Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/59197
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dc.contributor.authorAdak, Shubhadeep-
dc.contributor.authorAhmad, Md Sarfaraz-
dc.contributor.authorSadhu, Souvik-
dc.contributor.authorKhatun, Rubina-
dc.contributor.authorPrasad, V V D N-
dc.contributor.authorBal, Rajaram-
dc.date.accessioned2022-02-16T07:19:59Z-
dc.date.available2022-02-16T07:19:59Z-
dc.date.issued2022-02-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/59197-
dc.description121-126en_US
dc.description.abstractPreferential oxidation of carbon monoxide in presence of excess hydrogen is a promising alternative to restrict the CO deposition in the Pt-anode in the practical polymer electrolyte membrane fuel cell application. In the present work, nanocrystalline copper-ceria catalysts have been synthesized by hydrothermal method, wet impregnation method and urea nitrate combustion method. Their characterizations have been carried out by using X-ray diffraction, transmission electron microscopy, X . ray photoelectron spectroscopy- It has been found that Cu2+ replaced Ce4+ in cerium oxide, creating oxygen vacancy. The formation of more nano-sized CeO2 leads to more oxygen vacancies in CeO2 through the formation of interfacial Cu1+ ions, which also enhances the CO oxidation activity. Among the synthesized Cu-CeO2 catalysts, the catalyst prepared by hydrothermal method have shown both CO conversion andC O2 selectivity as 100% towards CO oxidation at 373 K in the presence of excess H2 making this catalyst viable for practical fuel cell application..en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR, Indiaen_US
dc.sourceIJC Vol.61(02) [February 2022]en_US
dc.subjectCu-CeO2en_US
dc.subjectPROXen_US
dc.subjectCuOen_US
dc.subjectCeO2en_US
dc.subjectNanoparticlesen_US
dc.subjectOxygen vacancyen_US
dc.titleComparison study of preferential oxidation of CO over nanocrystalline Cu/CeO2 catalysts synthesized by different preparation methodsen_US
dc.typeArticleen_US
Appears in Collections:IJC Vol.61(02) [February 2022]

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