Geometric magnetic frustration in the hexagonal perovskite (La,Sr)4-zRuO7+δ

被引:9
作者
Ebbinghaus, Stefan G.
Scheidt, Ernst-Wilhelm
Goetzfried, Thomas
机构
[1] Univ Augsburg, Inst Phys, Lehrstuhl Festkorperchem, D-86159 Augsburg, Germany
[2] Univ Augsburg, Inst Phys, Chem Phys & Mat Wissensch, D-86159 Augsburg, Germany
来源
PHYSICAL REVIEW B | 2007年 / 75卷 / 14期
关键词
CRYSTAL-STRUCTURE; STRUCTURAL RELATIONSHIPS; RUTHENIUM(V) OXIDE; PEROXIDE IONS; RU; MEMBER; BA5RU2O9(O-2); BA5RU2O10; SERIES; SYSTEM;
D O I
10.1103/PhysRevB.75.144414
中图分类号
T [工业技术];
学科分类号
120111 [工业工程];
摘要
The hexagonal perovskite (La,Sr)(4-z)RuO7+delta exhibits a strong magnetic frustration due to the geometric arrangement of the paramagnetic Ru5+ ions, which form a network of edge-sharing elongated tetrahedra. In this magnetic sublattice, frustration may either be restricted to the crystallographic ab plane, in which the ruthenium ions form a triangle lattice, or concern the entire tetrahedra. Crystals of (La,Sr)(4-z)RuO7+delta were grown by the floating zone method, and their magnetic properties were measured with respect to the crystallographic axes. Magnetic ordering was only detected for the external magnetic field parallel to the ab plane, while for B parallel to c the samples showed no magnetic transition down to 2 K. Heat capacity measurements revealed a magnetic entropy corresponding to a spin of 1/2, a value much smaller than the S=3/2 expected for the (t(2g))(3) configuration of Ru5+ ions. From symmetry considerations, we conclude that only the orbitals corresponding to the irreducible representation A(1g) mediate the cooperative interaction between the magnetic moments, giving rise to an orbitally ordered state.
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页数:8
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