Localized-itinerant dichotomy and unconventional magnetism in SrRu2O6
Abstract
Electron correlations tend to generate local magnetic moments that usually order if the lattices are not too frustrated. The hexagonal compound SrRu2O6 has a relatively high Neel temperature but small local moments, which seem to be at odds with the nominal valence of Ru5+ in the t2g3 configuration. Here, we investigate the electronic property of SrRu2O6 using density functional theory (DFT) combined with dynamical-mean-field theory (DMFT). We find that the strong hybridization between Ru d and O p states results in a Ru valence that is closer to +4, leading to the small ordered moment 1.2μB. While this is consistent with a DFT prediction, correlation effects are found to play a significant role. The local moment per Ru site remains finite 2.3μB in the whole temperature range investigated. Due to the lower symmetry, the t2g manifold is split and the quasiparticle weight is renormalized significantly in the a1g state, while the renormalization in eg' states is about a factor of 2--3 weaker. Our theoretical Neel temperature 700~K is in reasonable agreement with experimental observations. SrRu2O6 is a unique system in which localized and itinerant electrons coexist with the proximity to an orbitally-selective Mott transition within the t2g sector.
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