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Synergistic Effects of a CeO2/SmMn2O5-H Diesel Oxidation Catalyst Induced by Acid-Selective Dissolution Drive the Catalytic Oxidation Reaction.

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A diesel oxidation catalyst (DOC) is installed upstream of an exhaust after-treatment line to remove CO and hydrocarbons and generate NO2. The catalyst should possess both good oxidation ability and… Click to show full abstract

A diesel oxidation catalyst (DOC) is installed upstream of an exhaust after-treatment line to remove CO and hydrocarbons and generate NO2. The catalyst should possess both good oxidation ability and thermal stability because it sits after the engine. We present a novel high-performance DOC with high steam resistance and thermal stability. A selective dissolution method is adopted to modify the surface physicochemical environment of CeO2-SmMn2O5. The X-ray photoelectron spectroscopy, X-ray absorption spectroscopy, Raman, electron paramagnetic resonance, hydrogen temperature-programmed reduction, and temperature-programmed desorption results reveal that surface Sm cations are partially removed with the exposure of more Mn4+ and Ce3+ cations and the presence of active surface oxygen species. This mechanism benefits the oxygen transformation from Ce to Mn and promotes the Ce3+ + Mn4+ ↔ Ce4+ + Mn3+ redox cycle according to the in situ near-ambient pressure X-ray photoelectron spectroscopy and in situ diffuse reflectance infrared Fourier transformation spectroscopy results. Under laboratory-simulated diesel combustion conditions, the catalyst demonstrates excellent low-temperature oxidation catalytic activity (CO and C3H6 conversion: T100 = 250 °C) compared to a Pt-based catalyst (CO and C3H6 conversion: T100 = 310 °C) with a WHSV of 120,000 mL g-1 h-1. Specifically, NO conversion reaches 68% when the temperature is approximately 300 °C.

Keywords: spectroscopy; oxidation; diesel oxidation; oxidation catalyst

Journal Title: ACS applied materials & interfaces
Year Published: 2022

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