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Investigating charge-up and fragmentation dynamics of oxygen molecules after interaction with strong X-ray free-electron laser pulses
- Kastirke, G;
- Ota, F;
- Rezvan, DV;
- Schöffler, MS;
- Weller, M;
- Rist, J;
- Boll, R;
- Anders, N;
- Baumann, TM;
- Eckart, S;
- Erk, B;
- De Fanis, A;
- Fehre, K;
- Gatton, A;
- Grundmann, S;
- Grychtol, P;
- Hartung, A;
- Hofmann, M;
- Ilchen, M;
- Janke, C;
- Kircher, M;
- Kunitski, M;
- Li, X;
- Mazza, T;
- Melzer, N;
- Montano, J;
- Music, V;
- Nalin, G;
- Ovcharenko, Y;
- Pier, A;
- Rennhack, N;
- Rivas, DE;
- Dörner, R;
- Rolles, D;
- Rudenko, A;
- Schmidt, Ph;
- Siebert, J;
- Strenger, N;
- Trabert, D;
- Vela-Perez, I;
- Wagner, R;
- Weber, Th;
- Williams, JB;
- Ziolkowski, P;
- Schmidt, L Ph H;
- Czasch, A;
- Tamura, Y;
- Hara, N;
- Yamazaki, K;
- Hatada, K;
- Trinter, F;
- Meyer, M;
- Ueda, K;
- Demekhin, Ph V;
- Jahnke, T
- et al.
Published Web Location
https://doi.org/10.1039/d2cp02408jAbstract
During the last decade, X-ray free-electron lasers (XFELs) have enabled the study of light-matter interaction under extreme conditions. Atoms which are subject to XFEL radiation are charged by a complex interplay of (several subsequent) photoionization events and electronic decay processes within a few femtoseconds. The interaction with molecules is even more intriguing, since intricate nuclear dynamics occur as the molecules start to dissociate during the charge-up process. Here, we demonstrate that by analyzing photoelectron angular emission distributions and kinetic energy release of charge states of ionic molecular fragments, we can obtain a detailed understanding of the charge-up and fragmentation dynamics. Our novel approach allows for gathering such information without the need of complex ab initio modeling. As an example, we provide a detailed view on the processes happening on a femtosecond time scale in oxygen molecules exposed to intense XFEL pulses.
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