Modelling of warm dense hydrogen via explicit real time electron dynamics: Electron transport properties

(2024)

Authors:

Pontus Svensson, Patrick Hollebon, Daniel Plummer, Sam M Vinko, Gianluca Gregori

Ionisation Calculations using Classical Molecular Dynamics

(2024)

Authors:

Daniel Plummer, Pontus Svensson, Dirk O Gericke, Patrick Hollebon, Sam M Vinko, Gianluca Gregori

A molecular dynamics framework coupled with smoothed particle hydrodynamics for quantum plasma simulations

(2024)

Authors:

Thomas Campbell, Pontus Svensson, Brett Larder, Daniel Plummer, Sam M Vinko, Gianluca Gregori

Ionic structure, Liquid-liquid phase transitions, X-Ray diffraction, and X-Ray Thomson scattering in shock compressed liquid Silicon in the 100-200 GPa regime

(2024)

Authors:

MWC Dharma-wardana, Dennis D Klug, Hannah Poole, G Gregori

Resonant inelastic x-ray scattering in warm-dense Fe compounds beyond the SASE FEL resolution limit

Communications Physics Nature Research 7:1 (2024) 266

Authors:

Alessandro Forte, Thomas Gawne, Karim K Alaa El-Din, Oliver S Humphries, Thomas R Preston, C茅line Cr茅pisson, Thomas Campbell, Pontus Svensson, Sam Azadi, Patrick Heighway, Yuanfeng Shi, David A Chin, Ethan Smith, Carsten Baehtz, Victorien Bouffetier, Hauke H枚ppner, Alexis Amouretti, David McGonegle, Marion Harmand, Gilbert W Collins, Justin S Wark, Danae N Polsin, Sam M Vinko

Abstract:

Resonant inelastic x-ray scattering (RIXS) is a widely used spectroscopic technique, providing access to the electronic structure and dynamics of atoms, molecules, and solids. However, RIXS requires a narrow bandwidth x-ray probe to achieve high spectral resolution. The challenges in delivering an energetic monochromated beam from an x-ray free electron laser (XFEL) thus limit its use in few-shot experiments, including for the study of high energy density systems. Here we demonstrate that by correlating the measurements of the self-amplified spontaneous emission (SASE) spectrum of an XFEL with the RIXS signal, using a dynamic kernel deconvolution with a neural surrogate, we can achieve electronic structure resolutions substantially higher than those normally afforded by the bandwidth of the incoming x-ray beam. We further show how this technique allows us to discriminate between the valence structures of Fe and Fe2O3, and provides access to temperature measurements as well as M-shell binding energies estimates in warm-dense Fe compounds.