Cooperative effects of lattice and spin-orbit coupling on the electronic structure of orthorhombic SrIrO3
arXiv:1507.05704 · doi:10.1088/0953-8984/27/33/335502
Abstract
Orthorhombic SrIrO3 subjected to strain show tunable transport properties. With underlying symmetry remaining invariant, these properties are associated with IrO6 octahedral tilting. Adopting to first-principles methods, the effects of crystal field, spin-orbit coupling, and Coulomb correlations, on comparable interaction length scales, are discussed. While tilting induces a t2g-eg crystal-field splitting and band narrowing, spin-orbit coupling induces a partial splitting of the Jeff bands rendering SrIrO3 a semi-metallic ground state. The SOC enhanced hybridization of Ir-O orbitals, serve as a explanation to why the critical Hubbard correlation strength increases with increasing SOC strength in SrIrO3 to induce an insulating phase.
References in corpus (13)
- Mott Insulators in the Strong Spin-Orbit Coupling Limit: From Heisenberg to a Quantum Compass and Kitaev Models
- Novel Jeff = 1/2 Mott State Induced by Relativistic Spin-Orbit Coupling in Sr2IrO4
- Bandwidth-Controlled Insulator-Metal Transition and Correlated Metallic State in 5 Transition Metal Oxides SrIrO (=1, 2, and )
- Twisted Hubbard Model for Sr2IrO4: Magnetism and Possible High Temperature Superconductivity
- Interplay of Spin-Orbit Interactions, Dimensionality, and Octahedral Rotations in Semimetallic SrIrO
- Microscopic study of spin-orbit-induced Mott insulator in Ir oxides
- Metal insulator transitions in perovskite SrIrO3 thin films
- Non-Fermi-liquid behavior in nearly ferromagnetic metallic SrIrO3 single crystals
- Electronic structures of layered perovskite Sr2MO4 (M=Ru, Rh, and Ir)
- Compressive strain-induced metal-insulator transition in orthorhombic SrIrO3 thin films
- Tunable Semimetallic State in Compressive-strained SrIrO3 Films Revealed by Transport Behaviors
- On the magnetic structure of Sr3Ir2O7: an x-ray resonant scattering study
- The J_{eff}=1/2 insulator Sr3Ir2O7 studied by means of angle-resolved photoemission spectroscopy