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Bottom-up design of spin-split and reshaped electronic band structures in antiferromagnets without spin-orbit coupling: Procedure on the basis of augmented multipoles

机译:无旋转轨道耦合的反铁渣中的自旋分流和重塑电子频带结构的自下而上的设计:基于增强多元化的程序

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摘要

We propose an efficient microscopic design procedure of electronic band structures having intrinsic spin and momentum dependences in spin-orbit-coupling free antiferromagnets. Our bottom-up design approach to creating desired spin-split and reshaped electronic band structures could result in further findings of practical spin-orbit-coupling free materials exhibiting a giant spin-dependent and/or nonreciprocal transport, magneto-electric and elastic responses, and so on, as a consequence of such band structures. We establish a systematic guideline to construct symmetric/antisymmetric spin-split and antisymmetrically deformed spin-independent band structures in spin-orbit-coupling free systems by using two polar multipole degrees of freedom, i.e., electric and magnetic toroidal multipoles. The two polar multipoles constitute a complete set and describe arbitrary degrees of freedom in the hopping Hamiltonian, whose onsite and offsite degrees of freedom in a cluster are described as the so-called cluster and bond multipoles, respectively, and another degree of freedom connecting between clusters is expressed as momentum multipoles. By using these multipole descriptions, we elucidate simple microscopic conditions to realize intrinsic band deformations in magnetically ordered states: The symmetric spin splitting is realized in collinear magnets when cluster and bond multipoles contain the same symmetry of multipoles. The antisymmetric spin splitting occurs in noncollinear antiferromagnets when a bond-type magnetic toroidal multipole is present. Furthermore, the antisymmetric band deformation with spin degeneracy is realized in noncoplanar antiferromagnets. We exemplify three lattice systems formed by a triangle unit, triangular, kagome, and breathing kagome structures, to demonstrate the band deformations under the magnetic ordering. On the basis of the proposed procedure, we list up various candidate materials showing intrinsic band deformations in accordance with MAGNDATA, magnetic structures database.
机译:我们提出了一种高效的微观设计程序,其具有内在的旋转和动量依赖性在旋转轨道耦合的自由杀剂中。我们的自下而上的设计方法来创建所需的旋转分流和重塑电子频带结构可能导致实际旋转轨道偶联的自由材料的进一步发现,其呈巨型旋转依赖性和/或非抗钙传输,磁电和弹性响应,因此,作为这种乐队结构的结果。我们通过使用两个极性多极自由度,即电和磁环形多元化,建立一个系统的指南,以构建旋转轨道耦合自由系统中的对称/反对二手旋转和防旋旋转型旋转型频带结构。两个极性多人构成一个完整的集合,并描述跳跃汉密尔顿人的任意自由度,其现场和群集中的现场自由度分别被描述为所谓的群集和债券多元化,以及两者之间的自由度群集表示为动量多人。通过使用这些多极描述,我们阐明简单的微观条件,以实现磁有序状态下的内在带变形:当簇和粘合多孔包含相同的多极对称时,在共线磁体中实现对称自旋分裂。当存在粘合型磁环形多极时,在非可口压反铁渣中发生反对称旋转分裂。此外,在非平板上的反铁磁体中实现了与旋转退化的反对称带状变形。我们举例说明了三角形单元,三角形,kagome和呼吸kagome结构形成的三个晶格系统,以展示磁性排序下的带状变形。在拟议的程序的基础上,我们列出了各种候选材料,示出了根据Magndata,磁性结构数据库的内在频带变形。

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  • 来源
    《Physical review》 |2020年第14期|144441.1-144441.24|共24页
  • 作者单位

    Department of Applied Physics The University of Tokyo Bunkyo Tokyo 113-8656 Japan;

    Center for Computational Materials Science Institute for Materials Research Tohoku University Sendai Miyagi 950-8577 Japan;

    Department of Phxsics Meiji University Kawasaki 214-8571 Japan;

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