Nitrogen Vacancy Induced Coordinative Reconstruction of Single‐Atom Ni Catalyst for Efficient Electrochemical CO2 Reduction

Abstract Transition metal nitrogen carbon based single‐atom catalysts (SACs) have exhibited superior activity and selectivity for CO 2 electroreduction to CO. A favorable local nitrogen coordination environment is key to construct efficient metal‐N moieties. Here, a facile plasma‐assisted and nitrogen vacancy (NV) induced coordinative reconstruction strategy is reported for this purpose. Under continuous plasma striking, the preformed pentagon pyrrolic N‐defects around Ni sites can be transformed to a stable pyridinic N dominant Ni‐N 2 coordination structure with promoted kinetics toward the CO 2 ‐to‐CO conversion. Both the CO selectivity and productivity increase markedly after the reconstruction, reaching a high CO Faradaic efficiency of 96% at mild overpotential of 590 mV and a large CO current density of 33 mA cm ‐2 at 890 mV. X‐ray adsorption spectroscopy and density functional theory (DFT) calculations reveal this defective local N environment decreases the restraint on central Ni atoms and provides enough space to facilitate the adsorption and activation of CO 2 molecule, leading to a reduced energy barrier for CO 2 reduction.