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Ultra-intense lasers that ionize and accelerate electrons in solids to near the speed of light can lead to kinetic instabilities that alter the laser absorption and subsequent electron transport, isochoric heating, and ion acceleration. These instabilities can be difficult to characterize, but a novel approach using X-ray scattering at keV energies allows for their visualization with femtosecond temporal resolution on the few nanometer mesoscale. Our experiments on laser-driven flat silicon membranes show the development of structure with a dominant scale of $~60\unit{nm}$ in the plane of the laser axis and laser polarization, and $~95\unit{nm}$ in the vertical direction with a growth rate faster than $0.1/\mathrm{fs}$. Combining the XFEL experiments with simulations provides a complete picture of the structural evolution of ultra-fast laser-induced instability development, indicating the excitation of surface plasmons and the growth of a new type of filamentation instability. These findings provide new insight into the ultra-fast instability processes in solids under extreme conditions at the nanometer level with important implications for inertial confinement fusion and laboratory astrophysics.

Controlling the formation and stoichiometric content of desired phases of materials has become a central interest for the study of a variety of fields, notably high temperature superconductivity under extreme pressures. The further possibility of accessing metastable states by initiating reactions by x-ray triggered mechanisms over ultra-short timescales is enabled with the development of x-ray free electron lasers (XFEL). Utilizing the exceptionally high brilliance x-ray pulses from the EuXFEL, we report the synthesis of a previously unobserved yttrium hydride under high pressure, along with non-stoichiometric changes in hydrogen content as probed at a repetition rate of 4.5\,MHz using time-resolved x-ray diffraction. Exploiting non-equilibrium pathways we synthesize and characterize a hydride with yttrium cations in an \textit{A}15 structure type at 125\,GPa, predicted using crystal structure searches, with a hydrogen content between 4.0--5.75 hydrogens per cation, that is enthalpically metastable on the convex hull. We demonstrate a tailored approach to changing hydrogen content using changes in x-ray fluence that is not accessible using conventional synthesis methods, and reveals a new paradigm in metastable chemical physics.

The new generation of multi-petawatt (PW) class laser systems will generally combine several beamlines. We here investigate how to arrange their irradiation geometry in order to optimize their coupling with solid targets, as well as the yields and beam quality of the produced particles. We first report on a proof-of-principle experiment, performed at the Rutherford Appleton Laboratory Vulcan laser facility, where two intense laser beams were overlapped in a mirror-like configuration onto a solid target, preceded by a long preplasma. We show that when the laser beams were close enough to each other, the generation of hot electrons at the target front was much improved and so was the ion acceleration at the target backside, both in terms of their maximum energy and collimation. The underlying mechanism is pinpointed with multidimensional particle-in-cell simulations, which demonstrate that the magnetic fields self-induced by the electron currents driven by the two laser beams at the target front can reconnect, thereby enhancing the production of hot electrons, and favoring their subsequent magnetic guiding across the target. Our simulations also reveal that the laser coupling with the target can be further improved when overlapping more than two beamlines. This multi-beam scheme would obviously be highly beneficial to the multi-PW laser projects proposed now and in the near future worldwide.

Extreme states of matter exist throughout the universe e.g. inside planetary cores, stars or astrophysical jets. Such conditions are generated in the laboratory in the interaction of powerful lasers with solids, and their evolution can be probed with femtosecond precision using ultra-short X-ray pulses to study laboratory astrophysics, laser-fusion research or compact particle acceleration. X-ray scattering (SAXS) patterns and their asymmetries occurring at X-ray energies of atomic bound-bound transitions contain information on the volumetric nanoscopic distribution of density, ionization and temperature. Buried heavy ion structures in high intensity laser irradiated solids expand on the nanometer scale following heat diffusion, and are heated to more than 2 million Kelvin. These experiments demonstrate resonant SAXS with the aim to better characterize dynamic processes in extreme laboratory plasmas.

Observing ultrafast laser-induced structural changes in nanoscale systems is essential for understanding the dynamics of intense light-matter interactions. For laser intensities on the order of $10^{14} \, \rm W/cm^2$, highly-collisional plasmas are generated at and below the surface. Subsequent transport processes such as heat conduction, electron-ion thermalization, surface ablation and resolidification occur at picosecond and nanosecond time scales. Imaging methods, e.g. using x-ray free-electron lasers (XFEL), were hitherto unable to measure the depth-resolved subsurface dynamics of laser-solid interactions with appropriate temporal and spatial resolution. Here we demonstrate picosecond grazing-incidence small-angle x-ray scattering (GISAXS) from laser-produced plasmas using XFEL pulses. Using multi-layer (ML) samples, both the surface ablation and subsurface density dynamics are measured with nanometer depth resolution. Our experimental data challenges the state-of-the-art modeling of matter under extreme conditions and opens new perspectives for laser material processing and high-energy-density science., Comment: 16 pages, 4 figures. This is the version of the article before peer review, as submitted by authors. There is a Supplementary Information file in the Ancillary files directory