The tuned selective catalytic reduction behaviors of NO over the Pt/CeO2 catalysts by preferentially exposing different facets of CeO2 supports

被引:3
作者
Wang, Kaiqiang [1 ]
Zhang, Roujia [1 ]
Wu, Songze [1 ]
Chen, Mengyin [1 ]
Tang, Jie [1 ]
Zhao, Liming [2 ]
Liu, Yubing [1 ]
Fan, Yining [1 ]
机构
[1] Nanjing Univ, Sch Chem & Chem Engn, Nanjing 210023, Peoples R China
[2] China Jiliang Univ, Coll Standardisat, Hangzhou 310018, Peoples R China
基金
中国国家自然科学基金;
关键词
NO plus CO reaction; Pt catalyst; CeO2; support; Different exposed facet; Oxygen vacancy; PLATINUM SINGLE ATOMS; CO OXIDATION; CERIA; SHAPE; PERFORMANCE; REACTIVITY; STABILITY; KINETICS; WATER;
D O I
10.1016/j.catcom.2022.106530
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
For the Pt catalysts supported on CeO2 nanosheet (NS), nanopolyhedron (NP) and nanorod (NR) with preferentially exposed {100}, {111} and {110} facets, respectively, the NO conversion and N-2 selectivity for NO + CO reaction at 100-250 degrees C exhibit the order as Pt/CeO2-NS{100} > Pt/CeO2-NP{111} > Pt/CeO2-NR{110}. The higher surface concentration of oxygen vacancies on CeO2 (NS) can promote the dissociation of NO and result in the highest performance of Pt/CeO2-NS{100} catalyst. Moreover, CO intensively chemisorbs on the Pt2+ ions on CeO2 (NR) support, suppressing the dissociative chemisorption of NO and leading to lower reaction performance of Pt/CeO2-NR{110} catalyst.
引用
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页数:5
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