Ni‐Based Catalysts for CO2 Methanation: Exploring the Support Role in Structure‐Activity Relationships

This research highlights the significance of solvothermal technique and how it can be used to synthesize the catalyst with morphologies. Extensive advanced characterizations have been utilized to explain the role of support in structure-activity relationship during CO₂ methanation.

Abstract

The catalytic hydrogenation of CO₂ to methane is one of the highly researched areas for the production of chemical fuels. The activity of catalyst is largely affected by support type and metal-support interaction deriving from the special method during catalyst preparation. Hence, we employed a simple solvothermal technique to synthesize Ni-based catalysts with different supports and studied the support role (CeO₂, Al₂O₃, ZrO₂, and La₂O₃) on structure-activity relationships in CO₂ methanation. It is found that catalyst morphology can be altered by only changing the support precursors during synthesis, and therefore their catalytic behaviours were significantly affected. The Ni/Al₂O₃ with a core-shell morphology prepared herein exhibited a higher activity than the catalyst prepared with a common wet impregnation method. To have a comprehensive understanding for structure-activity relationships, advanced characterization (e. g., synchrotron radiation-based XAS and photoionization mass spectrometry) and in-situ diffuse reflectance infrared Fourier transform spectroscopy experiments were conducted. This research opens an avenue to further delve into the role of support on morphologies that can greatly enhance catalytic activity during CO₂ methanation.

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