催化作用
碳纤维
选择性催化还原
金属
还原(数学)
化学
无机化学
材料科学
冶金
有机化学
几何学
数学
复合数
复合材料
作者
Rucheng Duan,Yu Fu,Zhuocan Li,Xin Wang,Meng Gao,Yunbo Yu,Guangzhi He,Hong He
标识
DOI:10.1021/acs.est.4c14482
摘要
Catalysts operating at low temperatures are imperative for the denitrification of flue gases from various non-electric industries. Current catalysts typically exhibit significant activity for the selective catalytic reduction of NOx with NH3 (NH3–SCR) at temperatures above 100 °C. Here, we observed for the first time remarkable room-temperature NH3–SCR activity on the surface of carbon-based catalysts. The oxidation of NO to NO2 by surface C–O–C groups at room temperature serves as a key initial step, triggering a fast SCR reaction. The C–OH groups, as active sites, directly participate in the elementary reaction pathways of the SCR through an H migration process, significantly reducing the energy barrier of the rate-determining step to below 1 eV, thereby enabling fast SCR to occur at room temperature. The room-temperature SCR and its novel reaction mechanism reported in this study would inevitably expand the research boundaries of NOx abatement.
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