在URu2Si2的隐藏阶段中,旋转对称性被打破
R Okazaki1, T Shibauchi, H J Shi
1Department of Physics, Kyoto University, Kyoto 606-8502, Japan.
概括
在URu(2) Si(2) 中的隐藏顺序相表现出被破坏的旋转对称性,暗示一个电子阴性相. 这一发现解决了重子化合物中长期存在的.
科学领域:
- 凝聚物质物理学 凝聚物质物理学
- 材料科学 材料科学 材料科学
- 量子材料是一种量子材料.
背景情况:
- 第二阶段过渡涉及自发的对称性破坏.
- 在URu(2) Si(2) (URu2Si2) 中的隐藏顺序阶段,对它的折叠对称性构成了一个长期存在的.
- 对于重子系统来说,了解这个阶段至关重要.
研究的目的:
- 为了阐明URu的隐性阶段中破坏对称性的性质(2)Si(2).
- 为了研究在过渡温度T (h) = 17.5K以下的对称性破坏.
主要方法:
- 在平面内测量磁性易感性异质性.
- 使用平面内场旋转检测磁力扭矩的两倍振荡.
- 在小,纯净的URu(2) Si(2) 水晶上进行的实验.
主要成果:
- 观察到在T (h) 下的平面内磁感应性异质的出现.
- 检测到磁力扭矩的两倍振荡,证实四倍旋转对称性被打破.
- 在隐藏顺序阶段,URu(2) Si(2) 的四角对称被打破.
结论:
- 在URu(2)Si(2) 中的隐藏顺序阶段被确定为电子阴性阶段.
- 这一阶段的特点是旋转对称性的自发破坏,同时保持转换不变.
- 这些发现为重子材料中对称性破坏提供了新的理解.
更多相关视频
09:06Visualizing Uniaxial-strain Manipulation of Antiferromagnetic Domains in Fe1+YTe Using a Spin-polarized Scanning Tunneling Microscope
Published on: March 24, 2019
04:51Comparison of Two Different Synthesis Methods of Single Crystals of Superconducting Uranium Ditelluride
Published on: July 8, 2021
相关概念视频
Symmetry Elements in a Crystal
Crystal symmetry operations are isometric transformations that map objects onto indistinguishable copies while preserving distances, angles, and volumes. The simplest symmetry operation is translation, which shifts the entire infinite crystal lattice parallelly by a translation vector.Crystallographic rotations involve rotations by an angle of 2π/n around an axis without changing the positions of points on the axis. It is called the rotational axis of the symmetry, denoted by n. The combination...
Woodward–Hoffmann Selection Rules and Microscopic Reversibility
Electrocyclic reactions, cycloadditions, and sigmatropic rearrangements are concerted pericyclic reactions that proceed via a cyclic transition state. These reactions are stereospecific and regioselective. The stereochemistry of the products depends on the symmetry characteristics of the interacting orbitals and the reaction conditions. Accordingly, pericyclic reactions are classified as either symmetry-allowed or symmetry-forbidden. Woodward and Hoffmann presented the selection criteria for...
Thermal Sigmatropic Reactions: Overview
Sigmatropic rearrangements are a class of pericyclic reactions in which a σ bond migrates from one part of a π system to another. These are intramolecular rearrangements where the total number of σ and π bonds remain unchanged.
Sigmatropic shifts are classified based on an order term [i, j ], where i and j indicate the number of atoms across which each end of the σ bond migrates. Below are examples of a [3,3] sigmatropic shift in 1,5-hexadiene, referred to as...
Sigmatropic shifts are classified based on an order term [i, j ], where i and j indicate the number of atoms across which each end of the σ bond migrates. Below are examples of a [3,3] sigmatropic shift in 1,5-hexadiene, referred to as...
Stereoisomerism of Cyclic Compounds
In this lesson, we delve into the role of ring conformation and its stability, which determines the spatial arrangement and, consequently, the molecular symmetry and stereoisomerism of cyclic compounds. 1,2-Dimethylcyclohexane is used as a case study to evaluate the possible number of stereoisomers. Here, given the multiple (n = 2) chiral centers, there are 2n = 4 possible configurations that lack a plane of symmetry, as the ring skeleton exists in a non-planar chair conformation. In addition,...
Crystallographic Point Groups
Crystallographic point groups represent the various symmetry operations that can occur within crystals. They are unique in that at least one point will always remain unchanged during these actions. For instance, consider the triclinic system. This system, devoid of any axis or plane of symmetry, aligns with the C1 and Ci point groups.where Cᵢ is characterized solely by a center of inversion.Contrastingly, the monoclinic system introduces an element of symmetry. This system with one plane and...
Chirality at Nitrogen, Phosphorus, and Sulfur
Chirality is most prevalent in carbon-based tetrahedral compounds, but this important facet of molecular symmetry extends to sp3-hybridized nitrogen, phosphorus and sulfur centers, including trivalent molecules with lone pairs. Here, the lone pair behaves as a functional group in addition to the other three substituents to form an analogous tetrahedral center that can be chiral.
A consequence of chirality is the need for enantiomeric resolution. While this is theoretically possible for all...
A consequence of chirality is the need for enantiomeric resolution. While this is theoretically possible for all...
