arXiv subjects

Sae Hwan Chun

Publications and source records attributed to Sae Hwan Chun.

At least 19 recordsLinked to original sources

arXiv2026

Atomically Resolved Acoustic Dynamics Coupled with Magnetic Order in a van der Waals Antiferromagnet

Magnetoelastic coupling in van der Waals (vdW) magnetic materials enables a unique interplay between the spin and lattice degrees of freedom. Characterizing the elastic responses with atomic and femtosecond resolution across the magnetic transition is essential for guiding the design of magnetically tunable actuators and strain-mediated spintronic devices. Here, ultrafast x-ray diffraction employed at a free-electron laser reveals that the atomic displacements, wave vectors, and dispersion relations of acoustic phonon modes in a vdW antiferromagnet FePS$_3$ are coupled with the magnetic order, by tracking both in-plane and out-of-plane Bragg peaks upon optical excitation across the Néel temperature (T$_N$). One transverse mode shows that a quasi-out-of-plane atomic displacement undergoes a significant directional change across T$_N$. Its quasi-in-plane wave vector is derived by the comparison between the measured sound velocity and the first-principles calculations. The other transverse mode is an interlayer shear acoustic mode whose amplitude is strongly enhanced in the antiferromagnetic phase, exhibiting eight times stronger amplitude than the longitudinal acoustic mode below T$_N$. The atomically resolved characterization of acoustic phonon dynamics that couple with magnetic ordering opens opportunities for harnessing unique magnetoelastic coupling in vdW magnets on ultrafast timescales.

cond-mat.mtrl-sci↗

arXiv2025

Photo-induced Dynamics and Momentum Distribution of Chiral Charge Density Waves in 1T-TiSe$_{2}$

Exploring the photoinduced dynamics of chiral states offers promising avenues for advanced control of condensed matter systems. Photoinduced or photoenhanced chirality in 1T-TiSe$_{2}$ has been suggested as a fascinating platform for optical manipulation of chiral states. However, the mechanisms underlying chirality training and its interplay with the charge density wave (CDW) phase remain elusive. Here, we use time-resolved X-ray diffraction (tr-XRD) with circularly polarized pump lasers to probe the photoinduced dynamics of chirality in 1T-TiSe$_{2}$. We observe a notable ($\sim$20%) difference in CDW intensity suppression between left- and right-circularly polarized pumps. Additionally, we reveal momentum-resolved circular dichroism arising from domains of different chirality, providing a direct link between CDW and chirality. An immediate increase in CDW correlation length upon laser pumping is detected, suggesting the photoinduced expansion of chiral domains. These results both advance the potential of light-driven chirality by elucidating the mechanism driving chirality manipulation in TiSe$_2$, and they demonstrate that tr-XRD with circularly polarized pumps is an effective tool for chirality detection in condensed matter systems.

cond-mat.str-el↗

arXiv2024

Signatures of Floquet Engineering in the proximal Kitaev Quantum Spin Liquid H$_3$LiIr$_2$O$_6$ by tr-RIXS

We present the first circularly polarized Floquet engineering time-resolved Resonant Inelastic X-ray Scattering (tr-RIXS) experiment in H$_3$LiIr$_2$O$_6$, an iridium-based Kitaev system. Our calculations and experimental results are consistent with the modification of the low energy magnetic excitations in H$_3$LiIr$_2$O$_6$ only during illumination by the laser pulse, consistent with the Floquet engineering of the exchange interactions. However, the penetration length mismatch between the X-ray probe and laser pump and the intrinsic complexity of Kitaev magnets prevented us from unequivocally extracting towards which ground H$_3$LiIr$_2$O$_6$ was driven. We outline possible solutions to these challenges for Floquet stabilization and observation of the Kitaev Quantum Spin Liquid limit by RIXS.

