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Coherent structural trapping through wave packet dispersion during photoinduced spin state switching

Lemke, Henrik T. (author)
Paul Scherrer Institute,Stanford Linear Accelerator Center (SLAC)
Kjær, Kasper S. (author)
Lund University,Lunds universitet,Kemisk fysik,Enheten för fysikalisk och teoretisk kemi,Kemiska institutionen,Institutioner vid LTH,Lunds Tekniska Högskola,Chemical Physics,Physical and theoretical chemistry,Department of Chemistry,Departments at LTH,Faculty of Engineering, LTH,Stanford University,Stanford Linear Accelerator Center (SLAC),Technical University of Denmark
Hartsock, Robert W. (author)
Stanford Linear Accelerator Center (SLAC),Stanford University
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van Driel, Tim B (author)
Technical University of Denmark,Stanford Linear Accelerator Center (SLAC)
Chollet, Matthieu (author)
Stanford Linear Accelerator Center (SLAC)
Glownia, James M. (author)
Stanford Linear Accelerator Center (SLAC)
Song, Sanghoon (author)
Stanford Linear Accelerator Center (SLAC)
Zhu, Diling (author)
Stanford Linear Accelerator Center (SLAC)
Pace, Elisabetta (author)
INFN Frascati National Laboratory
Matar, Samir F. (author)
University of Bordeaux
Nielsen, Martin M. (author)
Technical University of Denmark
Benfatto, Maurizio (author)
INFN Frascati National Laboratory
Gaffney, Kelly J. (author)
Stanford Linear Accelerator Center (SLAC)
Collet, Eric (author)
Institut de Physique de Rennes
Cammarata, Marco (author)
Institut de Physique de Rennes
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 (creator_code:org_t)
2017-05-24
2017
English.
In: Nature Communications. - : Springer Science and Business Media LLC. - 2041-1723. ; 8
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • The description of ultrafast nonadiabatic chemical dynamics during molecular photo-transformations remains challenging because electronic and nuclear configurations impact each other and cannot be treated independently. Here we gain experimental insights, beyond the Born-Oppenheimer approximation, into the light-induced spin-state trapping dynamics of the prototypical [Fe(bpy) 3 ] 2+ compound by time-resolved X-ray absorption spectroscopy at sub-30-femtosecond resolution and high signal-to-noise ratio. The electronic decay from the initial optically excited electronic state towards the high spin state is distinguished from the structural trapping dynamics, which launches a coherent oscillating wave packet (265 fs period), clearly identified as molecular breathing. Throughout the structural trapping, the dispersion of the wave packet along the reaction coordinate reveals details of intramolecular vibronic coupling before a slower vibrational energy dissipation to the solution environment. These findings illustrate how modern time-resolved X-ray absorption spectroscopy can provide key information to unravel dynamic details of photo-functional molecules.

Subject headings

NATURVETENSKAP  -- Fysik -- Atom- och molekylfysik och optik (hsv//swe)
NATURAL SCIENCES  -- Physical Sciences -- Atom and Molecular Physics and Optics (hsv//eng)

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