氮氧化物
催化作用
活动站点
化学
协调数
硫酸盐
选择性催化还原
纳米技术
材料科学
有机化学
燃烧
离子
作者
Lupeng Han,Xiyang Wang,Fuli Wang,Yongjie Shen,Hengxiang Zhang,Weiwei Hu,Min Gao,Yimin A. Wu,MING XIE,Jianfu Chen,Dengsong Zhang,Lupeng Han,Xiyang Wang,Fuli Wang,Yongjie Shen,Hengxiang Zhang,Weiwei Hu,Min Gao,Yimin A. Wu,MING XIE
标识
DOI:10.1021/acs.est.4c11440
摘要
Nowadays, it is challenging to achieve SO2-tolerant environmental catalysis for NOx reduction because of the thermodynamically favorable transformation of reactive sites to inactive sulfate species in the presence of SO2. Herein, we achieve enhanced low-temperature SO2-tolerant NOx reduction by manipulating the dynamic coordination environment of active sites. Engineered by coordination chemistry, SiO2-CeO2 composite oxides with a short-range ordered Ce-O-Si structure were elaborately constructed on a TiO2 support. A dynamic coordination environment of active sites is demonstrated from a Ce-O-Si local structure to a low-coordinated Ce-SO42- species in the presence of SO2. The low-coordinated Ce-SO42- species as new active sites maintain a high NO removal efficiency by preserving the good adsorption and activation capacity of NO and NH3 reactants. This work proposes a new notion to improve the SO2 resistance of catalysts by regulating the coordination environment of sulfated active sites, which is of significance for SO2-tolerant environmental catalysis in practical applications.
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