TY - JOUR
T1 - XUV pump-XUV probe transient absorption spectroscopy at FELs
AU - Ding, Thomas
AU - Rebholz, Marc
AU - Aufleger, Lennart
AU - Hartmann, Maximilian
AU - Stooß, Veit
AU - Magunia, Alexander
AU - Birk, Paul
AU - Borisova, Gergana Dimitrova
AU - Da Costa Castanheira, Carina
AU - Rupprecht, Patrick
AU - Mi, Yonghao
AU - Gaumnitz, Thomas
AU - Loh, Zhi Heng
AU - Roling, Sebastian
AU - Butz, Marco
AU - Zacharias, Helmut
AU - Düsterer, Stefan
AU - Treusch, Rolf
AU - Ott, Christian
AU - Pfeifer, Thomas
N1 - Publisher Copyright:
© 2021 The Royal Society of Chemistry.
PY - 2021
Y1 - 2021
N2 - The emergence of ultra-intense extreme-ultraviolet (XUV) and X-ray free-electron lasers (FELs) has opened the door for the experimental realization of non-linear XUV and X-ray spectroscopy techniques. Here we demonstrate an experimental setup for an all-XUV transient absorption spectroscopy method for gas-phase targets at the FEL. The setup combines a high spectral resolving power of E/ΔE ≈ 1500 with sub-femtosecond interferometric resolution, and covers a broad XUV photon-energy range between approximately 20 and 110 eV. We demonstrate the feasibility of this setup firstly on a neon target. Here, we intensity- and time-resolve key aspects of non-linear XUV-FEL light-matter interactions, namely the non-resonant ionization dynamics and resonant coupling dynamics of bound states, including XUV-induced Stark shifts of energy levels. Secondly, we show that this setup is capable of tracking the XUV-initiated dissociation dynamics of small molecular targets (oxygen and diiodomethane) with site-specific resolution, by measuring the XUV transient absorption spectrum. In general, benefitting from a single-shot detection capability, we show that the setup and method provides single-shot phase-locked XUV pulse pairs. This lays the foundation to perform, in the future, experiments as a function of the XUV interferometric time delay and the relative phase, which enables advanced coherent non-linear spectroscopy schemes in the XUV and X-ray spectral range.
AB - The emergence of ultra-intense extreme-ultraviolet (XUV) and X-ray free-electron lasers (FELs) has opened the door for the experimental realization of non-linear XUV and X-ray spectroscopy techniques. Here we demonstrate an experimental setup for an all-XUV transient absorption spectroscopy method for gas-phase targets at the FEL. The setup combines a high spectral resolving power of E/ΔE ≈ 1500 with sub-femtosecond interferometric resolution, and covers a broad XUV photon-energy range between approximately 20 and 110 eV. We demonstrate the feasibility of this setup firstly on a neon target. Here, we intensity- and time-resolve key aspects of non-linear XUV-FEL light-matter interactions, namely the non-resonant ionization dynamics and resonant coupling dynamics of bound states, including XUV-induced Stark shifts of energy levels. Secondly, we show that this setup is capable of tracking the XUV-initiated dissociation dynamics of small molecular targets (oxygen and diiodomethane) with site-specific resolution, by measuring the XUV transient absorption spectrum. In general, benefitting from a single-shot detection capability, we show that the setup and method provides single-shot phase-locked XUV pulse pairs. This lays the foundation to perform, in the future, experiments as a function of the XUV interferometric time delay and the relative phase, which enables advanced coherent non-linear spectroscopy schemes in the XUV and X-ray spectral range.
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U2 - 10.1039/d0fd00107d
DO - 10.1039/d0fd00107d
M3 - Article
C2 - 33575691
AN - SCOPUS:85105993713
SN - 1359-6640
VL - 228
SP - 519
EP - 536
JO - Faraday Discussions
JF - Faraday Discussions
ER -