ترغب بنشر مسار تعليمي؟ اضغط هنا

High--field NMR of the quasi--1D antiferromagnet LiCuVO$_4$

170   0   0.0 ( 0 )
 نشر من قبل Norbert Buettgen
 تاريخ النشر 2012
  مجال البحث فيزياء
والبحث باللغة English




اسأل ChatGPT حول البحث

We report on NMR studies of the quasi one--dimensional (1D) antiferromagnetic $S=1/2$ chain cuprate LiCuVO$_4$ in magnetic fields $H$ up to $mu_0H$ = 30 T ($approx 70$% of the saturation field $H_{rm sat}$). NMR spectra in fields higher than $H_{rm c2}$ ($mu_0H_{rm c2} approx 7.5$ T) and temperatures $T<T_{rm N}$ can be described within the model of a spin-modulated phase in which the magnetic moments are aligned parallel to the applied field $H$ and their values alternate sinusoidally along the magnetic chains. Based on theoretical concepts about magnetically frustrated 1D chains, the field dependence of the modulation strength of the magnetic structure is deduced from our experiments. Relaxation time $T_2$ measurements of the $^{51}$V nuclei show that $T_2$ depends on the particular position of the probing $^{51}$V nucleus with respect to the magnetic copper moments within the 1D chains: the largest $T_2$ value is observed for the vanadium nuclei which are very next to the magnetic Cu$^{2+}$ ion with largest ordered magnetic moment. This observation is in agreement with the expectation for the spin-modulated magnetic structure. The $(H,T)$ magnetic phase diagram of LiCuVO$_4$ is discussed.



قيم البحث

اقرأ أيضاً

We report on NMR studies of the quasi--1D antiferromagnetic $S=1/2$ chain cuprate LiCuVO$_4$, focusing on the high--field spin--modulated phase observed recently in applied magnetic fields $H > H_{rm c2}$ ($mu_0H_{rm c2} approx 7.5$ T). The NMR spect ra of $^7$Li and $^{51}$V around the transition from the ordered to the paramagnetic state were measured. It is shown that the spin--modulated magnetic structure forms with ferromagnetic interactions between spins of neighboring chains within the {bf ab}--plane at low temperatures 0.6 K $ < T < T_{rm N}$. The best fit provides evidence that the mutual orientation between spins of neighboring {bf ab}--planes is random. For elevated temperatures $T_{rm N} < T lesssim 15$ K, short--range magnetic order occurs at least on the characteristic time scale of the NMR experiment.
We report on magnetic resonance studies within the magnetically ordered phase of the quasi-1D antiferromagnet LiCuVO_4. Our studies reveal a spin reorientational transition at a magnetic field H_c1 ~ 25 kOe applied within the crystallographical (ab)- plane in addition to the recently observed one at H_c2 ~75 kOe [ M.G. Banks et al., cond-mat/0608554 (2006)]. Spectra of the antiferromagnetic resonance (AFMR) along low-frequency branches can be described in the frame of a macroscopic theory of exchange-rigid planar magnetic structures. These data allow to obtain the anisotropy of the exchange interaction together with a constant of the uniaxial anisotropy. Spectra of 7Li nuclear magnetic resonance (NMR) show that, within the magnetically ordered phase of LiCuVO_4 in the low-field range H < H_c1, a planar spiral spin structure is realized with the spins lying in the (ab)-plane in agreement with neutron scattering studies of B.J. Gibson et al. [Physica B Vol. 350, 253 (2004)]. Based on NMR spectra simulations, the transition at H_c1 can well be described as a spin-flop transition, where the spin plane of the magnetically ordered structure rotates to be perpendicular to the direction of the applied magnetic field. For H > H_c2 ~ 75 kOe, our NMR spectra simulations show that the magnetically ordered structure exhibits a modulation of the spin projections along the direction of the applied magnetic field H.
CaV$_2$O$_4$ is a spin-1 antiferromagnet, where the magnetic vanadium ions are arranged on quasi-one-dimensional (1D) zig-zag chains with potentially frustrated antiferromagnetic exchange interactions. High temperature susceptibility and single-cryst al neutron diffraction measurements are used to deduce the non-collinear magnetic structure, dominant exchange interactions and orbital configurations. The results suggest that at high temperatures CaV$_2$O$_4$ behaves as a Haldane chain, but at low temperatures, orbital ordering lifts the frustration and it becomes a spin-1 ladder.
123 - R. Coldea 1997
Magnetic excitations of the quasi-1D S=1/2 Heisenberg antiferromagnet (HAF) Cs2CuCl4 have been measured as a function of magnetic field using neutron scattering. For T<0.62 K and B=0 T the weak inter-chain coupling produces 3D incommensurate ordering . Fields greater than Bc =1.66 T, but less than the field (~8 T) required to fully align the spins, are observed to decouple the chains, and the system enters a disordered intermediate-field phase (IFP). The IFP excitations are in agreement with the predictions of Muller et al. for the 1D S=1/2 HAF, and Talstra and Haldane for the related 1/r^2 chain (the Haldane-Shastry model). This behaviour is inconsistent with linear spin-wave theory.
We investigated the magnetoelastic properties of the quasi-one-dimensional spin-1/2 frustrated magnet LiCuVO$_4$. Longitudinal-magnetostriction experiments were performed at 1.5 K in high magnetic fields of up to 60 T applied along the $b$ axis, i.e. , the spin-chain direction. The magnetostriction data qualitatively resemble the magnetization results, and saturate at $H_{text{sat}} approx 54$ T, with a relative change in sample length of $Delta L/L approx 1.8times10^{-4}$. Remarkably, both the magnetostriction and the magnetization evolve gradually between $H_{text{c3}} approx 48$ T and $H_{text{sat}}$, indicating that the two quantities consistently detect the spin-nematic phase just below the saturation. Numerical analyses for a weakly coupled spin-chain model reveal that the observed magnetostriction can overall be understood within an exchange-striction mechanism. Small deviations found may indicate nontrivial changes in local correlations associated with the field-induced phase transitions.
التعليقات
جاري جلب التعليقات جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا