arXiv subjects

Claus Ropers

Publications and source records attributed to Claus Ropers.

At least 37 records · Page 2Linked to original sources

arXiv2023

Laser-induced real-space topology control of spin wave resonances

Femtosecond laser excitation of materials that exhibit magnetic spin textures promises advanced magnetic control via the generation of ultrafast and non-equilibrium spin dynamics. We explore such possibilities in ferrimagnetic [Fe(0.35 nm)/Gd(0.40 nm)]$_{160}$ multilayers, which host a rich diversity of magnetic textures from stripe domains at low magnetic fields, a dense bubble/skyrmion lattice at intermediate fields, and a single domain state for high magnetic fields. Using femtosecond magneto-optics, we observe distinct coherent spin wave dynamics in response to a weak laser excitation allowing us to unambiguously identify the different magnetic spin textures. Moreover, employing strong laser excitation we show that we achieve versatile control of the coherent spin dynamics via non-equilibrium and ultrafast transformation of magnetic spin textures by both creating and annihilating bubbles/skyrmions. We corroborate our findings by micromagnetic simulations and by Lorentz transmission electron microscopy before and after laser exposure.

cond-mat.mtrl-sci↗

arXiv2023

Coherent x-ray magnetic imaging with 5 nm resolution

Soft x-ray microscopy plays an important role in modern spintronics. However, the achievable resolution of most x-ray magnetic imaging experiments is above 10 nm, limiting access to fundamental and technologically relevant length scales. Here, we demonstrate x-ray magnetic microscopy with 5 nm resolution by combining holography-assisted coherent diffractive imaging with heterodyne amplification of the weak magnetic signal. The gain in resolution and contrast allows direct access to key magnetic properties, including domain wall profiles and the position of pinning sites. The ability to detect and map such properties with photons opens new horizons for element-specific, time-resolved, and in-operando research on magnetic materials and beyond.

cond-mat.mtrl-sci↗

arXiv2023

Free-electron interaction with nonlinear optical states in microresonators

The short de Broglie wavelength and strong interaction empower free electrons to probe scattering and excitations in materials and resolve the structure of biomolecules. Recent advances in using nanophotonic structures to mediate bilinear electron-photon interaction have brought novel optical manipulation schemes to electron beams, enabling high space-time-energy resolution electron microscopy, quantum-coherent optical modulation, attosecond metrology and pulse generation, transverse electron wavefront shaping, dielectric laser acceleration, and electron-photon pair generation. However, photonic nanostructures also exhibit nonlinearities, which have to date not been exploited for electron-photon interactions. Here, we report the interaction of electrons with spontaneously generated Kerr nonlinear optical states inside a continuous-wave driven photonic chip-based microresonator. Optical parametric processes give rise to spatiotemporal pattern formation, or dissipative structures, corresponding to coherent or incoherent optical frequency combs. By coupling such microcombs in situ to electron beams, we demonstrate that different dissipative structures induce distinct fingerprints in the electron spectra and Ramsey-type interference patterns. In particular, using spontaneously formed femtosecond temporal solitons, we achieve ultrafast temporal gating of the electron beam without the necessity of a pulsed laser source or a pulsed electron source. Our work elucidates the interaction of free electrons with a variety of nonlinear dissipative states, demonstrates the ability to access solitons inside an electron microscope, and extends the use of microcombs to unexplored territories, with ramifications in novel ultrafast electron microscopy, light-matter interactions driven by on-chip temporal solitons, and ultra-high spatiotemporal resolution sampling of nonlinear optical dynamics and devices.

physics.optics↗

arXiv2023

Attosecond electron microscopy by free-electron homodyne detection

Time-resolved electron microscopy aims at tracking nanoscale excitations and dynamic states of matter with a temporal resolution ultimately reaching the attosecond regime. Periodically time-varying fields in an illuminated specimen cause free-electron inelastic scattering, which enables the spectroscopic imaging of near-field intensities. However, access to the evolution of nanoscale fields and structures within the light cycle requires a sensitivity to the optical phase. Here, we introduce Free-Electron Homodyne Detection (FREHD) as a universally applicable approach to electron microscopy of phase-resolved optical responses at high spatiotemporal resolution. In this scheme, a phase-controlled reference interaction serves as the local oscillator to extract arbitrary sample-induced modulations of a free-electron wave function. We demonstrate this principle through the phase-resolved imaging of plasmonic fields with few-nanometer spatial and sub-cycle temporal resolutions. Due to its sensitivity to both phase- and amplitude-modulated electron beams, FREHD measurements will be able to detect and amplify weak signals stemming from a wide variety of microscopic origins, including linear and nonlinear optical polarizations, atomic and molecular resonances and attosecond-modulated structure factors.

