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Electrochemical reduction of CO2 by renewable electricity offers a promising way to settle excessive greenhouse gases and achieve carbon neutrality under a mild environment. Cu-based catalysts have a unique catalytic activity towards multicarbon (C2+) products in the CO2 electroreduction reaction and are widely studied to promote the corresponding selectivity and activity. Here we report a F-doped Cu (F–Cu) catalyst to improve C2+ products in CO2 electroreduction. A high C2+ product (mainly ethylene and ethanol) faradaic efficiency of 70.4% was achieved on the F–Cu catalyst with a high current density (above 400 mA cm−2) in the flow-cell system. The in situ surface enhanced Raman spectroscopy results and electrochemical performance analysis demonstrated that CO2 could be reduced into CO at low potentials and the adsorption of CO could be strengthened on F–Cu, which is beneficial to the subsequent C–C coupling step and formation of the C2+ products. [ABSTRACT FROM AUTHOR]

Cu(OH)2/CuO nanocomposite-derived Cu2O/Cu was highly efficient for CO2 electroreduction to C2 products. The highest faradaic efficiency and current density could reach 64.5% and 26.2 mA cm−2, respectively. By changing the calcination time, moderate grain boundary density and the Cu+/Cu0 ratio in catalysts can be controlled, leading to a large number of active sites and low interfacial charge transfer resistance. [ABSTRACT FROM AUTHOR]

Acetic acid is an important bulk chemical and synthesis of acetic acid via methanol hydrocarboxylation with CO2 and H2 is a very promising route. In this work, we studied the reaction over a number of catalytic systems. It was found that Rh2(CO)4Cl2 with 4-methylimidazole (4-MI) as the ligand was very efficient in the presence of LiCl and LiI. Acetic acid began to form at 150 °C. The TOF was as high as 26.2 h−1 and the yield of acetic acid could reach 81.8% at 180 °C. The catalytic system had obvious advantages, such as simplicity, high activity and selectivity, milder reaction conditions, and less corrosiveness. The excellent cooperation of CO and Cl− in Rh2(CO)4Cl2, suitable basicity and aromaticity of the ligand 4-MI, and the hydrogen bonding ability of Cl− were crucial for the outstanding performance of the catalytic system. The control experiments showed that the reaction did not proceed via the CO pathway. [ABSTRACT FROM AUTHOR]