Tracking polar solvation dynamics of a photoexcited organic chromophore with ultrafast X-ray scattering
Abstract
Abstract Solvation plays a key role in many photochemical and biological processes. Yet, direct atomic-scale observation of solvent reorganization around photoexcited molecules containing only light atoms has so far remained elusive. Here, we use time-resolved X-ray scattering at an X-ray free-electron laser to track with a ~ 120 fs time resolution the photoinduced ultrafast rearrangement of polar acetonitrile solvent molecules around an organic hemithioindigo chromophore. The experiments reveal that the solvation shell reorganizes with a ~ 0.3 ps time constant driven by photoinduced charge transfer in the chromophore, and then reequilibrates over ~ 3 ps as the excited state population returns to the ground state. These results demonstrate the viability of using ultrashort X-ray pulses to directly visualize the motion of light atoms in solution, paving the way for atomic-scale understanding and control of photoinduced processes in biological and synthetic photoactive organic molecules.
Article Details
Authors (20)
Kerstin M. Mitterer
Elli Selenius
Morten L. Haubro
Magnus A. H. Christiansen
Verena Markmann
Department of Physics, Technical University of Denmark 1 , DK-2800 Kgs. Lyngby,
Bianca L. Hansen
Department of Physics, Technical University of Denmark 1 , DK-2800 Kgs. Lyngby,
Mikkel Krell-Jørgensen
Joseph G. F. Hoock
Victor Lorentzen
Emma V. Beale
Philip J. M. Johnson
Paul-Scherrer Institute
David J. Gosztola
Center for Nanoscale Materials, Argonne National Laboratory, 9700 S Cass Ave, Lemont, Illinois 60439, United States
Claudio Cirelli
Paul-Scherrer Institute
Camila Bacellar
Paul-Scherrer Institute
Asmus O. Dohn
Luca Laraia
Department of Chemistry
Klaus B. Møller
Kristoffer Haldrup
Department of Physics, Technical University of Denmark 1 , DK-2800 Kgs. Lyngby,
Gianluca Levi
Science Institute and Faculty of Physical Sciences, University of Iceland 1 , Reykjavík,
Martin M. Nielsen