physics.optics↗

arXiv2023

High-sensitivity extreme-ultraviolet transient absorption spectroscopy enabled by machine learning

We introduce a machine-learning-based approach to enhance the sensitivity of optical-extreme ultraviolet (XUV) transient absorption spectroscopy. A reference spectrum is used as input to a three-layer feed-forward neural network, allowing for an efficient elimination of source noise from measurement data. In pump-probe experiments using high-harmonic radiation, we show a more than tenfold improvement in noise suppression in XUV transient absorption spectra compared to conventional referencing. Utilizing strong spectral correlations in the source fluctuations, the network facilitates a pixel-wise noise reduction without the need for wavelength calibration of the reference spectrum. The presented method can be adapted to a wide range of beam lines and enables the investigation of subtle electron and lattice dynamics in the weak excitation regime, relevant for the study of photovoltaics and photoinduced phase transitions of strongly correlated materials.

physics.optics↗

arXiv2023

Coulomb-correlated electron number states in a transmission electron microscope beam

We demonstrate the generation of Coulomb-correlated pair, triple and quadruple states of free electrons by femtosecond photoemission from a nanoscale field emitter inside a transmission electron microscope. Event-based electron spectroscopy allows a spatial and spectral characterization of the electron ensemble emitted by each laser pulse. We identify distinctive energy and momentum correlations arising from acceleration-enhanced interparticle energy exchange, revealing strong few-body Coulomb interactions at an energy scale of about two electronvolts. State-sorted beam caustics show a discrete increase in virtual source size and longitudinal source shift for few-electron states, associated with transverse momentum correlations. We observe field-controllable electron antibunching, attributed primarily to transverse Coulomb deflection. The pronounced spatial and spectral characteristics of these electron number states allow filtering schemes that control the statistical distribution of the pulse charge. In this way, the fraction of specific few-electron states can be actively suppressed or enhanced, facilitating the preparation of highly non-Poissonian electron beams for microscopy and lithography, including future heralding schemes and correlated multi-electron probing.

cond-mat.mes-hall↗

arXiv2023

Spatiotemporal Electron-Beam Focusing through Parallel Interactions with Shaped Optical Fields

The ability to modulate free electrons with light has emerged as a powerful tool to produce attosecond electron wavepackets. However, research has so far aimed at the manipulation of the longitudinal wave function component, while the transverse degrees of freedom have primarily been utilized for spatial rather than temporal shaping. Here, we show that the coherent superposition of parallel light-electron interactions in separate spatial zones allows for a simultaneous spatial and temporal compression of a convergent electron wave function, enabling the formation of sub-Ångström focal spots of attosecond duration. The proposed approach will facilitate the exploration of previously inaccessible ultrafast atomic-scale phenomena in particular enabling attosecond scanning transmission electron microscopy.

physics.optics↗

arXiv2022

Quantum state heralding using photonic integrated circuits with free electrons

Recently, integrated photonic circuits have brought new capabilities to electron microscopy and been used to demonstrate efficient electron phase modulation and electron-photon correlations. Here, we quantitatively analyze the feasibility of high fidelity and high purity quantum state heralding using a free electron and a photonic integrated circuit with parametric coupling, and propose schemes to shape useful electron and photonic states in different application scenarios. Adopting a dissipative quantum electrodynamics treatment, we formulate a framework for the coupling of free electrons to waveguide spatial-temporal modes. To avoid multimode-coupling induced state decoherence, we show that with proper waveguide design, the interaction can be reduced to a single-mode coupling to a quasi-TM00 mode. In the single-mode coupling limit, we go beyond the conventional state ladder treatment, and show that the electron-photon energy correlations within the ladder subspace can still lead to a fundamental purity and fidelity limit on complex optical and electron state preparations through heralding schemes. We propose applications that use this underlying correlation to their advantage, but also show that the imposed limitations for general applications can be overcome by using photonic integrated circuits with an experimentally feasible interaction length, showing its promise as a platform for free-electron quantum optics.

quant-ph↗

arXiv2022

Electronic and structural fingerprints of charge density wave excitations in extreme ultraviolet transient absorption spectroscopy

Femtosecond core-level transient absorption spectroscopy is utilized to investigate photoinduced dynamics of the charge density wave in 1T-TiSe2 at the Ti M2,3 edge (30-50 eV). Photoexcited carriers and phonons are found to primarily induce spectral red-shifts of core-level excitations, and a carrier relaxation time and phonon heating time of approximately 360 fs and 1.0 ps are extracted, respectively. Pronounced oscillations in delay-dependent absorption spectra are assigned to coherent excitations of the optical $A_{1g}$ phonon (6.0 THz) and the $A_{1g}^*$ charge density wave amplitude mode (3.3 THz). By comparing the measured spectra with time-dependent density functional theory simulations, we determine the directions of the momentary atomic displacements of both coherent modes and estimate their amplitudes. This work presents a first look on charge density wave excitations with table-top core-level transient absorption spectroscopy, enabling simultaneous access to electronic and lattice excitation and relaxation.

