The Development of the Regenerable Catalytic System in Selective Catalytic Oxidation of Ammonia with High N2Selectivity

Supported particulate noble-metal catalysts are widely used in industrial catalytic reactions. However, these metal species, whether in the form of nanoparticles or highly dispersed entities, tend to aggregate during reactions, leading to a reduced activity or selectivity. Addressing the frequent necessity for the replacement of industrial catalysts remains a significant challenge. Herein, we demonstrate the feasibility of the ‘regenerable catalytic system’ exemplified by selective catalytic oxidation of ammonia (NH3–SCO) employing Ag/Al2O3catalysts. Results demonstrate that our highly dispersed Ag catalyst (Ag HD) maintains >90% N2selectivity at 80% NH3conversion and >80% N2selectivity at 100% NH3conversion after enduring 5 cycles of reducible aggregation and oxidative dispersion. Moreover, it consistently upholds over 98% N2selectivity at 100% NH3conversion after 10 cycles of Ar treatment. During the aggregation–dispersion process, the Ag HD catalyst intentionally aggregated into Ag nanoparticles (Ag NP) after H2reduction and exhibited remarkable regenerable capabilities, returning to the Ag HD state after calcination in the air. This structural evolution was characterized through in situ transmission electron microscopy, atomically resolved high-angle annular dark-field scanning transmission electron microscopy, and X-ray absorption spectroscopy, revealing the on-site oxidative dispersion of Ag NP. Additionally, in situ diffuse reflectance infrared Fourier transform spectroscopy provided insights into the exceptional N2selectivity on Ag HD catalysts, elucidating the critical role of NO+intermediates. Our findings suggest a sustainable and cost-effective solution for various industry applications.