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Intermolecular Coulombic Decay in water dimers -
observation of an ultrafast decay mechanism

We observed a novel decay mechanism called "Intermolecular Coulombic Decay" (ICD) in water dimers. The process is triggered by removing an inner valence electron from one of the water molecules of the dimer (a). As the ionized molecule deexcites, the deexcitation energy is transferred to the neighboring molecule (b). That neighbor to the initially ionized molecule emits a low energy electron, the so called ICD electron. Our investigations reveal that the decay process is ultrafast, it happens even before the water molecules are able to rearrange: usually a protonated water molecule, i.e. H3O+ is formed after ionization of compounds of water molecules. As the proton rearrangement happens typically on a time scale of 50 fs, ICD seems to be a highly efficient mechanism to "convert" incoming radiation into a low energy electron. This fact might be of interest to other disciplines: during the last years low energy electrons have been observed to efficiently cause single and double strand breaks in DNA. As bio matter is often surrounded by water, ICD in water may be a so far overseen source for radiation damage of living tissue.

More details can be found here:

Ultrafast Energy Transfer between Water Molecules
T. Jahnke, H. Sann, T. Havermeier, K. Kreidi, C. Stuck, M. Meckel, M. Schöffler, N. Neumann, R. Wallauer, S. Voss, A. Czasch, O. Jagutzki, A. Malakzadeh, F. Afaneh, Th. Weber, H. Schmidt-Böcking, and R. Dörner
Nature Physics (2010), doi:10.1038/NPHYS1498

Available on the preprint server of Nature Physics (the link above will lead you to the Nature Physics Magazine website).

Download a PDF file of the original submitted version of the paper here (273 kB).
Please note that this text is not identical with the final paper published by Nature.