2020
DOI: 10.1016/j.mcat.2019.110704
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Role of oxygen vacancies and Mn4+/Mn3+ ratio in oxidation and dry reforming over cobalt-manganese spinel oxides

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Cited by 17 publications
(15 citation statements)
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“…These defect sites on the surface of metal oxides adsorb oxygen from the air and transform it into catalytically active species. Similarly to our results,Mitran et al recently observed that replacing of Co 3+ with Mn 4+ in Co-Mn oxides up to Mn 0.15 Co 2.85 leads to the formation of active sites for ethanol oxidation(Mitran et al, 2020). Interaction of Co 3+ and Mn 4+ with lattice oxygen created oxygen vacancies, which served as catalytically active sites.…”
supporting
confidence: 90%
“…These defect sites on the surface of metal oxides adsorb oxygen from the air and transform it into catalytically active species. Similarly to our results,Mitran et al recently observed that replacing of Co 3+ with Mn 4+ in Co-Mn oxides up to Mn 0.15 Co 2.85 leads to the formation of active sites for ethanol oxidation(Mitran et al, 2020). Interaction of Co 3+ and Mn 4+ with lattice oxygen created oxygen vacancies, which served as catalytically active sites.…”
supporting
confidence: 90%
“…In addition, the concentrations of Mn 4+ and O α species of oxidizing catalyst were crucial for the oxidative degradation of VOCs [43,49]. The order of the O β /O α follows in descending order as Mn 4+ /Mn 3+ , which was depicted as TP-Mn2Zr3 > MP-Mn2Zr3 > CP-Mn2Zr3, indicating the concentration of Mn 4+ was positively correlated with the content of oxygen vacancy [40]. In combination with the results of catalytic activity and components of active phase, the improved catalytic activity should be attributed to the promoted effects of the solid solution of Mn x Zr 1−x O 2 .…”
Section: Discussionmentioning
confidence: 96%
“…183 eV), and Mn (ca. 642 eV) (Figure 4a) [30,40]. Figure 4b shows the XPS spectra of Mn 2p; it was integrated into two characteristic peaks by deconvolution.…”
Section: Xps Analysismentioning
confidence: 99%
“…The H 2 -TPR pro les of 0.2, 0.4, 0.6, and 0.8 samples revealed shift of the lowtemperature maximum reduction to 335°C. Furthermore, the 0.5 catalyst exhibited a shoulder at about 227°C, which was tentatively ascribed to reduction of Co 4+ components(Mitran et al, 2020). Thus, the high catalytic activity of the 0.5 catalyst could be connected with its improved reduction behavior.…”
mentioning
confidence: 84%