2,159 research outputs found

    Quantum Phase Transition from a Spin-liquid State to a Spin-glass State in the Quasi-1D Spin-1 System Sr1-xCaxNi2V2O8

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    We report a quantum phase transition from a spin-liquid state to a spin-glass state in the quasi-one dimensional (1D) spin-1 system Sr1-xCaxNi2V2O8, induced by a small amount of Ca-substitution at Sr site. The ground state of the parent compound (x = 0) is found to be a spin-liquid type with a finite energy gap of 26.6 K between singlet ground state and triplet excited state. Both dc-magnetization and ac-susceptibility studies on the highest Ca-substituted compound (x = 0.05) indicate a spin-glass type magnetic ground state. With increasing Ca-concentration, the spin-glass ordering temperature increases from 4.5 K (for the x = 0.015 compound) to 6.25 K (for the x = 0.05 compound). The observed results are discussed in the light of the earlier experimental reports and the theoretical predictions for a quasi-1D spin-1 system.Comment: 26 pages, 8 figures, 3 table

    Enhanced Raman and photoluminescence response in monolayer MoS2_2 due to laser healing of defects

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    Bound quasiparticles, negatively charged trions and neutral excitons, are associated with the direct optical transitions at the K-points of the Brillouin zone for monolayer MoS2_2. The change in the carrier concentration, surrounding dielectric constant and defect concentration can modulate the photoluminescence and Raman spectra. Here we show that exposing the monolayer MoS2_2 in air to a modest laser intensity for a brief period of time enhances simultaneously the photoluminescence (PL) intensity associated with both trions and excitons, together with \sim 3 to 5 times increase of the Raman intensity of first and second order modes. The simultaneous increase of PL from trions and excitons cannot be understood based only on known-scenario of depletion of electron concentration in MoS2_2 by adsorption of O2_2 and H2_2O molecules. This is explained by laser induced healing of defect states resulting in reduction of non-radiative Auger processes. This laser healing is corroborated by an observed increase of intensity of both the first order and second order 2LA(M) Raman modes by a factor of \sim 3 to 5. The A1g_{1g} mode hardens by \sim 1.4 cm1^{-1} whereas the E2g1^1_{2g} mode softens by \sim 1 cm1^{-1}. The second order 2LA(M) Raman mode at \sim 440 cm1^{-1} shows an increase in wavenumber by \sim 8 cm1^{-1} with laser exposure. These changes are a combined effect of change in electron concentrations and oxygen-induced lattice displacements.Comment: 15 pages, 5 figures, Journal of Raman Spectroscopy, 201

    Magnetic correlations of the quasi-one-dimensional half-integer spin-chain antiferromagnets SrM2M_2V2_2O8_8 (MM = Co, Mn)

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    Magnetic correlations of two iso-structural quasi-one-dimensional (1D) antiferromagnetic spin-chain compounds SrM2M_2V2_2O8_8 (MM = Co, Mn) have been investigated by magnetization and powder neutron diffraction. Two different collinear antiferromagnetic (AFM) structures, characterized by the propagation vectors, kk = (0 0 1) and kk = (0 0 0), have been found below \sim 5.2 K and \sim 42.2 K for the Co- and Mn-compounds, respectively. For the Mn-compound, AFM chains (along the cc axis) order ferromagnetically within the abab plane, whereas, for the Co-compound, AFM chains order ferro-/antiferromagnetically along the a/ba/b direction. The critical exponent study confirms that the Co- and Mn-compounds belong to the Ising and Heisenberg universality classes, respectively. For both compounds, short-range spin-spin correlations are present over a wide temperature range above TNT_N. The reduced ordered moments at base temperature (1.5 K) indicate the presence of quantum fluctuations in both compounds due to the quasi-1D magnetic interactions.Comment: 14 pages, 10 figures, 9 table
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