<?xml version="1.0" encoding="UTF-8"?>
<resource xmlns="http://datacite.org/schema/kernel-4" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://datacite.org/schema/kernel-4 http://schema.datacite.org/meta/kernel-4.1/metadata.xsd">
  <identifier identifierType="DOI">10.18453/rosdok_id00004614</identifier>
  <creators>
    <creator>
      <creatorName nameType="Personal">Cisneros, Sebastian</creatorName>
      <givenName>Sebastian</givenName>
      <familyName>Cisneros</familyName>
      <nameIdentifier nameIdentifierScheme="GND" schemeURI="http://d-nb.info/gnd/">http://d-nb.info/gnd/1333898908</nameIdentifier>
    </creator>
  </creators>
  <titles>
    <title>Structure-reactivity relationships in heterogeneous catalytic CO2 hydrogenation to CH4 and CO on low loaded precious metal catalysts</title>
  </titles>
  <publisher>Universität Rostock</publisher>
  <publicationYear>2023</publicationYear>
  <resourceType resourceTypeGeneral="Text" />
  <subjects>
    <subject xml:lang="en" schemeURI="http://dewey.info/" subjectScheme="dewey">540 Chemistry &amp; allied sciences</subject>
  </subjects>
  <dates>
    <date dateType="Created">2023</date>
  </dates>
  <language>en</language>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="PURL">https://purl.uni-rostock.de/rosdok/id00004614</alternateIdentifier>
    <alternateIdentifier alternateIdentifierType="URN">urn:nbn:de:gbv:28-rosdok_id00004614-6</alternateIdentifier>
  </alternateIdentifiers>
  <descriptions>
    <description descriptionType="Abstract">The production of CH4 and CO via CO2 hydrogenation was studied on catalysts with low precious metal loading. CO2 methanation was investigated on Ru/TiO2 und Ru/ZrO2 catalysts with Ru &lt; 1 wt.%. CO production was investigated on Au/ZrO2 and Au/TiO2 catalysts with &lt; 0.1 wt.% Au. Notably the most O-defective catalysts showed the highest rates. In-situ spectroscopic assessments revealed distinct electronic metal-support interactions induced by electron transfer from the defects to the supported metal entities. This effect is proposed as driver for the catalytic enhancement.</description>
  </descriptions>
</resource>
