Cobalt-Based Nonprecious Metal Catalysts Derived from Metal-Organic Frameworks for High-Rate Hydrogenation of Carbon Dioxide

The development of cost-effective catalysts with both high activity and selectivity for carbon-oxygen bond activation is a major challenge and has important ramifications for making value-added chemicals from carbon dioxide (CO₂). Herein, we present a one-step pyrolysis of metal organic frameworks that yields highly dispersed cobalt nanoparticles embedded in a carbon matrix which shows exceptional catalytic activity in the reverse water gas shift reaction. Incorporation of nitrogen into the carbon-based supports resulted in increased reaction activity and selectivity toward carbon monoxide (CO), likely because of the formation of a Mott-Schottky interface. At 300 °C and a high space velocity of 300 000 mL g^-1 h^-1, the catalyst exhibited a CO₂ conversion rate of 122 μmol_CO2 g^-1s^-1, eight times higher than that of a reference Cu/ZnO/Al₂O₃ catalyst. Our experimental and computational results suggest that nitrogen-doping lowers the energy barrier for the formation of formate intermediates (CO2∗ + H∗ → COOH∗ +∗), in addition to the redox mechanism (CO2∗ + ∗ → CO∗ + O∗). This enhancement is attributed to the efficient electron transfer at the cobalt-support interface, leading to higher hydrogenation activity and opening new avenues for the development of CO₂ conversion technology.