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Register a new userDynamic symmetry breaking in chiral magnetic systems
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The Dzyaloshinskii-Moriya interaction (DMI) in magnetic systems stabilizes spin textures with preferred chirality, applicable to next-generation memory and computing architectures. In perpendicularly magnetized heavy-metal/ferromagnet films, the interfacial DMI originating from structural inversion asymmetry and strong spin-orbit coupling favors chiral Neel-type domain walls (DWs) whose energetics and mobility remain at issue. Here, we characterize a new effect in which domains expand unidirectionally in response to a combination of out-of-plane and in-plane magnetic fields, with the growth direction controlled by the in-plane field strength. These growth directionalities and symmetries with applied fields cannot be understood from static treatments alone. We theoretically demonstrate that perpendicular field torques stabilize steady-state magnetization profiles highly asymmetric in elastic energy, resulting in a dynamic symmetry breaking consistent with the experimental findings. This phenomenon sheds light on the mechanisms governing the dynamics of Neel-type DWs and expands the utility of field-driven DW motion to probe and control chiral DWs.
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We discovered in simulations of sliding coaxial nanotubes an unanticipated example of dynamical symmetry breaking taking place at the nanoscale. While both nanotubes are perfectly left-right symmetric and nonchiral, a nonzero angular momentum of phonon origin appears spontaneously at a series of critical sliding velocities, in correspondence with large peaks of the sliding friction. The non-linear equations governing this phenomenon resemble the rotational instability of a forced string. However, several new elements, exquisitely nano appear here, with the crucial involvement of Umklapp and of sliding nanofriction.
We report on the linear optical properties of the chiral magnet Cu2OSeO3, specifically associated with the absence of inversion symmetry, the chiral crystallographic structure, and magnetic order. Through spectroscopic ellipsometry, we observe local crystal-field excitations below the charge-transfer gap. These crystal-field excitations are optically allowed due to the lack of inversion symmetry at the Cu sites. Optical polarization rotation measurements were used to study the structural chirality and magnetic order. The temperature dependence of the natural optical rotation, originating in the chiral crystal structure, provides evidence for a finite magneto-electric effect in the helimagnetic phase. We find a large magneto-optical susceptibility on the order of V(540nm)~10^4 rad/(T*m) in the helimagnetic phase and a maximum Faraday rotation of ~165deg/mm in the ferrimagnetic phase. The large value of V can be explained by considering spin cluster formation and the relative ease of domain reorientation in this metamagnetic material. The magneto-optical activity allows us to map the magnetic phase diagram, including the skyrmion lattice phase. In addition to this, we probe and discuss the nature of the various magnetic phase transitions in Cu2OSeO3.
Metal halide perovskites exhibit a materials physics that is distinct from traditional inorganic and organic semiconductors. While materials such as CH3NH3PbI3 are non-magnetic, the presence of heavy elements (Pb and I) in a non-centrosymmetric crystal environment result in a significant spin-splitting of the frontier electronic bands through the Rashba-Dresselhaus effect. We show, from a combination of textit{ab initio} molecular dynamics, density-functional theory, and relativistic quasi-particle textit{GW} theory, that the nature (magnitude and orientation) of the band splitting depends on the local asymmetry around the Pb and I sites in the perovskite structure. The potential fluctuations vary in time as a result of thermal disorder and a dynamic lone pair instability of the Pb(II) 6s$^{2}$6p$^{0}$ ion. We show that the same physics emerges both for the organic-inorganic CH3NH3PbI3 and the inorganic CsPbI3 compound. The results are relevant to the photophysics of these compounds and are expected to be general to other lead iodide containing perovskites.
The bulk band topology of symmetry invariant adiabatic systems in the thermodynamic limit are considered to be determined by the hopping energy. In this work, we present that in closed classical systems, due to generalized chiral symmetry broken, the on-site energy cannot always be regarded as identical and can crucially impact the topological properties of the systems. Based on a finite one-dimensional chain, we demonstrate that the non-equivalent on-site energy of bulk lattices affects the topological phases of the bands, and the on-site energy of end lattices affects the existence of the topological states. Along these lines, the correspondence with generalized chiral symmetry in acoustic system is rigorously proposed. Our work provides a new degree of freedom for topological classical systems, and can be generalized to higher-dimensions and non-Hermitian conditions.
Using the nonperturbative Schwinger-Dyson equation, we show that chiral symmetry is dynamically broken in QED at weak couplings when an external magnetic field is present, and that chiral symmetry is restored at temperatures above $T_c simeq alphapi^2/sqrt{2 pi |eH|}$, where $alpha$ is the fine structure constant and $H$ is the magnetic field strength.
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