Enhancement of CO2 Hydrogenation to LightOlefins by Developing a Higher Alcohols-Intermediate Route

CO₂ hydrogenation to light olefins generally occurs via Fischer–Tropsch (FT) synthesis and methanol-intermediate routes. However, these two routes usually give low light olefin yields, although large numbers of catalysts have been fabricated. This results from the limitation of the Anderson–Schulz–Flory (ASF) law or the formation of initial C–C bond and hydrocarbon pool (HCP) species. To overcome these problems, a higher alcohol-intermediate route is developed here as these alcoholic products are rapidly dehydrated to light olefins. The designed Na-CuFeO_x/H-GeAPO-34 composite shows CO₂ conversion of 75.1% and light olefins selectivity in all products (including CO) of 48.7%, thus resulting in an unprecedentedly high yield of 36.6%. In situ spectroscopy and DFT calculation results reveal that the metallic copper (Cu) species not only promotes iron (Fe) species reduction and carbonization by overflowing active hydrogen species and transferring electrons but also provides an effective site for stabilizing nondissociative CO* species. This enhances formation of CH_x* and nondissociative CO* species, which are coupled to generate large amounts of higher alcohols intermediates that are facilely dehydrated into light olefins on weakly acidic H-GeAPO-34. This work confirms that the higher alcohols-intermediate route is highly effective for converting CO₂ into light olefins.