Single-atom catalysts reveal the dinuclear characteristic of active sites in NO selective reduction with NH3

被引:183
|
作者
Qu, Weiye [1 ]
Liu, Xiaona [1 ]
Chen, Junxiao [1 ]
Dong, Yangyang [1 ]
Tang, Xingfu [1 ,2 ]
Chen, Yaxin [1 ]
机构
[1] Fudan Univ, Dept Environm Sci & Engn, Shanghai 200433, Peoples R China
[2] Nanjing Univ Informat Sci & Technol, Jiangsu Collaborat Innovat Ctr Atmospher Environm, Nanjing 210044, Peoples R China
基金
中国国家自然科学基金;
关键词
VANADIA-TITANIA CATALYSTS; RAY-ABSORPTION SPECTROSCOPY; NITRIC-OXIDE; ACID SITES; AMMONIA; SCR; MECHANISM; V2O5/TIO2; SUPPORT; FE2O3;
D O I
10.1038/s41467-020-15261-5
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
High-performance catalysts are extremely required for controlling NO emission via selective catalytic reduction (SCR), and to acquire a common structural feature of catalytic sites is one key prerequisite for developing such catalysts. We design a single-atom catalyst system and achieve a generic characteristic of highly active SCR catalytic sites. A single-atom Mo-1/Fe2O3 catalyst is developed by anchoring single acidic Mo ions on (001) surfaces of reducible alpha-Fe2O3, and the individual Mo ion and one neighboring Fe ion are thus constructed as one dinuclear site. As the number of the dinuclear sites increases, SCR rates increase linearly but the apparent activation energy remains almost unchanged, evidencing the identity of the dinuclear active sites. We further design W-1/Fe2O3 and Fe-1/WO3 and find that tuning acid or/and redox properties of dinuclear sites can alter SCR rates. Therefore, this work provides a design strategy for developing improved SCR catalysts via optimizing acid-redox properties of dinuclear sites.
引用
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页数:7
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