cond-mat.str-el↗

arXiv2023

Non-local features of the spin-orbit exciton in Kitaev materials

A comparative resonant inelastic x-ray scattering (RIXS) study of three well-known Kitaev materials is presented: $α$-Li$_2$IrO$_3$, Na$_2$IrO$_3$, and $α$-RuCl$_3$. Despite similar low-energy physics, these materials show distinct electronic properties, such as the large difference in the size of the charge gap. The RIXS spectra of the spin-orbit exciton for these materials show remarkably similar three-peak features, including sharp low energy peak (peak A) as well as transitions between $j_{\text{eff}}=1/2$ and $j_{\text{eff}}=3/2$ states. Comparison of experimental spectra with cluster calculations reveals that the observed three-peak structure reflects the significant role that non-local physics plays in the electronic structure of these materials. In particular, the low-energy peak A arises from a holon-doublon pair rather than a conventional particle-hole exciton as proposed earlier. Our study suggests that while spin-orbit assisted Mott insulator is still the best description for these materials, electron itinerancy cannot be ignored when formulating low-energy Hamiltonian of these materials.

cond-mat.str-el↗

arXiv2022

Optically Induced Picosecond Lattice Compression in the Dielectric Component of a Strongly Coupled Ferroelectric/Dielectric Superlattice

Above-bandgap femtosecond optical excitation of a ferroelectric/dielectric BaTiO3/CaTiO3 superlattice leads to structural responses that are a consequence of the screening of the strong electrostatic coupling between the component layers. Time-resolved x-ray free-electron laser diffraction shows that the structural response to optical excitation includes a net lattice expansion of the superlattice consistent with depolarization-field screening driven by the photoexcited charge carriers. The depolarization-field-screening-driven expansion is separate from a photoacoustic pulse launched from the bottom electrode on which the superlattice was epitaxially grown. The distribution of diffracted intensity of superlattice x-ray reflections indicates that the depolarization-field-screening-induced strain includes a photoinduced expansion in the ferroelectric BaTiO3 and a contraction in CaTiO3. The magnitude of expansion in BaTiO3 layers is larger than the contraction in CaTiO3. The difference in the magnitude of depolarization-field-screening-driven strain in the BaTiO3 and CaTiO3 components can arise from the contribution of the oxygen octahedral rotation patterns at the BaTiO3/CaTiO3 interfaces to the polarization of CaTiO3. The depolarization-field-screening-driven polarization reduction in the CaTiO3 layers points to a new direction for the manipulation of polarization in the component layers of a strongly coupled ferroelectric/dielectric superlattice.

cond-mat.mtrl-sci↗

arXiv2022

Magnetic excitations in double perovskite iridates La$_{2}$$\mathit{M}$IrO$_{6}$ ($\mathit{M}$ = Co, Ni, and Zn) mediated by 3$\mathit{d}$-5$\mathit{d}$ hybridization

By performing resonant inelastic x-ray scattering (RIXS) measurements at the Ir $\mathit{L_{\mathrm{3}}}$ edge, we have investigated the low-energy elementary excitations in a series of double perovskite iridate single crystals, La$_{2}$$\mathit{M}$IrO$_{6}$ ($\mathit{M}$ = Co, Ni, and Zn). Almost dispersionless magnetic excitations at $\sim$ 42(6) meV and $\sim$ 35(5) meV have been observed in crystals containing magnetic 3$\mathit{d}$ ions, La$_{2}$CoIrO$_{6}$ and La$_{2}$NiIrO$_{6}$, respectively. In contrast, this low-energy magnetic excitation is absent in La$_{2}$ZnIrO$_{6}$ in which the 3$\mathit{d}$ ions are non-magnetic, suggesting the importance of 3$\mathit{d}$-5$\mathit{d}$ hybridization in the magnetic properties of these double perovskite iridates. The magnetic excitation is suppressed completely above the magnetic ordering temperature, suggesting the inadequacy of using a simple spin Hamiltonian to describe magnetism of these materials.

cond-mat.str-el↗

arXiv2021

Optical excitation of electromagnons in hexaferrite

Understanding ultrafast magnetization dynamics on the microscopic level is of strong current interest due to the potential for applications in information storage. In recent years, the spin-lattice coupling has been recognized to be essential for ultrafast magnetization dynamics. Magnetoelectric multiferroics of type II possess intrinsic correlations among magnetic sublattices and electric polarization (P) through spin-lattice coupling, enabling fundamentally coupled dynamics between spins and lattice. Here we report on ultrafast magnetization dynamics in a room-temperature multiferroic hexaferrite possessing ferrimagnetic and antiferromagnetic sublattices, revealed by time-resolved resonant x-ray diffraction. A femtosecond above-bandgap excitation triggers a coherent magnon in which the two magnetic sublattices entangle and give rise to a transient modulation of P. A novel microscopic mechanism for triggering the coherent magnon in this ferrimagnetic insulator based on the spin-lattice coupling is proposed. Our finding opens up a novel but general pathway for ultrafast control of magnetism.

