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Unlocking Optimal Performance of PGM-Free CeCuOx Mixed Oxide Catalysts for CO and C3H6 Emission Conversion
Unlocking Optimal Performance of PGM-Free CeCuOx Mixed Oxide Catalysts for CO and C3H6 Emission Conversion
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Unlocking Optimal Performance of PGM-Free CeCuOx Mixed Oxide Catalysts for CO and C3H6 Emission Conversion
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Unlocking Optimal Performance of PGM-Free CeCuOx Mixed Oxide Catalysts for CO and C3H6 Emission Conversion
Unlocking Optimal Performance of PGM-Free CeCuOx Mixed Oxide Catalysts for CO and C3H6 Emission Conversion

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Unlocking Optimal Performance of PGM-Free CeCuOx Mixed Oxide Catalysts for CO and C3H6 Emission Conversion
Unlocking Optimal Performance of PGM-Free CeCuOx Mixed Oxide Catalysts for CO and C3H6 Emission Conversion
Journal Article

Unlocking Optimal Performance of PGM-Free CeCuOx Mixed Oxide Catalysts for CO and C3H6 Emission Conversion

2025
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Overview
A sustainable and cost-effective alternative for environmental applications is the use of PGM-free catalysts, which are crucial for pollutant removal. This research employed the sol-gel method to synthesize stable and effective mesoporous CeCuO x mixed oxide catalysts to facilitate the oxidation of CO and C 3 H 6 emissions at lower temperatures. Additionally, pure CeO 2 and CuO were also synthesized for comparative analysis. Catalytic performance was considerably increased by doping CeO 2 with Cu, whereas pure CuO and CeO 2 showed modest activity. XRD, SEM, BET, XPS, Raman spectroscopy, H 2 -TPR, and CO-TPD showed that increasing Ce content produced a consistent pore structure without aggregation. In contrast, higher Cu concentration resulted in bulk CuO production, which led to decreased catalytic performance. In particular, the production of isolated CuO x species partly covered or clogged pores when the Cu level was above 20 wt%, which reduced the total number of effective sites for O 2 activation. Compared to other mixed and pure oxides, the ideal catalyst, Ce 7 Cu 3 Ox (T 90, CO = 178 °C), showed smaller particle size, higher specific surface area, and a larger lattice oxygen species and oxygen vacancies concentration. Additionally, it showed the best CO and C 3 H 6 conversion due to its high Ce 3+ concentration and interfacial active Cu species ratio. H 2 -TPR and CO-TPD analyses demonstrated that Ce-Cu mixed oxides with optimal Ce/Cu ratios, particularly Ce 7 Cu 3 O x and Ce 5 Cu 5 O x , achieve enhanced reducibility and balanced CO adsorption, which are critical for maximizing catalytic reactivity. The catalytic activity exhibited the following sequence: Ce 7 Cu 3 O x  > Ce 5 Cu 5 O x  > Ce 9 Cu 1 O x  > Ce 3 Cu 7 O x  > Ce 1 Cu 9 O x  > CuO > CeO 2 . This investigation offers a valuable perspective on the mechanisms of Ce-Cu interaction, which contributes to developing high-performance CeCuOx catalysts that are free of PGMs and operate under realistic reaction conditions. Graphical abstract