Professor Justin Wark

Abstract:

<jats:p>We present measurements on <a:math xmlns:a="http://www.w3.org/1998/Math/MathML"><a:mrow><a:msub><a:mi>Fe</a:mi><a:mn>2</a:mn></a:msub><a:msub><a:mi mathvariant="normal">O</a:mi><a:mn>3</a:mn></a:msub></a:mrow></a:math> amorphization and melt under laser-driven shock compression up to 209(10) GPa via time-resolved x-ray diffraction. At 122(3) GPa, a diffuse signal is observed indicating the presence of a noncrystalline phase. Structure factors have been extracted up to 182(6) GPa showing the presence of two well-defined peaks. A rapid change in the intensity ratio of the two peaks is identified between 145(12) and 151(12) GPa, indicative of a phase change. The noncrystalline diffuse scattering is consistent with shock amorphization of <c:math xmlns:c="http://www.w3.org/1998/Math/MathML"><c:mrow><c:msub><c:mi>Fe</c:mi><c:mn>2</c:mn></c:msub><c:msub><c:mi mathvariant="normal">O</c:mi><c:mn>3</c:mn></c:msub></c:mrow></c:math> between 122(3) and 145(12) GPa, followed by an amorphous-to-liquid transition above 151(12) GPa. Upon release, a noncrystalline phase is observed alongside crystalline <e:math xmlns:e="http://www.w3.org/1998/Math/MathML"><e:mrow><e:mi>α</e:mi><e:mtext>−</e:mtext><e:msub><e:mi>Fe</e:mi><e:mn>2</e:mn></e:msub><e:msub><e:mi mathvariant="normal">O</e:mi><e:mn>3</e:mn></e:msub></e:mrow></e:math>. The extracted structure factor and pair distribution function of this release phase resemble those reported for <g:math xmlns:g="http://www.w3.org/1998/Math/MathML"><g:mrow><g:msub><g:mi>Fe</g:mi><g:mn>2</g:mn></g:msub><g:msub><g:mi mathvariant="normal">O</g:mi><g:mn>3</g:mn></g:msub></g:mrow></g:math> melt at ambient pressure.</jats:p> <jats:sec> <jats:title/> <jats:supplementary-material> <jats:permissions> <jats:copyright-statement>Published by the American Physical Society</jats:copyright-statement> <jats:copyright-year>2025</jats:copyright-year> </jats:permissions> </jats:supplementary-material> </jats:sec>

Abstract:

We posit the existence of a nonthermal phase transition in iron, driven by a loss of ferromagnetic ordering on ultrafast timescales with increasing electron temperature. The transition corresponds to a solid-solid BCC to FCC phase transformation and takes place at an electron temperature of 0.62 eV while the ion lattice remains near room temperature. The BCC structure initially undergoes phonon softening during the magnetic transformation, followed by a solid-solid phase transition to the FCC structure, and a subsequent hardening of phonon modes. We present a detailed physical picture of the process, supported by finite-temperature density functional theory simulations of the phonon dispersion curves, electronic density of states, and thermodynamic free energy.

Abstract:

Knowing the characteristic relaxation time of free electrons in a dense plasma is crucial to our understanding of plasma equilibration and transport. However, experimental investigations of electron relaxation dynamics have been hindered by the ultrafast, sub-femtosecond timescales on which these interactions typically take place. Here, we propose a novel approach that uses x rays from a free electron laser to generate well-defined non-thermal electron distributions, which can then be tracked via emission spectroscopy from radiative recombination as they thermalize. Collisional radiative simulations reveal how this method can enable the measurement of electron relaxation timescales in situ, shedding light on the applicability and accuracy of the Coulomb logarithm framework for modeling collisions in dense plasmas.

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.