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Development of effective and stable catalysts for CO2 hydrogenation into ethanol remains a challenge. Herein, we report that Rh1 /CeTiOx single-atom catalyst constructed by embedding monoatomic Rh onto Ti-doped CeO2 support has shown a super high ethanol selectivity (≈99.1 %), record-breaking turnover frequency (493.1 h-1 ), and outstanding stability. Synergistic effects of Ti-doption and monoatomic Rh contribute to this excellent catalytic performance by firstly facilitating oxygen vacancies formation to generate oxygen-vacancy-Rh Lewis-acid-base pairs, which favor CO2 adsorption and activation, cleavage of C-O bonds in CHx OH* and COOH* into CHx * and CO* species, subsequent C-C coupling and hydrogenation into ethanol, and secondly generating strong Rh-O bond by Ti-doping-induced crystal reconstruction, which contributes to striking stability. This work highlights the importance of support elaborating regulation for single-atom catalyst design to substantially improve the catalytic performance.
Zheng et al. (Fri,) studied this question.