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5d(2) Sr2MgOsO6 中各向异性、基态和磁阻的自旋轨道耦合控制。

Spin-orbit coupling control of anisotropy, ground state and frustration in 5d(2) Sr2MgOsO6.

机构信息

Department of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio 43210-1185, USA.

Quantum Condensed Matter Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831, USA.

出版信息

Sci Rep. 2016 Aug 30;6:32462. doi: 10.1038/srep32462.

Abstract

The influence of spin-orbit coupling (SOC) on the physical properties of the 5d(2) system Sr2MgOsO6 is probed via a combination of magnetometry, specific heat measurements, elastic and inelastic neutron scattering, and density functional theory calculations. Although a significant degree of frustration is expected, we find that Sr2MgOsO6 orders in a type I antiferromagnetic structure at the remarkably high temperature of 108 K. The measurements presented allow for the first accurate quantification of the size of the magnetic moment in a 5d(2) system of 0.60(2) μB -a significantly reduced moment from the expected value for such a system. Furthermore, significant anisotropy is identified via a spin excitation gap, and we confirm by first principles calculations that SOC not only provides the magnetocrystalline anisotropy, but also plays a crucial role in determining both the ground state magnetic order and the size of the local moment in this compound. Through comparison to Sr2ScOsO6, it is demonstrated that SOC-induced anisotropy has the ability to relieve frustration in 5d(2) systems relative to their 5d(3) counterparts, providing an explanation of the high TN found in Sr2MgOsO6.

摘要

通过磁强计、比热测量、弹性和非弹性中子散射以及密度泛函理论计算的组合,研究了自旋轨道耦合(SOC)对 5d(2) 体系 Sr2MgOsO6 物理性质的影响。尽管预计会有很大程度的受挫,但我们发现 Sr2MgOsO6 在高达 108 K 的温度下以 I 型反铁磁结构有序。所提出的测量允许首次准确量化 5d(2) 系统中磁矩的大小为 0.60(2) μB-与这样的系统的预期值相比,磁矩显著减小。此外,通过自旋激发能隙确定了显著的各向异性,我们通过第一性原理计算证实 SOC 不仅提供了磁晶各向异性,而且在确定该化合物的基态磁序和局域磁矩大小方面也起着至关重要的作用。通过与 Sr2ScOsO6 的比较,证明 SOC 诱导的各向异性能够缓解 5d(2) 体系相对于其 5d(3) 对应物的受挫,这解释了 Sr2MgOsO6 中发现的高 TN。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d168/5004149/67faed390efe/srep32462-f1.jpg

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