cond-mat.str-el↗

arXiv2021

4D visualization of the photoexcited coherent magnon by an X-ray free electron laser

X-ray free electron lasers (XFEL) create femtosecond X-ray pulses with high brightness and high longitudinal coherence allowing to extend X-ray spectroscopy and scattering techniques into the ultrafast time-domain. These X-rays are a powerful probe for studying coherent quasiparticle excitations in condensed matter triggered by an impulsive optical laser pump. However, unlike coherent phonons, other quasiparticles have been rarely observed due to small signal changes and lack of standards for the identification. Here, we exploit resonant magnetic X-ray diffraction using an XFEL to visualize a photoexcited coherent magnon in space and time. Large intensity oscillations in antiferromagnetic and ferromagnetic Bragg reflections from precessing moment are observed in a multiferroic Y-type hexaferrite. The precession trajectory reveals that a large, long-lived, photoinduced magnetic-field changes the net magnetization substantially through the large-amplitude of the magnon. This work demonstrates an efficient XFEL probe for the coherent magnon in the spotlight for opto-spintronics application.

cond-mat.str-el↗

arXiv2021

Structural evidence for ultrafast polarization rotation in ferroelectric/dielectric superlattice nanodomains

Weakly coupled ferroelectric/dielectric superlattice thin film heterostructures exhibit complex nanoscale polarization configurations that arise from a balance of competing electrostatic, elastic, and domain-wall contributions to the free energy. A key feature of these configurations is that the polarization can locally have a significant component that is not along the thin-film surface normal direction, while maintaining zero net in-plane polarization. PbTiO3/SrTiO3 thin-film superlattice heterostructures on a conducting SrRuO3 bottom electrode on SrTiO3 have a room-temperature stripe nanodomain pattern with nanometer-scale lateral period. Ultrafast time-resolved x-ray free electron laser diffraction and scattering experiments reveal that above-bandgap optical pulses induce rapidly propagating acoustic pulses and a perturbation of the domain diffuse scattering intensity arising from the nanoscale stripe domain configuration. With 400 nm optical excitation, two separate acoustic pulses are observed: a high-amplitude pulse resulting from strong optical absorption in the bottom electrode and a weaker pulse arising from the depolarization field screening effect due to absorption directly within the superlattice. The picosecond scale variation of the nanodomain diffuse scattering intensity is consistent with a larger polarization change than would be expected due to the polarization-tetragonality coupling of uniformly polarized ferroelectrics. The polarization change is consistent instead with polarization rotation facilitated by the reorientation of the in-plane component of the polarization at the domain boundaries of the striped polarization structure. The complex steady-state configuration within these ferroelectric heterostructures leads to polarization rotation phenomena that have been previously available only through the selection of bulk crystal composition.

cond-mat.mtrl-sci↗

arXiv2021

Ultrafast carrier-lattice interactions and interlayer modulations of Bi2Se3 by X-ray free electron laser diffraction

As a 3D topological insulator, bismuth selenide (Bi2Se3) has potential applications for electrically and optically controllable magnetic and optoelectronic devices. How the carriers interact with lattice is important to understand the coupling with its topological phase. It is essential to measure with a time scale smaller than picoseconds for initial interaction. Here we use an X-ray free-electron laser to perform time-resolved diffraction to study ultrafast carrier-induced lattice contractions and interlayer modulations in Bi2Se3 thin films. The lattice contraction depends on the carrier concentration and is followed by an interlayer expansion accompanied by oscillations. Using density functional theory (DFT) and the Lifshitz model, the initial contraction can be explained by van der Waals force modulation of the confined free carrier layers. Band inversion, related to a topological phase transition, is modulated by the expansion of the interlayer distance. These results provide insight into instantaneous topological phases on ultrafast timescales.

cond-mat.mtrl-sci↗

arXiv2021

Optical magnons with dominant bond-directional exchange interactions in a honeycomb lattice iridate $α$-Li$_{2}$IrO$_{3}$

