2020
DOI: 10.1016/j.mtener.2020.100557
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Low-temperature synthesis of PdO-CeO2/C toward efficient oxygen reduction reaction

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Cited by 14 publications
(6 citation statements)
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“…All voltages mentioned below were referred to the 4b). 54 Only the Pd-O reduction peak (0.70 V) was observed in the N 2 -saturated electrolyte, confirming an apparent Pd-O reduction and surface oxygenation on the catalyst. Note that the current density of the Pd-O reduction peak in CV curves for PdNiMnO-PF is significantly higher than that for PdNiO-PF and PdNiMn metal porous film (PdNiMn-MPF, Fig.…”
Section: Papermentioning
confidence: 82%
“…All voltages mentioned below were referred to the 4b). 54 Only the Pd-O reduction peak (0.70 V) was observed in the N 2 -saturated electrolyte, confirming an apparent Pd-O reduction and surface oxygenation on the catalyst. Note that the current density of the Pd-O reduction peak in CV curves for PdNiMnO-PF is significantly higher than that for PdNiO-PF and PdNiMn metal porous film (PdNiMn-MPF, Fig.…”
Section: Papermentioning
confidence: 82%
“…[27] The close interfacial binding and complex hierarchical structure of MEA-oxide-carbon is difficult to achieve using conventional wet chemistry or thermal reduction methods featuring low synthesis temperature (<600 K). [28][29][30][31] Note that the formation of MEA generally requires high temperature due to drastically physicochemical differences for each element. In comparison, our approach realizes the stable configuration of MEA-oxidecarbon as promising catalysts in a rapid and scalable manner.…”
Section: Resultsmentioning
confidence: 99%
“…Unlike the previous chemical oxidation of Pd to PdO at 500 °C, Pd is electrochemically oxidized to PdO in pairs with CeO 2 /CeO 2− x at 250 °C. 198 Compared with commercial Pt/C, PdO–CeO 2 /C exhibits excellent ORR activity in alkaline media, with a significant mass activity of 1103 mA mg Pd −1 (relative to reversible hydrogen electrodes at 0.9 V), which is 5.9 times higher than commercial Pt/C. DFT shows that the high ORR activity may be due to the appropriate oxygen adsorption strength at the PdO–CeO 2 interface.…”
Section: Electrochemical Applicationsmentioning
confidence: 95%