cond-mat.mtrl-sci↗

arXiv2022

Light-induced hexatic state in a layered quantum material

The tunability of materials properties by light promises a wealth of future applications in energy conversion and information technology. Strongly correlated materials such as transition-metal dichalcogenides (TMDCs) offer optical control of electronic phases, charge ordering and interlayer correlations by photodoping. Here, we find the emergence of a transient hexatic state in a TMDC thin-film during the laser-induced transformation between two charge-density wave (CDW) phases. Introducing tilt-series ultrafast nanobeam electron diffraction, we reconstruct CDW rocking curves at high momentum resolution. An intermittent suppression of three-dimensional structural correlations promotes a loss of in-plane translational order characteristic of a hexatic intermediate. Our results demonstrate the merit of tomographic ultrafast structural probing in tracing coupled order parameters, heralding universal nanoscale access to laser-induced dimensionality control in functional heterostructures and devices.

cond-mat.mtrl-sci↗

arXiv2022

Mode-selective ballistic pathway to a metastable electronic phase

Exploiting vibrational excitation for the dynamic control of material properties is an attractive goal with wide-ranging technological potential. Most metal-to-insulator transitions are mediated by few structural modes and are thus ideal candidates for the selective driving towards a desired electronic phase. Such targeted navigation within a generally multi-dimensional potential energy landscape requires microscopic insight into the non equilibrium pathway. However, the exact role of coherent inertial motion across the transition state has remained elusive. Here, we demonstrate mode-selective control over the metal-to-insulator phase transition of atomic indium wires on the Si(111) surface, monitored by ultrafast low-energy electron diffraction. We use tailored pulse sequences to individually enhance or suppress key phonon modes and thereby steer the collective atomic motion within the potential energy surface underlying the structural transformation. Ab initio molecular dynamics simulations demonstrate the ballistic character of the structural transition along the deformation vectors of the Peierls amplitude modes. Our work illustrates that coherent excitation of collective modes via exciton-phonon interactions evades entropic barriers and enables the dynamic control of materials functionality.

cond-mat.mes-hall↗

arXiv2021

Tailored high-contrast attosecond electron pulses for coherent excitation and scattering

Temporally shaping the density of electron beams using light forms the basis for a wide range of established and emerging technologies, including free-electron lasers and attosecond electron microscopy. The modulation depth of compressed electron pulses is a key figure of merit limiting applications. In this work, we present an approach for generating background-free attosecond electron pulse trains by sequential inelastic electron-light scattering. Harnessing quantum interference in the fractional Talbot effect, we suppress unwanted background density in electron compression by several orders of magnitude. Our results will greatly enhance applications of coherent electron-light scattering, such as stimulated cathodoluminescence and streaking.

quant-ph↗

arXiv2021

Chiral high-harmonic generation and spectroscopy on solid surfaces using polarization-tailored strong fields

Strong-field methods in solids enable new strategies for ultrafast nonlinear spectroscopy and provide all-optical insights into the electronic properties of condensed matter in reciprocal and real space. Additionally, solid-state media offers unprecedented possibilities to control high-harmonic generation using modified targets or tailored excitation fields. Here we merge these important points and demonstrate circularly-polarized high-harmonic generation with polarization-matched excitation fields for spectroscopy of chiral electronic properties at surfaces. The sensitivity of our approach is demonstrated for structural helicity and termination-mediated ferromagnetic order at the surface of silicon-dioxide and magnesium oxide, respectively. Circularly polarized radiation emanating from a solid sample now allows to add basic symmetry properties as chirality to the arsenal of strong-field spectroscopy in solids. Together with its inherent temporal (femtosecond) resolution and non-resonant broadband spectrum, the polarization control of high harmonics from condensed matter can illuminate ultrafast and strong field dynamics of surfaces, buried layers or thin films.

physics.optics↗

arXiv2021

Pinning and gyration dynamics of magnetic vortices revealed by correlative Lorentz and bright-field imaging

