Photoelectron Diffraction Imaging of a Molecular Breakup Using an X-Ray Free-Electron Laser

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 fr...

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Veröffentlicht in:Physical review. X 2020-06, Vol.10 (2), p.021052, Article 021052
Hauptverfasser: 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
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Sprache:eng
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Zusammenfassung: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 anO2molecule. By measuring the molecular-frame photoelectron emission patterns for a two-photon sequentialK-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.
ISSN:2160-3308
2160-3308
DOI:10.1103/PhysRevX.10.021052