Scalable synthesis of coordinatively unsaturated metal-nitrogen sites for large-scale CO(2) electrolysis.

Practical electrochemical CO(2)-to-CO conversion requires a non-precious catalyst to react at high selectivity and high rate. Atomically dispersed, coordinatively unsaturated metal-nitrogen sites have shown great performance in CO(2) electroreduction; however, their controllable and large-scale fabrication still remains a challenge. Herein, we report a general method to fabricate coordinatively unsaturated metal-nitrogen sites doped within carbon nanotubes, among which cobalt single-atom catalysts can mediate efficient CO(2)-to-CO formation in a membrane flow configuration, achieving a current density of 200 mA cm(-2) with CO selectivity of 95.4% and high full-cell energy efficiency of 54.1%, outperforming most of CO(2)-to-CO conversion electrolyzers. By expanding the cell area to 100 cm(2), this catalyst sustains a high-current electrolysis at 10 A with 86.8% CO selectivity and the single-pass conversion can reach 40.4% at a high CO(2) flow rate of 150 sccm. This fabrication method can be scaled up with negligible decay in CO(2)-to-CO activity. In situ spectroscopy and theoretical results reveal the crucial role of coordinatively unsaturated metal-nitrogen sites, which facilitate CO(2) adsorption and key *COOH intermediate formation.