Abstract
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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