Axial coordination regulation of MOF-based single-atom Ni catalysts by halogen atoms for enhanced CO2 electroreduction

Single-atom catalysts (SACs), with the utmost atom utilization, have attracted extensive interests for various catalytic applications. The coordination environment of SACs has been recognized to play a vital role in catalysis while their precise regulation at atomic level remains an immense challenge. Herein, a post metal halide modification (PMHM) strategy has been developed to construct Ni-N-4 sites with axially coordinated halogen atoms, named Ni1N-C (X) (X = Cl, Br, and I), on pre-synthetic nitrogen-doped carbon derived from metal-organic frameworks. The axial halogen atoms with distinct electronegativity can break the symmetric charge distribution of planar Ni-N-4 sites and regulate the electronic states of central Ni atoms in Ni1N-C (X) (X = Cl, Br, and I). Significantly, the Ni1N-C (Cl) catalyst, decorated with the most electronegative Cl atoms, exhibits Faradaic efficiency of CO up to 94.7% in electrocatalytic CO2 reduction, outperforming Ni1N-C (Br) and Ni1N-C (I) catalysts. Moreover, Ni1N-C (Cl) also presents superb performance in Zn-CO2 battery with ultrahigh CO selectivity and great durability. Theoretical calculations reveal that the axially coordinated Cl atom remarkably facilitates *COOH intermediate formation on single-atom Ni sites, thereby boosting the CO2 reduction performance of Ni1N-C (Cl). This work offers a facile strategy to tailor the axial coordination environments of SACs at atomic level and manifests the crucial role of axial coordination microenvironments in catalysis.

Automated summary

In this study, a post metal halide modification strategy was developed to construct Ni-N-4 sites with axially coordinated halogen atoms, which can regulate the electronic states of Ni atoms. The Ni1N-C (Cl) catalyst, decorated with Cl atoms, showed excellent performance in CO2 reduction and Zn-CO2 battery.