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Photoelectron Diffraction Imaging of a Molecular Breakup Using an X-Ray Free-Electron Laser
- Kastirke, Gregor;
- Schöffler, Markus S;
- Weller, Miriam;
- Rist, Jonas;
- Boll, Rebecca;
- Anders, Nils;
- Baumann, Thomas M;
- Eckart, Sebastian;
- Erk, Benjamin;
- De Fanis, Alberto;
- Fehre, Kilian;
- Gatton, Averell;
- Grundmann, Sven;
- Grychtol, Patrik;
- Hartung, Alexander;
- Hofmann, Max;
- Ilchen, Markus;
- Janke, Christian;
- Kircher, Max;
- Kunitski, Maksim;
- Li, Xiang;
- Mazza, Tommaso;
- Melzer, Niklas;
- Montano, Jacobo;
- Music, Valerija;
- Nalin, Giammarco;
- Ovcharenko, Yevheniy;
- Pier, Andreas;
- Rennhack, Nils;
- Rivas, Daniel E;
- Dörner, Reinhard;
- Rolles, Daniel;
- Rudenko, Artem;
- Schmidt, Philipp;
- Siebert, Juliane;
- Strenger, Nico;
- Trabert, Daniel;
- Vela-Perez, Isabel;
- Wagner, Rene;
- Weber, Thorsten;
- Williams, Joshua B;
- Ziolkowski, Pawel;
- Schmidt, Lothar Ph H;
- Czasch, Achim;
- Trinter, Florian;
- Meyer, Michael;
- Ueda, Kiyoshi;
- Demekhin, Philipp V;
- Jahnke, Till
- et al.
Published Web Location
https://doi.org/10.1103/physrevx.10.021052Abstract
A central motivation for the development of x-ray free-electron lasers has been the prospect of time-resolved single-molecule imaging with atomic resolution. Here, we show that x-ray photoelectron diffraction - where a photoelectron emitted after x-ray absorption illuminates the molecular structure from within - can be used to image the increase of the internuclear distance during the x-ray-induced fragmentation of an O2 molecule. By measuring the molecular-frame photoelectron emission patterns for a two-photon sequential K-shell ionization in coincidence with the fragment ions, and by sorting the data as a function of the measured kinetic energy release, we can resolve the elongation of the molecular bond by approximately 1.2 a.u. within the duration of the x-ray pulse. The experiment paves the road toward time-resolved pump-probe photoelectron diffraction imaging at high-repetition-rate x-ray free-electron lasers.
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