26 research outputs found

    Novel Crossover in Coupled Spin Ladders

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    We report a novel crossover behavior in the long-range-ordered phase of a prototypical spin-1/21/2 Heisenberg antiferromagnetic ladder compound (C7H10N)2CuBr4\mathrm{(C_7H_{10}N)_2CuBr_4}. The staggered order was previously evidenced from a continuous and symmetric splitting of 14^{14}N NMR spectral lines on lowering temperature below Tc≃330T_c\simeq 330 mK, with a saturation towards ≃150\simeq 150 mK. Unexpectedly, the split lines begin to further separate away below T∗∼100T^*\sim 100 mK while the line width and shape remain completely invariable. This crossover behavior is further corroborated by the NMR relaxation rate T1−1T_1^{-1} measurements. A very strong suppression reflecting the ordering, T1−1∼T5.5T_1^{-1}\sim T^{5.5}, observed above T∗T^*, is replaced by T1−1∼TT_1^{-1}\sim T below T∗T^*. These original NMR features are indicative of unconventional nature of the crossover, which may arise from a unique arrangement of the ladders into a spatially anisotropic and frustrated coupling network.Comment: 5 pages, 3 figure

    ESR study of the spin ladder with uniform Dzyaloshinskii-Moria interaction

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    Evolution of the ESR absorption in a strong-leg spin ladder magnet (C7_7H10_{10}N2_2)2_2CuBr4_4 (abbreviated as DIMPY) is studied from 300K to 400mK. Temperature dependence of the ESR relaxation follows a staircase of crossovers between different relaxation regimes. We ague that the main mechanism of ESR line broadening in DIMPY is uniform Dzyaloshinskii-Moria interaction (∣D⃗∣=0.20|\vec{D}|=0.20K) with an effective longitudinal component along an exchange bond of Cu ions within the legs resulting from the low crystal symmetry of DIMPY and nontrivial orbital ordering. The same Dzyaloshinskii-Moriya interaction results in the lifting of the triplet excitation degeneracy, revealed through the weak splitting of the ESR absorption at low temperatures.Comment: 13 pages, submitted to PRB, Fig.3 update

    Spectrum of a magnetized strong-leg quantum spin ladder

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    Inelastic neutron scattering is used to measure the spin excitation spectrum of the Heisenberg S=1/2S=1/2 ladder material (C7_7H10_10N)2_2CuBr4_4 in its entirety, both in the gapped spin-liquid and the magnetic field induced Tomonaga-Luttinger spin liquid regimes. A fundamental change of the spin dynamics is observed between these two regimes. DMRG calculations quantitatively reproduce and help understand the observed commensurate and incommensurate excitations. The results validate long-standing quantum field theoretical predictions, but also test the limits of that approach

    Symmetric and asymmetric excitations of a strong-leg quantum spin ladder

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    The zero-field excitation spectrum of the strong-leg spin ladder (C7_7H10_10N)2_2CuBr4_4 (DIMPY) is studied with a neutron time-of-flight technique. The spectrum is decomposed into its symmetric and asymmetric parts with respect to the rung momentum and compared with theoretical results obtained by the density matrix renormalization group method. Additionally, the calculated dynamical correlations are shown for a wide range of rung and leg coupling ratios in order to point out the evolution of arising excitations, as e.g. of the two-magnon bound state from the strong to the weak coupling limit

    Long-lived magnons throughout the Brillouin zone of the strong-leg spin ladder (C7_7H10_{10}N)2_2CuBr4_4

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    Inelastic neutron scattering is used to measure spin excitations in fully deuterated single crystal samples of the strong-leg antiferromagnetic S=1/2 spin ladder compound (C7_7H10_{10}N)2_2CuBr4_4. Sharp resolution-limited magnons are observed across the entire one-dimensional Brillouin zone. The results validate the previously proposed {\it symmetric} spin ladder model and provide a reliable estimate of the relevant exchange interactions.Comment: 5 pages, 5 figure

    Crystals for neutron scattering studies of quantum magnetism

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    We review a strategy for targeted synthesis of large single crystal samples of prototype quantum magnets for inelastic neutron scattering experiments. Four case studies of organic copper halogenide S=1/2 systems are presented. They are meant to illustrate that exciting experimental results pertaining to forefront many-body quantum physics can be obtained on samples grown using very simple techniques, standard laboratory equipment, and almost no experience in in advanced crystal growth techniques.Comment: 16 pages, 10 figure

    Extracellular matrix-induced GM-CSF and hypoxia promote immune control of; Mycobacterium tuberculosis; in human; in vitro; granulomas

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    Several in vitro cellular models have been developed with the aim to reproduce and dissect human granulomatous responses, the hallmark of tuberculosis (TB) immunopathogenesis. In that context, we compared two- (2D) versus three-dimensional (3D) granuloma models resulting from infection of human peripheral blood mononuclear cells with M. tuberculosis (Mtb) in the absence or presence of a collagen-based extracellular matrix (ECM). Granuloma formation was found to be significantly enhanced in the 2D model. This feature was associated with an earlier chemokine production and lymphocyte activation, but also a significantly increased bacterial burden. Remarkably, the reduction in Mtb burden in the 3D model correlated with an increase in GM-CSF production. GM-CSF, which is known to promote macrophage survival, was found to be inherently induced by the ECM. We observed that only 3D in vitro granulomas led to the accumulation of lipid inclusions within Mtb. Our data suggest that a hypoxic environment within the ECM could be responsible for this dormant-like Mtb phenotype. Furthermore, exposure to a TNF-alpha antagonist reverted Mtb dormancy, thereby mimicking the reactivation of TB observed in rheumatic patients receiving this therapy. To conclude, we showed that only in vitro granulomas generated in the presence of an ECM could recapitulate some clinically relevant features of granulomatous responses in TB. As such, this model constitutes a highly valuable tool to study the interplay between immunity and Mtb stress responses as well as to evaluate novel treatment strategies
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