催化作用
拉曼光谱
漫反射红外傅里叶变换
吸附
材料科学
氧化还原
傅里叶变换红外光谱
选择性
化学工程
化学
无机化学
光催化
物理化学
有机化学
工程类
物理
光学
作者
Wei Tan,Yi Cai,Shaohua Xie,Juntian Xu,Kaili Ma,Kailong Ye,Lu Ma,Steven N. Ehrlich,Weixin Zou,Fei Gao,Lin Dong,Fudong Liu
标识
DOI:10.1016/j.cej.2022.140807
摘要
CuO-CeO2 based materials have been recognized as promising substitutes for precious metal catalysts in emission control field due to their superior redox property and low cost. Herein, by optimizing the deposition process of CeO2 and CuO onto γ-Al2O3, highly dispersed CuO clusters on unique CeO2-Al2O3 support with small CeO2 particles (7Cu-Ce/CeAl) were successfully constructed for efficient NO reduction by CO, which exhibited much higher NO removal efficiency and N2 selectivity than CuO catalysts supported on γ-Al2O3 (7Cu/Al) and conventional CeO2-Al2O3 support (7Cu/CeAl). Moreover, H2O showed limited inhibition effect on the catalytic performance of 7Cu-Ce/CeAl catalyst. With the help of Raman spectra, X-ray absorption spectroscopy, in situ diffuse reflectance infrared Fourier transform spectroscopy, etc., it was clearly revealed that the abundant Cu+/Ce3+ paired sites with surface synergetic oxygen vacancies (SSOV) on 7Cu-Ce/CeAl catalyst could effectively facilitate the adsorption and activation of CO and NO, thus significantly enhancing the NO removal efficiency.
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