arXiv subjects

Sebastian T. Weber

Publications and source records attributed to Sebastian T. Weber.

10 recordsLinked to original sources

arXiv2026

Interplay of non-local transport and local scattering during electron thermalization and spatial equilibration in laser-excited metals

Ultrafast laser excitation of metals induces electronic nonequilibrium both in space and locally in the energy distribution. The subsequent dynamics are governed by the interplay between non-local transport and local scattering of hot electrons, yet combined microscopic descriptions of these processes remain sparse. Here, we disentangle the influence of these processes on thermalization using a reformulation of the Boltzmann transport equation in energy space that consistently describes both spatial equilibration and scattering through full collision integrals. Our results reveal that transport accelerates the apparent thermalization observed at the irradiated surface by removing athermal carriers, while the same spatial redistribution delays complete equilibration of the full electron system. We analyze the experimentally accessible energy-dependent dynamics at the front and back surface and find that the dominant process varies, depending on both position and on the energetic window. Overall, our work improves the understanding of the interplay of electronic nonequilibrium processes occurring in optically thick laser-driven systems with relevant implications for future electronic applications.

cond-mat.mtrl-sci↗

arXiv2026

From Code to Figure: A FAIR-Aligned Data Provenance Chain for Reproducible Simulation Research in Numerical Physics

Computational physics increasingly depends on large simulation datasets generated by software that remains under active development for many years. In such settings, reproducibility requires not only well documented data but also explicit links between code versions, simulation inputs, generated outputs, analysis steps, and published figures. Here, we present an integrated workflow for reproducible and FAIR-aligned simulation research in numerical physics. We describe how version control, code review, automated testing, structured logging, metadata-rich output, and standardized post-processing can be combined to support traceability from software development to publication. The presented concepts demonstrated for one particular simulation framework are broadly applicable to computational physics and other data-intensive areas of scientific computing.

physics.comp-ph↗

arXiv2026

Thermalization of Optically Excited Fermi Systems: Electron-Electron Collisions in Solid Metals

Ultrafast optical excitation of metals induces a non-equilibrium energy distribution in the electronic system, with a characteristic step-structure determined by Pauli blocking. On a femtosecond timescale, electron-electron scattering drives the electrons towards a hot Fermi distribution. In this work, we present a derivation of the full electron-electron Boltzmann collision integral within the random-k approximation. Building on this approach, we trace the temporal evolution of the electron energy distribution towards equilibrium, for an excited but strongly degenerate Fermi system. Furthermore, we examine to which extent the resulting dynamics can be captured by the numerically simpler relaxation time approach, applying a constant and an energy-dependent relaxation time derived from Fermi-liquid theory. We find a better agreement with the latter, while specific features caused by the balance of scattering and reoccupation can only be captured with a full collision integral.

cond-mat.mtrl-sci↗

arXiv2025

Probing laser-driven surface and subsurface dynamics via grazing-incidence XFEL scattering and diffraction

We demonstrate a grazing-incidence x-ray platform that simultaneously records time-resolved grazing-incidence small-angle x-ray scattering (GISAXS) and grazing-incidence x-ray diffraction (GID) from a femtosecond laser-irradiated gold film above the melting threshold, with picosecond resolution at an x-ray free-electron laser (XFEL). By tuning the x-ray incidence angle, the probe depth is set to tens of nanometers, enabling depth-selective sensitivity to near-surface dynamics. GISAXS resolves ultrafast changes in surface nanomorphology (correlation length, roughness), while GID quantifies subsurface lattice compression, grain orientation, melting, and recrystallization. The approach overcomes photon-flux limitations of synchrotron grazing-incidence geometries and provides stringent, time-resolved benchmarks for complex theoretical models of ultrafast laser-matter interaction and warm dense matter. Looking ahead, the same depth-selective methodology is well suited to inertial confinement fusion (ICF): it can visualize buried-interface perturbations and interfacial thermal resistance on micron to sub-micron scales that affect instability seeding and burn propagation.

physics.optics↗

arXiv2023

Influence of band occupation on electron-phonon coupling in gold

Electron-phonon coupling is a fundamental process that governs the energy relaxation dynamics of solids excited by ultrafast laser pulses. It has been found to strongly depend on electron temperature as well as on nonequilibrium effects. Recently, the effect of occupational nonequilibrium in noble metals, which outlasts the fully kinetic stage, has come into increased focus. In this work, we investigate the influence of nonequilibrium density distributions in gold on the electron-phonon coupling. We find a large effect on the coupling parameter which describes the energy exchange between the two subsystems. Our results challenge the conventional view that electron temperature alone is a sufficient predictor of electron-phonon coupling.

