Angewandte Chemie International Edition · 2018 · 355 citations · 27 references
Methods for the hydrogenation of CO<sub>2</sub> into valuable chemicals are in great demand but their development is still challenging. Herein, we report the selective hydrogenation of CO<sub>2</sub> into ethanol over non-noble cobalt catalysts (CoAlO<sub>x</sub> ), presenting a significant advance for the conversion of CO<sub>2</sub> into ethanol as the major product. By adjusting the composition of the catalysts through the use of different prereduction temperatures, the efficiency of CO<sub>2</sub> to ethanol hydrogenation was optimized; the catalyst reduced at 600 ° gave an ethanol selectivity of 92.1 % at 140 °C with an ethanol time yield of 0.444 mmol g<sup>-1</sup> h<sup>-1</sup> . Operando FT-IR spectroscopy revealed that the high ethanol selectivity over the CoAlO<sub>x</sub> catalyst might be due to the formation of acetate from formate by insertion of *CH<sub>x</sub> , a key intermediate in the production of ethanol by CO<sub>2</sub> hydrogenation.
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Active sites for CO <sub>2</sub> hydrogenation to methanol on Cu/ZnO catalysts
Shyam Kattel, Pedro J. Ramírez, Jingguang G. Chen et al. · Science · 2017 · 1.7K citations · Full text