RESUMO
The Femtosecond X-ray Experiments (FXE) instrument at the European X-ray Free-Electron Laser (EuXFEL) provides an optimized platform for investigations of ultrafast physical, chemical and biological processes. It operates in the energy range 4.7-20â keV accommodating flexible and versatile environments for a wide range of samples using diverse ultrafast X-ray spectroscopic, scattering and diffraction techniques. FXE is particularly suitable for experiments taking advantage of the sub-MHz repetition rates provided by the EuXFEL. In this paper a dedicated setup for studies on ultrafast biological and chemical dynamics in solution phase at sub-MHz rates at FXE is presented. Particular emphasis on the different liquid jet sample delivery options and their performance is given. Our portfolio of high-speed jets compatible with sub-MHz experiments includes cylindrical jets, gas dynamic virtual nozzles and flat jets. The capability to perform multi-color X-ray emission spectroscopy (XES) experiments is illustrated by a set of measurements using the dispersive X-ray spectrometer in von Hamos geometry. Static XES data collected using a multi-crystal scanning Johann-type spectrometer are also presented. A few examples of experimental results on ultrafast time-resolved X-ray emission spectroscopy and wide-angle X-ray scattering at sub-MHz pulse repetition rates are given.
RESUMO
Recent advances in high-harmonic generation gave rise to soft X-ray pulses with higher intensity, shorter duration and higher photon energy. One of the remaining shortages of this source is its restriction to linear polarization, since the yield of generation of elliptically polarized high harmonics has been low so far. We here show how this limitation is overcome by using a cross-polarized two-colour laser field. With this simple technique, we reach high degrees of ellipticity (up to 75%) with efficiencies similar to classically generated linearly polarized harmonics. To demonstrate these features and to prove the capacity of our source for applications, we measure the X-ray magnetic circular dichroism (XMCD) effect of nickel at the M2,3 absorption edge around 67 eV. There results open up the way towards femtosecond time-resolved experiments using high harmonics exploiting the powerful element-sensitive XMCD effect and resolving the ultrafast magnetization dynamics of individual components in complex materials.
RESUMO
The current density limit for photoemission from metals was measured in an rf photogun to be below 10(9) A/m2. We have achieved 1.6×10(11) A/m2 by photofield emission from a new type of photocathode made from a metallic-composite, multifilamentary Nb3Sn wire driven by a 266 nm picosecond laser pulse and a 2 ns, 50 kV accelerating voltage. This cathode has a micrometer arrayed structure with tens of thousands of Nb/Nb3Sn filaments embedded in a bronze matrix. Our measurements revealed the existence of a new electron emission regime at high laser fluence (100 mJ/cm2). We have extracted stably, and without any surface ablation, up to 4800 pC of charge. This corresponds to 0.9% quantum efficiency, 100 times larger than what is measured from conventional metallic photocathodes. The unexpected large and stable charge extraction cannot be explained by the 3-step model. Thanks to the small emitting area, the measured emittance (0.6 mm·mrad) is low in spite of the high current density and space charge effects. This cathode will be of benefit for many applications based on short and bright electron bunches.
