arXiv subjects

C. Strohm

Publications and source records attributed to C. Strohm.

5 recordsLinked to original sources

arXiv2026

Nanosecond timescale plasticity in shock-compressed polycrystalline MgO: evidence for transition in mechanism above 100 GPa

The mechanical properties of ceramics under extreme conditions directly impact applications ranging from shielding spacecrafts, designing plasma facing materials in nuclear fusion to understanding the rheology of deep planetary interiors. Here, we use polycrystalline MgO as a model ceramic to understand the high-pressure-temperature mechanical behaviour of such materials under extreme strain rates. We use laser-driven shock compression up to 175(15) GPa on the principal Hugoniot along with ultrafast diagnostics at the European X-ray Free Electron Laser to probe the dominant deformation mechanisms with changing P -T conditions. These near-instantaneous time-resolved snapshots, coupled with elasto-viscoplastic self-consistent (EVPSC) simulations, strongly suggest that MgO attains plastic regime in the nanoseconds scale accompanied by a pressure-mediated change in dominant slip system between 95 and 175 GPa. This work provides a new direct window into the deformation dynamics of polycrystalline ceramics under high-velocity impacts.

cond-mat.mtrl-sci↗

arXiv2026

Volume Collapse Without a Structural Transition in Shock-Compressed FeO

We report x-ray diffraction and emission spectroscopy of FeO under laser-driven shock compression between 31-199 GPa. FeO retains the B1 (rocksalt) structure along the Hugoniot to the melt boundary at 191 GPa. While the phase and volume are broadly consistent with results from static compression, we observe an anomalous 7-10% volume collapse around 60 GPa absent in static experiments. We identify this as an isostructural high-spin to low-spin metallic transition in FeO. The low-spin state is directly evidenced by x-ray emission spectroscopy at 180 GPa.

cond-mat.mtrl-sci↗

arXiv2020

Coherent x-ray-optical control of nuclear excitons with zeptosecond phase-stability

Coherent control of quantum dynamics is key to a multitude of fundamental studies and applications alike. In the visible or longer-wavelength domains, near-resonant light fields have become the primary tool to control electron dynamics. Recently, coherent control in the extreme-ultraviolet range was demonstrated, with timing stability of the applied light fields in the few-attosecond range. At hard x-ray energies, M\"ossbauer nuclei feature narrow nuclear resonances, and spectroscopy of these resonances is a widespread tool to study magnetic, structural and dynamical properties of matter. It has been shown that the power and scope of M\"ossbauer spectroscopy can be significantly advanced using various control techniques. However, the coherent control of atomic nuclei using near-resonant x-ray fields remains an open challenge, also because of the extreme stability requirements on the x-ray light in the few-zeptosecond range. Here, we demonstrate such control, and use the relative phase of two x-ray pulses to switch the nuclear dynamics between stimulated emission and enhanced coherent excitation. For this, we suggest and implement a method to shape single pulses delivered by modern x-ray facilities into tunable double-pulses, with the desired stability on the few-zeptosecond level. Our results unlock coherent optical control for nuclei, and pave the way for nuclear Ramsey spectroscopy and spin-echo-like techniques, which not only provide key concepts for advancing nuclear quantum optics, but also essential ingredients for possible x-ray clocks and frequency standards. As a long-term perspective, we envision time-resolved studies of nuclear out-of-equilibrium dynamics, which is a long-standing open challenge in M\"ossbauer science.

quant-ph↗

arXiv2012

Tuning the Eu valence in EuPd_3B_x: pressure versus valence electron count - a combined computational and experimental study

In a joint theoretical and experimental study we investigate the pressure dependence of the Eu valence in EuPd_3B_x (0 <= x <= 1). Density functional band structure calculations are combined with x-ray absorption and x-ray diffraction measurements under hydrostatic pressures up to 30 GPa. It is observed that the heterogenous mixed-valence state of Eu in EuPd_3B_x (x >= 0.2) can be suppressed partially in this pressure range. From the complementary measurements we conclude that the valence change in EuPd_3B_x is mainly driven by the number of additional valence electrons due to the insertion of boron, whereas the volume change is a secondary effect. A similar valence change of Eu in Eu_{1-x}La_xPd_3 is predicted for x >= 0.4, in line with the suggested electron count scenario.

cond-mat.str-el↗

arXiv2009

High-field recovery of the undistorted triangular lattice in the frustrated metamagnet CuFeO2

Pulsed field magnetization experiments extend the typical metamagnetic staircase of CuFeO2 up to 58 T to reveal an additional first order phase transition at high field for both the parallel and perpendicular field configuration. Virtually complete isotropic behavior is retrieved only above this transition, indicating the high-field recovery of the undistorted triangular lattice. A consistent phenomenological rationalization for the field dependence and metamagnetism crossover of the system is provided, demonstrating the importance of both spin-phonon coupling and a small field-dependent easy-axis anisotropy in accurately describing the magnetization process of CuFeO2.

cond-mat.str-el↗