Regulating the Coordination Environment of Single-Atom Catalysts Anchored on Thiophene Linked Porphyrin for an Efficient Nitrogen Reduction Reaction

The electrochemical nitrogen reduction reaction (NRR) offers a promising strategy to resolve high energy consumption in the nitrogen industry. Recently, the regulation of the electronic structure of single-atom catalysts (SACs) by adjusting their coordination environment has emerged as a rather promising strategy to further enhance their electrocatalytic activity. Herein, we design novel SACs supported by thiophene-linked porphyrin (TM–N 4 /TP and TM–N 4- x B x /TP, where TM = Sc to Au) as potential NRR catalysts using density functional theory calculations. Among these catalysts, TM–N 4 /TP (TM = Ti, Nb, Mo, Ta, W, and Re) and TM–N 4 /TP with a water bilayer (TM = Nb, Mo, W, and Re) show excellent activity (low limiting potential) but low selectivity. Encouragingly, we find that Mo–N 3 B/TP, Mo–N 2 B 2 -2/TP, W–N 3 B/TP, W–N 2 B 2 -2/TP, Re–N 3 B/TP, Re–N 2 B 2 -2/TP, and Re–N 2 B 2 -1/TP serve as the most efficient NRR electrocatalysts, as they present stability, superior activity, better selectivity with low limiting potentials (−0.18 ∼ −0.90 V), and high Faradaic efficiencies (>99.80%). Based on microkinetic modeling, kinetic analysis of the NRR is performed and shows that the Re–N 2 B 2 -1/TP catalyst is more efficient for NH 3 formation. Additionally, multiple-level descriptors provide insight into the origin of NRR activity and enable fast prescreening among numerous candidates. This work provides a new perspective to design highly efficient catalysts for the NRR under ambient conditions.