Effect of Pr in CO2 Methanation Ru/CeO2 Catalysts

CO2 methanation has been studied with Pr-doped Ru/CeO2 catalysts, and a dual effect of Pr has been observed. For low Pr content (i.e., 3 wt %) a positive effect in oxygen mobility prevails, while for high Pr doping (i.e., 25 wt %) a negative effect in the Ru-CeO2 interaction is more relevant. Isotopic experiments evidenced that Pr hinders the dissociation of CO2, which takes place at the Ru-CeO2 interface. However, once the temperature is high enough (200 degrees C), Pr improves the oxygen mobility in the CeO(2 )support, and this enhances CO2 dissociation because the oxygen atoms left are delivered faster to the support sink and the dissociation sites at the interface are cleaned up faster. In situ Raman spectroscopy experiments confirmed that Pr improves the creation of oxygen vacancies on the ceria lattice but hinders their reoxidation by CO2, and both opposite effects reach an optimum balance for 3 wt % Pr doping. In addition, in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) experiments showed that Pr doping, regardless of the amount, decreases the population of surface carbon species created on the catalysts surface upon CO2 chemisorption under methanation reaction conditions, affecting both productive reaction intermediates (formates and carbonyls) and unproductive carbonates.

Automated summary

The study showed a dual effect of Pr-doped Ru/CeO2 catalysts on CO2 methanation, with low Pr content enhancing oxygen mobility but high Pr content hindering CO2 dissociation. At high temperatures, Pr improves oxygen mobility which promotes CO2 dissociation, balancing out the negative effects of hindering dissociation at the interface.