اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدNovel ordering of an S = 1/2 quasi one-dimensional Ising-like anitiferromagnet in magnetic field
405
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
High-field specific heat measurements on BaCo2V2O8, which is a good realization of an S = 1/2 quasi one-dimensional Ising-like antifferomagnet, have been performed in magnetic fields up to 12 T along the chain and at temperature down to 200 mK. We have found a new magnetic ordered state in the field-induced phase above Hc ~ 3.9 T. We suggest that a novel type of the incommensurate order, which has no correspondence to the classical spin system, is realized in the field-induced phase.
قيم البحث
اقرأ أيضاً
We report on magnetization, sound velocity, and magnetocaloric-effect measurements of the Ising-like spin-1/2 antiferromagnetic chain system BaCo$_2$V$_2$O$_8$ as a function of temperature down to 1.3 K and applied transverse magnetic field up to 60
T. While across the N{e}el temperature of $T_Nsim5$ K anomalies in magnetization and sound velocity confirm the antiferromagnetic ordering transition, at the lowest temperature the field-dependent measurements reveal a sharp softening of sound velocity $v(B)$ and a clear minimum of temperature $T(B)$ at $B^{c,3D}_perp=21.4$ T, indicating the suppression of the antiferromagnetic order. At higher fields, the $T(B)$ curve shows a broad minimum at $B^c_perp = 40$ T, accompanied by a broad minimum in the sound velocity and a saturation-like magnetization. These features signal a quantum phase transition which is further characterized by the divergent behavior of the Gr{u}neisen parameter $Gamma_B propto (B-B^{c}_perp)^{-1}$. By contrast, around the critical field, the Gr{u}neisen parameter converges as temperature decreases, pointing to a quantum critical point of the one-dimensional transverse-field Ising model.
CuSiO_3, isotypic to the spin - Peierls compound CuGeO_3, was discovered recently as a metastable decomposition product of the silicate mineral dioptase, Cu_6Si_6O_{18}cdot6H_2O. We investigated the physical properties of CuSiO_3 using susceptibility
, magnetization and specific heat measurements on powder samples. The magnetic susceptibility chi(T) is reproduced very well above T = 8 K by theoretical calculations for an S=1/2 antiferromagnetic Heisenberg linear chain without frustration (alpha = 0) and a nearest - neighbor exchange coupling constant of J/k_{B} = 21 K, much weaker than in CuGeO_3. Below 8 K the susceptibility exhibits a substantial drop. This feature is identified as a second - order phase transition at T_{0} = 7.9 K by specific heat measurements. The influence of magnetic fields on T_{0} is weak, and ac - magnetization measurements give strong evidence for a spin - flop - phase at mu_0H_{SF} ~ 3 T. The origin of the magnetic phase transition at T_{0} = 7.9 K is discussed in the context of long - range antiferromagnetic order (AF) versus spin - Peierls(SP)order. Susceptibility and specific heat results support the AF ordered ground state. Additional temperature dependent ^{63,65}Cu nuclear quadrupole resonance experiments have been carried out to probe the Cu^{2+} electronic state and the spin dynamics in CuSiO_3.
BaCo2V2O8 is a nice example of a quasi-one-dimensional quantum spin system that can be described in terms of Tomonaga-Luttinger liquid physics. This is explored in the present study where the magnetic field-temperature phase diagram is thoroughly est
ablished up to 12 T using single-crystal neutron diffraction. The transition from the Neel phase to the incommensurate longitudinal spin density wave (LSDW) phase through a first-order transition, as well as the critical exponents associated with the paramagnetic to ordered phase transitions, and the magnetic order both in the Neel and in the LSDW phase are determined, thus providing a stringent test for the theory.
We investigate magnetic, thermal, and dielectric properties of SrCuTe2O6, which is isostructural to PbCuTe2O6, a recently found, Cu-based 3D frustrated magnet with a corner sharing triangular spin network having dominant first and second nearest neig
hbor (nn) couplings [B. Koteswararao, et al. Phys. Rev. B 90, 035141 (2014)]. Although SrCuTe2O6 has a structurally similar spin network, but the magnetic data exhibit the characteristic features of a typical quasi -one-dimensional magnet, which mainly resulted from the magnetically dominant third nn coupling, uniform chains. The magnetic properties of this system are studied via magnetization (M), heat capacity (Cp), dielectric constant, measurements along with ab-initio band structure calculations. Magnetic susceptibility chi(T) data show a broad maximum at 32 K and the system orders at low temperatures TN1=5.5 K and TN2=4.5 K, respectively. The analysis of chi(T) data gives an intra-chain coupling, J3/kB, to be about - 42 K with non-negligible frustrated inter-chain couplings (J1/kB and J2/kB). The hopping parameters obtained from LDA band structure calculations also suggest the presence of coupled uniform chains. The observation of simultaneous anomalies in dielectric constant at TN1 and TN2 suggests the presence of magneto-dielectric effect in SrCuTe2O6. A magnetic phase diagram is also built based on M, C p, and dielectric constant results.
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.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
