Multifunctional long-lived catalysts for direct hydrogenative conversion of CO₂ to liquid hydrocarbons with upscaling C₅₊ productivity

Abstract

Rationally designed K-promoted Fe/CuAl 2 O 4 acts as a tandem catalyst for CO 2 conversion to C 5+ hydrocarbons via the reverse water–gas shift reaction and Fischer–Tropsch synthesis consecutively, achieving upscaling C 5+ productivity and stability.