51st Annual Meeting of the APS Division of Atomic, Molecular and Optical Physics
Volume 65, Number 4
Monday–Friday, June 1–5, 2020;
Portland, Oregon
Session G04: Attosecond Transient Absorption and Four-Wave Mixing Spectroscopies
8:00 AM–10:00 AM,
Wednesday, June 3, 2020
Room: D137-138
Co-Sponsoring
Unit:
DCMP
Chair: Agnieszka Jaron-Becker, University of Colorado Boulder
Abstract: G04.00004 : Attosecond soft-X-ray spectroscopy in the gas and liquid phases
9:30 AM–10:00 AM
Live
Preview Abstract
Abstract
Author:
Hans Jakob Wörner
(ETH Zurich)
Attosecond spectroscopy has the potential to address fundamental questions
in molecular sciences. A promising approach is offered by the element- and
site-sensitivity of X-ray spectroscopy. We have recently demonstrated the
potential of table-top X-ray absorption spectroscopy with a water-window
high-harmonic source, observing the temporal evolution of unoccupied
molecular orbitals and molecular shape resonances during chemical reactions
[1]. Compressing the mid-infrared driving pulses to less than 2 optical
cycles, we have demonstrated the extension of this light source to fully
cover the oxygen K-edge [2]. Using the same technique, we have also
demonstrated the generation of isolated attosecond pulses, which have
established a new record of the shortest light pulses ever measured (43
attoseconds) [3].
Since the vast majority of chemical processes takes place in the liquid
phase, the extension of attosecond spectroscopy to liquids is desirable. I
will discuss the first observation of extreme-ultraviolet high-harmomic
generation from liquids, achieved through the application of ultrathin
(0.6-2 $\mu $m) flat microjets [4]. I will also present the extension of
attosecond time-resolved spectroscopy from molecules [5] to liquids [6]. The
time delays between photoemission from gaseous and liquid water range from
50-70 attoseconds and are shown to mainly originate from the solvation of
water molecules, with liquid-phase electron scattering playing a minor role.
These developments set the stage for attosecond time-resolved studies of
molecular systems of chemical complexity.
\textless br/\textgreater
[1] Y. Pertot et al., \textit{Science }\textbf{355}, 264 (2017)
[2] C. Schmidt et al., \textit{Opt. Exp. }\textbf{26}, 11834 (2018)
[3] T. Gaumnitz et al., \textit{Opt. Exp }\textbf{25}, 27506 (2017)
[4] T. T. Luu et al., \textit{Nature Communications }\textbf{9,} 3723 (2018)
[5] M. Huppert et al., \textit{Phys. Rev. Lett.} \textbf{117}, 093001 (2016)
[6] I. Jordan et al., \textit{submitted }(2019)