Abstract
The conversion of C1 molecules, COx (CO and CO2), to valuable chemical products has garnered ever-increasing attention. Among many routes, the hydrogenation via thermal catalysis is particularly promising as a key clean energy technology with the increasing supply of green H2. Zinc-based mixed oxide catalysts exhibit exceptional catalytic performance in the COx hydrogenation to value-added hydrocarbons, especially in combination with zeolite. This review overviews the recent achievements in understanding the active sites and reaction mechanisms of COx hydrogenation on zinc-based mixed oxide catalysts, focusing on three most-studied zinc-based mixed oxide catalysts, namely ZnCrOx, ZnAlOx and ZnZrOx. The challenges and future directions are also discussed.
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Acknowledgements
This work was supported by the National Natural Science Foundation of China (12188101, 91745201, 91945301, 22203101, and 22033003), the Fundamental Research Funds for the Central Universities (20720220011), the Youth Innovation Promotion Association CAS (2023265), the Science & Technology Commission of Shanghai Municipality (23ZR1476100), and the Tencent Foundation for EXPLORER PRIZE.
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Yao, ZY., Ma, S. & Liu, ZP. Active sites and reaction mechanisms of COx hydrogenation on zinc-based mixed oxide catalysts. Sci. China Chem. (2024). https://doi.org/10.1007/s11426-024-2212-0
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DOI: https://doi.org/10.1007/s11426-024-2212-0