Zn promoted GaZrOx Ternary Solid Solution Oxide Combined with SAPO‐34 Effectively Converts CO2 to Light Olefins with Low CO Selectivity

We proposed a new strategy for CO2 hydrogenation to prepare light olefins by introducing Zn into GaZrOx to construct ZnGaZrOx ternary oxides, which was combined with SAPO‐34 to prepare a high–performance ZnGaZrOx/SAPO‐34 tandem catalyst for CO2 hydrogenation to light olefins. By optimizing the Zn doping content, the ratio and mode of the two–phase composite, and the process conditions, the 3.5 %ZnGaZrOx/SAPO‐34 tandem catalyst showed excellent catalytic performance and good high–temperature inhibition of the reverse water–gas shift (RWGS) reaction. The catalyst achieved 26.6 % CO2 conversion, 82.1 % C2=−C4= selectivity and 11.8 % light olefins yield. The ZnGaZrOx formed by introducing an appropriate amount of Zn into GaZrOx significantly enhanced the spillover H2 effect and also induced the generation of abundant oxygen vacancies to effectively promote the activation of CO2. Importantly, the RWGS reaction was also significantly suppressed at high temperatures, with the CO selectivity being only 46.1 % at 390 °C. In this paper, Zn was introduced into GaZrOx to construct ZnGaZrOx ternary oxides, which was combined with SAPO‐34 for CO2 hydrogenation to light olefins. The ZnGaZrOx significantly enhanced the spillover H2 effect and also induced the generation of abundant oxygen vacancies to effectively promote the activation of CO2, thereby the ZnGaZrOx/SAPO‐34 bifunctional catalysts exhibited excellent catalytic performance.