Spin dynamics in frustrated magnets: from edge- to corner-sharing geometries

被引:17
作者
Mendels, P.
Olariu, A.
Bert, F.
Bono, D.
Limot, L.
Collin, G.
Ueland, B.
Schiffer, P.
Cava, R. J.
Blanchard, N.
Duc, F.
Trombe, J. C.
机构
[1] Univ Paris 11, Phys Solides Lab, CNRS, UMR 8502, F-91405 Orsay, France
[2] CEA, CNRS, Lab Leon Brillouin, F-91191 Gif Sur Yvette, France
[3] Penn State Univ, Dept Phys, University Pk, PA 16802 USA
[4] Penn State Univ, Mat Res Inst, University Pk, PA 16802 USA
[5] Princeton Univ, Dept Chem, Princeton, NJ 08540 USA
[6] CNRS, Ctr Elaborat Mat & Etud Struct, UPR 8011, F-31055 Toulouse, France
关键词
D O I
10.1088/0953-8984/19/14/145224
中图分类号
O469 [凝聚态物理学];
学科分类号
070205 ;
摘要
Our work in the past few years has been focused on local NMR ( nuclear magnetic resonance) and mu SR (muon spin resonance) studies of pure Heisenberg isotropic triangular lattices with nearest neighbour couplings, a prerequisite for reaching the ideal spin liquid case. In the case of chromates, although S = 3/2, the combination of the weakness of the Cr3+ single-ion anisotropy and that of an exchange interaction resulting from a direct overlap of the Cr3+ orbitals allows us to tackle these properties. We were recently able to single out, in the triangular compound NaCrO2, an original dynamical crossover regime in a broad range of T between the peak in specific heat and a low T static ground state. Moving to the corner-sharing geometry of Kagome bilayers (Ba2Sn2ZnGa10-7pCr7pO22 and SrCr9pGa12-9pO19), we illustrate all the potential of local studies ( NMR and mu SR) for revealing some key aspects of the physics of these compounds, namely T -> 0 fluctuations, susceptibility, the impact of dilution defects which generate an extended response of the spin lattice as well as their puzzling spin glass state. These results are compared to the case of volborthite which features S = 1/2 spins on a corner-sharing, probably anisotropic, antiferromagnetic Kagome lattice.
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页数:9
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