Structural and metal-insulator transitions in rhenium based double perovskites via orbital ordering
arXiv:1708.07798 · doi:10.1103/PhysRevB.97.045102
Abstract
Re-based double perovskites (DPs) exhibit a complex interplay of structural and metal-insulator transitions. Here we systematically study the ground state electronic and structural properties for a family of Re-based DPs ReO (=Sr, Ca and =Cr, Fe), which are related by a common low energy Hamiltonian, using density functional theory + calculations. We show that the on-site interaction of Re induces orbital ordering (denoted COO), with each Re site having an occupied orbital and a C-type alternation among , resulting in an insulating state consistent with experimentally determined insulators SrCrReO, CaCrReO, and CaFeReO. The threshold value of for orbital ordering is reduced by inducing octahedral distortions of the same C-type wavelength (denoted COD), which serves as a structural signature of the orbital ordering; octahedral tilting also reduces the threshold. The COO, and the concomitant COD, are a spontaneously broken symmetry for the Sr based materials (i.e. tilt pattern), while not for the Ca based systems (i.e. tilt pattern). Spin-orbit coupling does not qualitatively change the physics of the COO/COD, but can induce relevant quantitative changes. We prove that a single set of ,, capture the experimentally observed metallic state in SrFeReO and insulating states in the other three systems. We predict that the COO is the origin of the insulating state in SrCrReO, and that the concomitant COD may be experimentally observed at sufficiently low temperatures (ie. space group P). Additionally, given our prescribed values of , we show that the COO induced insulating state in CaCrReO will survive even if the COD amplitude is suppressed (e.g. due to thermal fluctuations).
arXiv comment29 pages, 20 figures, 7 tables
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