Enhanced CO2 Methanation Activity of Sm0.25Ce0.75O2-δ-Ni by Modulating the Chelating Agents-to-Metal Cation Ratio and Tuning Metal-Support Interactions.

Abstract

Highly active and selective CO2 methanation catalysts are critical to CO2 upgrading, synthetic natural gas production, and CO2 emission reduction. Wet impregnation is widely used to synthesize oxide-supported metallic nanoparticles as the catalyst for CO2 methanation. However, as the reagents cannot be homogeneously mixed at an atomic level, it is challenging to modulate the microstructure, crystal structure, chemical composition, and electronic structure of catalysts via wet impregnation. Herein, a scalable and straightforward catalyst fabrication approach has been designed and validated to produce Sm0.25Ce0.75O2-δ-supported Ni (SDC-Ni) as the CO2 methanation catalyst. By varying the chelating agents-to-total metal cations ratio (C/I ratio) during the catalyst synthesis, we can readily and simultaneously modulate the microstructure, metallic surface area, crystal structure, chemical composition, and electronic structure of SDC-Ni, consequently fine-tuning the oxide-support interactions and CO2 methanation activity. The optimal C/I ratio (0.1) leads to an SDC-Ni catalyst that facilitates C-O bond cleavage and significantly improves CO2 conversion at 250 °C. A CO2-to-CH4 yield of >73% has been achieved at 250 °C. Furthermore, a stable operation of >1500 hours has been demonstrated, and no degradation is observed. Extensive characterizations were performed to fundamentally understand how to tune and enhance CO2 methanation activity of SDC-Ni by modulating the C/I ratio. The correlation of physical, chemical, and catalytic properties of SDC-Ni with the C/I ratio is established and thoroughly elaborated in this work. This study could be applied to tune the oxide-support interactions of various catalysts for enhancing the catalytic activity.