Dataset Open Access
Rabe, Anna;
Elsherif, Ahmed Gamal Attallah;
Eggert, Benedikt;
Hirschmann, Eric;
Salamon, Soma;
Landers, Joachim;
Kämmerer, Lea;
Cosanne, Nicolas;
Koul, Adarsh;
Budiyanto, Eko;
Schuhmann, Wolfgang;
Behrens, Malte;
Wende, Heiko
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<identifier identifierType="DOI">10.14278/rodare.4326</identifier>
<creators>
<creator>
<creatorName>Rabe, Anna</creatorName>
<givenName>Anna</givenName>
<familyName>Rabe</familyName>
<affiliation>aculty of Physics and Center for Nanointegration Duisburg-Essen (CENIDE),University of Duisburg-Essen, Duisburg, Germany</affiliation>
</creator>
<creator>
<creatorName>Elsherif, Ahmed Gamal Attallah</creatorName>
<givenName>Ahmed Gamal Attallah</givenName>
<familyName>Elsherif</familyName>
<nameIdentifier nameIdentifierScheme="ORCID" schemeURI="http://orcid.org/">0000-0002-7759-0315</nameIdentifier>
</creator>
<creator>
<creatorName>Eggert, Benedikt</creatorName>
<givenName>Benedikt</givenName>
<familyName>Eggert</familyName>
<affiliation>aculty of Physics and Center for Nanointegration Duisburg-Essen (CENIDE),University of Duisburg-Essen, Duisburg, Germany</affiliation>
</creator>
<creator>
<creatorName>Hirschmann, Eric</creatorName>
<givenName>Eric</givenName>
<familyName>Hirschmann</familyName>
<nameIdentifier nameIdentifierScheme="ORCID" schemeURI="http://orcid.org/">0000-0001-5782-9627</nameIdentifier>
</creator>
<creator>
<creatorName>Salamon, Soma</creatorName>
<givenName>Soma</givenName>
<familyName>Salamon</familyName>
<affiliation>aculty of Physics and Center for Nanointegration Duisburg-Essen (CENIDE),University of Duisburg-Essen, Duisburg, Germany</affiliation>
</creator>
<creator>
<creatorName>Landers, Joachim</creatorName>
<givenName>Joachim</givenName>
<familyName>Landers</familyName>
<affiliation>aculty of Physics and Center for Nanointegration Duisburg-Essen (CENIDE),University of Duisburg-Essen, Duisburg, Germany</affiliation>
</creator>
<creator>
<creatorName>Kämmerer, Lea</creatorName>
<givenName>Lea</givenName>
<familyName>Kämmerer</familyName>
<affiliation>aculty of Physics and Center for Nanointegration Duisburg-Essen (CENIDE),University of Duisburg-Essen, Duisburg, Germany</affiliation>
</creator>
<creator>
<creatorName>Cosanne, Nicolas</creatorName>
<givenName>Nicolas</givenName>
<familyName>Cosanne</familyName>
<affiliation>nstitute for Inorganic Chemistry, Christian-Albrechts-Universität zu Kiel, Kiel24148, German</affiliation>
</creator>
<creator>
<creatorName>Koul, Adarsh</creatorName>
<givenName>Adarsh</givenName>
<familyName>Koul</familyName>
<affiliation>Analytical Chemistry – Center for Electrochemical Sciences (CES), Faculty ofChemistry and Biochemistry, Ruhr University Bochum, Bochum 44780,Germany</affiliation>
</creator>
<creator>
<creatorName>Budiyanto, Eko</creatorName>
<givenName>Eko</givenName>
<familyName>Budiyanto</familyName>
<affiliation>Max-Planck Institute für Kohlenforschung, Mülheim an der Ruhr 45470,Germany</affiliation>
</creator>
<creator>
<creatorName>Schuhmann, Wolfgang</creatorName>
<givenName>Wolfgang</givenName>
<familyName>Schuhmann</familyName>
<affiliation>Analytical Chemistry – Center for Electrochemical Sciences (CES), Faculty ofChemistry and Biochemistry, Ruhr University Bochum, Bochum 44780,Germany</affiliation>
</creator>
<creator>
<creatorName>Behrens, Malte</creatorName>
<givenName>Malte</givenName>
<familyName>Behrens</familyName>
<affiliation>nstitute for Inorganic Chemistry, Christian-Albrechts-Universität zu Kiel, Kiel24148, German</affiliation>
</creator>
<creator>
<creatorName>Wende, Heiko</creatorName>
<givenName>Heiko</givenName>
<familyName>Wende</familyName>
<affiliation>Faculty of Physics and Center for Nanointegration Duisburg-Essen (CENIDE),University of Duisburg-Essen, Duisburg, Germany</affiliation>
</creator>
</creators>
<titles>
<title>Data publication: Catalytic Activity of Cobalt Ferrites in Water Oxidation Reactions and Its Defect Dependency</title>
</titles>
<publisher>Rodare</publisher>
<publicationYear>2026</publicationYear>
<dates>
<date dateType="Issued">2026-01-06</date>
</dates>
<resourceType resourceTypeGeneral="Dataset"/>
<alternateIdentifiers>
<alternateIdentifier alternateIdentifierType="url">https://rodare.hzdr.de/record/4326</alternateIdentifier>
</alternateIdentifiers>
<relatedIdentifiers>
<relatedIdentifier relatedIdentifierType="DOI" relationType="IsReferencedBy">10.1002/cctc.202501270</relatedIdentifier>
<relatedIdentifier relatedIdentifierType="URL" relationType="IsIdenticalTo">https://www.hzdr.de/publications/Publ-42663</relatedIdentifier>
<relatedIdentifier relatedIdentifierType="URL" relationType="IsReferencedBy">https://www.hzdr.de/publications/Publ-42662</relatedIdentifier>
<relatedIdentifier relatedIdentifierType="DOI" relationType="IsVersionOf">10.14278/rodare.4325</relatedIdentifier>
<relatedIdentifier relatedIdentifierType="URL" relationType="IsPartOf">https://rodare.hzdr.de/communities/rodare</relatedIdentifier>
</relatedIdentifiers>
<rightsList>
<rights rightsURI="https://creativecommons.org/licenses/by/4.0/legalcode">Creative Commons Attribution 4.0 International</rights>
<rights rightsURI="info:eu-repo/semantics/openAccess">Open Access</rights>
</rightsList>
<descriptions>
<description descriptionType="Abstract"><p>CoFe2O4 (CFO) nanoparticles were synthesized via controlled co-precipitation with subsequent calcination at 400 &deg;C, 500 &deg;C, and 600 &deg;C to systematically investigate the influence of thermal treatment on mesostructure, catalytic performance, and especially defect landscape. Structural characterization revealed enhanced crystallinity, sintering, and reduced defect concentration with increasing calcination temperature. M&ouml;ssbauer spectroscopy and magnetometry indicated increased inversion parameters, improved magnetic alignment, and reduced spin canting, which is consistent with enhanced atomic diffusion during calcination and structural ordering. Positron annihilation lifetime spectroscopy confirmed a calcination-dependent decrease in vacancy-type defects. Catalytic testing showed diverging trends: chemical water oxidation (CAN test) activity increased with calcination temperature, but electrochemical oxygen evolution (OER) activity decreased. The opposing behavior is attributed to distinct differences in mechanism: CAN test reactivity is dominated by surface site availability, whereas OER benefits from defect mediated conductivity and charge-transfer. These results underline the pivotal role of defect engineering while tailing spinel catalysts and highlight that optimal mesostructures depend strongly on the target reaction</p></description>
</descriptions>
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