<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>Błachucki, Wojciech</dc:creator>
  <dc:creator>Szlachetko, Jakub</dc:creator>
  <dc:creator>Kayser, Yves</dc:creator>
  <dc:creator>Dousse, Jean-Claude</dc:creator>
  <dc:creator>Hoszowska, Joanna</dc:creator>
  <dc:creator>Zeeshan, Faisal</dc:creator>
  <dc:creator>Sá, Jacinto</dc:creator>
  <dc:date>2017-11-15</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">In the present work high energy resolution off-resonant X-ray spectroscopy (HEROS)  was employed at a synchrotron to study a silica supported Ta(V) bisalkyl catalyst  activated in hydrogen. The Ta Lα1 HEROS spectra were measured during oxidation of  the starting complex and the relative species’ concentration was successfully retrieved  as a function of time using the fingerprint HEROS spectra measured for the  unoxidized and the oxidized catalyst. Based on the experimental data and theory- based calculations, it was shown that oxidation of the active Ta catalyst leads to the  formation of mono- and di-meric species on the SiO2 surface. The obtained results  were compared to those of the previously reported time-resolved HEROS study on an  inactive silica supported Ta(V) bisalkyl catalyst’s concentration evolution during its  oxidation Błachucki et al. (2015). The study allowed observation of an immediate  transition of the active Ta catalyst from its unoxidized form to the oxidized one. This  finding is dissimilar to the result of the study on the inactive Ta catalyst, where the  oxidation led through an intermediate step.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/306288</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/306288/files/dou_ish.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1016/j.nimb.2016.11.029</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Nuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms. - 2017, vol. 411, no. Supplement C, p. 63–67</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Synchrotron radiationTime-resolved high energy resolution off-resonant X-ray spectroscopyCatalysts</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/53</dc:subject>
  <dc:title xmlns:ns2="xml" ns2:lang="en">In situ high energy resolution off-resonant spectroscopy applied to a time-resolved study of single site Ta catalyst during oxidation</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
