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@ARTICLE{Magunia:599079,
      author       = {Magunia, Alexander and Rebholz, Marc and Appi, Elisa and
                      Papadopoulou, Christina C. and Lindenblatt, Hannes and
                      Trost, Florian and Meister, Severin and Ding, Thomas and
                      Straub, Michael and Borisova, Gergana D. and Lee, Junhee and
                      Jin, Rui and von der Dellen, Alexander and Kaiser, Christian
                      and Braune, Markus and Düsterer, Stefan and Alisauskas,
                      Skirmantas and Lang, Tino and Heyl, Christoph and
                      Manschwetus, Bastian and Grunewald, Sören and Fruehling,
                      Ulrike and Tajalli, Ayhan and Wahid, Ammar Bin and Silletti,
                      Laura and Calegari, Francesca and Mosel, Philip and Morgner,
                      Uwe and Kovacev, Milutin and Thumm, Uwe and Hartl, Ingmar
                      and Treusch, Rolf and Moshammer, Robert and Ott, Christian
                      and Pfeifer, Thomas},
      title        = {{T}ime-resolving state-specific molecular dissociation with
                      {XUV} broadband absorption spectroscopy},
      journal      = {Science advances},
      volume       = {9},
      number       = {47},
      issn         = {2375-2548},
      address      = {Washington, DC [u.a.]},
      publisher    = {Assoc.},
      reportid     = {PUBDB-2023-07145},
      pages        = {eadk1482},
      year         = {2023},
      abstract     = {The electronic and nuclear dynamics inside molecules are
                      essential for chemical reactions, where different pathways
                      typically unfold on ultrafast timescales. Extreme
                      ultraviolet (XUV) light pulses generated by free-electron
                      lasers (FELs) allow atomic-site and electronic-state
                      selectivity, triggering specific molecular dynamics while
                      providing femtosecond resolution. Yet, time-resolved
                      experiments are either blind to neutral fragments or limited
                      by the spectral bandwidth of FEL pulses. Here, we combine a
                      broadband XUV probe pulse from high-order harmonic
                      generation with an FEL pump pulse to observe dissociation
                      pathways leading to fragments in different quantum states.
                      We temporally resolve the dissociation of a specific
                      O$_2$$^+$ state into two competing channels by measuring the
                      resonances of ionic and neutral fragments. This scheme can
                      be applied to investigate convoluted dynamics in larger
                      molecules relevant to diverse science fields.},
      cin          = {DOOR ; HAS-User / FS-FLASH-O / FS-FLASH-D / FS-LA /
                      FS-ATTO},
      ddc          = {500},
      cid          = {I:(DE-H253)HAS-User-20120731 /
                      I:(DE-H253)FS-FLASH-O-20160930 /
                      I:(DE-H253)FS-FLASH-D-20160930 / I:(DE-H253)FS-LA-20130416 /
                      I:(DE-H253)FS-ATTO-20170403},
      pnm          = {631 - Matter – Dynamics, Mechanisms and Control
                      (POF4-631) / 6G2 - FLASH (DESY) (POF4-6G2) / DFG project
                      G:(GEPRIS)390837967 - EXC 2123: QuantumFrontiers - Licht und
                      Materie an der Quantengrenze (390837967) / DFG project
                      G:(GEPRIS)390900948 - EXC 2181: STRUKTUREN: Emergenz in
                      Natur, Mathematik und komplexen Daten (390900948)},
      pid          = {G:(DE-HGF)POF4-631 / G:(DE-HGF)POF4-6G2 /
                      G:(GEPRIS)390837967 / G:(GEPRIS)390900948},
      experiment   = {EXP:(DE-H253)F-FL26-20150901},
      typ          = {PUB:(DE-HGF)16},
      pubmed       = {37992169},
      UT           = {WOS:001116509200020},
      doi          = {10.1126/sciadv.adk1482},
      url          = {https://bib-pubdb1.desy.de/record/599079},
}