arXiv subjects

Christoph Sahle

Publications and source records attributed to Christoph Sahle.

5 recordsLinked to original sources

arXiv2025

A Momentum-Resolved X-ray Thomson Scattering Benchmark of Electronic-Response Models in Warm Dense Aluminium

The robust diagnosis of conditions generated in warm dense matter (WDM) experiments remains a persistent challenge. Here we describe the measurement of shock-compressed aluminium at 50 GPa with angle-resolved femtosecond x-ray Thomson scattering (XRTS) over a wide range of scattering wavevectors at the European XFEL. The measured plasmon dispersion and line shape show that the de facto standard approach for analysing XRTS spectra, based on uniform-electron-gas models, systematically overestimates the resonance energy by up to 8 eV. We present an ab initio approach that agrees within the experimental uncertainty and demonstrates that accounting for shock-induced disorder is critical for interpreting shock-compressed systems, providing evidence that ab initio treatments are required for reliable XRTS inference in warm dense aluminium.

physics.plasm-ph↗

arXiv2025

Multichannel active-space embedding of atomic multiplets in plane-wave DFT/PAW for core-level spectroscopies

We introduce an active-space embedding framework for core-level spectroscopies that connects localized atomic multiplets to continuum resonances within a plane-wave DFT/PAW description. The approach is complementary to widely used core-level Bethe--Salpeter implementations based on a two-particle (core-exciton) picture with typically static screening: here a correlated multiplet manifold of the absorber (including the core hole and open-shell configurations) is coherently coupled to a plane-wave photoelectron, enabling a unified treatment of localized multiplet structure and continuum lineshapes. Spectra are computed in a general time-domain formulation equivalent to Fermi's golden rule: a transition operator tailored to the specific spectroscopy technique is applied to the correlated ground state to generate an excited wavepacket, and the corresponding wavepacket autocorrelation function is evaluated without explicit real-time propagation, using Lanczos tridiagonalization or the kernel polynomial method; the spectral intensity follows from its Fourier representation. We validate the method at the Ce $N_{4,5}$ edges, reproducing in quantitative agreement with experiment both high-$Q$ multiplet features and the low-$Q$ giant dipole resonance continuum, including a characteristic low-energy shoulder relevant for robust Ce valence assignments. The implementation is available open-source within the Quantum ESPRESSO XSPECTRA package (xspectruplet mode), together with reproducible inputs and scripts.

cond-mat.str-el↗

arXiv2024

Coexistence of insulator-like paramagnon and metallic spin-orbit exciton modes in SrIrO$_3$

We probe the spectrum of elementary excitations in SrIrO$_3$ by using heterostructured [(SrIrO$_3$)$_m$/(SrTiO$_3$)$_l$] samples to approach the bulk limit. Our resonant inelastic x-ray scattering (RIXS) measurements at the Ir $L_3$-edge reveal a robust low-lying collective magnetic mode with an antiferromagnetic (AF) dispersion similar to the insulators Sr$_2$IrO$_4$ and Sr$_3$Ir$_2$O$_7$, albeit with a large gap and much larger linewidth. At higher energies we find the spin-orbit exciton, also strongly broadened, but with an inverted dispersion and doubled periodicity that are controlled by the charge hopping. These results demonstrate that the AF paramagnon persists, somewhat counterintuitively, far into the metallic regime of the insulator-metal transition driven by the degree of confinement in the heterostructure. We conclude that these two excitations, which are contrasting but coexisting hallmarks of strong AF pseudospin and charge fluctuations in a spin-orbit-coupled Mott-Slater material, are properties intrinsic to the ground state of semimetallic perovskite SrIrO$_3$.

cond-mat.str-el↗

arXiv2024

Understanding the irreversible lithium loss in silicon anodes using multi-edge X-ray scattering analysis

During the first charge-discharge cycle, silicon-based batteries show an important capacity loss because of the formation of the solid electrolyte interphase (SEI) and morphological changes due to expansion-contraction sequence upon alloying. To understand this first-cycle irreversibility, quantitative methods are needed to characterize the chemical environment of silicon and lithium in the bulk of the cycled electrodes. Here we report a methodology based on multi-edge X-ray Raman Scattering performed on model silicon electrodes prepared in fully lithiated and fully delithiated states after the first cycle. The spectra were recorded at the C, O, F and Li K edges, as well as Si L2,3 edge. They were analysed using linear combinations of both experimental and computed reference spectra. We used prototypical SEI compounds as Li2CO3, LiF and LiPF6, as well as electrode constituents as binder and conductive carbon, cristalline Si, native SiO2,LixSi phases (x being the lithiation index) to identify the main species, isolate their relative contributions, and quantitatively evaluate the proportions of organic and inorganic products. We find that 30% of the carbonates formed in the SEI during the lithiation are dissolved on delithiation, and that part of the Li15Si4 alloys remain present after delithiation. By combining electrochemical analysis and XRS results, we identify that 17% of the lithium lost in the first cycle is trapped in disconnected silicon particles, while 30% form a fluorine-rich stable SEI and 53% a carbonate-rich partially-dissolvable SEI. These results pave the way to systematic, reference data-informed, and modelling assisted studies of SEI characteristics in the bulk of electrodes prepared under controlled state-of-charge and state-of-health conditions.

cond-mat.mtrl-sci↗

arXiv2023

Absence of localized $5d^1$ electrons in KTaO$_3$ interface superconductors

Recently, an exciting discovery of orientation-dependent superconductivity was made in two-dimensional electron gas (2DEG) at the interfaces of LaAlO$_3$/KTaO$_3$ (LAO/KTO) or EuO/KTaO$_3$ (EuO/KTO). The superconducting transition temperature can reach a $T_c$ of up to $\sim$ 2.2 K, which is significantly higher than its 3$d$ counterpart LaAlO$_3$/SrTiO$_3$ (LAO/STO) with a $T_c$ of $\sim$ 0.2 K. However, the underlying origin remains to be understood. To uncover the nature of electrons in KTO-based interfaces, we employ x-ray absorption spectroscopy (XAS) and resonant inelastic x-ray spectroscopy (RIXS) to study LAO/KTO and EuO/KTO with different orientations. We reveal the absence of $dd$ orbital excitations in all the measured samples. Our RIXS results are well reproduced by calculations that considered itinerant $5d$ electrons hybridized with O $2p$ electrons. This suggests that there is a lack of localized Ta $5d^1$ electrons in KTO interface superconductors, which is consistent with the absence of magnetic hysteresis observed in magneto-resistance (MR) measurements. These findings offer new insights into our understanding of superconductivity in Ta $5d$ interface superconductors and their potential applications.

cond-mat.supr-con↗