Impact of inversion symmetry on a quasi-1D S=1 system

被引:0
|
作者
Kim, J. K. [1 ,2 ]
Ranjith, K. M. [1 ]
Burkhardt, U. [1 ]
Prots, Yu [1 ]
Baenitz, M. [1 ]
Valldor, M. [1 ,3 ]
机构
[1] Max Planck Inst Chem Phys Solids, Nothnitzer Str 40, D-01187 Dresden, Germany
[2] Pohang Univ Sci & Technol, Dept Phys, Pohang 790784, South Korea
[3] Univ Oslo, Ctr Mat Sci & Nanotechnol SMN, Dept Chem, POB 1033 Blindern, N-0315 Oslo, Norway
关键词
low-dimesional magnetism; S=1; inversion symmetry; magneto-electric coupling; HALDANE-GAP; TRANSITION; CHAINS; SPIN; FERROMAGNETISM; FE; CR;
D O I
10.1088/1361-648X/ab7134
中图分类号
O469 [凝聚态物理学];
学科分类号
070205 ;
摘要
Here, we report the synthesis and magnetic properties of a novel, centrosymmetric, quasi-1D spin chain system La3VWS3O6, with hexagonal crystal structure (P6(3)/m, a = 9.460 76(3), c = 5.518 09(2) angstrom). Pure powders were obtained by solid-state reactions from La2O3, WO3 and metal powders of V and W. X-ray powder diffraction, specific heat, magnetization, La-139-nuclear magnetic resonance (NMR), and electric resistivity measurements indicate that the compound is a low dimensional magnet with an S = 1 spin chain that exhibits no sign of magnetic ordering above 2 K. A single ion anisotropy (D/k(B) similar to 10 K), caused by magneto-crystalline effects, is probably responsible for a thermodynamic entropy release at lower temperatures, which concurs with La-139-NMR data. By detailed comparison with non-centrosymmetric Ba3V2S4O3, having a very similar magnetic lattice, it is obvious that the presence of crystallographic inversion symmetry has an effect on the behaviour of the magnetic chains.
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页数:9
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