期刊
PHYSICAL CHEMISTRY CHEMICAL PHYSICS
卷 17, 期 24, 页码 15996-16006出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c5cp02158h
关键词
-
资金
- National Natural Science Foundation of China [21273110, 21403134]
- National Basic Research Program of China (973 Program) [2010CB732300]
- Shandong Province Development Program of Science and Technology [2014GGX102019]
- Shandong Province Advanced School Program of Science and Technology [J12LD09]
Two different precursors, manganese nitrate (MN) and manganese acetate (MA), were employed to prepare two series of catalysts, i.e., xCuyMn(N)/TiO2 and xCuyMn(A)/TiO2, by a co-impregnation method. The catalysts were characterized by XRD, LRS, CO-TPR, XPS and EPR spectroscopy. The results suggest that: (1) both xCuyMn(N)/TiO2 and xCuyMn(A)/TiO2 catalysts exhibit much higher catalytic activities than an unmodified Cu/TiO2 catalyst in the NO + CO reaction. Furthermore, the activities of catalysts modified with the same amount of manganese are closely dependent on manganese precursors. (2) The enhancement of activities for Mn-modified catalysts should be attributed to the formation of the surface synergetic oxygen vacancy (SSOV) Cu+-square-Mny+ in the reaction process. Moreover, since the formation of the SSOV (Cu+-square-Mn-3(+)) in the xCuyMn(N)/TiO2 catalyst is easier than that (Cu+-square-Mn2+) in the xCuyMn(A)/TiO2 catalyst, the activity of the xCuyMn(N)/TiO2 catalyst is higher than that of the xCuyMn(A)/TiO2 catalyst. This conclusion is well supported by the XPS and EPR results.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据