论文标题

I型抗铁磁weyl semimetal inmnti $ _2 $

The type-I antiferromagnetic Weyl semimetal InMnTi$_2$

论文作者

Grassano, Davide, Binci, Luca, Marzari, Nicola

论文摘要

拓扑材料在过去十年中一直是研究的主要重点,因为它们的受保护特性可以用于制造新设备。其中,Weyl半学是一类拓扑半学,非平凡的线性带越过靠近费米水平。这种交叉的存在需要破坏时间反转或反转对称性,并负责外来物理特性。在这项工作中,我们确定了全赫斯勒的复合inmnti $ _2 $,是一种有希望的,易于合成的,$ t $ - 和$ i $ $ $ $ $ - 破坏Weyl Semimetal。为了正确捕获磁状态的性质,我们采用了一种新颖的$ \ mathrm {dft}+u $计算设置,其中所有哈伯德参数均可从第一原则评估;从而保留了理论的真正预测性\ textit {ab inoio}特征。我们证明,这种材料在其他已知的Weyl半学方面表现出相对更为有趣的功能:两个相邻节点之间的距离足够大,可以观察到频段中的各种线性分散体,并且只有一种这种节点的对存在于Brillouin区域中。我们还显示了在广泛的化学势范围内的费米弧稳定的存在。最后,从微不足道到低能特性的缺乏贡献使材料成为实践设备的有前途的候选人。

Topological materials have been a main focus of studies in the past decade due to their protected properties that can be exploited for the fabrication of new devices. Among them, Weyl semimetals are a class of topological semimetals with non-trivial linear band crossing close to the Fermi level. The existence of such crossings requires the breaking of either time-reversal or inversion symmetry and is responsible for the exotic physical properties. In this work we identify the full-Heusler compound InMnTi$_2$, as a promising, easy to synthesize, $T$- and $I$-breaking Weyl semimetal. To correctly capture the nature of the magnetic state, we employed a novel $\mathrm{DFT}+U$ computational setup where all the Hubbard parameters are evaluated from first-principles; thus preserving a genuinely predictive \textit{ab initio} character of the theory. We demonstrate that this material exhibits several features that are comparatively more intriguing with respect to other known Weyl semimetals: the distance between two neighboring nodes is large enough to observe a wide range of linear dispersions in the bands, and only one kind of such node's pairs is present in the Brillouin zone. We also show the presence of Fermi arcs stable across a wide range of chemical potentials. Finally, the lack of contributions from trivial points to the low-energy properties makes the materials a promising candidate for practical devices.

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