Professor Justin Wark

Abstract:

We present new exclusion bounds obtained at the European X-Ray Free Electron Laser facility (EuXFEL) on axionlike particles in the mass range $10^{-3}\,\mathrm{eV} \lesssim m_a \lesssim 10^{4}\,\mathrm{eV}$. Our experiment exploits the Primakoff effect via which photons can, in the presence of a strong external electric field, decay into axions, which then convert back into photons after passing through an opaque wall. While similar searches have been performed previously at a third-generation synchrotron [Yamaji et al., Phys.\ Lett.\ B 782, 523 (2018)], our work demonstrates improved sensitivity, exploiting the higher brightness of x-rays at EuXFEL.

Abstract:

We present measurements on Fe₂O₃ amorphization and melt under laser-driven shock compression up to 209(10) GPa via time-resolved in situ 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 Fe₂O₃ 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 α-Fe₂O₃. The extracted structure factor and pair distribution function of this release phase resemble those reported for Fe₂O₃ melt at ambient pressure.

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.