论文标题

方格抗晶格晶格抗fiferromagnet lasrcro4

Anticollinear order and degeneracy lifting in square lattice antiferromagnet LaSrCrO4

论文作者

Zhou, Jing, Quirion, Guy, Quilliam, Jeffrey A., Cao, Huibo, Ye, Feng, Stone, Matthew B., Huang, Qing, Zhou, Haidong, Cheng, Jinguang, Bai, Xiaojian, Mourigal, Martin, Wan, Yuan, Dun, Zhiling

论文摘要

我们报告了Lasrcro $ _4 $的静态和动态磁性特性,这是一种看似典型的Spin-3/2平方晶格抗fiferromagnet,由于其AB堆积而在磁性层之间表现出挫败感 - 并提供了稀有的测试床,以研究磁力中的偶然降低磁性提升。在单晶样品上进行的中子衍射实验发现了低于$ t_n $ = 170 K的显着抗线磁序,其特征是每一层内的旋转和相邻层之间的正交布置。为了理解这种异常磁性结构的起源,我们通过非弹性中子散射和大量测量来分析自旋波激发光谱。光谱间隙为0.5 MeV,以及3.2 \,t的自旋触发转变反映了与退化延伸相关的能量尺度。解释这些观察结果的最小模型既需要呈阳性的层间层交换和偶性相互作用,这两者都按10 $^{-4} $ MEV的顺序,只有每百万个主导交易交互$ J_1 $ J_1 \约11 $ 11 $ MEV。这些结果通过两个不同的退化提升相互作用的综合效应,为选择非类别磁性结构提供了直接的证据。

We report the static and dynamic magnetic properties of LaSrCrO$_4$, a seemingly canonical spin-3/2 square-lattice antiferromagnet that exhibits frustration between magnetic layers -- owing to their AB stacking -- and offers a rare testbed to investigate accidental-degeneracy lifting in magnetism. Neutron diffraction experiments on single-crystal samples uncover a remarkable anticollinear magnetic order below $T_N$ = 170 K characterized by a Néel arrangement of the spins within each layer and an orthogonal arrangement between adjacent layers. To understand the origin of this unusual magnetic structure, we analyze the spin-wave excitation spectrum by means of inelastic neutron scattering and bulk measurements. A spectral gap of 0.5 meV, along with a spin-flop transition at 3.2\, T, reflect the energy scale associated with the degeneracy-lifting. A minimal model to explain these observations requires both a positive biquadratic interlayer exchange and dipolar interactions, both of which are on the order of 10$^{-4}$ meV, only a few parts per million of the dominant exchange interaction $J_1 \approx 11$ meV. These results provide direct evidence for the selection of a non-collinear magnetic structure by the combined effect of two distinct degeneracy lifting interactions.

扫码加入交流群

加入微信交流群

微信交流群二维码

扫码加入学术交流群,获取更多资源