Origin of the N-coordinated single-atom Ni sites in heterogeneous electrocatalysts for CO2 reduction reaction

Abstract

Heterogeneous Ni–N–C single-atom catalysts (SACs) have attracted great research interest regarding their capability in facilitating the CO₂ reduction reaction (CO₂RR), with CO accounting for the major product. However, the fundamental nature of their active Ni sites remains controversial, since the typically proposed pyridinic-type Ni configurations are inactive, display low selectivity, and/or possess an unfavorable formation energy. Herein, we present a constant-potential first-principles and microkinetic model to study the CO₂RR at a solid–water interface, which shows that the electrode potential is crucial for governing CO₂ activation. A formation energy analysis on several NiN_xC_4−x (x = 1–4) moieties indicates that the predominant Ni moieties of Ni–N–C SACs are expected to have a formula of NiN₄. After determining the potential-dependent thermodynamic and kinetic energy of these Ni moieties, we discover that the energetically favorable pyrrolic-type NiN₄ moiety displays high activity for facilitating the selective CO₂RR over the competing H₂ evolution. Moreover, model polarization curves and Tafel analysis results exhibit reasonable agreement with existing experimental data. This work highlights the intrinsic tetrapyrrolic coordination of Ni for facilitating the CO₂RR and offers practical guidance for the rational improvement of SACs, and this model can be expanded to explore mechanisms of other electrocatalysis in aqueous solutions.