Lattice-Site-Specific Spin Dynamics in Double Perovskite Sr2CoOsO6

被引:65
|
作者
Yan, Binghai [1 ,2 ]
Paul, Avijit Kumar [1 ]
Kanungo, Sudipta [1 ]
Reehuis, Manfred [3 ]
Hoser, Andreas [3 ]
Toebbens, Daniel M. [3 ]
Schnelle, Walter [1 ]
Williams, Robert C. [4 ]
Lancaster, Tom [4 ]
Xiao, Fan [4 ]
Moeller, Johannes S. [5 ]
Blundell, Stephen J. [5 ]
Hayes, William [5 ]
Felser, Claudia [1 ,6 ]
Jansen, Martin [1 ,7 ]
机构
[1] Max Planck Inst Chem Phys Fester Stoffe, D-01187 Dresden, Germany
[2] Max Planck Inst Phys Komplexer Syst, D-01187 Dresden, Germany
[3] Helmholtz Zentrum Mat & Energie, D-14109 Berlin, Germany
[4] Univ Durham, Dept Phys, Durham DH1 3LE, England
[5] Univ Oxford, Dept Phys, Clarendon Lab, Oxford OX1 3PU, England
[6] Johannes Gutenberg Univ Mainz, Inst Anorgan Chem & Analyt Chem, D-55128 Mainz, Germany
[7] Max Planck Inst Festkorperforsch, D-70569 Stuttgart, Germany
基金
英国工程与自然科学研究理事会;
关键词
FRUSTRATED MAGNETS; CRYSTAL-STRUCTURE; ICE;
D O I
10.1103/PhysRevLett.112.147202
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
Magnetic properties and spin dynamics have been studied for the structurally ordered double perovskite Sr2CoOsO6. Neutron diffraction, muon-spin relaxation, and ac-susceptibility measurements reveal two antiferromagnetic (AFM) phases on cooling from room temperature down to 2 K. In the first AFM phase, with transition temperature T-N1 = 108 K, cobalt (3d(7), S = 3/2) and osmium (5d(2), S = 1) moments fluctuate dynamically, while their average effective moments undergo long-range order. In the second AFM phase below T-N2 = 67 K, cobalt moments first become frozen and induce a noncollinear spin-canted AFM state, while dynamically fluctuating osmium moments are later frozen into a randomly canted state at T approximate to 5 K. Ab initio calculations indicate that the effective exchange coupling between cobalt and osmium sites is rather weak, so that cobalt and osmium sublattices exhibit different ground states and spin dynamics, making Sr2CoOsO6 distinct from previously reported double-perovskite compounds.
引用
收藏
页数:6
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