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@PHDTHESIS{Yang:825919,
      author       = {Yang, Xiaosheng},
      othercontributors = {Tautz, Frank Stefan and Stadtmüller, Benjamin},
      title        = {{I}nvestigating the interaction between π-conjugated
                      organic molecules and metal surfaces with photoemission
                      tomography},
      school       = {RWTH Aachen University},
      type         = {Dissertation},
      address      = {Aachen},
      publisher    = {RWTH Aachen University},
      reportid     = {RWTH-2021-08602},
      pages        = {1 Online-Ressource : Illustrationen},
      year         = {2021},
      note         = {Veröffentlicht auf dem Publikationsserver der RWTH Aachen
                      University; Dissertation, RWTH Aachen University, 2021},
      abstract     = {Photoemission tomography (PT) is a combined experimental
                      and theoretical technique applied to molecule–metal
                      interfaces which uses angle-resolved photoemission
                      spectroscopy over a wide angular range, while the
                      photoelectron angular distributions in reciprocal space
                      (momentum maps, or called k-maps) are interpreted in terms
                      of the molecular orbital structure of the initial state.
                      This thesis uses PT to investigate various aspects of the
                      interaction between π-conjugated organic molecular
                      adsorbates and metal surfaces: PT was successfully used to
                      identify the exact products of chemical reactions at
                      surfaces and their local bonding. The measured k-maps
                      confirm a modification of the orbital structure of
                      dibromo-bianthracene on Cu(110) in the thermal reaction and
                      the fully hydrogenated bisanthene is found to be the correct
                      reaction intermediate. To decouple molecular adsorbates from
                      the metal substrate, PT was employed to gauge whether charge
                      is transferred through the interface. Oxygen adsorbed on the
                      Cu(100) surface immobilizes the surface electrons in the
                      Cu–O covalent bonds, thus achieving electronic and
                      physical decoupling of perylene-tetracarboxylic-dianhydride
                      as determined by combined results of PT and normal incidence
                      X-ray standing waves. A special example of an electronically
                      inhomogeneous unary molecular layer on a metal surface is
                      showcased in the saturated monolayer of tetracene on
                      Ag(110). With the help of PT, two highest occupied molecular
                      orbital peaks in the photoemission spectra were found,
                      indicating that two molecular species coexist in the
                      tetracene layer. While one molecule remains neutral, another
                      is charged. Finally, we applied PT to study photoelectron
                      angular distributions for highly-hybridized molecule–metal
                      systems, monolayers of p-sexiphenyl, p-quinquephenyl, and
                      pentacene on Cu(110) and on Ag(110), respectively. In k-maps
                      measured for the lowest unoccupied molecular orbital , PT
                      has identified the scattering of either the Shockley surface
                      states or the states around the projected bulk band gap. The
                      scattering vectors can be directly related to reciprocal
                      lattice vectors of the overlayer structure.},
      cin          = {134110 / 130000},
      ddc          = {530},
      cid          = {$I:(DE-82)134110_20140620$ / $I:(DE-82)130000_20140620$},
      typ          = {PUB:(DE-HGF)11},
      doi          = {10.18154/RWTH-2021-08602},
      url          = {https://publications.rwth-aachen.de/record/825919},
}