Femtosecond Soft-X-ray Absorption Spectroscopy of Liquids with a Water-Window High-Harmonic Source
Author(s) -
Adam Smith,
Tadas Balčiūnas,
Yi–Ping Chang,
Cédric Schmidt,
Kristina S. Zinchenko,
Fernanda Brandalise Nunes,
Emanuele Rossi,
Vít Svoboda,
Zhong Yin,
JeanPierre Wolf,
Hans Jakob Wörner
Publication year - 2020
Publication title -
the journal of physical chemistry letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.563
H-Index - 203
ISSN - 1948-7185
DOI - 10.1021/acs.jpclett.9b03559
Subject(s) - femtosecond , x ray absorption spectroscopy , spectroscopy , absorption spectroscopy , ionization , water window , materials science , absorption (acoustics) , analytical chemistry (journal) , laser , atomic physics , chemistry , optics , ion , physics , chromatography , quantum mechanics , organic chemistry
Femtosecond X-ray absorption spectroscopy (XAS) is a powerful method to investigate the dynamical behavior of a system after photoabsorption in real time. So far, the application of this technique has remained limited to large-scale facilities, such as femtosliced synchrotrons and free-electron lasers (FEL). In this work, we demonstrate femtosecond time-resolved soft-X-ray absorption spectroscopy of liquid samples by combining a sub-micrometer-thin flat liquid jet with a high-harmonic tabletop source covering the entire water-window range (284-538 eV). Our work represents the first extension of tabletop XAS to the oxygen edge of a chemical sample in the liquid phase. In the time domain, our measurements resolve the gradual appearance of absorption features below the carbon K-edge of ethanol and methanol during strong-field ionization and trace the valence-shell ionization dynamics of the liquid alcohols with a temporal resolution of ∼30 fs. This technique opens unique opportunities to study molecular dynamics of chemical systems in the liquid phase with elemental, orbital, and site sensitivity.
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