文献类型：期刊文献

英文题名：Insight into the NH3-Assisted Selective Catalytic Reduction of NO on β-MnO2(110): Reaction Mechanism, Activity Descriptor, and Evolution from a Pristine State to a Steady State

作者：Yuan, Haiyang[1,2];Sun, Ningning[1,2];Chen, Jianfu[1,2];Jin, Jiamin[1,2];Wang, Haifeng[1,2];Hu, Peijun[1,2,3]

机构：[1]East China Univ Sci & Technol, Key Lab Adv Mat, Ctr Computat Chem, Shanghai 200237, Peoples R China;[2]East China Univ Sci & Technol, Sch Chem & Mol Engn, Res Inst Ind Catalysis, Shanghai 200237, Peoples R China;[3]Queens Univ Belfast, Sch Chem & Chem Engn, Belfast BT9 5AG, Antrim, North Ireland

年份：2018

卷号：8

期号：10

起止页码：9269

外文期刊名：ACS CATALYSIS

收录：;EI(收录号：20184205941286);WOS:【SCI-EXPANDED(收录号:WOS:000447224100032)】；

基金：This project was supported by the NSFC of China (21333003, 21622305), National Ten Thousand Talent Program for Young Top-notch Talents in China, The Shanghai Shuguang scholar program (17SG30), and the Fundamental Research Funds for the Central Universities (WJ1616007).

语种：英文

外文关键词：density functional theory; selective catalytic reduction; nitrogen oxides; MnO2; catalytic mechanism; activity descriptor

摘要：To understand the molecular-level reaction mechanism and crucial activity-limiting factors of the NH3-SCR process catalyzed by MnO2-based oxide to eliminate NO (4NH(3) + 4NO + O-2 -> 4N(2) + 6H(2)O) at middle-low temperature, a systematic computational investigation is performed on beta-MnO2(110) by first-principles calculations together with microkinetic analysis. Herein, the favored reaction pathways are unveiled. (i) NH3 tends to adsorb at the unsaturated Lewis acid Mnsc site on MnO2(110) and then partially dissociates into NH2* (assisted by the surface lattice Ob,) at the steady state, triggering the subsequent reactions. (ii) Interestingly, NO, either in the gas phase or at the adsorbed state, can readily react with NH2* to give the key intermediate NH2NO, with the former (i.e., the Eley-Rideal pathway) being slightly more kinetically preferred. (iii) NH2NO conversion is identified to proceed easily to N-2 through the dehydrogenation/hydrogenation processes NH2NO -> NHNO -> NHNOH -> N-2 + H2O. (iv) The removal of the accumulated surface H into H2O, assisted by O-2, is relatively difficult, which preferentially occurs via the Mars-van Krevelen mechanism. Quantitatively, a kinetic analysis is conducted to deal with such a complex reaction network, revealing that the rate-limiting steps are NH2* + NO(g) -> NH2NO* and ObriH + O-2# -> OOH# + O-bri. Moreover, a sensitivity analysis shows that the adsorption strengths of H on O-bri and O-2 in the Obri vacancy (O-vac) are two main activity-determining factors for the overall NH3-SCR on MnO2(110); notably, it is further found that the O-vac formation energy correlates well with both factors and can thus serve as a unified activity descriptor. In addition, the effects of catalyst surface environment under the reaction conditions on the NH3-SCR activity and selectivity are discussed. In comparison with the pristine state of MnO2(110), both the overall activity and N-2 selectivity (versus N2O) would be interestingly enhanced when it arrives at the kinetically steady state that the surface O-bri, are largely covered by H. These results could provide a consolidated theoretical basis for understanding and optimizing MnO2 catalysts for the NH3-SCR process.