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首页> 外文期刊>Physical review >Field-induced magnetic ordering and single-ion anisotropy in the quasi-one-dimensional Haldane chain compound SrNi_2V_2O_8: A single-crystal investigation
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Field-induced magnetic ordering and single-ion anisotropy in the quasi-one-dimensional Haldane chain compound SrNi_2V_2O_8: A single-crystal investigation

机译:准一维Haldane链化合物SrNi_2V_2O_8中的场致磁有序性和单离子各向异性:单晶研究

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Field-induced magnetic ordering in the Haldane chain compound SrNi_2 V_2O_8 and the effect of anisotropy have been investigated using single crystals. Static susceptibility, inelastic neutron scattering, high-field magnetization, and low-temperature heat-capacity studies confirm a nonmagnetic spin-singlet ground state and a gap between the singlet ground state and triplet excited states. The intrachain exchange interaction is estimated to be J ~ 8.9 ± 0.1 meV. Splitting of the dispersions into two modes with minimum energies 1.57 and 2.58 meV confirms the existence of single-ion anisotropy D(S~z)~2. The value of D is estimated to be -0.51 ±0.01 meV and the easy axis is found to be along the crystallographic c axis. Field-induced magnetic ordering has been found with two critical fields (_(μ0)H~(⊥c)_c = 12.0 ± 0.2 T and _(μ0)H~(⊥c)_c = 20.8 ± 0.5 T at 4.2 K). Field-induced three-dimensional magnetic ordering above the critical fields is evident from the heat-capacity, susceptibility, and high-field magnetization study. The phase diagram in the H-T plane has been obtained from the high-field magnetization. The observed results are discussed in the light of theoretical predictions as well as earlier experimental reports on Haldane chain compounds.
机译:使用单晶研究了Haldane链化合物SrNi_2 V_2O_8中的场致磁有序性和各向异性的影响。静态磁化率,非弹性中子散射,高场磁化强度和低温热容量研究确认了非磁性自旋单基态和单重态与三重态激发态之间的间隙。链内交换相互作用估计为J〜8.9±0.1 meV。将分散体分为两种具有最小能量1.57和2.58 meV的模式,证实了单离子各向异性D(S〜z)〜2的存在。 D的值估计为-0.51±0.01meV,并且易轴沿结晶c轴。发现了两个感应场的磁场感应磁排序(_(μ0)H〜(⊥c)_c = 12.0±0.2 T和_(μ0)H〜(⊥c)_c = 20.8±0.5 T在4.2 K下) 。从热容量,磁化率和高磁场磁化研究可以清楚地看到,在临界磁场之上的磁场感应三维磁序。 H-T平面中的相图是从高磁场磁化获得的。观察到的结果将根据理论预测以及有关Haldane链化合物的早期实验报告进行讨论。

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