1. Femtosecond-resolved observation of the fragmentation of buckminsterfullerene following X-ray multiphoton ionization
- Author
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Berrah, N., Sanchez-Gonzalez, A., Jurek, Z., Obaid, R., Xiong, H., Squibb, R. J., Osipov, T., Lutman, A., Fang, L., Barillot, T., Bozek, J. D., Cryan, J., Wolf, T. J. A., Rolles, D., Coffee, R., Schnorr, K., Augustin, S., Fukuzawa, H., Motomura, K., Niebuhr, N., Frasinski, L. J., Feifel, R., Schulz, C. P., Toyota, K., Son, S.-K., Ueda, K., Pfeifer, T., Marangos, J. P., and Santra, R.
- Abstract
X-ray free-electron lasers have, over the past decade, opened up the possibility of understanding the ultrafast response of matter to intense X-ray pulses. In earlier research on atoms and small molecules, new aspects of this response were uncovered, such as rapid sequences of inner-shell photoionization and Auger ionization. Here, we studied a larger molecule, buckminsterfullerene (C60), exposed to 640 eV X-rays, and examined the role of chemical effects, such as chemical bonds and charge transfer, on the fragmentation following multiple ionization of the molecule. To provide time resolution, we performed femtosecond-resolved X-ray pump/X-ray probe measurements, which were accompanied by advanced simulations. The simulations and experiment reveal that despite substantial ionization induced by the ultrashort (20 fs) X-ray pump pulse, the fragmentation of C60is considerably delayed. This work uncovers the persistence of the molecular structure of C60, which hinders fragmentation over a timescale of hundreds of femtoseconds. Furthermore, we demonstrate that a substantial fraction of the ejected fragments are neutral carbon atoms. These findings provide insights into X-ray free-electron laser-induced radiation damage in large molecules, including biomolecules.
- Published
- 2019
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