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作 者:李金兵[1] 姜志全[2] 王坤[2] 黄伟新[2]
机构地区:[1]中国石化北京北化院燕山分院,北京102500 [2]中国科学技术大学合肥微尺度物质科学国家实验室(筹)中国科学院能量转换材料重点实验室化学物理系,合肥230026
出 处:《Chinese Journal of Chemical Physics》2012年第1期103-109,I0004,共8页化学物理学报(英文)
摘 要:Co3O4/SiO2 catalysts for CO oxidation were prepared by conventional incipient wetness impregnation followed by calcination at various temperatures. Their structures were char- acterized with X-ray diffraction (XRD), laser Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), temperature-programmed reduction (TPR) and X-ray absorption fine structure (XAFS) spectroscopy. Both XRD and Raman spectroscopy only detect the existence of Co3O4 crystallites in all catalysts. However, XPS results indicate that excess Co2+ ions are present on the surface of Co3O4 in Co3O4(200)/Si02 as compared with bulk Co3O4. Meanwhile, TPR results suggest the presence of surface oxygen vacancies on Co3O4 in Co3O4(200)/SiO2, and XAFS results demonstrate that Co3O4 in Co3O4(200)/SIO2 contains excess Co2+. Increasing calcination temperature results in oxidation of excess Co2+ and the decrease of the concentration of surface oxygen vacancies, consequently the for- mation of stoichiometric Co3O4 on supported catalysts. Among all Co3O4/SiO2 catalysts, Co3O4(200)/SiO2 exhibits the best catalytic performance towards CO oxidation, demonstrating that excess Co2+ and surface oxygen vacancies can enhance the catalytic activity of Co3O4 towards CO oxidation. These results nicely demonstrate the effect of calcination temperature on the structure and catalytic performance towards CO oxidation of silicasupported Co3O4 catalysts and highlight the important role of surface oxygen vacancies on Co3O4.
关 键 词:Co3O4/8iO2 catalyst CO oxidation Calcination temperature Surface oxygen vacancies
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