Efficient photo-thermal catalytic CO2 methanation and dynamic structural evolution over Ru/Mg-CeO2 single-atom catalyst.

[Display omitted] • Atomically dispersed Ru/Mg-CeO 2 catalyst was prepared and possessed excellent catalytic performance for photo-thermal catalytic CO 2 methanation reaction. • The photo-electron excitation/migration path and the surface structure changes induced by light were systematically characterized by operando experiments. • All potential micro-reaction steps and light intensification steps were determined by in situ DRIFTs experiments. • The reversible dynamic structural evolution between Ru-O-Ce structure and Ru-O v -Ce structure could be induced by light. It is a promising green technology to reduce CO 2 to CH 4 by using renewable solar energy driving photo-thermal catalysis route. However, the efficiency of photo-thermal catalytic CO2 methanation remained to be improved, and the mechanism of this reaction still required further investigation. In this paper, a Ru/Mg-CeO 2 catalyst was designed based on the concepts of single atom catalyst and photo-thermal catalysis concept. The catalyst achieved the CH 4 formation rate of 469 mmol·gcat−1·h−1 at 400 °C under photo-thermal conditions with good catalytic stability. Besides, the superiority of the single-atom of Ru, Ru-O-Ce structure and doping of alkaline metals in catalytic process was proved by a series of physicochemical and optical characterization, and electron migration direction from Ce and Mg elements to Ru sites through Ru-O-Ce and Ru-O-Mg path under photo-thermal catalysis was determined by ISI-XPS experiment. Finally, the comprehensive reaction mechanism and reversible dynamic structural evolution process between Ru-O-Ce and Ru-O v -Ce structures were investigated by in situ DRIFTs experiments, and the source of the excellent performance and structure-function relationship of the catalyst was explored, which provided the theoretical and practical basis for the development of catalyst and industrial application of the reaction. [ABSTRACT FROM AUTHOR]