<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Allan, Michael</dc:creator>
  <dc:creator>Čurík, Roman</dc:creator>
  <dc:creator>Čársky, Petr</dc:creator>
  <dc:date>2019-08-13</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">We present calculated and measured elastic and vibrational excitation cross sections  in benzene with the objective to assess the reliability of the theoretical method and to  shed more light on how the electronic motion of the incoming electron is coupled with  the nuclear motion of the vibrations. The calculation employed the discrete  momentum representation method which involves solving the two-channel Lippmann- Schwinger equation in the momentum space. The electron-molecule interaction was  described by the exact static-exchange potential extended by a density-functional  theory correlation-polarization interaction that models the molecular response in the  field of the incoming electron. Cross sections were calculated for all 20 vibrational  modes from near threshold until 20 eV. They were convoluted with a simulated  instrumental profile for comparison with electron energy-loss spectra or appropriately  summed for overlapping vibrations for comparison with measured cross sections  plotted as a function of electron energy. An electron spectrometer with hemispherical  analyzers was employed for the measurements. Good agreement of theory with  experiment was obtained for the spectral profiles at 8 eV, and a nearly quantitative  agreement was obtained at 3 and 4.8 eV. The theoretical results provided new insight  into the excitation process, and it showed that more modes are excited than predicted  by simple symmetry rules. Spectra showing the details of boomerang structure in the  1.15 eV π* resonance were recorded and are presented, although this aspect of  experiment cannot be compared with the current theory.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/308197</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/308197/files/all_cen.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1063/1.5110677</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>The Journal of Chemical Physics. - 2019, vol. 151, no. 6, p. 064119</dc:source>
  <dc:subject>info:eu-repo/classification/udc/54</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Coupling of electronic and nuclear motion in a negative ion resonance: Experimental and theoretical study of benzene</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
