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Title: Attosecond transient absorption of a bound wave packet coupled to a smooth continuum

Abstract

Here, we investigate the possibility of using transient absorption of a coherent bound electron wave packet in hydrogen as an attosecond pulse characterization technique. In a recent work, we have shown that photoionization of such a coherent bound electron wave packet opens up for pulse characterization with unprecedented temporal accuracy—independent of the atomic structure—with maximal photoemission at all kinetic energies given a wave packet with zero relative phase. Here, we perform numerical propagation of the time-dependent Schrödinger equation and analytical calculations based on perturbation theory to show that the energy-resolved maximal absorption of photons from the attosecond pulse does not uniquely occur at a zero relative phase of the initial wave packet. Instead, maximal absorption occurs at different relative wave packet phases, distributed as a non-monotonous function with a smooth $$-\pi /2$$ shift across the central photon energy (given a Fourier-limited Gaussian pulse). Similar results are also found in helium. Our finding is surprising, because it implies that the energy-resolved photoelectrons are not mapped one-to-one with the energy-resolved absorbed photons of the attosecond pulse.

Authors:
ORCiD logo [1]; ORCiD logo [2]; ORCiD logo [3]
  1. Lund Univ., Lund (Sweden); Stockholm Univ., Stockholm (Sweden)
  2. Harvard-Smithsonian Center for Astrophysics, Cambridge, MA (United States); SLAC National Accelerator Lab., Menlo Park, CA (United States)
  3. Stockholm Univ., Stockholm (Sweden)
Publication Date:
Research Org.:
SLAC National Accelerator Lab., Menlo Park, CA (United States)
Sponsoring Org.:
USDOE
OSTI Identifier:
1410602
Grant/Contract Number:  
AC02-76SF00515; 2014-3724; 2016-03789
Resource Type:
Accepted Manuscript
Journal Name:
Journal of Optics
Additional Journal Information:
Journal Volume: 19; Journal Issue: 11; Journal ID: ISSN 2040-8978
Publisher:
IOP Publishing
Country of Publication:
United States
Language:
English
Subject:
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY; 72 PHYSICS OF ELEMENTARY PARTICLES AND FIELDS; attosecond; transient absorption; ATAS; pulse characterization; continuum transition

Citation Formats

Dahlström, Jan Marcus, Pabst, Stefan, and Lindroth, Eva. Attosecond transient absorption of a bound wave packet coupled to a smooth continuum. United States: N. p., 2017. Web. https://doi.org/10.1088/2040-8986/aa8a93.
Dahlström, Jan Marcus, Pabst, Stefan, & Lindroth, Eva. Attosecond transient absorption of a bound wave packet coupled to a smooth continuum. United States. https://doi.org/10.1088/2040-8986/aa8a93
Dahlström, Jan Marcus, Pabst, Stefan, and Lindroth, Eva. Mon . "Attosecond transient absorption of a bound wave packet coupled to a smooth continuum". United States. https://doi.org/10.1088/2040-8986/aa8a93. https://www.osti.gov/servlets/purl/1410602.
@article{osti_1410602,
title = {Attosecond transient absorption of a bound wave packet coupled to a smooth continuum},
author = {Dahlström, Jan Marcus and Pabst, Stefan and Lindroth, Eva},
abstractNote = {Here, we investigate the possibility of using transient absorption of a coherent bound electron wave packet in hydrogen as an attosecond pulse characterization technique. In a recent work, we have shown that photoionization of such a coherent bound electron wave packet opens up for pulse characterization with unprecedented temporal accuracy—independent of the atomic structure—with maximal photoemission at all kinetic energies given a wave packet with zero relative phase. Here, we perform numerical propagation of the time-dependent Schrödinger equation and analytical calculations based on perturbation theory to show that the energy-resolved maximal absorption of photons from the attosecond pulse does not uniquely occur at a zero relative phase of the initial wave packet. Instead, maximal absorption occurs at different relative wave packet phases, distributed as a non-monotonous function with a smooth $-\pi /2$ shift across the central photon energy (given a Fourier-limited Gaussian pulse). Similar results are also found in helium. Our finding is surprising, because it implies that the energy-resolved photoelectrons are not mapped one-to-one with the energy-resolved absorbed photons of the attosecond pulse.},
doi = {10.1088/2040-8986/aa8a93},
journal = {Journal of Optics},
number = 11,
volume = 19,
place = {United States},
year = {2017},
month = {10}
}

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Cited by: 3 works
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    Pulse analysis by delayed absorption from a coherently excited atom
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