Strong Stabilization of Co Nanoparticles by CeO<sub>2-x</sub> Clusters in Inverse CeO<sub>x</sub>/Co Catalysts for Enhanced CO<sub>2</sub> Methanation.

Gao, Yu; Muravev, Valery; Fan, Yonghui; Zhang, Hao; Wagemakers, Jorden; Parastaev, Alexander; Kosinov, Nikolay; Hensen, Emiel J M · Adv Mater · 2026

basic_science · Level V

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Abstract

Inverse catalysts, where metal oxide species are dispersed over metallic nanoparticles, represent a promising class of materials for accelerating various chemical reactions. However, stabilizing metal nanoparticles with a small amount of oxide clusters remains a significant challenge, as the metallic phase tends to sinter under reaction conditions due to insufficient immobilization. In this study, flame spray pyrolysis is employed to synthesize uniformly sized inverse CeO<sub>x</sub>/Co catalysts for CO<sub>2</sub> methanation (Sabatier reaction). It is found that small, highly reducible CeO<sub>2-x</sub> clusters effectively stabilize metallic cobalt nanoparticles, thereby preventing sintering even during hydrogen reduction at 500 °C and during CO<sub>2</sub> hydrogenation. Detailed operando characterization demonstrates that this stabilization leads to a high density of metallic Co sites interfaced with CeO<sub>2-x</sub> clusters, which facilitates CO<sub>2</sub> activation into carbonyl (CO<sup>*</sup>) intermediates, resulting in significantly enhanced CH<sub>4</sub> formation rates. Notably, an inverse CeO<sub>x</sub>/Co catalyst containing 20 mol% Ce exhibits a methanation rate an order of magnitude higher than that of a CeO<sub>2</sub>-free Co catalyst. These findings highlight the dual role of CeO<sub>2-x</sub> clusters in both stabilizing Co nanoparticles and enhancing catalytic performance, offering a robust strategy for improving CO<sub>2</sub> hydrogenation performance.