Actions for Decoupling of the antiferromagnetic and insulating states in Tb-doped Sr2IrO4 [electronic resource].
Decoupling of the antiferromagnetic and insulating states in Tb-doped Sr2IrO4 [electronic resource].
- Published
- Washington, D.C. : United States. Dept. of Energy. Office of Basic Energy Sciences, 2015.
Oak Ridge, Tenn. : Distributed by the Office of Scientific and Technical Information, U.S. Dept. of Energy - Physical Description
- Article numbers 214,411 : digital, PDF file
- Additional Creators
- Argonne National Laboratory, United States. Department of Energy. Office of Basic Energy Sciences, and United States. Department of Energy. Office of Scientific and Technical Information
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- Free-to-read Unrestricted online access
- Summary
- Sr2IrO4 is a spin-orbit coupled insulator with an antiferromagnetic (AFM) transition at TN = 240 K. We report results of a comprehensive study of single-crystal Sr2Ir1-xTbxO4 (0≤x≤0.03). This study found that mere 3% (x=0.03) tetravalent Tb4+(4f7) substituting for Ir4+ (rather than Sr2+) completely suppresses the long-range collinear AFM transition but retains the insulating state, leading to a phase diagram featuring a decoupling of magnetic interactions and charge gap. The insulating state at x = 0.03 is characterized by an unusually large specific heat at low temperatures and an incommensurate magnetic state having magnetic peaks at (0.95, 0, 0) and (0, 0.95, 0) in the neutron diffraction, suggesting a spiral or spin density wave order. It is apparent that Tb doping effectively changes the relative strength of the SOI and the tetragonal CEF and enhances the Hund’s rule coupling that competes with the SOI, and destabilizes the AFM state. However, the disappearance of the AFM accompanies no metallic state chiefly because an energy level mismatch for the Ir and Tb sites weakens charge carrier hopping and renders a persistent insulating state. Furthermore, this work highlights an unconventional correlation between the AFM and insulating states in which the magnetic transition plays no critical role in the formation of the charge gap in the iridate.
- Report Numbers
- E 1.99:1248025
- Subject(s)
- Note
- Published through SciTech Connect.
12/08/2015.
"125825"
Physical Review. B, Condensed Matter and Materials Physics 92 21 ISSN 1098-0121 AM
J. C. Wang; S. Aswartham; Feng Ye; J. Terzic; H. Zheng; Daniel Haskel; Shalinee Chikara; Yong Choi; P. Schlottmann; Radu Custelcean; S. J. Yuan; G. Cao. - Funding Information
- AC02-06CH11357
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