Catalytic Role of Adsorption of Electrolyte/Molecules as Functional Ligands on Two-Dimensional TM-N4 Monolayer Catalysts for the Electrocatalytic Nitrogen Reduction Reaction

Two-dimensional single-atom catalysts (2D SACs) have been widely studied on the nitrogen reduction reaction (NRR). The characteristics of 2D catalysts imply that both sides of the monolayer can be catalytic sites and adsorb electrolyte ions or molecules from solutions. Overstrong adsorption of electrolyte ions or molecules on both sides of the catalyst site will poison the catalyst, while the adsorbate on one side of the catalytic site will modify the activity and selectivity of the other side for NRR. Discovering the influence of adsorption of electrolyte ions or molecules as a functional ligand on catalyst performance on the NRR is crucial to improve NRR efficiency. Here, we report this work using the density functional theory (DFT) method to investigate adsorption of electrolyte ions or molecules as a functional ligand. Among all of the studied 18 functional ligands and 3 transition metals (TMs), the results showed that Ru&F, Ru&COOH, and Mo&H2O combinations were screened as electrocatalysis systems with high activity and selectivity. Particularly, the Mo&H2O combination possesses the highest activity with a low ΔGMAX of 0.44 eV through the distal pathway. The superior catalytic performance of the Mo&H2O combination is mainly attributed to the electron donation from the metal d orbital. Furthermore, the functional ligands can occupy the active sites and block the competing vigorous hydrogen evolution reaction. Our findings offer an effective and practical strategy to design the combination of the catalyst and electrolyte to improve electrocatalytic NRR efficiency.