Low-Temperature Thermocatalytic Coupling of CH4 and CO2 to Ethanol over Zn–Ce/ZSM-5 by a Stepwise Technique

Direct thermocatalytic coconversion of CH4 and CO2 to C2 oxygenates at low temperatures has attracted extensive attention but is challenged due to being thermodynamically unfavorable. Herein, we report the direct coupling of CH4 and CO2 to ethanol as the sole liquid product on the Zn–Ce/ZSM-5 catalyst by a two-stepwise technique at 150 °C. The unexpected results toward ethanol are attributed to the special technique and Zn–O–Ce interfaces, which ensure the preferential adsorption and dehydrogenation of CH4 on ZnOH+ sites, while CO2 is adsorbed on the oxygen vacancies of Ce sites. It is found that the formation rate of ethanol is closely related to the number of medium strong acids and medium strong bases in zeolite. In situ DRIFTS experiments demonstrate that C–C is respectively realized by the coupling of CH3* and CO2* as well as the insertion of CO* into the CH2* to form CH3COO* and CH2CO* intermediates, which undergo finally hydrogenation to achieve ethanol. This study pioneers an attractive route for the direct synthesis of ethanol from CH4–CO2 under mild conditions.