arXiv subjects

X. J. Wang

Publications and source records attributed to X. J. Wang.

At least 19 recordsLinked to original sources

arXiv2025

Probing the atomic dynamics of ultrafast melting with femtosecond electron diffraction

Melting is an everyday phase transition that is determined by thermodynamic parameters like temperature and pressure. In contrast, ultrafast melting is governed by the microscopic response to a rapid energy input and, thus, can reveal the strength and dynamics of atomic bonds as well as the energy flow rate to the lattice. Accurately describing these processes remains challenging and requires detailed insights into transient states encountered. Here, we present data from femtosecond electron diffraction measurements that capture the structural evolution of copper during the ultrafast solid to liquid phase transformations. At absorbed energy densities 2 to 4 times the melting threshold, melting begins at the surface slightly below the nominal melting point followed by rapid homogeneous melting throughout the volume. Molecular dynamics simulations reproduce these observations and reveal a weak electron lattice energy transfer rate for the given experimental conditions. Both simulations and experiments show no indications of rapid lattice collapse when its temperature surpasses proposed limits of superheating, providing evidence that inherent dynamics limits the speed of disordering in ultrafast melting of metals.

cond-mat.mtrl-sci↗

arXiv2025

Performance Study of a Position-sensitive Plastic Scintillator Detector

For a long time, scintillator detectors have suffered from relatively weak spatial resolution due to various influencing factors. Additionally, the high cost of photomultiplier tubes (PMTs) has limited the widespread adoption of scintillator detectors as position-sensitive detectors in particle and nuclear physics experiments. In recent years, thanks to the rapid development of silicon photomultipliers (SiPMs), their excellent cost-performance ratio has led to a renewed interest in scintillator detectors in particle and nuclear physics. This project provides a detailed discussion of a detector based on scintillators coupled with SiPMs, focusing on how to improve the detector's position accuracy. By developing algorithms based on traditional optical propagation, a position resolution of mm level has been achieved. Furthermore, the introduction of a machine learning CNN algorithm has further enhanced the detector's position resolution.

physics.ins-det↗

arXiv2024

I-mode Plasma Confinement Improvement by Real-time Lithium Injection and its Classification on EAST Tokamak

I-mode is a promising regime for future fusion reactors due to the high energy confinement and the moderate particle confinement. However, the effect of lithium, which has been widely applied for particle recycling and impurity control, on I-mode plasma is still unclear. Recently, experiments of real-time lithium powder injection on I-mode plasma have been carried out in EAST Tokamak. It was found that the confinement performance of the I-mode can be improved by the lithium powder injection, which can strongly reduce electron turbulence (ET) and then trigger ion turbulence (IT). Four different regimes of I-mode have been identified in EAST. The Type I I-mode plasma is characterized by the weakly coherent mode (WCM) and the geodesic-acoustic mode (GAM). The Type II I-mode is featured as the WCM and the edge temperature ring oscillation (ETRO). The Type III I-mode corresponds to the plasma with the co-existence of ETRO, GAM, and WCM. The Type IV I-mode denotes the plasma with only WCM but without ETRO and GAM. It has been observed that WCM and ETRO are increased with lithium powder injection due to the reduction of ion and electron turbulence, and the enhancement of the pedestal electron temperature gradient. EAST experiments demonstrate that lithium powder injection is an effective tool for real-time control and confinement improvement of I-mode plasma.

physics.plasm-ph↗

arXiv2024

Robust globally divergence-free weak Galerkin methods for stationary incompressible convective Brinkman-Forchheimer equations

This paper develops a class of robust weak Galerkin methods for the stationary incompressible convective Brinkman-Forchheimer equations. The methods adopt piecewise polynomials of degrees $m\ (m\geq1)$ and $m-1$ respectively for the approximations of velocity and pressure variables inside the elements and piecewise polynomials of degrees $k \ ( k=m-1,m)$ and $m$ respectively for their numerical traces on the interfaces of elements, and are shown to yield globally divergence-free velocity approximation. Existence and uniqueness results for the discrete schemes, as well as optimal a priori error estimates, are established. A convergent linearized iterative algorithm is also presented. Numerical experiments are provided to verify the performance of the proposed methods

math.NA↗

arXiv2022

Characterization of Pedestal Burst Instabilities during I-mode to H-mode Transition in the EAST Tokamak

