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@PHDTHESIS{Mller:230028,
      author       = {Müller, Mirko},
      othercontributors = {Tautz, Stefan},
      title        = {{S}trukturelle und chemische {C}harakterisierung von
                      selbst-assemblierten {M}onolagen organischer {M}oleküle auf
                      {O}berflächen},
      volume       = {66},
      address      = {Jülich},
      publisher    = {Forschungszentrum Jülich, Zentralbibliothek},
      reportid     = {RWTH-CONV-144811},
      series       = {Schriften des Forschungszentrums Jülich : Reihe
                      Schlüsseltechnologien},
      pages        = {168 S. : Ill., graph. Darst.},
      year         = {2013},
      note         = {Zugl.: Aachen, Techn. Hochsch., Diss., 2013},
      abstract     = {In this thesis self-assembled monolayers (SAM) of
                      4(4´methylbiphenyl4yl)butane 1thiol (BP4) on a gold(111)
                      surface were fabricated. The deposited amount of molecules
                      could be adjusted very precisely, using an upstream vessel.
                      Two coverage depending phases could be observed: the
                      alpha-Phase and the delta-phase. The letter has a lower
                      areal density. BP4 adsorbs on a gold(111) surface in an
                      Au-S-C-angle of 104° due to the sp3 hybridization of
                      sulfur. Starting from a coverage of 0.07 island formation of
                      the delta-phase occurs. The unit cell can be described with
                      an unit cell. the film thickness is 6.4 Å. Two
                      perpendicular glide planes parallel to the unit cell axes
                      give rise to systematically vanishing LEED-Spots. At a
                      coverage of 0.16 a homogenous film of the delta-phase
                      exists. Adsorbing additional molecules leads to a disordered
                      phase. At a coverage of 0.33 a chemisorbed monolayer is
                      achieved. Only few weakly physisorbed molecules can be
                      additionally deposited. Short time heating at 330 K leads to
                      desorption of these molecules. The chemisorbed molecules
                      desorb at temperatures between 340 and 380 K (DeltaH: AuS ~
                      184 kJ/mol). Higher temperatures lead to dissociation of the
                      BP4 molecules (DeltaH: CS = 289 kJ/mol). Heating between 340
                      and 380 K also leads to a deformation of the Au-S-C-angle
                      from 104° to 144°. Therefore the molecules can arrange in
                      the alpha-Phase. The more upright standing molecules give
                      rise to a stronger intermolecular interaction. A homogenous
                      chemisorbed monolayer of the alpha-phase exist at a coverage
                      of 0.33. It can be described with an unit cell consisting of
                      16 molecules. The film thickness is 13.4 Å and thereby
                      twice as much as in the delta-phase. At coverages between
                      0.19 and 0.22 both Phases can coexist. The transition from
                      the alpha-Phase to the delta-Phase is thermic irreversible.
                      Both phases can be distinct by their S2p binding energy. Due
                      to the deformation of the Au-S-C-angle the electron density
                      at the sulfur is higher in the alpha-phase. Therefore the
                      S2p binding energy is higher in the alpha-phase. Further
                      phases of BP4 on gold(111) could not be observed. Hence it
                      is assumed that the previously observed beta- and
                      gamma-phases are contaminated. The volume density of both
                      observed phases is nearly the same: rho(alpha) = 1,46 g/cm3
                      vs. rho(delta) = 1,50 g/cm3. The molecules in the
                      alpha-phase are standing more upright. Therefore it is
                      assumed, that there is a better intermolecular interaction
                      in the alpha-phase. For this reason it can be assumed, that
                      the electronic properties are different in both phases.},
      keywords     = {CVD-Verfahren (SWD) / Röntgen-Photoelektronenspektroskopie
                      (SWD) / LEED (SWD) / Monoschicht (SWD)},
      cin          = {130000 / 134110},
      ddc          = {530},
      cid          = {$I:(DE-82)130000_20140620$ / $I:(DE-82)134110_20140620$},
      typ          = {PUB:(DE-HGF)11 / PUB:(DE-HGF)3},
      urn          = {urn:nbn:de:hbz:82-opus-46947},
      url          = {https://publications.rwth-aachen.de/record/230028},
}