Single Ru(II) Ions on Ceria as a Highly Active Catalyst for Abatement of NO

Atom trapping leads to catalysts with atomically dispersed Ru₁O₅ sites on (100) facets of ceria, as identified by spectroscopy and DFT calculations. This is a new class of ceria-based materials with Ru properties drastically different from the known M/ceria materials. They show excellent activity in catalytic NO oxidation, a critical step that requires use of large loadings of expensive noble metals in diesel aftertreatment systems. Ru₁/CeO₂ is stable during continuous cycling, ramping, and cooling as well as the presence of moisture. Furthermore, Ru₁/CeO₂ shows very high NO storage properties due to formation of stable Ru-NO complexes as well as a high spill-over rate of NO onto CeO₂. Only ∼0.05 wt % of Ru is required for excellent NO storage. Ru₁O₅ sites exhibit much higher stability during calcination in air/steam up to 750 °C in contrast to RuO₂ nanoparticles. We clarify the location of Ru(II) ions on the ceria surface and experimentally identify the mechanism of NO storage and oxidation using DFT calculations and in situ DRIFTS/mass spectroscopy. Moreover, we show excellent reactivity of Ru₁/CeO₂ for NO reduction by CO at low temperatures: only 0.1-0.5 wt % of Ru is sufficient to achieve high activity. Modulation-excitation in situ infrared and XPS measurements reveal the individual elementary steps of NO reduction by CO on an atomically dispersed Ru ceria catalyst, highlighting unique properties of Ru₁/CeO₂ and its propensity to form oxygen vacancies/Ce⁺³ sites that are critical for NO reduction, even at low Ru loadings. Our study highlights the applicability of novel ceria-based single-atom catalysts to NO and CO abatement.