Quasi-periodic Pedestal Burst Instabilities (PBIs), featuring alternative turbulence suppression and bursts, have been clearly identified by various edge diagnostics during I-mode to H-mode transition in the EAST Tokamak. The radial distribution of the phase perturbation caused by PBI shows that PBI is localized in the pedestal. Prior to each PBI, a significant increase of density gradient close to the pedestal top can be clearly distinguished, then the turbulence burst is generated, accompanied by the relaxation of the density profile, and then induces an outward particle flux. The relative density perturbation caused by PBIs is about $6 \sim 8\%$. Statistic analyses show that the pedestal normalized density gradient triggering the first PBI has a threshold value, mostly in the range of $22 \sim 24$, suggesting that a PBI triggering instability could be driven by the density gradient. And the pedestal normalized density gradient triggering the last PBI is about $30 \sim 40$ and seems to increase with the loss power and the chord-averaged density. In addition, the frequency of PBI is likely to be inversely proportional to the chord-averaged density and the loss power. These results suggest that PBIs and the density gradient prompt increase prior to PBIs can be considered as the precursor for controlling I-H transition.

physics.plasm-ph↗

arXiv2021

Non-equilibrium self-assembly of spin-wave solitons in FePt nanoparticles

Magnetic nanoparticles such as FePt in the L10-phase are the bedrock of our current data storage technology. As the grains become smaller to keep up with technological demands, the superparamagnetic limit calls for materials with higher magneto-crystalline anisotropy. This in turn reduces the magnetic exchange length to just a few nanometers enabling magnetic structures to be induced within the nanoparticles. Here we describe the existence of spin-wave solitons, dynamic localized bound states of spin-wave excitations, in FePt nanoparticles. We show with time-resolved X-ray diffraction and micromagnetic modeling that spin-wave solitons of sub-10 nm sizes form out of the demagnetized state following femtosecond laser excitation. The measured soliton spin-precession frequency of 0.1 THz positions this system as a platform to develop miniature devices capable of filling the THz gap.

cond-mat.mtrl-sci↗

arXiv2021

Conformer-specific Chemistry Imaged in Real Space and Time

Conformational isomers or conformers of molecules play a decisive role in chemistry and biology. However, experimental methods to investigate chemical reaction dynamics are typically not conformer-sensitive. Here, we report on a gas-phase megaelectronvolt ultrafast electron diffraction investigation of α-phellandrene undergoing an electrocyclic ring-opening reaction. We directly image the evolution of a specific set of α-phellandrene conformers into the product isomer predicted by the Woodward-Hoffmann rules in real space and time. Our experimental results are in quantitative agreement with nonadiabatic quantum molecular dynamics simulations, which provide unprecedented detail of how conformation influences time scale and quantum efficiency of photoinduced ring-opening reactions. Due to the prevalence of large numbers of conformers in organic chemistry, our findings impact our general understanding of reaction dynamics in chemistry and biology.

physics.chem-ph↗

arXiv2021

Effect of lattice excitations on transient near edge X-ray absorption spectroscopy

Time-dependent and constituent-specific spectral changes in soft near edge X-ray spectroscopy (XAS) of an [Fe/MgO]$_8$ metal/insulator heterostructure upon laser excitation are analyzed at the O K-edge with picosecond time resolution. The oxygen absorption edge of the insulator features a uniform intensity decrease of the fine structure at elevated phononic temperatures, which can be quantified by a simple simulation and fitting procedure presented here. Combining X-ray absorption spectroscopy with ultrafast electron diffraction measurements and ab initio calculations demonstrate that the transient intensity changes in XAS can be assigned to a transient lattice temperature. Thus, the sensitivity of transient near edge XAS to phonons is demonstrated.

