氧化还原
催化作用
活动站点
离子
选择性催化还原
化学
Atom(片上系统)
材料科学
组合化学
无机化学
有机化学
计算机科学
嵌入式系统
作者
Weiye Qu,Xiaona Liu,Junxiao Chen,Yangyang Dong,Xingfu Tang,Yaxin Chen
标识
DOI:10.1038/s41467-020-15261-5
摘要
Abstract 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 /Fe 2 O 3 catalyst is developed by anchoring single acidic Mo ions on (001) surfaces of reducible α-Fe 2 O 3 , 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 /Fe 2 O 3 and Fe 1 /WO 3 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.
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