Attosecond Transient Absorption Spectrum of Argon at the L$_{2,3}$-edge

ORAL

Abstract

Attosecond transient absorption, or time-resolved pump-probe spectroscopy, has made it possible to study fast electron dynamics in atomic and molecular systems within subfemtosecond timescales. With the emergence of table-top attosecond sources with spectra that extend into the water window, it is now possible to study atoms and molecules with absorption edges at higher energies than before. One such atom is the Argon L$_{2,3}$ edge, that lies near 250 eV, where the autoionization states approaching the 2p$^{-1}$ 2P$^{o}_{3/2}$ decay most notably through Auger processes. We present here the first Attosecond Transient Absorption Spectrum of the Argon atom in the vicinity of the 2p$^{-1}$ 2P$^{o}_{3/2}$ threshold, dressed by a strong shortwave infra-red pulse, with sub-cycle time resolution and high energy resolution. Our spectra resolve the dynamics of autoionizing states converging to the 2p$^{-1}$ 2P$^{o}_{3/2}$ threshold. Comparison with theoretical simulations indicates that the measured resonant profiles display ac-Stark shift and bear the signature of simultaneous Auger decay and tunneling ionization.

Authors

  • Andrew Chew

    Univ of Central Florida

  • Nicolas Douguet

    Univ of Central Florida, University of Central Florida

  • C Cariker

    Univ of Central Florida, Univ. Central Florida, USA, Dept. of Physics, Univ. of Central Florida, FL, USA, Dept. Physics, Univ. Central Florida, FL, USA

  • Jie Li

    Univ of Central Florida

  • Eva Lindroth

    Stockholm University

  • Xiaoming Ren

    Univ of Central Florida

  • Yanchun Yin

    Univ of Central Florida

  • Luca Argenti

    Univ of Central Florida

  • Wendell Hill

    University of Maryland

  • Zenghu Chang

    Univ of Central Florida