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个人信息Personal Information
教授
博士生导师
硕士生导师
性别:女
毕业院校:中科院大连化学物理研究所
学位:博士
所在单位:环境学院
学科:环境科学与工程. 环境工程. 环境科学
办公地点:环境楼B511
电子邮箱:quzhenping@dlut.edu.cn
Enhancement of toluene oxidation performance over Pt/MnO2@Mn3O4 catalyst with unique interfacial structure
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论文类型:期刊论文
发表时间:2020-02-15
发表刊物:APPLIED SURFACE SCIENCE
收录刊物:EI、SCIE
卷号:503
ISSN号:0169-4332
关键字:Pt/MnO2@Mn3O4 catalyst; In situ synthesis; Three-phase interface; Strong metal-support interaction; Toluene oxidation
摘要:Bi-component MnO2 and Mn3O4 supported Pt catalyst (Pt/MnO2@Mn3O4-I) with low Pt loading (0.25 wt%) was synthesized by a facile in situ liquid-phase reduction strategy. The synchronous reduction of segmental MnO2 and Pt precursor by NaBH4 during the preparation process formed a novel interfacial structure in the catalyst. From the results of XRD, HRTEM and XPS, it was found that Pt nanoparticles were highly dispersed on interface of MnO2@Mn3O4 and the unique three-phase interfacial structure of Pt and MnO2@Mn3O4 existed in Pt/MnO2@Mn3O4-I. Meanwhile, the obtained Pt/MnO2@Mn3O4-I catalyst showed excellent catalytic activity for toluene oxidation, which was better than that of single manganese oxide supported Pt catalysts (Pt/MnO2, Pt/Mn3O4), and toluene could be completely oxidized into H2O and CO2 at 160 degrees C under the weight hourly space velocity (WHSV) of 22500 mL g(-1)h(-1). Higher proportions of Pt-o and fine interaction between Pt and MnO2@Mn3O4 at the interface were responsible for the superior catalytic activity and stability of the catalyst. Thus, it was suggested that the in situ fabrication of bi-component manganese oxides supported Pt catalysts with special interfacial structure was a feasible way to enhance toluene catalytic oxidation performances.