cond-mat.mtrl-sci↗

arXiv2020

Photoinduced Dirac semimetal in ZrTe5

Novel phases of matter with unique properties that emerge from quantum and topological protection present an important thrust of modern research. Of particular interest is to engineer these phases on demand using ultrafast external stimuli, such as photoexcitation, which offers prospects of their integration into future devices compatible with optical communication and information technology. Here, we use MeV Ultrafast Electron Diffraction (UED) to show how a transient three-dimensional (3D) Dirac semimetal state can be induced by a femtosecond laser pulse in a topological insulator ZrTe$_5$. We observe marked changes in Bragg diffraction, which are characteristic of bond distortions in the photoinduced state. Using the atomic positions refined from the UED, we perform density functional theory (DFT) analysis of the electronic band structure. Our results reveal that the equilibrium state of ZrTe$_5$ is a topological insulator with a small band gap of $\sim$25 meV, consistent with angle-resolved photoemission (ARPES) experiments. However, the gap is closed in the presence of strong spin-orbit coupling (SOC) in the photoinduced transient state, where massless Dirac fermions emerge in the chiral band structure. The time scale of the relaxation dynamics to the transient Dirac semimetal state is remarkably long, $τ\sim$160 ps, which is two orders of magnitude longer than the conventional phonon-driven structural relaxation. The long relaxation is consistent with the vanishing density of states in Dirac spectrum and slow spin-repolarization of the SOC-controlled band structure accompanying the emergence of Dirac fermions.

cond-mat.str-el↗

arXiv2019

Microscopic non-equilibrium energy transfer dynamics in a photoexcited metal/insulator heterostructure

The element specificity of soft X-ray spectroscopy makes it an ideal tool for analyzing the microscopic origin of ultrafast dynamics induced by localized optical excitation in metal-insulator heterostructures. Using [Fe/MgO]$_n$ as a model system, we perform ultraviolet pump/soft X-ray probe experiments, which are sensitive to all constituents of these heterostructures, to probe both electronic and lattice excitations. Complementary ultrafast electron diffraction experiments independently analyze the lattice dynamics of the Fe constituent, and together with ab initio calculations yield comprehensive insight into the microscopic processes leading to local relaxation within a single constituent or non-local relaxation between two constituents. Besides electronic excitations in Fe, which are monitored at the Fe L$_3$ absorption edge and relax within 1 ps by electron-phonon coupling, soft X-ray analysis identifies a change at the oxygen K absorption edge of the MgO layers which occurs within 0.5 ps. This ultrafast energy transfer across the Fe-MgO interface is mediated by high-frequency, interface vibrational modes, which are excited by hot electrons in Fe and couple to vibrations in MgO in a mode-selective, non-thermal manner. A second, slower timescale is identified at the oxygen K pre-edge and the Fe L$_3$ edge. The slower process represents energy transfer by acoustic phonons and contributes to thermalization of the entire heterostructure. We thus find that the interfacial energy transfer is associated with non-equilibrium behavior in the phonon system. Because our experiments lack signatures of charge transfer across the interface, we conclude that phonon-mediated processes dominate the competition of electronic and lattice excitations in these non-local, non-equilibrium dynamics.

cond-mat.mtrl-sci↗

arXiv2019

Tracking the Ultrafast Non-Equilibrium Energy Flow between Electronic and Lattice Degrees of Freedom in Crystalline Nickel

