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Thomas Fennel

Publications and source records attributed to Thomas Fennel.

31 records · Page 2Linked to original sources

Fast reconstruction of single-shot wide-angle diffraction images through deep learning

Single-shot X-ray imaging of short-lived nanostructures such as clusters and nanoparticles near a phase transition or non-crystalizing objects such as large proteins and viruses is currently the most elegant method for characterizing their structure. Using hard X-ray radiation provides scattering images that encode two-dimensional projections, which can be combined to identify the full three-dimensional object structure from multiple identical samples. Wide-angle scattering using XUV or soft X-rays, despite yielding lower resolution, provides three-dimensional structural information in a single shot and has opened routes towards the characterization of non-reproducible objects in the gas phase. The retrieval of the structural information contained in wide-angle scattering images is highly non-trivial, and currently no efficient rigorous algorithm is known. Here we show that deep learning networks, trained with simulated scattering data, allow for fast and accurate reconstruction of shape and orientation of nanoparticles from experimental images. The gain in speed compared to conventional retrieval techniques opens the route for automated structure reconstruction algorithms capable of real-time discrimination and pre-identification of nanostructures in scattering experiments with high repetition rate -- thus representing the enabling technology for fast femtosecond nanocrystallography.

physics.atm-clus↗

Quantum coherent diffractive imaging

Coherent diffractive imaging has enabled the structural analysis of individual free nanoparticles in a single shot and offers the tracking of their light induced dynamics with unprecedented spatial and temporal resolution. The retrieval of structural information from scattering images in CDI experiments is so far mostly based on the assumption of classical scattering in linear response. For strong laser fields and in particular for resonant excitations, both the linear and the classical description may no longer be valid as population depletion and stimulated emission become important. Here we develop a density-matrix-based scattering model in order to include such quantum effects in the local medium response and explore the transition from linear to non-linear CDI for the resonant scattering from Helium nanodroplets. We find substantial departures from the linear response case already for experimentally reachable pulse parameters and show that non-linear spatio-temporal excitation dynamics results in rich features in the scattering, leading to the proposal of quantum coherent diffractive imaging (QCDI) as a promising novel branch in strong-field XUV and x-ray physics.

physics.optics↗

A DFT-based Tight-Binding Approach to the Self-consistent Description of Molecule Metal-Nanoparticle Interactions

The interaction within a hybrid system consisting of a spherical metal nanoparticle and a nearby organic dye molecule is formulated in a combined quantum-classical approach. Whereas the nanoparticle's polarization field is treated in classical multipole form, the electronic charge density of the molecule is described quantum mechanically. An efficient solution of the resulting self-consistency problem becomes possible by using the discrete representation of the charge density in terms of atom-centered Mulliken charges within the density functional theory-based tight binding (DFTB) approach. Results for two different dye molecules are presented, which focus on the dependence of the interaction on the nanoparticle's radius, the distance between nanoparticle and molecule and their mutual orientation.

physics.chem-ph↗

Three-Dimensional Shapes of Spinning Helium Nanodroplets

A significant fraction of superfluid helium nanodroplets produced in a free-jet expansion have been observed to gain high angular momentum resulting in large centrifugal deformation. We measured single-shot diffraction patterns of individual rotating helium nanodroplets up to large scattering angles using intense extreme ultraviolet light pulses from the FERMI free-electron laser. Distinct asymmetric features in the wide-angle diffraction patterns enable the unique and systematic identification of the three-dimensional droplet shapes. The analysis of a large dataset allows us to follow the evolution from axisymmetric oblate to triaxial prolate and two-lobed droplets. We find that the shapes of spinning superfluid helium droplets exhibit the same stages as classical rotating droplets while the previously reported metastable, oblate shapes of quantum droplets are not observed. Our three-dimensional analysis represents a valuable landmark for clarifying the interrelation between morphology and superfluidity on the nanometer scale.

physics.atm-clus↗

High-order above-threshold photoemission from nanotips controlled with two-color laser fields

