arXiv subjects

Steffen Peer Zeuschner

Publications and source records attributed to Steffen Peer Zeuschner.

5 recordsLinked to original sources

arXiv2025

Experimental evidence of dominant ultrafast diffusive energy transport by hot electrons in Cu

When the dimensions of structures shrink to the order of the inelastic mean free path of the energy-carrying quasi-particles, the character of energy transport changes from diffusive to ballistic. However, the point of transition remains a matter of debate. Here, we determine the dominant channel of energy transport through a nanoscale Cu layer as a function of its thickness. The energy rapidly transferred across Cu via hot electrons from a photo-excited Pt layer into a buried Ni detection layer translates into a rapid expansion of the Ni layer probed via ultrafast x-ray diffraction. The non-linear dependence of the Ni strain amplitude on the absorbed laser fluence indicates that the transport through Cu becomes more efficient with increasing fluence. This fluence-dependent transport efficiency is reproduced by a diffusive energy transport model and serves as a generally applicable experimental approach to distinguish diffusion from ballistic transport. Following this approach, we identify diffusive electronic energy transport to govern the spatial energy distribution for Cu layer thicknesses larger than twice the electronic inelastic mean free path.

cond-mat.mtrl-sci↗

arXiv2025

Non-thermal electrons open the non-equilibrium pathway of the phase transition in FeRh

We use ultrafast x-ray diffraction to study non-equilibrium pathways of the phase transition in FeRh parametrized by the structural response. By increasing the pump-pulse duration beyond the electron-phonon coupling time, we suppress the electron-phonon non-equilibrium present upon femtosecond laser excitation but still photoexcite electrons to non-thermal states. Irrespective of the pump pulse duration, we find an optically induced nucleation of ferromagnetic domains on an $8\,\text{ps}$ timescale that starts as soon as the successively deposited energy surpasses the site-specific threshold energy. If in contrast, FeRh is only indirectly excited by diffusion of thermalized electrons from an opaque Pt cap layer, the ferromagnetic phase rises on a $50\,\text{ps}$ timescale. These findings unambiguously identify the photo-excitation of non-thermal electrons and not electron-phonon non-equilibria to enable the non-equilibrium pathway of the phase transition in FeRh.

cond-mat.mtrl-sci↗

arXiv2024

Unveiling the nanomorphology of HfN thin films by ultrafast reciprocal space mapping

Hafnium Nitride (HfN) is a promising and very robust alternative to gold for applications of nanoscale metals. Details of the nanomorphology related to variations in strain states and optical properties can be crucial for applications in nanophotonics and plasmon-assisted chemistry. We use ultrafast reciprocal space mapping (URSM) with hard x-rays to unveil the nanomorphology of thin HfN films. Static high-resolution x-ray diffraction reveals a twofold composition of the thin films being separated into regions with identical lattice constant and similar out-of-plane but hugely different in-plane coherence lengths. URSM upon femtosecond laser excitation reveals different transient strain dynamics for the two respective Bragg peak components. This unambiguously locates the longer in-plane coherence length in the first 15\,nm of the thin film adjacent to the substrate. The transient shift of the broad diffraction peak displays the strain dynamics of the entire film, implying that the near-substrate region hosts nanocrystallites with small and large coherence length, whereas the upper part of the film grows in small columnar grains. Our results illustrate that URSM is a suitable technique for non-destructive investigations of the depth-resolved nanomorphology of nanostructures.

cond-mat.mtrl-sci↗

arXiv2023

Concepts and use cases for picosecond ultrasonics with x-rays

This review discusses picosecond ultrasonics experiments using ultrashort hard x-ray probe pulses to extract the transient strain response of laser-excited nanoscopic structures from Bragg-peak shifts. This method provides direct, layer-specific, and quantitative information on the picosecond strain response for structures down to few-nm thickness. We model the transient strain using the elastic wave equation and express the driving stress using Grüneisen parameters stating that the laser-induced stress is proportional to energy density changes in the microscopic subsystems of the solid, i.e., electrons, phonons and spins. The laser-driven strain response can thus serve as an ultrafast proxy for local energy-density and temperature changes, but we emphasize the importance of the nanoscale morphology for an accurate interpretation due to the Poisson effect. The presented experimental use cases encompass ultrathin and opaque metal heterostructures, continuous and granular nanolayers as well as negative thermal expansion materials, that each pose a challenge to established all-optical techniques.

cond-mat.mtrl-sci↗

arXiv2022

Standing spin wave excitation in Bi:YIG films via temperature induced anisotropy changes and magnetoacoustic coupling

Based on micromagnetic simulations and experimental observations of the magnetization and lattice dynamics following the direct optical excitation of the magnetic insulator Bi:YIG or indirect excitation via an optically opaque Pt/Cu double layer, we disentangle the dynamical effects of magnetic anisotropy and magnetoelastic coupling. The strain and temperature of the lattice are quantified via modeling ultrafast x-ray diffraction data. Measurements of the time-resolved magneto-optical Kerr effect agree well with the magnetization dynamics simulated according to the excitation via two mechanisms: The magneto-acoustic coupling to the experimentally verified strain dynamics and the ultrafast temperature-induced transient change in the magnetic anisotropy. The numerical modeling proves that for direct excitation both mechanisms drive the fundamental mode with opposite phase. The relative ratio of standing spin-wave amplitudes of higher order modes indicates that both mechanisms are substantially active.

cond-mat.other↗