Femtosecond laser excitation of solid-state systems creates non-equilibrium hot electrons that cool down by transferring their energy to other degrees of freedom and ultimately to lattice vibrations of the solid. By combining ab initio calculations with ultrafast diffuse electron scattering we gain a detailed understanding of the complex non-equilibrium energy transfer between electrons and phonons in laser-excited Ni metal. Our experimental results show that the wavevector resolved population dynamics of phonon modes is distinctly different throughout the Brillouin zone and are in remarkable agreement with our theoretical results. We find that zone-boundary phonon modes become occupied first. As soon as the energy in these modes becomes larger than the average electron energy a backflow of energy from lattice to electronic degrees of freedom occurs. Subsequent excitation of lower-energy phonon modes drives the thermalization of the whole system on the picosecond timescale. We determine the evolving non-equilibrium phonon occupations which we find to deviate markedly from thermal occupations.

cond-mat.mtrl-sci↗

arXiv2019

Femtosecond compression dynamics and timing jitter suppression in a terahertz-driven electron bunch compressor

We present the first demonstration of THz-driven bunch compression and timing stabilization of a few-fC relativistic electron beam with kinetic energy of 2.5 MeV using quasi-single-cycle strong field THz radiation in a shorted parallel-plate structure. Compression by nearly a factor of 3 produced a 39 fs rms bunch length and a reduction in timing jitter by more than a factor of 2, to 31 fs rms, offering a significant improvement to beam performance for applications like ultrafast electron diffraction. This THz-driven technique provides a critical step towards unprecedented timing resolution in ultrafast sciences and other accelerator applications using femtosecond-scale electron beams.

physics.acc-ph↗

arXiv2019

Parallel-Plate Waveguides for Terahertz-Driven MeV Electron Bunch Compression

We demonstrate the electromagnetic performance of waveguides for femtosecond electron beam bunch manipulation and compression with strong-field terahertz (THz) pulses. The compressor structure is a dispersion-free exponentially-tapered parallel-plate waveguide (PPWG) that can focus single-cycle THz pulses along one dimension. We show test results of the tapered PPWG structure using electro-optic sampling (EOS) at the interaction region with peak fields of at least 300 kV/cm given 0.9 uJ of incoming THz energy. We also present a modified shorted design of the tapered PPWG for better beam manipulation and reduced magnetic field as an alternative to a dual-feed approach. As an example, we demonstrate that with 5 uJ of THz energy, the PPWG compresses a 2.5 MeV electron bunch by a compression factor of more than 4 achieving a bunch length of about 18 fs.

physics.acc-ph↗

arXiv2019

Photoinduced ultrafast dynamics of local nematicity and lattice distortions in FeSe crystals

Formation of electronic nematicity is a common thread of unconventional superconductors. In iron-based materials, the long-range nematic order is revealed by the orthorhombic lattice distortion, which importance is a highly controversial topic due the small magnitude of the distortion. Here, we study the local crystal structure of FeSe and its interaction with electronic degrees of freedom using ultrafast electron diffraction, x-ray pair distribution function analysis, and transmission electron microscopy and find a significant lattice response to local nematicity. The study demonstrates how local lattice distortions, which exist even at temperatures above the nematic phase transition, can be released by photoexcitation, leading to an enhancement of the crystalline order. The observed local atomic structures and their out-of-equilibrium behavior unravel a sophisticated coupling between the lattice and nematic order parameter in FeSe.

cond-mat.supr-con↗

arXiv2018

Imaging the Photochemical Ring-Opening of 1,3-Cyclohexadiene by Ultrafast Electron Diffraction

The ultrafast photoinduced ring-opening of 1,3-cyclohexadiene constitutes a textbook example of electrocyclic reactions in organic chemistry and a model for photobiological reactions in vitamin D synthesis. Here, we present direct and unambiguous observation of the ring-opening reaction path on the femtosecond timescale and sub-Ångström length scale by megaelectronvolt ultrafast electron diffraction. We follow the carbon-carbon bond dissociation and the structural opening of the 1,3-cyclohexadiene ring by direct measurement of time-dependent changes in the distribution of interatomic distances. We observe a substantial acceleration of the ring-opening motion after internal conversion to the ground state due to steepening of the electronic potential gradient towards the product minima. The ring-opening motion transforms into rotation of the terminal ethylene groups in the photoproduct 1,3,5-hexatriene on the sub-picosecond timescale. Our work demonstrates the potential of megaelectronvolt ultrafast electron diffraction to elucidate photochemical reaction paths in organic chemistry.

