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Raman scattering for triangular lattices spin-1/2 Heisenberg antiferromagnets

134   0   0.0 ( 0 )
 Added by Francois Vernay
 Publication date 2006
  fields Physics
and research's language is English




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Motivated by various spin-1/2 compounds like Cs$_2$CuCl$_4$ or $kappa$-(BEDT-TTF)$_2$Cu$_2$(CN)$_3$, we derive a Raman-scattering operator {it `a la} Shastry and Shraiman for various geometries. For T=0, the exact spectra is computed by Lanczos algorithm for finite-size clusters. We perform a systematic investigation as a function of $J_2/J_1$, the exchange constant ratio: ranging from $J_2=0$, the well known square-lattice case, to $J_2/J_1=1$ the isotropic triangular lattice. We discuss the polarization dependence of the spectra and show how it can be used to detect precursors of the instabilities of the ground state against quantum fluctuations.



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We numerically study the Heisenberg models on triangular lattices by extending it from the simplest equilateral lattice with only the nearest-neighbor exchange interaction. We show that, by including an additional weak next-nearest-neighbor interaction, a quantum spin-liquid phase is stabilized against the antiferromagnetic order. The spin gap (triplet excitation gap) and spin correlation at long distances decay algebraically with increasing system size at the critical point between the antiferromagnetic phase and the spin-liquid phase. This algebraic behavior continues in the spin-liquid phase as well, indicating the presence of an unconventional critical (algebraic spin-liquid) phase characterized by the dynamical and anomalous critical exponents $z+etasim1$. Unusually small triplet and singlet excitation energies found in extended points of the Brillouin zone impose constraints on this algebraic spin liquid.
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We report a muSR study of LiCrO2, which has a magnetic lattice made up of a stacking of triangular Heisenberg antiferromagnetic (Cr3+, S = 3/2) layers. A static magnetically ordered state is observed below the transition temperature T_N = 62 K, while the expected peak of the relaxation rate is slightly shifted downward by a few kelvins below T_N. We draw a comparison with the isostructural compound NaCrO2, where an exotic broad fluctuating regime has been observed [A. Olariu, P. Mendels, F. Bert, B. G. Ueland, P. Schiffer, R. F. Berger, and R. J. Cava, Phys. Rev. Lett. 97, 167203 (2006)] and was suggested to originate from topological excitations of the triangular lattice. Replacing Na by Li strongly narrows the exotic fluctuating regime formerly observed in NaCrO2, which we attribute to a more pronounced inter-plane coupling in LiCrO2.
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