Topological magnetic textures are of great interest in various scientific and technological fields. To allow for precise control of nanoscale magnetism, it is of great importance to understand the role of intrinsic defects in the host material. Here, we use conventional and time-resolved Lorentz microscopy to study the effect of grain size in polycrystalline permalloy films on the pinning and gyration orbits of vortex cores inside magnetic nanoislands. To assess static pinning, we use in-plane magnetic fields to shift the core across the island while recording its position. This enables us to produce highly accurate two-dimensional maps of pinning sites. Based on this technique, we can generate a quantitative map of the pinning potential for the core, which we identify as being governed by grain boundaries. Furthermore, we investigate the effects of pinning on the dynamic behavior of the vortex core using stroboscopic Lorentz microscopy, harnessing a new photoemission source that accelerates image acquisition by about two orders of magnitude. We find characteristic changes to the vortex gyration in the form of increased dissipation and enhanced bistability in samples with larger grains.

cond-mat.mes-hall↗

arXiv2021

Coherent control of a structural phase transition in a solid-state surface system

The desire to exert active optical control over matter is a unifying theme across multiple scientific disciplines, as exemplified by all-optical magnetic switching, light-induced metastable or exotic phases of solids and the coherent control of chemical reactions. Typically, these approaches dynamically steer a system towards states or reaction products far from equilibrium. In solids, metal-insulator transitions are an important target for optical manipulation, offering dramatic and ultrafast changes of the electronic and lattice properties. In this context, essential questions concern the role of coherence in the efficiencies and thresholds of such transitions. Here, we demonstrate coherent vibrational control over a metal-insulator structural phase transition in a quasi-one-dimensional solid-state surface system. An optical double-pulse excitation scheme is used to drive the system from the insulating to a metastable metallic state, and the corresponding structural changes are monitored by ultrafast low-energy electron diffraction. We observe strong oscillations in the switching efficiency as a function of the double-pulse delay, revealing the importance of vibrational coherence in two key structural modes governing the transition on a femtosecond timescale. This mode-selective coherent control of solids and surfaces could open new routes to switching chemical and physical functionalities, facilitated by metastable and non-equilibrium states.

cond-mat.str-el↗

arXiv2021

Modulation of Cathodoluminescence Emission by Interference with External Light

Spontaneous processes triggered in a sample by free electrons are commonly regarded as incoherent, and therefore unable to interfere with external light sources. Here, we challenge this concept by showing through first-principles theory that light and free-electron pulses can interfere when interacting with a nanostructure, giving rise to a modulation in the spectral distribution of the cathodoluminescence light emission that is strongly dependent on the electron wave function. Specifically, for a temporally focused electron, cathodoluminescence can be cancelled upon illumination with a spectrally modulated dimmed laser that is phase-locked relative to the electron density profile. We illustrate this idea with realistic simulations under attainable conditions in currently available ultrafast electron microscopes. We further argue that the interference between excitations produced by light and free electrons opens a new window to manipulate the ultrafast materials response by combining the spectral and temporal selectivity of the light with the atomic resolution of electron beams.

physics.optics↗

arXiv2020

Optical coherence transfer mediated by free electrons

We investigate theoretically the quantum-coherence properties of the cathodoluminescence (CL) emission produced by a temporally modulated electron beam. Specifically, we consider the quantum-optical correlations of CL from electrons that are previously shaped by a laser field. The main prediction here is the presence of phase correlations between the emitted CL field and the electron-modulating laser, even though the emission intensity and spectral profile are independent of the electron state. In addition, the coherence of the CL field extends to harmonics of the laser frequency. Since electron beams can be focused to below one Angstrom, their ability to transfer optical coherence could enable ultra precise excitation, manipulation, and spectroscopy of nanoscale quantum systems.

quant-ph↗

arXiv2020

Ultrafast high-harmonic nanoscopy of magnetization dynamics

Light-induced magnetization changes, such as all-optical switching, skyrmion nucleation, and intersite spin transfer, unfold on temporal and spatial scales down to femtoseconds and nanometers, respectively. Pump-probe spectroscopy and diffraction studies indicate that spatio-temporal dynamics may drastically affect the non-equilibrium magnetic evolution. Yet, direct real-space magnetic imaging on the relevant timescale has remained challenging. Here, we demonstrate ultrafast high-harmonic nanoscopy employing circularly polarized high-harmonic radiation for real-space imaging of femtosecond magnetization dynamics. We observe the reversible and irreversible evolution of nanoscale spin textures following femtosecond laser excitation. Specifically, we map quenched magnetic domains and localized spin structures in Co/Pd multilayers with a sub-wavelength spatial resolution down to 16 nm, and strobosocopically trace the local magnetization dynamics with 40 fs temporal resolution. Our approach enables the highest spatio-temporal resolution of magneto-optical imaging to date. Facilitating ultrafast imaging with an extreme sensitivity to various microscopic degrees of freedom expressed in chiral and linear dichroism, we envisage a wide range of applications spanning magnetism, phase transitions, and carrier dynamics.

physics.optics↗