cond-mat.mtrl-sci↗

arXiv2023

Time-resolved spectral densities of non-thermal electrons in gold

Noble-metal nanoparticles for photocatalysis have become a major research object in recent years due to their plasmon-enhanced strong light-matter interaction. The dynamics of the hot electrons in the noble metal are crucial for the efficiency of the photocatalysis and for the selective control of reactions. In this work, we present a kinetic description of the non-equilibrium electron distribution created by photoexcitation, based on full energy-resolved Boltzmann collision integrals for the laser excitation as well as for the electron-electron thermalization. The laser-induced electronic non-equilibrium and the inherently included secondary electron generation govern the dynamics of non-thermal electrons. Applying our method to gold, we show a significant dependence of hot electron dynamics on kinetic energy. Specifically, the timescales of the relaxation as well as the qualitative behavior are depending on the evaluated energy window. During the thermalization processes there are cases of increasing electron density as well as of decreasing electron density. Studying the influence of excitation parameters, we find that the photon energy and the fluence of the exciting laser can be tuned to influence not only the initial excitation but also the subsequent characteristics of the time-resolved electronic spectral density dynamics. The electronic thermalization including secondary electron generation leads to time-dependent spectral densities which differ from their specific final equilibrium values for picoseconds after irradiation ended.

physics.app-ph↗

arXiv2023

Competing signatures of intersite and interlayer spin transfer in the ultrafast magnetization dynamics

Optically driven intersite and interlayer spin transfer are individually known as the fastest processes for manipulating the spin order of magnetic materials on the sub 100 fs time scale. However, their competing influence on the ultrafast magnetization dynamics remains unexplored. In our work, we show that optically induced intersite spin transfer (also known as OISTR) dominates the ultrafast magnetization dynamics of ferromagnetic alloys such as Permalloy (Ni80Fe20) only in the absence of interlayer spin transfer into a substrate. Once interlayer spin transfer is possible, the influence of OISTR is significantly reduced and interlayer spin transfer dominates the ultrafast magnetization dynamics. This provides a new approach to control the magnetization dynamics of alloys on extremely short time scales by fine-tuning the interlayer spin transfer.

cond-mat.mtrl-sci↗

arXiv2021

Control of transport phenomena in magnetic heterostructures by wavelength modulation

We demonstrate the tuneablity of the ultrafast energy flow in magnetic/non-magnetic bilayer structures by changing the wavelength of the optical excitation. This is achieved by an advanced description of the temperature based $μ$T-model that explicitly considers the wavelength- and layer-dependent absorption profile within multilayer structures. For the exemplary case of a Ni/Au bilayer, our simulations predict that the energy flow from Ni to Au is reversed when changing the wavelength of the excitation from the infrared to the ultraviolet spectral range. These predictions are fully supported by characteristic signatures in the magneto-optical Kerr traces of the Ni/Au model system. Our results will open up new avenues to steer and control the energy transport in designed magnetic multilayer for ultrafast spintronic applications.

cond-mat.mes-hall↗

arXiv2021

Implementation of the electronic non-equilibrium in the two-temperature model

We investigate a temperature-based model, called extended two-temperature model (eTTM), that describes the electronic non-equilibrium and its effect on energy dissipation in metals after ultrashort laser excitation. We derive and discuss improvements in comparison to published versions of this model [E. Carpene, Phys. Rev. B 2006, 74, 024301; G. Tsibidis, Appl. Phys. A 2018, 124, 311]. The comparison of the results of the eTTM with results of the well-known two-temperature model (TTM) shows a delayed increase of the electronic temperature when being calculated with the eTTM. We find a good agreement in the non-equilibrium energy distribution after absorption of photons with results from a kinetic description using a Boltzmann collision term. The model provides a convenient tool for fast calculation of features of the non-equilibrium electrons. As an example we inspect the dynamics of high-energy electrons observable in photo-electron spectroscopy and demonstrate the advantage of the eTTM over the conventional two-temperature model.

cond-mat.mtrl-sci↗

arXiv2018

Phonon-induced long-lasting nonequilibrium in the electron system of a laser-excited solid

Electron-electron thermalization and electron-phonon relaxation processes in laser-excited solids are often assumed to occur on different timescales. This is true for the majority of the conduction band electrons in a metal. However, electron-phonon interactions can influence the thermalization process of the excited electrons. We study the interplay of the underlying scattering mechanisms for the case of a noble metal with help of a set of complete Boltzmann collision integrals. We trace the transient electron distribution in copper and its deviations from a Fermi-Dirac distribution due to the excitation with an ultrashort laser pulse. We investigate the different stages of electronic nonequilibrium after an excitation with an ultrashort laser-pulse of 800 nm wavelength and 10 fs pulse duration. Our calculations show a strong nonequilibrium during and directly after the end of the laser pulse. Subsequently, we find a fast thermalization of most electrons. Surprisingly, we observe a long-lasting nonequilibrium, which can be attributed to the electron-phonon scattering. This nonequilibrium establishes at energies around peaks in the density of states of the electrons and persists on the timescale of electron-phonon energy relaxation. It influences in turn the electron phonon coupling strength.

cond-mat.mes-hall↗