2021, Chardonnet, Valentin, Hennes, Marcel, Jarrier, Romain, Delaunay, Renaud, Jaouen, Nicolas, Kuhlmann, Marion, Ekanayake, Nagitha, Léveillé, Cyril, von Korff Schmising, Clemens, Schick, Daniel, Yao, Kelvin, Liu, Xuan, Chiuzbăian, Gheorghe S., Lüning, Jan, Vodungbo, Boris, Jal, Emmanuelle

During the last two decades, a variety of models have been developed to explain the ultrafast quenching of magnetization following femtosecond optical excitation. These models can be classified into two broad categories, relying either on a local or a non-local transfer of angular momentum. The acquisition of the magnetic depth profiles with femtosecond resolution, using time-resolved x-ray resonant magnetic reflectivity, can distinguish local and non-local effects. Here, we demonstrate the feasibility of this technique in a pump–probe geometry using a custom-built reflectometer at the FLASH2 free-electron laser (FEL). Although FLASH2 is limited to the production of photons with a fundamental wavelength of 4 nm (≃310 eV), we were able to probe close to the Fe L3 edge (706.8 eV) of a magnetic thin film employing the third harmonic of the FEL. Our approach allows us to extract structural and magnetic asymmetry signals revealing two dynamics on different time scales which underpin a non-homogeneous loss of magnetization and a significant dilation of 2 Å of the layer thickness followed by oscillations. Future analysis of the data will pave the way to a full quantitative description of the transient magnetic depth profile combining femtosecond with nanometer resolution, which will provide further insight into the microscopic mechanisms underlying ultrafast demagnetization.

2021, Kleine, Carlo, Ekimova, Maria, Winghart, Marc-Oliver, Eckert, Sebastian, Reichel, Oliver, Löchel, Heike, Probst, Jürgen, Braig, Christoph, Seifert, Christian, Erko, Alexei, Sokolov, Andrey, Vrakking, Marc J. J., Nibbering, Erik T. J., Rouzée, Arnaud

We present a novel soft x-ray spectrometer for ultrafast absorption spectroscopy utilizing table-top femtosecond high-order harmonic sources. Where most commercially available spectrometers rely on spherical variable line space gratings with a typical efficiency on the order of 3% in the first diffractive order, this spectrometer, based on a Hettrick-Underwood design, includes a reflective zone plate as a dispersive element. An improved efficiency of 12% at the N K-edge is achieved, accompanied by a resolving power of 890. The high performance of the soft x-ray spectrometer is further demonstrated by comparing nitrogen K-edge absorption spectra from calcium nitrate in aqueous solution obtained with our high-order harmonic source to previous measurements performed at the electron storage ring facility BESSY II.