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Structure symmetry determination and magnetic evolution inSr2Ir1−xRhxO4

2015/10/26 by Feng Ye, Xiaoping Wang, Christina Hoffmann +8 · 1 citation
Chemistry · Materials Science · Physics and Astronomy · #Advanced Condensed Matter Physics #Chemistry #Condensed matter physics #Crystal structure #Crystallography #Doping #Magnetic and transport properties of perovskites and related materials #Magnetic moment #Neutron diffraction #Physics #Physics of Superconductivity and Magnetism #Tetragonal crystal system #cond-mat.str-el

paper · pdf · doi:10.1103/physrevb.92.201112

published as Phys. Rev. B 92, 201112(R), 2015 · Accepted for publication in Phys. Rev. B

arxiv created 2015/10/26 · openalex publication_date 2015/11/23 · arxiv updated 2015/11/30 · openalex created_date 2016/06/24 · openalex updated_date 2026/08/06

Abstract

We use single-crystal neutron diffraction to determine the crystal structure symmetry and the magnetic evolution in the rhodium-doped iridates Sr2Ir_1\ensuremath-xRhxO4 (0\ensuremath≤x\ensuremath≤0.16). Throughout this doping range, the crystal structure retains a tetragonal symmetry (space group I41/a) with two distinct magnetic Ir sites in the unit cell forming staggered IrO6 rotation. Upon Rh doping, the magnetic order is suppressed and the magnetic moment of Ir4+ is reduced from 0.21\ensuremathμB/Ir for x=0 to 0.18\ensuremathμB/Ir for x=0.12. The magnetic structure at x=0.12 is different from that of the parent compound, while the moments remain in the basal plane.

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