近程
催化作用
高分辨率透射电子显微镜
化学吸附
吸附
微晶
氧化还原
氧气
X射线光电子能谱
解吸
吸附
材料科学
无机化学
化学
化学工程
一氧化碳
纳米技术
物理化学
结晶学
透射电子显微镜
生物化学
有机化学
工程类
作者
Shanghong Zeng,Yan Wang,Suping Ding,Jesper J. H. B. Sättler,Elena Borodina,Lu Zhang,Bert M. Weckhuysen,Haiquan Su
标识
DOI:10.1016/j.jpowsour.2014.01.098
摘要
A series of CuO/CeO2 and inverse CeO2/CuO catalysts are prepared by the surfactant-templated method and characterized via XRD, HRTEM, H2-TPR, SEM, XPS, in situ XRD, in situ UV–Vis and N2 adsorption–desorption techniques. It is found that there are two kinds of surface sites in the CuO–CeO2 system, including CuO surface sites for CO chemisorption and CeO2 surface sites with oxygen vacancies for oxygen sorption. The active sites for CO oxidation are located on the contact interface of two-kind surface sites and the lattice oxygen can make a significant contribution to the CO-PROX reaction. The resistance to H2O and CO2 is related to BET surface area, the crystallite sizes of CuO and the reduction behavior of catalysts. The Ce4Cu4 and Ce4Cu1 catalysts exhibit the best resistance against H2O and CO2.
科研通智能强力驱动
Strongly Powered by AbleSci AI