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@ARTICLE{Aeschlimann:618790,
      author       = {Aeschlimann, Martin and Bange, Jan Philipp and Bauer,
                      Michael and Bovensiepen, Uwe and Elmers, Hans-Joachim and
                      Fauster, Thomas and Gierster, Lukas and Höfer, Ulrich and
                      Huber, Rupert and Li, Andi and Li, Xintong and Mathias,
                      Stefan and Morgenstern, Karina and Petek, Hrvoje and
                      Reutzel, Marcel and Rossnagel, Kai and Schoenhense, Gerd and
                      Scholz, Markus and Stadtmüller, Benjamin and Stähler,
                      Julia and Tan, Shijing and Wang, Bing and Wang, Zehua and
                      Weinelt, Martin},
      title        = {{T}ime-resolved photoelectron spectroscopy at surfaces},
      journal      = {Surface science},
      volume       = {753},
      issn         = {0039-6028},
      address      = {Amsterdam},
      publisher    = {Elsevier},
      reportid     = {PUBDB-2024-07151},
      pages        = {122631},
      year         = {2025},
      note         = {Waiting for fulltext},
      abstract     = {Light is a preeminent spectroscopic tool for investigating
                      the electronic structure of surfaces. Time-resolved
                      photoelectron spectroscopy has mainly been developed in the
                      last 30 years. It is therefore not surprising that the topic
                      was hardly mentioned in the issue on “The first thirty
                      years” of surface science. In the second thirty years,
                      however, we have seen tremendous progress in the development
                      of time-resolved photoelectron spectroscopy on surfaces.
                      Femtosecond light pulses and advanced photoelectron
                      detection schemes are increasingly being used to study the
                      electronic structure and dynamics of occupied and unoccupied
                      electronic states and dynamic processes such as the energy
                      and momentum relaxation of electrons, charge transfer at
                      interfaces and collective processes such as plasmonic
                      excitation and optical field screening. Using spin- and
                      time-resolved photoelectron spectroscopy, we were able to
                      study ultrafast spin dynamics, electron–magnon scattering
                      and spin structures in magnetic and topological materials.
                      Light also provides photon energy as well as electric and
                      magnetic fields that can influence molecular surface
                      processes to steer surface photochemistry and
                      hot-electron-driven catalysis. In addition, we can consider
                      light as a chemical reagent that can alter the properties of
                      matter by creating non-equilibrium states and ultrafast
                      phase transitions in correlated materials through the
                      coupling of electrons, phonons and spins. Electric fields
                      have also been used to temporarily change the electronic
                      structure. This opened up new methods and areas such as high
                      harmonic generation, light wave electronics and attosecond
                      physics. This overview certainly cannot cover all these
                      interesting topics. But also as a testimony to the cohesion
                      and constructive exchange in our ultrafast community, a
                      number of colleagues have come together to share their
                      expertise and views on the very vital field of dynamics at
                      surfaces. Following the introduction, the interested reader
                      will find a list of contributions and a brief summary in
                      Section 1.3.},
      cin          = {FS-SXQM / DOOR ; HAS-User / FS-FLASH},
      ddc          = {530},
      cid          = {I:(DE-H253)FS-SXQM-20190201 / I:(DE-H253)HAS-User-20120731
                      / I:(DE-H253)FS-FLASH-20140814},
      pnm          = {632 - Materials – Quantum, Complex and Functional
                      Materials (POF4-632) / 6G2 - FLASH (DESY) (POF4-6G2) /
                      05K22FK2 - Verbundprojekt 05K2022 - 10K-THz-k-ToF: 10K
                      ToF-Impulsmikroskop für FLASH mit Terahertz Anregung und
                      Raumladungsunterdrückung. Teilprojekt 2. (BMBF-05K22FK2) /
                      05K22KE2 - Messplatz für ultraschnelle Spindynamik bei
                      FLASH (BMBF-05K22KE2) / 05K22UM4 - Verbundprojekt 05K2022 -
                      ToFPAXRIXS: In-situ Kombination von RIXS und ARPES mit
                      Flugzeit basierter Photoelektronen Detektion. Teilprojekt 1.
                      (BMBF-05K22UM4) / 05K22UM2 - Verbundprojekt 05K2022 -
                      10K-THz-k-ToF: 10K ToF-Impulsmikroskop für FLASH mit
                      Terahertz Anregung und Raumladungsunterdrückung.
                      Teilprojekt 3. (BMBF-05K22UM2) / DFG project
                      G:(GEPRIS)390677874 - EXC 2033: RESOLV (Ruhr Explores
                      Solvation) (390677874) / DFG project G:(GEPRIS)278162697 -
                      SFB 1242: Nichtgleichgewichtsdynamik kondensierter Materie
                      in der Zeitdomäne (278162697)},
      pid          = {G:(DE-HGF)POF4-632 / G:(DE-HGF)POF4-6G2 /
                      G:(DE-Ds200)BMBF-05K22FK2 / G:(DE-Ds200)BMBF-05K22KE2 /
                      G:(DE-Ds200)BMBF-05K22UM4 / G:(DE-Ds200)BMBF-05K22UM2 /
                      G:(GEPRIS)390677874 / G:(GEPRIS)278162697},
      experiment   = {EXP:(DE-H253)F-PG2-20150101},
      typ          = {PUB:(DE-HGF)16},
      UT           = {WOS:001367868300001},
      doi          = {10.1016/j.susc.2024.122631},
      url          = {https://bib-pubdb1.desy.de/record/618790},
}