arXiv subjects

Meng-Jie Huang

Publications and source records attributed to Meng-Jie Huang.

9 recordsLinked to original sources

arXiv2026

Emergent Chaos-Like Dynamics of Spin-Orbit Torque-Driven Magnetic Transitions

Spin-orbit torques (SOTs) are widely used to control magnetization in nanoscale electric systems and are typically assumed to drive skyrmion nucleation and motion in a deterministic manner, especially in materials with strong Dzyaloshinskii-Moriya interaction. Here, using time-resolved holography-based x-ray microscopy supported by micromagnetic simulations, we reveal that on nano- to picosecond timescales the actual dynamics can deviate strikingly from this expectation by producing transient regimes of chaos-like behavior. By exploiting deterministic skyrmion generation at an anisotropy-engineered defect and implementing a high-resolution pump-probe scheme, we directly track the magnetization evolution in real space. This approach uncovers a dynamic phase transition that separates coherent SOT-driven motion from a regime of transient instability characterized by picosecond-scale fluctuations, strong domain disorder, topological instabilities, and skyrmion shedding, experimentally observed here for the first time. During SOT actuation, the system briefly enters this instability regime, showing short-lived chaos-like behavior, yet it reliably relaxes into robust and reproducible final states. Our results demonstrate a powerful methodology for accessing time-averaged nano- to picosecond dynamics in magnetic systems and reveal a previously hidden layer of transient, topologically rich behavior underlying nominally deterministic skyrmion control.

cond-mat.mes-hall↗

arXiv2026

Quantifying quasiparticle chirality in a chiral topological semimetal

Recently, the projection of the electron's spin on its crystal momentum has been proposed as a metric to quantify electronic chirality of Bloch states in crystals, which is expected to affect a wide range of physical properties, such as magnetoelectric and optical responses. However, a direct experimental quantification of this chirality metric over an entire iso-energy surface has remained elusive. Here, we have used spin- and angle-resolved photoemission spectroscopy to directly probe the electronic chirality by measuring the bulk spin texture of Kramers-Weyl and Weyl cones in RhSi, a chiral topological semimetal with strong spin-orbit coupling (SOC). After quantifying the SOC splitting of Weyl cones, we determine their spin direction along different azimuthal angles to extract energy dependent the deviations (up to ~40°) from perfect parallel spin-momentum locking. From these deviations we define an energy-dependent normalized electron chirality density (NECD), a directly accessible metric of bulk electronic chirality. In RhSi, the NECD decreases from 1 at the Kramers-Weyl point to ~0.8 at ~200 meV below it. Finally, we show that this experimentally grounded NECD provides predictive power for magneto-optical and transport responses of chiral materials, exemplified by the longitudinal Edelstein effect.

cond-mat.mes-hall↗

arXiv2026

Electronic Structure and Resonant Circular Dichroism of La$_{0.7}$Sr$_{0.3}$MnO$_3$ from Soft X-ray Angle-Resolved Photoemission

Coupling between spin, orbital, charge, and lattice degrees of freedom in transition-metal oxides produces a variety of electronic and magnetic phenomena of importance for future technologies. Here, we explore the electronic band structure of a (111)-oriented La0.7Sr0.3MnO3 thin film through soft X-ray angle-resolved photoemission spectroscopy (ARPES). The measurements agree with the electronic band structure calculated with density functional theory using Hubbard U correction. Furthermore, we probe the circular dichroism in ARPES, and observe a pronounced momentum- resolved magnetic circular dichroism in resonant photoemission from the Mn L-edge. The approach combines the momentum- and spin-selectivity of ARPES and X-ray magnetic circular dichroism, respectively, which could provide a useful approach for the study of unconventional magnetism.

cond-mat.str-el↗

arXiv2024

Chirality-Driven Orbital Angular Momentum and Circular Dichroism in CoSi

Chiral crystals and molecules were recently predicted to form an intriguing platform for unconventional orbital physics. Here, we report the observation of chirality-driven orbital textures in the bulk electronic structure of CoSi, a prototype member of the cubic B20 family of chiral crystals. Using circular dichroism in soft X-ray angle-resolved photoemission, we demonstrate the formation of a bulk orbital-angular-momentum texture and monopole-like orbital-momentum locking that depends on crystal handedness. We introduce the intrinsic chiral circular dichroism, icCD, as a differential photoemission observable and a natural probe of chiral electron states. Our findings render chiral crystals promising for spin-orbitronics applications.

cond-mat.mtrl-sci↗

arXiv2024

A compact approach to higher-resolution resonant inelastic X-ray scattering detection using photoelectrons

