Single-metal-atom site with high-spin state embedded in defective BN nanosheet promotes electrocatalytic nitrogen reduction

Single-atom catalysts (SACs) especially supported on two-dimensional nitrogen-doped carbon substrate have been widely reported to be able to effectively promote electrocatalytic N 2 reduction reaction (eNRR). The precise design of single-metal-atom active site (SMAS) calls for fundamental understanding of its working mechanism for enhanced eNRR performance. Herein, by means of density functional theory calculations, we theoretically investigate the eNRR performance of nine prototypical SMAS, namely, MN 2 B 2 (M: transition metals of IIIB, IVB and VB groups) which comprises of asymmetric ligands of N 2 B 2 embedded in defective BN nanosheet. Our results reveal the significant role of spin state of SMAS in tuning the potential-determining steps of eNRR, in which MN 2 B 2 site with higher spin magnetic moment ( μ ) is beneficial to reducing limiting potentials ( U L ) of eNRR. Specially, CrN 2 B 2 ( μ = 4 μ B ), VN 2 B 2 ( μ = 3 μ B ) and MoN 2 B 2 ( μ = 2 μ B ) demonstrate high activity and selectivity to eNRR. The asymmetric ligands of N 2 B 2 are deemed to be superior over mono-symmetric ligands. More importantly, our results demonstrate that breaking (or deviating) of the scaling relations between key N-containing intermediates (*N 2 H/*N 2 and *NH 2 /*N 2 ) on MN 2 B 2 can be realized by enhancing spin state of SMAS which renders the active site a balanced N-affinity critical for efficient eNRR. This observation is validated by the calculated Sabatier volcano-shape relation between eNRR limiting potentials and N 2 adsorption energy. Our study develops the guidance for catalyst design to boost eNRR performance by tuning the spin state of an active site.