Abstract
Sr2IrO4 exhibits a novel insulating state assisted by spin-orbit interactions. A series of polycrystalline samples of Sr2-xIrO4 have been synthesized. It is found that deep Sr-vacancies of Sr2-xIrO4 greatly reduce the rotation of IrO6 octahedral, and more importantly, a significant structural change occurs around x = 0.48 in both the lattice constants and the Ir-O2 bond length. An insulator-metal transition (IMT) appears and a non-Fermi-liquid metallic electronic state has been proved at x>0.48 in Sr2-xIrO4. Furthermore, a sudden drop emerges of the localization temperature T0 and the antiferromagnetic (AFM) transition temperature TN in Sr1.5IrO4, together with the Curie-Weiss temperature reversing its sign. These abrupt changes are closely related with the reduction of the rotation crystal structure.
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