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Atomically Dispersed Pt-Triggered CZO/Cu-SSZ-13 Coupling Catalyst for the Efficient Low-Temperature Selective Catalytic Reduction of NO x
In this study, an atomically dispersed Pt-loaded Ce0.6Zr0.4O2/Cu-SSZ-13 (Pt-CZO/Cu-SSZ-13) coupling catalyst was fabricated by a facile grinding strategy, and its structure and catalytic performance for the selective catalytic reduction (SCR) of NO x by NH3 were systematically investigated. The results reveal that the resulting Pt-CZO/Cu-SSZ-13 shows outstanding catalytic activity, achieving almost complete conversion of NO x at 145 °C, notably lower as compared with that of Cu-SSZ-13 with approximately 100% NO x conversion at 200 °C. The reason should be originated from the coexistence of Pt species in both single-atom and nanocluster forms, which not only significantly enhance the reactivity of lattice oxygen in CZO but also considerably increase the number of Brønsted acid sites. Both of these factors coordinately aid the adsorption and thereafter the activation of NO x and NH3, and then promote the NH3–SCR activity of the Pt-CZO/Cu-SSZ-13 coupling sample noticeably at the low-temperature range. This study introduces a viable approach to address the pressing issue of NO x emissions during the idle and cold-start phases of diesel engines.
Atomically Dispersed Pt-Triggered CZO/Cu-SSZ-13 Coupling Catalyst for the Efficient Low-Temperature Selective Catalytic Reduction of NO x
In this study, an atomically dispersed Pt-loaded Ce0.6Zr0.4O2/Cu-SSZ-13 (Pt-CZO/Cu-SSZ-13) coupling catalyst was fabricated by a facile grinding strategy, and its structure and catalytic performance for the selective catalytic reduction (SCR) of NO x by NH3 were systematically investigated. The results reveal that the resulting Pt-CZO/Cu-SSZ-13 shows outstanding catalytic activity, achieving almost complete conversion of NO x at 145 °C, notably lower as compared with that of Cu-SSZ-13 with approximately 100% NO x conversion at 200 °C. The reason should be originated from the coexistence of Pt species in both single-atom and nanocluster forms, which not only significantly enhance the reactivity of lattice oxygen in CZO but also considerably increase the number of Brønsted acid sites. Both of these factors coordinately aid the adsorption and thereafter the activation of NO x and NH3, and then promote the NH3–SCR activity of the Pt-CZO/Cu-SSZ-13 coupling sample noticeably at the low-temperature range. This study introduces a viable approach to address the pressing issue of NO x emissions during the idle and cold-start phases of diesel engines.
Atomically Dispersed Pt-Triggered CZO/Cu-SSZ-13 Coupling Catalyst for the Efficient Low-Temperature Selective Catalytic Reduction of NO x
Jia, Lingfeng (author) / Shao, Yuankai (author) / Li, Zhenguo (author) / Li, Kaixiang (author) / Ren, Xiaoning (author) / Wu, Hanming (author) / Li, Huiquan (author) / Cheng, Kai (author) / Cheng, Huifang (author) / Liu, Jian (author)
ACS ES&T Engineering ; 4 ; 1007-1015
2024-05-10
Article (Journal)
Electronic Resource
English
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