The detection of inelastically scattered soft X-rays with high energy resolution usually requires large grating spectrometers. Recently, photoelectron spectrometry for analysis of X-rays (PAX) has been rediscovered for modern spectroscopy experiments at synchrotron light sources. By converting scattered photons to electrons and using an electron energy analyser, the energy resolution for resonant inelastic X-ray scattering (RIXS) becomes decoupled from the X-ray spot size and instrument length. In this work, we develop PAX towards high energy resolution using a modern photoemission spectroscopy setup studying Ba2Cu3O4Cl2 at the Cu L3-edge. We measure a momentum transfer range of 24% of the first Brillouin zone simultaneously. Our results hint at the observation of a magnon excitation below 100 meV energy transfer and show intensity variations related to the dispersion of dd-excitations. With dedicated setups, PAX can become an alternative to the best and largest RIXS instruments, while at the same time opening new opportunities to acquire RIXS at a range of momentum transfers simultaneously and combine it with angle-resolved photoemission spectroscopy in a single instrument.

cond-mat.mtrl-sci↗

arXiv2020

Revealing the site selective local electronic structure of Co$_{3}$O$_{4}$ using $2p3d$ resonant inelastic X-ray scattering

We investigate mixed-valence oxide Co$_3$O$_4$ using Co $2p3d$ resonant inelastic X-ray scattering (RIXS). By setting resonant edges at Co$^{2+}$ and Co$^{3+}$ ions, the $dd$ excitations on the two Co sites are probed selectively, providing detailed information on the local electronic structure of Co$_3$O$_4$. The $2p3d$ RIXS result reveals the $^4$T$_{2}$ excited state of tetrahedral Co$^{2+}$ site at 0.5 eV beyond the discriminative power of optical absorption spectroscopies. Additionally, the $^3$T$_{2g}$ excited stated at 1.3 eV is uniquely identified for the octahedral Co$^{3+}$ site. Guided by cluster multiplet simulations, the ground-state character of the Co$^{2+}$ and Co$^{3+}$ site is determined to be high-spin $^4$A$_{2}$(T$_d$) and low-spin $^1$A$_{1g}$(O$_h$), respectively. This indicates that only the Co$^{2+}$ site is magnetically active site at low-temperatures in Co$_3$O$_4$. The ligand-to-metal charge transfer analysis suggests a formation of a strong covalent bonding between Co and O ions at the Co$^{3+}$ site, while Co$^{2+}$ is rather ionic.

cond-mat.mtrl-sci↗

arXiv2012

Study the dynamics of the nonspreading Airy packets from the time evolution operator

Berry and Balazs showed that an initial Airy packet Ai(b x) under time evolution is nonspreading in free space and also in a homogeneous time-varying linear potential V(x,t)=-F(t) x. We find both results can be derived from the time evolution operator U(t). We show that U(t) can be decomposed into ordered product of operators and is essentially a shift operator in x; hence, Airy packets evolve without distortion. By writing the Hamiltonian H as H=H_b+H_i, where H_b is the Hamiltonian such that Ai(b x) is its eigenfunction. Then, H_i is shown to be as an interacting Hamiltonian that causes the Airy packet into an accelerated motion of which the acceleration a=(-H_i/( x))/m. Nonspreading Airy packet then acts as a classical particle of mass m, and the motion of it can be described classically by H_i.

quant-ph↗

arXiv2008

Nonspreading wave packets in a general potential V(x,t) in one dimension

We discuss nonspreading wave packets in one dimensional Schrödinger equation. We derive general rules for constructing nonspreading wave packets from a general potential $\textmd{V}(x,t)$. The essential ingredients of a nonspreading wave packet, the shape function $f(x)$, the motion $d(t)$, the phase function $ϕ(x,t)$ are derived. Since the form of the shape of a nonspreading wave packet does not change in time, the shape equation should be time independent. We show that the shape function $f(x)$ is the eigenfunction of the time independent Schrödinger equation with an effective potential $V_{\textmd{eff}}$ and an energy $E_{\textmd{eff}}$. We derive nonspreading wave packets found by Schrödinger, Senitzky, and Berry and Balazs as examples. We show that most stationary potentials can only support stationary nonspreading wave packets. We show how to construct moving nonspreading wave packets from time dependent potentials, which drive nonspreading wave packets into an arbitrary motion.

quant-ph↗

arXiv2004

Gravity waves over topographical bottoms: Comparison with the experiment

In this paper, the propagation of water surface waves over one-dimensional periodic and random bottoms is investigated by the transfer matrix method. For the periodic bottoms, the band structure is calculated, and the results are compared to the transmission results. When the bottoms are randomized, the Anderson localization phenomenon is observed. The theory has been applied to an existing experiment (Belzons, et al., J. Fluid Mech. {\bf 186}, 530 (1988)). In general, the results are compared favorably with the experimental observation.

physics.flu-dyn↗