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
离子
燃烧
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
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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