TM3 (TM = V, Fe, Mo, W) single-cluster catalyst confined on porous BN for electrocatalytic nitrogen reduction

Abstract

• Confined metal clusters in the triplet form as sub-nanometer reactors for NRR. • Mo 3 @p-BN exhibits excellent catalytic activity and selectivity. • A rather low limiting potential (−0.34 V) was obtained. • Mo atoms act as “cache” to accelerate electron transfer. • Synergistic effect makes the “donation–backdonation” mechanism more efficient. Confined metal clusters as sub-nanometer reactors for electrocatalytic N 2 reduction reaction (eNRR) have received increasing attention due to the unique metal-metal interaction and higher activity than single-atom catalysts. Herein, the inspiration of the superior capacitance and unique microenvironment with regular surface cavities of the porous boron nitride (p-BN) nanosheets, we systematically studied the catalytic activity for NRR of transition-metal single-clusters in the triplet form (V 3 , Fe 3 , Mo 3 and W 3 ) confined in the surface cavities of the p-BN sheets by spin-polarized density functional theory (DFT) calculations. After a two-step screening strategy, Mo 3 @p-BN was found to have high catalytic activity and selectivity with a rather low limiting potential (–0.34 V) for the NRR. The anchored Mo 3 single-cluster can be stably embedded on the surface cavities of the substrate preventing the diffusion of the active Mo atoms. More importantly, the Mo atoms in the Mo 3 single-cluster would act as “cache” to accelerate electron transfer between active metal centers and nitrogen-containing intermediates via the intimate Mo-Mo interactions. The cooperation of Mo atoms can also provide a large number of occupied and unoccupied d orbitals to make the "donation–backdonation" mechanism more effective. This work not only provides a quite promising electrocatalyst for NRR, but also brings new insights into the rational design of triple-atom NRR catalysts.