals, flashcards, a quiz, exercises, and on-demand deep dives per section. Grounded in the abstract, never invented.