Schick, DanielBorchert, MartinBraenzel, JuliaStiel, HolgerTümmler, JohannesBürgler, Daniel E.Firsov, AlexanderKorff Schmising, Clemens vonPfau, BastianEisebitt, Stefan2021-11-082021-11-082021-09https://depositonce.tu-berlin.de/handle/11303/13845http://dx.doi.org/10.14279/depositonce-12621Time-resolved resonant magnetic scattering in the soft-x-ray range is a powerful tool for accessing the spatially resolved and element-specific spin dynamics in magnetic materials. So far, the application of this photon-demanding technique was limited to large-scale facilities. However, upgrades to diffraction-limited storage rings supporting only x-ray pulses beyond 100 ps, and the shift of x-ray free-electron lasers toward attosecond pulses aggravate the competition for beamtime in the picosecond time window, which is of utmost relevance for magnetism research. Here we present the development of a lab-based instrument providing sufficient photon flux up to 1.5 keV photon energy covering the soft-x-ray resonances of transition and rare-earth metal atoms. Our setup features the mandatory tunability in energy and reciprocal space in combination with sub-10 ps temporal resolution, exploiting the broadband emission of a laser-driven plasma x-ray source, which is monochromatized to about 1 eV bandwidth by a reflection zone plate. We benchmark our approach against accelerator-based soft-x-ray sources by simultaneously probing the laser-induced magnetic and structural dynamics from an antiferromagnetically coupled Fe/Cr superlattice. Our development lays the foundation for laser-driven resonant scattering experiments to study ultrafast ordering phenomena of charges, spins, and orbitals.en530 Physiksoft-x-ray scatteringstructural dynamicsantiferromagnetic dynamicsmagnetic scatteringmagnetic materialsArticle2334-2536