Simultaneous metal-insulator and antiferromagnetic transitions in orthorhombic perovskite iridate S r0.94 i r0.78 O2.68 single crystals

H. Zheng, J. Terzic, Feng Ye, X. G. Wan, D. Wang, Jinchen Wang, Xiaoping Wang, P. Schlottmann, S. J. Yuan, G. Cao

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Abstract

The orthorhombic perovskite SrIrO3 is a semimetal, an intriguing exception in iridates where the strong spin-orbit interaction coupled with electron correlations tends to impose an insulating state. We report results of our investigation of bulk single-crystal Sr0.94Ir0.78O2.68 or Ir-deficient, orthorhombic perovskite SrIrO3. It retains the same crystal structure as stoichiometric SrIrO3 but exhibits a sharp, simultaneous antiferromagnetic (AFM) and metal-insulator (MI) transition occurring in the basal-plane resistivity at 185 K. Above it, the basal-plane resistivity features an extended regime of almost linear temperature dependence up to 800 K but the strong electronic anisotropy renders an insulating behavior in the out-of-plane resistivity. The Hall resistivity undergoes an abrupt sign change and grows below 40 K, which along with the Sommerfeld constant of 20mJ/molK2 suggests a multiband effect. All results including our first-principles calculations underscore a delicacy of the paramagnetic, metallic state in SrIrO3 that is in close proximity to an AFM insulating state. The contrasting ground states in isostructural Sr0.94Ir0.78O2.68 and SrIrO3 illustrate a critical role of lattice distortions and Ir deficiency in rebalancing the ground state in the iridates. Finally, the concurrent AFM and MI transitions reveal a direct correlation between the magnetic transition and formation of an activation gap in the iridate, which is conspicuously absent in Sr2IrO4.

Original languageEnglish
Article number235157
JournalPhysical Review B
Volume93
Issue number23
DOIs
StatePublished - Jun 27 2016

Funding

G.C. is very thankful for enlightening conversations with Professor Hae-Young Kee and Professor Yong-Baek Kim. This work was supported by NSF through Grant No. DMR-1265162 and the Department of Energy (BES) through Grant No. DE-FG02-98ER45707 (P.S.). X.G.W. acknowledges support by Natural Science Foundation of China via Grant No.11525417.

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