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Visualizing the non-equilibrium dynamics of photoinduced intramolecular electron transfer with femtosecond X-ray pulses.

Canton, Sophie (author)
Lund University,Lunds universitet,MAX IV-laboratoriet,MAX IV Laboratory
Kjær, Kasper S (author)
Vankó, György (author)
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van Driel, Tim B (author)
Adachi, Shin-Ichi (author)
Bordage, Amélie (author)
Bressler, Christian (author)
Chabera, Pavel (author)
Christensen, Morten (author)
Dohn, Asmus O (author)
Galler, Andreas (author)
Gawelda, Wojciech (author)
Gosztola, David (author)
Haldrup, Kristoffer (author)
Harlang, Tobias (author)
Liu, Yizhu (author)
Møller, Klaus B (author)
Németh, Zoltán (author)
Nozawa, Shunsuke (author)
Pápai, Mátyás (author)
Sato, Tokushi (author)
Sato, Takahiro (author)
Suarez Alcantara, Karina (author)
Lund University,Lunds universitet,MAX IV-laboratoriet,MAX IV Laboratory
Togashi, Tadashi (author)
Tono, Kensuke (author)
Uhlig, Jens (author)
Vithanage, Dimali A (author)
Wärnmark, Kenneth (author)
Yabashi, Makina (author)
Zhang, Jianxin (author)
Sundström, Villy (author)
Nielsen, Martin M (author)
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 (creator_code:org_t)
2015-03-02
2015
English.
In: Nature Communications. - : Springer Science and Business Media LLC. - 2041-1723. ; 6
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Ultrafast photoinduced electron transfer preceding energy equilibration still poses many experimental and conceptual challenges to the optimization of photoconversion since an atomic-scale description has so far been beyond reach. Here we combine femtosecond transient optical absorption spectroscopy with ultrafast X-ray emission spectroscopy and diffuse X-ray scattering at the SACLA facility to track the non-equilibrated electronic and structural dynamics within a bimetallic donor-acceptor complex that contains an optically dark centre. Exploiting the 100-fold increase in temporal resolution as compared with storage ring facilities, these measurements constitute the first X-ray-based visualization of a non-equilibrated intramolecular electron transfer process over large interatomic distances. Experimental and theoretical results establish that mediation through electronically excited molecular states is a key mechanistic feature. The present study demonstrates the extensive potential of femtosecond X-ray techniques as diagnostics of non-adiabatic electron transfer processes in synthetic and biological systems, and some directions for future studies, are outlined.

Subject headings

NATURVETENSKAP  -- Fysik (hsv//swe)
NATURAL SCIENCES  -- Physical Sciences (hsv//eng)

Publication and Content Type

art (subject category)
ref (subject category)

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