Development of Ni-doped A-site lanthanides-based perovskite-type oxide catalysts for CO 2 methanation by auto-combustion method.

Engineering the interfacial interaction between the active metal element and support material is a promising strategy for improving the performance of catalysts toward CO 2 methanation. Herein, the Ni-doped rare-earth metal-based A-site substituted perovskite-type oxide catalysts (Ni/AMnO 3 ; A = Sm, La, Nd, Ce, Pr) were synthesized by auto-combustion method, thoroughly characterized, and evaluated for CO 2 methanation reaction. The XRD analysis confirmed the perovskite structure and the formation of nano-size particles with crystallite sizes ranging from 18 to 47 nm. The Ni/CeMnO 3 catalyst exhibited a higher CO 2 conversion rate of 6.6 × 10 -5 mol CO 2 g cat -1 s -1 and high selectivity towards CH 4 formation due to the surface composition of the active sites and capability to activate CO 2 molecules under redox property adopted associative and dissociative mechanisms. The higher activity of the catalyst could be attributed to the strong metal-support interface, available active sites, surface basicity, and higher surface area. XRD analysis of spent catalysts showed enlarged crystallite size, indicating particle aggregation during the reaction; nevertheless, the cerium-containing catalyst displayed the least increase, demonstrating resilience, structural stability, and potential for CO 2 methanation reaction.