Design, Synthesis, and Insights into the Redox Mechanism of Highly Efficient One-Pot Cu-ZSM-5 Catalysts for the Reduction of NOx by NH3-SCR at Low Temperatures

催化作用 ZSM-5型 选择性催化还原 化学 氧化还原 电子顺磁共振 选择性 无机化学 沸石 物理化学 有机化学 物理 核磁共振
作者
Chengming Zhong,Yu Ren,Chengyang Yin,Ruidan Wang,Jiakai Hou,Lanyi Wang,Zhen Zhao,Bartosz Mozgawa,Piotr Pietrzyk,Zbigniew Sojka,Yangyang Song
出处
期刊:ACS Catalysis [American Chemical Society]
卷期号:13 (16): 10927-10944 被引量:20
标识
DOI:10.1021/acscatal.3c01619
摘要

Cu-ZSM-5 zeolites exhibit promising NH3-SCR activity in a wide temperature window. The current challenges in preparing Cu-ZSM-5 are reducing the cost and simplifying the preparation process. The one-pot method using the Cu-amine complex as the template is an excellent strategy for solving the above problems. However, the above method is still lacking in preparing Cu-ZSM-5. In this work, a one-pot method using the Cu-(EDA)2 complex as the template is developed to prepare the Cu-ZSM-5-O catalyst. According to the fundamental measurements, the high dispersion of copper(II) species, appropriate acidity, and Cu+ species are in favor of the NH3-SCR reaction. Among one-pot catalysts, Cu1.8-ZSM-5-O shows excellent NH3-SCR performance at low temperatures (NO conversion of about 87.5% at 150 °C and N2 selectivity above 95% over the entire temperature window). The boosting activity at low temperatures of one-pot catalysts is probably assigned to abundant [Cu(OH)]+ species and appropriate amounts of Cu+ species in Cu-ZSM-5-O. Moreover, the variable-temperature EPR and subsequent computer simulation are used first to quantify the content of [Cu(OH)]+ species in Cu-ZSM-5-O. The NH3-SCR mechanism at low temperatures (150 °C) on [Cu(OH)]+ species is also investigated by in situ DRIFT spectra and DFT calculations, which mainly follow the Eley–Rideal route. A complete catalytic cycle of the SCR reaction was proposed based on the [Cu(OH)]+ species by DFT calculations. Our results suggest that [Cu(OH)]+ species contribute to the adsorption and activation of NH3, thus boosting the catalytic performance.
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