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@ARTICLE{Rebholz:472030,
      author       = {Rebholz, Marc and Ding, Thomas and Aufleger, Lennart and
                      Hartmann, Maximilian and Meyer, Kristina and Stooß, Veit
                      and Magunia, Alexander and Wachs, David and Birk, Paul and
                      Mi, Yonghao and Borisova, Gergana Dimitrova and da Costa
                      Castanheira, Carina and Rupprecht, Patrick and
                      Magrakvelidze, Maia and Thumm, Uwe and Roling, Sebastian and
                      Butz, Marco and Zacharias, Helmut and Düsterer, Stefan and
                      Treusch, Rolf and Brenner, Günter and Ott, Christian and
                      Pfeifer, Thomas},
      title        = {{XUV}-{I}nitiated {D}issociation {D}ynamics of {M}olecular
                      {O}xygen ({O}$_2$)},
      journal      = {The journal of physical chemistry / A},
      volume       = {125},
      issn         = {1089-5639},
      address      = {Washington, DC},
      publisher    = {Soc.},
      reportid     = {PUBDB-2021-04797},
      pages        = {10138−10143},
      year         = {2021},
      abstract     = {We performed a time-resolved spectroscopy experixment on
                      the dissociation of oxygen molecules after the
                      interactionwith intense extreme-ultraviolet (XUV) light from
                      the free-electronlaser in Hamburg at Deutsches
                      Elektronen-Synchrotron. Using anXUV-pump/XUV-probe
                      transient-absorption geometry with asplit-and-delay unit, we
                      observe the onset of electronic transitionsin the O$^{2+}$
                      cation near 50 eV photon energy, marking the end ofthe
                      progression from a molecule to two isolated atoms. We
                      observetwo different time scales of 290 ± 53 and 180 ± 76
                      fs for theemergence of different ionic transitions,
                      indicating differentdissociation pathways taken by the
                      departing oxygen atoms.With regard to the emerging
                      opportunities of tuning the centralfrequencies of pump and
                      probe pulses and of increasing the probe−pulse bandwidth,
                      future pump−probe transient-absorptionexperiments are
                      expected to provide a detailed view of the coupled nuclear
                      and electronic dynamics during molecular dissociation},
      cin          = {DOOR ; HAS-User / FS-FLASH-D / MPG / FS-FLASH-B /
                      FS-FLASH-O},
      ddc          = {530},
      cid          = {I:(DE-H253)HAS-User-20120731 /
                      I:(DE-H253)FS-FLASH-D-20160930 / I:(DE-H253)MPG-20120806 /
                      I:(DE-H253)FS-FLASH-B-20160930 /
                      I:(DE-H253)FS-FLASH-O-20160930},
      pnm          = {631 - Matter – Dynamics, Mechanisms and Control
                      (POF4-631) / 6G2 - FLASH (DESY) (POF4-6G2)},
      pid          = {G:(DE-HGF)POF4-631 / G:(DE-HGF)POF4-6G2},
      experiment   = {EXP:(DE-H253)F-BL2-20150101},
      typ          = {PUB:(DE-HGF)16},
      pubmed       = {34788037},
      UT           = {WOS:000727425100004},
      doi          = {10.1021/acs.jpca.1c06033},
      url          = {https://bib-pubdb1.desy.de/record/472030},
}