Attosecond impulsive stimulated x-ray raman scattering in liquid water

We report the measurement of impulsive stimulated x-ray Raman scattering in neutral liquid water. An attosecond pulse drives the excitations of an electronic wavepacket, which comprises two steps: a transition to core-excited states near the oxygen atoms accompanied by transition to a valence-excite...

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Hauptverfasser: Alexander, Oliver, Egun, Felix, Rego, Laura, Martinez, Ana, Garratt, Douglas, Cardenes, Gustavo, Nogueira, Juan, Lee, Jacob, Zhao, Kaixiang, Wang, Ru-Pan, Ayuso, David, Barnard, Jonathan, Beauvarlet, Sandra, Bucksbaum, Philip, Cesar, David, Coffee, Ryan, Duris, Joseph, Frasinski, Leszek, Huse, Nils, Kowalczyk, Katarzyna, Larsen, Kirk, Matthews, Mary, Mukamel, Shaul, O'Neal, Jordan, Penfold, Thomas, Thierstein, Emily, Tisch, John, Turner, James, Vogwell, Joshua, Driver, Taran, Berrah, Nora, Lin, Ming-Fu, Dakovski, Georgi, Moeller, Stefan, Cryan, James, Marinelli, Agostino, Picon, Antonio, Marangos, Jon
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Sprache:eng
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Zusammenfassung:We report the measurement of impulsive stimulated x-ray Raman scattering in neutral liquid water. An attosecond pulse drives the excitations of an electronic wavepacket, which comprises two steps: a transition to core-excited states near the oxygen atoms accompanied by transition to a valence-excited states. Thus, the wavepacket is impulsively created at a specific atomic site within a few hundred attoseconds through a non-linear interaction between the water and the x-ray pulse. We observe this nonlinear signature in an intensity dependent Stokes Raman sideband at 526 eV. Our measurements are supported by our state-of-the-art calculations based on the polarisation response of water dimers in bulk solvation and propagation of attosecond x-ray pulses at liquid density.
DOI:10.5061/dryad.dv41ns26m