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Interdisciplinary Intelligence and Emerging Technologies

Metal–Oxide Promotion Effects in Inverse Cobalt Catalysts for Selective CO₂ Methanation

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Abstract

Inverse cobalt catalysts provide unique metal–oxide boundary sites for CO2 methanation, but the role of oxide promotion remains unclear. Herein, ZrOx-, CeOx-, and TiOx-decorated Co catalysts were synthesized and tested for CO2 methanation at 220–360°C and atmospheric pressure. The ZrOx-modified Co catalyst showed the highest CH4 formation rate of 7.8 mmol gcat⁻¹ h⁻¹ at 300°C, with CO2 conversion of 61.4% and CH4 selectivity of 96.2%. In situ DRIFTS revealed that ZrOx promoted the formation and hydrogenation of bicarbonate and formate intermediates, while CeOx enhanced oxygen storage but favored CO formation at higher temperatures. H2 chemisorption and XPS results showed that oxide decoration modified the electron density of surface Co and improved the resistance to oxidation. The study demonstrates that inverse oxide modification can regulate both CO2 activation and hydrogenation pathways in cobalt-based methanation catalysts.

Keywords
CO2 methanationinverse cobalt catalystoxide promotermethane selectivitymetal–oxide interfaceformate intermediate
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Publication details
Journal
Interdisciplinary Intelligence and Emerging Technologies
Volume
1 (2026)
Article number
ajg20260002
License
CC BY 4.0