Regulation of Coordination Number over Single Co Sites: Triggering the Efficient Electroreduction of CO2

Abstract

The design of active, selective, and stable CO₂ reduction electrocatalysts is still challenging. A series of atomically dispersed Co catalysts with different nitrogen coordination numbers were prepared and their CO₂ electroreduction catalytic performance was explored. The best catalyst, atomically dispersed Co with two‐coordinate nitrogen atoms, achieves both high selectivity and superior activity with 94 % CO formation Faradaic efficiency and a current density of 18.1 mA cm⁻² at an overpotential of 520 mV. The CO formation turnover frequency reaches a record value of 18 200 h⁻¹, surpassing most reported metal‐based catalysts under comparable conditions. Our experimental and theoretical results demonstrate that lower a coordination number facilitates activation of CO₂ to the CO₂^.− intermediate and hence enhances CO₂ electroreduction activity.