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Metal oxide/CeO(2) nanocomposites derived from Ce-benzene tricarboxylate (Ce-BTC) adsorbing with metal acetylacetonate complexes for catalytic oxidation of carbon monoxide

Herein, a series of metal oxide/CeO(2) (M/CeO(2)) nanocomposites derived from Ce-benzene tricarboxylate (Ce-BTC) adsorbing with different metal acetylacetonate complexes were prepared for CO oxidation under four different CO gas atmospheres. It was demonstrated that Cu/CeO(2) exhibited the highest c...

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Detalles Bibliográficos
Autores principales: Cai, Dongren, Chen, Bin, Huang, Zhongliang, Zeng, Xiaoli, Xiao, Jingran, Zhou, Shu-Feng, Zhan, Guowu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9034050/
https://www.ncbi.nlm.nih.gov/pubmed/35479346
http://dx.doi.org/10.1039/d1ra03319k
Descripción
Sumario:Herein, a series of metal oxide/CeO(2) (M/CeO(2)) nanocomposites derived from Ce-benzene tricarboxylate (Ce-BTC) adsorbing with different metal acetylacetonate complexes were prepared for CO oxidation under four different CO gas atmospheres. It was demonstrated that Cu/CeO(2) exhibited the highest catalytic activity and stability in CO oxidation. Remarkably, both O(2) selectivity and CO selectivity to CO(2) are 100% in most of the investigated conditions. Several analytical tools such as N(2) adsorption–desorption and powder X-ray diffraction, were employed to characterize the prepared catalysts. In addition, the excellent catalytic performance of Cu/CeO(2) in CO oxidation was revealed by H(2) temperature-program reduction experiment, X-ray photoelectron spectroscopy, and in situ diffuse reflectance infrared Fourier transform spectroscopy. The result showed that high oxygen vacancy and high CO adsorption capacity (Cu(+)–CO) caused by the electron exchanges of Cu(2+)/Cu(+) and Ce(3+)/Ce(4+) pairs (Ce(4+) + Cu(+) ⇆ Ce(3+) + Cu(2+)) are two key factors contributing to the high oxidation performance of Cu/CeO(2) catalyst.