RESUMO
The BESSY II synchrotron radiation source at Helmholtz-Zentrum Berlin (HZB) is an internationally leading facility playing to its strengths in the UV and soft X-ray regime, with the mission to enlight and enable materials discovery, develop solutions and answers to the societal challenges of this century, like Energy, Information and Health, and enable research and innovation along the entire value chain. To maintain BESSY II competitive while bridging to its successor source BESSY III, HZB is currently developing an ambitious strategic upgrade program of the facility which includes maintenance and modernization measures as well as the provision of new research opportunities with the focus on new operando capabilities for energy research and technology development. On the longer term, the 4th generation source BESSY III is needed to meet the requirements of the mission-oriented scientific focus fields Catalysis, Energy, Quantum and Information and Life Sciences as well as Metrology for Innovation.
RESUMO
The temporal evolution of the exchange-split Δ(2)-like Σ valence bands of the 4f-ferromagnet gadolinium after femtosecond laser excitation has been studied using angle-resolved photoelectron spectroscopy based on high-order harmonic generation. The ultrafast drop of the exchange splitting reflects the magnetic response seen in femtosecond magnetic dichroism experiments. However, while the minority valence band reacts immediately, the response of the majority counterpart is delayed by 1 picosecond and is only half as fast. These findings demonstrate that laser excitation drives the valence band structure out of magnetic equilibrium.
RESUMO
A laser-based tabletop approach to femtosecond time-resolved photoelectron spectroscopy with photons in the vacuum-ultraviolet (VUV) energy range is described. The femtosecond VUV pulses are produced by high-order harmonic generation (HHG) of an amplified femtosecond Ti:sapphire laser system. Two generations of the same setup and results from photoelectron spectroscopy in the gas phase are discussed. In both generations, a toroidal grating monochromator was used to select one harmonic in the photon energy range of 20-30 eV. The first generation of the setup was used to perform photoelectron spectroscopy in the gas phase to determine the bandwidth of the source. We find that our HHG source has a bandwidth of 140 ± 40 meV. The second and current generation is optimized for femtosecond pump-probe photoelectron spectroscopy with high flux and a small spot size at the sample of the femtosecond probe pulses. The VUV radiation is focused into the interaction region with a toroidal mirror to a spot smaller than 100 × 100 µm(2) and the flux amounts to 10(10) photons/s at the sample at a repetition rate of 1 kHz. The duration of the monochromatized VUV pulses is determined to be 120 fs resulting in an overall pump-probe time resolution of 135 ± 5 fs. We show how this setup can be used to map the transient valence electronic structure in molecular dissociation.