双金属片
X射线光电子能谱
催化作用
材料科学
沸石咪唑盐骨架
钴
氧化钴
傅里叶变换红外光谱
透射电子显微镜
化学工程
拉曼光谱
扫描电子显微镜
铈
甲苯
程序升温还原
无机化学
化学
金属有机骨架
纳米技术
物理化学
吸附
有机化学
物理
光学
工程类
复合材料
作者
Wei Fang,Jinghuan Chen,Xiangyuan Zhou,Jianjun Chen,Zhiping Ye,Junhua Li
标识
DOI:10.1021/acs.iecr.9b07028
摘要
In this work, a core–shell structured CeO2@Co3O4 catalyst was successfully prepared by using a zeolitic imidazolate framework-based material as a sacrificial template. The structure, morphology, and physicochemical characteristics of these materials were investigated by X-ray diffraction, N2 sorption, Fourier transform infrared spectroscopy, Raman spectroscopy, field emission scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, temperature-programmed desorption, and temperature-programmed reduction studies. Compared with pure Co3O4 and CeO2, the CeO2@Co3O4 sample displayed superior catalytic performance (T90 = 225 °C) toward toluene oxidation. Results demonstrated that the CeO2@Co3O4 sample exhibited a core–shell structure, with hierarchically wrinkled surfaces. This unique structure, especially the interface between the core and the shell, endowed the CeO2@Co3O4 catalyst with better activity. In addition, there was a synergistic effect between cerium and cobalt oxides in the core–shell bimetallic sample, which was responsible for the improved performance of the material. Moreover, surface-active oxygen species involved and played a significant role in toluene oxidation.
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