催化作用
兴奋剂
色散(光学)
化学
选择性催化还原
无机化学
化学工程
材料科学
有机化学
光电子学
物理
光学
工程类
作者
Junqi Wang,Ruolan Jiang,Ruoxuan Bai,Fei Gao,Zixiao Yu,Jiangxiao Qiao,Yiqing Zeng,Shule Zhang,Zhaoxiang Zhong
标识
DOI:10.1016/j.seppur.2025.134952
摘要
• A strategy to achieve varied P-Mn interactions by modulating the dispersion of MnO x . • P-Mn interactions strength follows the order: Mn(A)/TiP > Mn(O)/TiP > Mn(N)/TiP. • Strong P-Mn interactions enhance the adsorption and activation rates of NH 3 and NO x . • Mn(A)/TiP achieved over 80% NO conversion across a temperature range of 145–300 ℃. Modification with strong acidic species serves as an effective strategy to broaden the active temperature window of MnO x based catalysts for ammonia selective catalytic reduction (NH 3 -SCR) of NO x . However, strong acidic species always decrease the redox properties of MnO x , which hinders the quest for better performance of MnO x based NH 3 -SCR catalysts. Herein, the dispersion of MnO x on P modified MnO x /TiO 2 (labeled as Mn(X)/TiP (X = O, A, N, represents the Mn precursors of manganese dioxide, manganese acetate and manganese nitrate, respectively)) catalysts were regulated via changing manganese precursors to investigate its effects on P-Mn interactions and catalytic performance. It is found that the low-temperature NH 3 -SCR performance follows the order Mn(A)/TiP > Mn(O)/TiP > Mn(N)/TiP, which is consistent with the degree of MnO x dispersion. The increase of MnO x dispersion can contribute to the formation of a large amount of isolated MnO x nanoparticles, which reduces the passivation of P on other active Mn sites due to the formation of P-Mn interactions and promotes the establishment of an efficient redox cycle between Mn and Ti (Ti 4+ + Mn 2+/3+ ↔ Ti 3+ + Mn 3+/4+ ), thereby promoting the NH 3 -SCR denitration reaction via enhancing the activation of NH 3 and NO x . This work sheds an insight into the effect of MnO x dispersion on regulating the NH 3 -SCR performance of P-modified MnO x /TiO 2 catalysts and provides an efficient strategy to solve the imbalance between acidity and redox property during the design and developments of efficient NH 3 -SCR catalysts.
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