Abstract
Pt and Ag nanoparticles (NPs) were synthesized by eco-friendly room-temperature chemical reduction routes based on trisodium citrate and L-ascorbic acid (for Pt NPs) and on gelatin and trisodium citrate (for Ag NPs). The as-prepared NPs were characterized by UV-visible absorption spectroscopy and transmission electron microscopy analyses, which confirmed the formation of sub-10 nm metal particles. Then, the colloidal solutions were used to obtain activated carbon-supported catalysts (metal/AC) for direct NO decomposition. X-ray photoelectron spectroscopy and x-ray diffraction measurements proved that the NPs hosted on the support surface were present in the metallic chemical state. In situ infrared absorption spectroscopy investigations during NO reduction catalytic reactions showed that the Pt/AC and Ag/AC catalysts were highly active at 373 K. At 573 K, we observed different behaviors for each catalyst. While Ag/AC performed similarly to the reaction at 373 K, Pt/AC was found to participate in a redox mechanism, where the catalyst’s active sites were oxidized by NO and reduced by carbon, thus emitting CO2 and enhancing its catalytic activity, an effect that we have also observed in carbon-supported Pd NPs.
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