Tuning the Jeff=1/2 insulating state via electron doping and pressure in the double-layered iridate Sr3Ir2O7

被引:50
作者
Li, L. [1 ,2 ]
Kong, P. P. [3 ]
Qi, T. F. [1 ,2 ]
Jin, C. Q. [3 ]
Yuan, S. J. [1 ,2 ,4 ]
DeLong, L. E. [1 ,2 ]
Schlottmann, P. [5 ]
Cao, G. [1 ,2 ]
机构
[1] Univ Kentucky, Dept Phys & Astron, Lexington, KY 40506 USA
[2] Univ Kentucky, Ctr Adv Mat, Lexington, KY 40506 USA
[3] Chinese Acad Sci, Inst Phys, Beijing 100080, Peoples R China
[4] Shanghai Univ, Dept Phys, Shanghai, Peoples R China
[5] Florida State Univ, Dept Phys, Tallahassee, FL 32306 USA
来源
PHYSICAL REVIEW B | 2013年 / 87卷 / 23期
基金
美国国家科学基金会;
关键词
SR2IRO4; TRANSITION;
D O I
10.1103/PhysRevB.87.235127
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Sr3Ir2O7 exhibits a novel J(eff) = 1/2 insulating state that features a splitting between Jeff = 1/2 and 3/2 bands due to spin-orbit interaction. We report a metal-insulator transition in Sr3Ir2O7 via either dilute electron doping (La3+ for Sr2+) or application of high pressure up to 35 GPa. Our study of single-crystal Sr3Ir2O7 and (Sr1-xLax)(3)Ir2O7 reveals that application of high hydrostatic pressure P leads to a drastic reduction in the electrical resistivity by as much as six orders of magnitude at a critical pressure P-C = 13.2 GPa, manifesting a closing of the gap; but further increasing P up to 35 GPa produces no fully metallic state at low temperatures, possibly as a consequence of localization due to a narrow distribution of bonding angles theta. In contrast, slight doping of La3+ ions for Sr2+ ions in Sr3Ir2O7 readily induces a robust metallic state in the resistivity at low temperatures; the magnetic ordering temperature is significantly suppressed but remains finite for (Sr0.95La0.05)(3)Ir2O7 where the metallic state occurs. The results are discussed along with comparisons drawn with Sr2IrO4, a prototype of the J(eff) = 1/2 insulator.
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页数:6
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