We investigate the process of phase-controlled high-order above-threshold photoemission from sharp metallic nanotips under bichromatic laser fields. Experimental photoelectron spectra resulting from two-color excitation with a moderately intense near-infrared fundamental field (1560 nm) and its weak second harmonic show a strong sensitivity on the relative phase and clear indications for a plateau-like structure that is attributed to elastic backscattering. To explore the relevant control mechanisms, characteristic features, and particular signatures from near-field inhomogeneity, we performed systematic quantum simulations employing a one-dimensional nanotip model. Besides rich phase-dependent structures in the simulated above-threshold ionization (ATI) photoelectron spectra we find ponderomotive shifts as well as substantial modifications of the rescattering cutoff as function of the decay length of the near-field. To explore the quantum or classical nature of the observed features and to discriminate the two-color effects stemming from electron propagation and from the ionization rate we compare the quantum results to classical trajectory simulations. We show that signatures from direct electrons as well as the modulations in the plateau region mainly stem from control of the ionization probability, while the modulation in the cutoff region can only be explained by the impact of the two-color field on the electron trajectory. Despite the complexity of the phase-dependent features that render two-color strong-field photoemission from nanotips intriguing for sub-cycle strong-field control, our findings support that the recollision features in the cutoff region provide a robust and reliable method to calibrate the relative two-color phase.

physics.atom-ph↗

Explicit formulation of second and third order optical nonlinearity in the FDTD framework

The finite-difference time-domain (FDTD) method is a flexible and powerful technique for rigorously solving Maxwell's equations. However, three-dimensional optical nonlinearity in current commercial and research FDTD softwares requires solving iteratively an implicit form of Maxwell's equations over the entire numerical space and at each time step. Reaching numerical convergence demands significant computational resources and practical implementation often requires major modifications to the core FDTD engine. In this paper, we present an explicit method to include second and third order optical nonlinearity in the FDTD framework based on a nonlinear generalization of the Lorentz dispersion model. A formal derivation of the nonlinear Lorentz dispersion equation is equally provided, starting from the quantum mechanical equations describing nonlinear optics in the two-level approximation. With the proposed approach, numerical integration of optical nonlinearity and dispersion in FDTD is intuitive, transparent, and fully explicit. A strong-field formulation is also proposed, which opens an interesting avenue for FDTD-based modelling of the extreme nonlinear optics phenomena involved in laser filamentation and femtosecond micromachining of dielectrics.

physics.optics↗

Coherent diffractive imaging of single helium nanodroplets with a high harmonic generation source

Coherent diffractive imaging of individual free nanoparticles has opened novel routes for the in-situ analysis of their transient structural, optical, and electronic properties. So far, single-shot single-particle diffraction was assumed to be feasible only at extreme ultraviolet (XUV) and X-ray free-electron lasers, restricting this research field to large-scale facilities. Here we demonstrate single-shot imaging of isolated helium nanodroplets using XUV pulses from a femtosecond-laser driven high harmonic source. We obtain bright wide-angle scattering patterns, that allow us to uniquely identify hitherto unresolved prolate shapes of superfluid helium droplets. Our results mark the advent of single-shot gas-phase nanoscopy with lab-based short-wavelength pulses and pave the way to ultrafast coherent diffractive imaging with phase-controlled multicolor fields and attosecond pulses.

physics.atm-clus↗

Ionization avalanching in clusters ignited by extreme-ultraviolet driven seed electrons

We study the ionization dynamics of Ar clusters exposed to ultrashort near-infrared (NIR) laser pulses for intensities well below the threshold at which tunnel ionization ignites nanoplasma formation. We find that the emission of highly charged ions up to Ar$^{8+}$ can be switched on with unit contrast by generating only a few seed electrons with an ultrashort extreme ultraviolet (XUV) pulse prior to the NIR field. Molecular dynamics simulations can explain the experimental observations and predict a generic scenario where efficient heating via inverse bremsstrahlung and NIR avalanching are followed by resonant collective nanoplasma heating. The temporally and spatially well-controlled injection of the XUV seed electrons opens new routes for controlling avalanching and heating phenomena in nanostructures and solids, with implications for both fundamental and applied laser-matter science.

physics.atm-clus↗

MeV femtosecond electron pulses from direct-field acceleration in low density atomic gases

Using three-dimensional particle-in-cell simulations, we show that few-MeV electrons can be produced by focusing tightly few-cycle radially-polarized laser pulses in a low-density atomic gas. In particular, it is observed that for the few-TW laser power needed to reach relativistic electron energies, longitudinal attosecond microbunching occurs naturally, resulting in femtosecond structures with high-contrast attosecond density modulations. The three-dimensional particle-in-cell simulations show that in the relativistic regime the leading pulse of these attosecond substructures survives to propagation over extended distances, suggesting that it could be delivered to a distant target, with the help of a properly designed transport beamline.