We have used resonant inelastic x-ray scattering to reveal optical magnons in a honeycomb lattice iridate $α$-Li$_{2}$IrO$_{3}$. The spectrum in the energy region 20-25 meV exhibits momentum dependence, of which energy is highest at the location of the magnetic Bragg peak, ($\textit{h}, \textit{k}$) = ($\pm$0.32, 0), and lowered toward (0, 0) and ($\pm$1, 0). We compare our data with a linear spin-wave theory based on a generic nearest-neighbor spin model. We find that a dominant bond-directional Kitaev interaction of order 20 meV is required to explain the energy scale observed in our study. The observed excitations are understood as stemming from optical magnon modes whose intensity is modulated by a structure factor, resulting in the apparent momentum dependence. We also observed diffuse magnetic scattering arising from the short-range magnetic correlation well above $\textit{T}_{N}$. In contrast to Na$_{2}$IrO$_{3}$, this diffuse scattering lacks the $C_3$ rotational symmetry of the honeycomb lattice, suggesting that the bond anisotropy is far from negligible in $α$-Li$_{2}$IrO$_{3}$.

cond-mat.str-el↗

arXiv2020

Robust Long Range Magnetic Correlation across Anti-phase Domain Boundaries in Sr$_2$CrReO$_6$

Anti-site disorder is one of the most important issues that arises in synthesis of double perovskite for spintronic applications. Although it is known that anti-site disorder leads to a proliferation of structural defects, known as the anti-phase boundaries that separate ordered anti-phase domains in the sample, little is known about the magnetic correlation across these anti-phase boundaries on a microscopic level. Motivated by this, we report resonant elastic X-ray scattering study of room temperature magnetic and structural correlation in a thin-film sample of Sr$_2$CrReO$_6$, which has one of the highest $\mathrm{T_C}$ among double perovskites. Structurally, we discovered existence of anti-phase nanodomains of $\sim$15~nm in the sample. Magnetically, the ordered moments are shown to lie perpendicular to the $c$ direction. Most remarkably, we found that the magnetic correlation length far exceeds the size of individual anti-phase nanodomains. Our results therefore provide conclusive proof for existence of robust magnetic correlation across the anti-phase boundaries in Sr$_2$CrReO$_6$.

cond-mat.mes-hall↗

arXiv2019

Non-thermal fluence threshold for femtosecond pulsed x-ray radiation damage in perovskite complex oxide epitaxial heterostructures

Intense hard x-ray pulses from a free-electron laser induce irreversible structural damage in a perovskite oxide epitaxial heterostructure when pulse fluences exceed a threshold value. The intensity of x-ray diffraction from a 25-nm thick epitaxial BiFeO$_{3}$ layer on a SrTiO$_{3}$ substrate measured using a series of pulses decreases abruptly with a per-pulse fluence of 2.7 x 10$^{6}$ photons $μ$m$^{-2}$ at 9.7 keV photon energy, but remains constant for 1.3 x 10$^{6}$ photons $μ$m$^{-2}$ or less. The damage resulted in the destruction of the BiFeO$_{3}$ thin film within the focal spot area and the formation of a deep cavity penetrating into the STO substrate via the removal of tens of nanometers of material per pulse. The damage threshold occurs at a fluence that is insufficient to heat the absorption volume to the melting point. The morphology of the ablated sample is consistent with fracture rather than melting. Together these results indicate that the damage occurs via a non-thermal process consistent with ultrafast ionization of the absorption volume.

cond-mat.mtrl-sci↗

arXiv2018

Evolution of Magnetic Excitations Across the Metal-Insulator Transition in a Pyrochlore Iridate Eu$_{2}$Ir$_{2}$O$_{7}$

We report Resonant Inelastic X-ray Scattering (RIXS) study of the magnetic excitation spectrum in a highly insulating Eu$_{2}$Ir$_{2}$O$_{7}$ single crystal that exhibits a metal-insulator transition at $T_{MI}$ = 111(7) K. A propagating magnon mode with 20 meV bandwidth and 28 meV magnon gap is found in the excitation spectrum at 7 K, which is expected in the all-in-all-out (AIAO) magnetically ordered state. This magnetic excitation exhibits substantial softening as temperature is raised towards $T_{MI}$, and turns into highly damped excitation in the paramagnetic phase. Remarkably, the softening occurs throughout the whole Brillouin zone including the zone boundary. This observation is inconsistent with magnon renormalization expected in a local moment system, and indicates that the strength of electron correlation in Eu$_{2}$Ir$_{2}$O$_{7}$ is only moderate, so that electron itinerancy should be taken into account in describing its magnetism.

