Slater Insulator in Iridate Perovskites with Strong Spin-Orbit Coupling
Q. Cui, J.-G. Cheng, W. Fan, A. E. Taylor, S. Calder, M.A. McGuire,, J.-Q. Yan, D. Meyers, X. Li, Y. Q. Cai, Y. Y. Jiao, Y. Choi, D. Haskel, H., Gotou, Y. Uwatoko, J. Chakhalian, A. D. Christianson, S. Yunoki, J. B., Goodenough, and J.-S. Zhou

TL;DR
This study demonstrates that substituting Sn for Ir in SrIrO3 induces a second-order metal-insulator transition with antiferromagnetic order, highlighting a Slater-type insulator driven by electron correlations and spin-orbit coupling effects.
Contribution
It reveals how Sn substitution in SrIrO3 induces a Slater insulator phase with antiferromagnetic order, expanding understanding of metal-insulator transitions in spin-orbit coupled systems.
Findings
Sn substitution causes a second-order metal-insulator transition.
Antiferromagnetic order develops below TN > 225 K.
Structural changes reduce SOC, leading to electron gap opening.
Abstract
The perovskite SrIrO3 is an exotic narrow-band metal owing to a confluence of the strengths of the spin-orbit coupling (SOC) and the electron-electron correlations. It has been proposed that topological and magnetic insulating phases can be achieved by tuning the SOC, Hubbard interactions, and/or lattice symmetry. Here, we report that the substitution of nonmagnetic, isovalent Sn4+ for Ir4+ in the SrIr1-xSnxO3 perovskites synthesized under high pressure leads to a metal-insulator transition to an antiferromagnetic (AF) phase at TN > 225 K. The continuous change of the cell volume as detected by x-ray diffraction and the lamda-shape transition of the specific heat on cooling through TN demonstrate that the metal-insulator transition is of second-order. Neutron powder diffraction results indicate that the Sn substitution enlarges an octahedral-site distortion that reduces the SOC relative…
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