physics.chem-ph↗

arXiv2018

Anisotropic spin-orbit torque generation in epitaxial SrIrO3 by symmetry design

Spin-orbit coupling (SOC), the interaction between the electron spin and the orbital angular momentum, can unlock rich phenomena at interfaces, in particular interconverting spin and charge currents. Conventional heavy metals have been extensively explored due to their strong SOC of conduction electrons. However, spin-orbit effects in classes of materials such as epitaxial 5d-electron transition metal complex oxides, which also host strong SOC, remain largely unreported. In addition to strong SOC, these complex oxides can also provide the additional tuning knob of epitaxy to control the electronic structure and the engineering of spin-to-charge conversion by crystalline symmetry. Here, we demonstrate room-temperature generation of spin-orbit torque on a ferromagnet with extremely high efficiency via the spin-Hall effect in epitaxial metastable perovskite SrIrO3. We first predict a large intrinsic spin-Hall conductivity in orthorhombic bulk SrIrO3 arising from the Berry curvature in the electronic band structure. By manipulating the intricate interplay between SOC and crystalline symmetry, we control the spin-Hall torque ratio by engineering the tilt of the corner-sharing oxygen octahedra in perovskite SrIrO3 through epitaxial strain. This allows the presence of an anisotropic spin-Hall effect due to a characteristic structural anisotropy in SrIrO3 with orthorhombic symmetry. Our experimental findings demonstrate the heteroepitaxial symmetry design approach to engineer spin-orbit effects. We therefore anticipate that these epitaxial 5d transition-metal oxide thin films can be an ideal building block for low-power spintronics.

cond-mat.mtrl-sci↗

arXiv2018

Terahertz-based attosecond metrology of relativistic electron beams

Photons, electrons, and their interplay are at the heart of photonic devices and modern instruments for ultrafast science [1-10]. Nowadays, electron beams of the highest intensity and brightness are created by photoemission with short laser pulses, and then accelerated and manipulated using GHz radiofrequency electromagnetic fields. The electron beams are utilized to directly map photoinduced dynamics with ultrafast electron scattering techniques, or further engaged for coherent radiation production at up to hard X-ray wavelengths [11-13]. The push towards improved timing precision between the electron beams and pump optical pulses though, has been stalled at the few tens of femtosecond level, due to technical challenges with synchronizing the high power rf fields with optical sources. Here, we demonstrate attosecond electron metrology using laser-generated single-cycle THz radiation, which is intrinsically phase locked to the optical drive pulses, to manipulate multi-MeV relativistic electron beams. Control and single-shot characterization of bright electron beams at this unprecedented level open up many new opportunities for atomic visualization.

physics.acc-ph↗

arXiv2018

Ultralow-temperature heat transport in the quantum spin liquid candidate Ca10Cr7O28 with bilayer kagome lattice

Recently, a novel material with bilayer kagome lattice Ca$_{10}$Cr$_7$O$_{28}$ was proposed to be a gapless quantum spin liquid, due to the lack of long-range magnetic order and the observation of broad diffuse excitations. Here, we present the ultralow-temperature thermal conductivity measurements on single crystals of Ca$_{10}$Cr$_7$O$_{28}$ to detect its low-lying magnetic excitations. At finite temperatures, with increasing the magnetic fields, the thermal conductivity exhibits a clear dip around 6 T, which may correspond to a crossover in the magnetic ground state. At the zero-temperature limit, no residual linear term is found at any fields, indicating the absence of gapless itinerant fermionic excitations. Therefore, if the spinons do exist, they are either localized or gapped. In the gapped case, the fitting of our data gives a small gap $Δ\sim$ 0.27(2) K. These results put strong constraints on the theoretical description of the ground state in this quantum spin liquid candidate.

cond-mat.str-el↗