cond-mat.str-el↗

arXiv2017

Observation of new magnetic ground state in frustrated quantum antiferromagnet spin liquid system Cs2CuCl4

Cs2CuCl4 is known to possess a quantum spin liquid phase with antiferromagnetic interaction below 2.8 K. We report the observation of a new metastable magnetic phase of the triangular frustrated quantum spin system Cs2CuCl4 induced by the application of hydrostatic pressure. We measured the magnetic properties of Cs2CuCl4 following the application and release of pressure after 3 days. We observed a previously unknown ordered magnetic phase with a transition temperature of 9 K. Furthermore, the recovered sample with new magnetic ground state possesses an equivalent crystal structure to the uncompressed one with antiferromagnetic quantum spin liquid phase.

cond-mat.str-el↗

arXiv2017

Quantitative measurements of size-dependent magnetoelectric coupling in Fe3O4 nanoparticles

Bulk magnetite (Fe3O4), the loadstone used in magnetic compasses, has been known to exhibit magnetoelectric (ME) properties below ~10 K; however, corresponding ME effects in Fe3O4 nanoparticles have been enigmatic. We investigate quantitatively the ME coupling of spherical Fe3O4 nanoparticles with uniform diameters (d) from 3 to 15 nm embedded in an insulating host, using a sensitive ME susceptometer. The intrinsic ME susceptibility (MES) of the Fe3O4 nanoparticles is measured, exhibiting a maximum value of ~0.6 ps/m at 5 K for d=15 nm. We found that the MES is reduced with reduced d but remains finite until d=~5 nm, which is close to the critical thickness for observing the Verwey transition. Moreover, with reduced diameter, the critical temperature below which the MES becomes conspicuous increased systematically from 9.8 K in the bulk to 19.7 K in the nanoparticles with d=7 nm, reflecting the core-shell effect on the ME properties. These results point to a new pathway for investigating ME effect in various nanomaterials.

cond-mat.str-el↗

arXiv2017

Microscopic Observation of Entangled Multi-Magnetoelectric Coupling Phenomenon

Searching for new functionality in next generation electronic devices is a principal driver of material physics research. Multiferroics simultaneously exhibit electric and magnetic order parameters that may be coupled through magnetoelectric (ME) effects. In single-phase materials the ME effect arises from one of three known mechanisms: inverse Dzyaloshinskii-Moriya (IDM) interaction, spin dependent ligand-metal (p-d) orbital hybridization, and exchange striction. However, the coupling among these mechanisms remains largely unexplored despite envisioned potential capabilities. Here, we present cooperative tuning between both IDM interaction and p-d hybridization that leads to discrete ME states in Ba0.5Sr2.5Co2Fe24O41. In-situ x-ray diffraction exposes the microscopic interplay between these two mechanisms, marked by a unique ME susceptibility upon electric and magnetic fields. The entangled multi-ME coupling phenomenon observed in this room-temperature ME hexaferrite offers a pathway to novel functional control for ME device applications.

cond-mat.mtrl-sci↗

arXiv2015

Direct Evidence for Dominant Bond-directional Interactions in a Honeycomb Lattice Iridate Na2IrO3

Heisenberg interactions are ubiquitous in magnetic materials and have been prevailing in modeling and designing quantum magnets. Bond-directional interactions offer a novel alternative to Heisenberg exchange and provide the building blocks of the Kitaev model, which has a quantum spin liquid (QSL) as its exact ground state. Honeycomb iridates, A2IrO3 (A=Na,Li), offer potential realizations of the Kitaev model, and their reported magnetic behaviors may be interpreted within the Kitaev framework. However, the extent of their relevance to the Kitaev model remains unclear, as evidence for bond-directional interactions remains indirect or conjectural. Here, we present direct evidence for dominant bond-directional interactions in antiferromagnetic Na2IrO3 and show that they lead to strong magnetic frustration. Diffuse magnetic x-ray scattering reveals broken spin-rotational symmetry even above Neel temperature, with the three spin components exhibiting nano-scale correlations along distinct crystallographic directions. This spin-space and real-space entanglement directly manifests the bond-directional interactions, provides the missing link to Kitaev physics in honeycomb iridates, and establishes a new design strategy toward frustrated magnetism.

cond-mat.mtrl-sci↗