Catalytic oxidation of CO over mesoporous copper-doped ceria catalysts via a facile CTAB-assisted synthesis. Issue 27 (19th April 2018)

• Record Type: Journal Article
• Authors: Zhu, Hongjian; Chen, Yingying; Wang, Zhongpeng; Liu, Wei; Wang, Liguo
• Is Part Of: RSC advances. Volume 8:Issue 27(2018)
• Page Start: 14888
• Page End: 14897
• Publication Date: 2018-04-19
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c8ra02327a
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : Surface Cu–O–Ce species can be reduced by CO and active oxygen can easily react with Cu + –CO to form CO2 . Abstract : Nanosized copper-doped ceria CuCe catalysts with a large surface area and well-developed mesoporosity were synthesized by a surfactant-assisted co-precipitation method. The prepared catalysts with different Cu doping concentrations were characterized by XRD, DLS analysis, TEM, BET, Raman, H2 -TPR and in situ DRIFTS techniques. The influence of Cu content on their catalytic performance for CO oxidation was also studied. The XRD results indicate that at a lower content, the Cu partially incorporates into the CeO2 lattice to form a CuCe solid solution, whereas a higher Cu doping causes the formation of bulk CuO. Copper doping favors an increase in the surface area of the CuCe catalysts and the formation of oxygen vacancies, thereby improving the redox properties. The CuCe samples exhibit higher catalytic performance compared to bare CeO2 and CuO catalysts. This is ascribed to the synergistic interaction between copper oxide and ceria. In particular, the Cu0.1 Ce catalyst shows the highest catalytic performance ( T 50 = 59 °C), as well as excellent stability. The in situ DRIFTS results show that CO adsorbed on surface Cu + (Cu + –CO species) can easily react with the active oxygen, while stronger adsorption of carbonate-like species causes catalyst deactivation during the reaction.