J = 0 nonmagnetic insulating state in KOs (X = F, Cl and Br)
arXiv:2206.05223 · doi:10.1103/PhysRevB.106.155148
Abstract
In transition-metal systems, many interesting physical properties arise from the interplay of bandwidth, electronic correlations, and spin-orbit interactions. Here, using {\it ab initio} density functional theory, we systematically study the double-perovskite-like system KOs (X = F, Cl, and Br) with a electronic configuration. Our main result is that the nonmagnetic insulating state develops in this system, induced by strong spin-orbital coupling. Specifically, the well-separated Os octahedra lead to the cubic crystal-field limit and result in dramatically decreasing hoppings in nearest neighbor Os-Os sites. In this case, the three degenerate orbitals are reconstructed into two ``effective'' ( and states) states separated by the strong SOC, opening a gap with four electrons occupying the orbitals. Furthermore, the hybridization between the Os orbitals and the ( = F, Cl, and Br) orbitals increases from F to Br, leading the electrons in KOsF to be more localized than in KOsCl and KOsBr, resulting in a smaller bandwidth for KOsF than in the Cl- or Br- cases. Our results provide guidance to experimentalists and theorists working on this interesting family of osmium halides.
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