physics.optics↗

Time-resolved analysis of strong-field induced plasmon oscillations in metal clusters by spectral interferometry with few-cycle laser fields

We propose a scheme for ultrafast real-time imaging of laser-induced collective electron oscillations (Mie plasmons) in gas phase metal clusters by interferometrically stable scanning of two intense few-cycle optical laser pulses. The feasibility of our nonlinear spectral interferometry method with experimentally accessible observables is tested in a theoretical case study on simple-metal clusters (Na$_{147}$). The results show that the plasmon period and lifetime as well as the phase and relative amplitude of the collective electron motion can be extracted with sub-fs resolution. The access to nonlinear response effects, as the demonstrated increase of the plasmon lifetime with laser intensity due to ionization-induced contraction of the electron cloud, opens up vast opportunities for interrogating ultrafast many-particle dynamics in nanosystems under strong laser fields with unprecedented resolution.

physics.atom-ph↗

Resonant charging of Xe clusters in Helium nanodroplets under intense laser fields

We theoretically investigate the impact of multiple plasmon resonances on the charging of Xe clusters embedded in He nanodroplets under intense pump-probe laser excitation. Our molecular dynamics simulations on Xe309He10000$ and comparison to results for free Xe309$ give clear evidence for selective resonance heating in the He shell and the Xe cluster, but no corresponding double hump feature in the final Xe charge spectra is found. Though the presence of the He shell substantially increases the maximum charge states, the pump-probe dynamics of the Xe spectra from embedded system is similar to that of the free species. In strong contrast to that, the predicted electron spectra do show well-separated and pronounced features from highly efficient plasmon assisted electron acceleration for both resonances in the embedded clusters. A detailed analysis of the underlying ionization and recombination dynamics is presented and explains the apparent disaccord between the resonance features in the ion and electron spectra.

physics.atm-clus↗

Rare-gas clusters in intense VUV, XUV and soft x-ray pulses: Signatures of the transition from nanoplasma-driven cluster expansion to Coulomb explosion in ion and electron spectra

We investigate the wavelength dependent ionization, heating, and expansion dynamics of medium-sized rare-gas clusters (Ar$_{923}$) under intense femtosecond short-wavelength free electron laser pulses by quasi-classical molecular dynamics simulations. A comparison of the interaction dynamics for pulses with $\hbarω$=20, 38, and 90\,eV photon energy at fixed total excitation energy indicates a smooth transition from plasma-driven cluster expansion, where predominantly surface ions are expelled by hydrodynamic forces, to quasi-electrostatic behavior with almost pure Coulomb explosion. Corresponding signatures in the time-dependent cluster dynamics as well as in the final ion and electron spectra support that this transition is linked to a crossover in the electron emission processes. The resulting signatures in the electron spectra are shown to be even more reliable for identifying the cluster expansion mechanisms than ion energy spectra itself.

physics.atm-clus↗

Ionization heating in rare-gas clusters under intense XUV laser pulses

The interaction of intense extreme ultraviolet (XUV) laser pulses ($λ=32\rm\,nm$, $I=10^{11-14}$\,W/cm$^2$) with small rare-gas clusters (Ar$_{147}$) is studied by quasi-classical molecular dynamics simulations. Our analysis supports a very general picture of the charging and heating dynamics in finite samples under short-wavelength radiation that is of relevance for several applications of free-electron lasers. First, up to a certain photon flux, ionization proceeds as a series of direct photoemission events producing a jellium-like cluster potential and a characteristic plateau in the photoelectron spectrum as observed in [Bostedt {\it et al.}, Phys. Rev. Lett. {\bf 100}, 013401 (2008)]. Second, beyond the onset of photoelectron trapping, nanoplasma formation leads to evaporative electron emission with a characteristic thermal tail in the electron spectrum. A detailed analysis of this transition is presented. Third, in contrast to the behavior in the infrared or low vacuum ultraviolet range, the nanoplasma energy capture proceeds via {\it ionization heating}, i.e., inner photoionization of localized electrons, whereas collisional heating of conduction electrons is negligible up to high laser intensities. A direct consequence of the latter is a surprising evolution of the mean energy of emitted electrons as function of laser intensity.

physics.atm-clus↗