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

Canton, S. E., Kjær, K. S., Vankó, G., van Driel, T. B., Adachi, S., Bordage, A., et al. (2015). Visualizing the non-equilibrium dynamics of photoinduced intramolecular electron transfer with femtosecond X-ray pulses. Nature Communications, 6: 6359. doi:10.1038/ncomms7359.

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Canton, S. E.1, Author           
Kjær, K. S., Author
Vankó, G., Author
van Driel, T. B., Author
Adachi, S., Author
Bordage, A., Author
Bressler, C., Author
Chabera, P., Author
Christensen, M., Author
Dohn, A. O., Author
Galler, A., Author
Gawelda, W., Author
Gosztola, D., Author
Haldrup, K., Author
Harlang, T., Author
Liu, Y., Author
Møller, K. B., Author
Németh, Z., Author
Nozawa, S.., Author
Pápai, M., Author
Sato, T., AuthorSato, T., AuthorSuarez-Alcantara, K., AuthorTogashi, T., AuthorTono, K., AuthorUhlig, J., AuthorVithanage, D. A., AuthorWärnmark, K., AuthorYabashi, M., AuthorZhang, J., AuthorSundström, V., AuthorNielsen, M. M., Author more..
Affiliations:
1Research Group of Structural Dynamics of (Bio)Chemical Systems, MPI for Biophysical Chemistry, Max Planck Society, ou_578564              

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Free keywords: Chemical sciences; catalysis; condensed matter
 Abstract: 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.

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Language(s): eng - English
 Dates: 2015-03-02
 Publication Status: Published online
 Pages: -
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 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1038/ncomms7359
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Title: Nature Communications
Source Genre: Journal
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Pages: 10 Volume / Issue: 6 Sequence Number: 6359 Start / End Page: - Identifier: ISSN: 2041-1723