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The efficient cleavage of the N≡N bond is vital to N2 fixation but remains challenging. In this issue of Chem, Zhang and co-workers report that the interfacial polarization fields triggered by protrusion-shaped Fe single atoms on monolayer MoS2 can promote N≡N splitting via electron injection, resulting in a praiseworthy nitrogen electroreduction.

The electroreduction of nitrogen (N2) to ammonia (NH3) is gravely restricted by its inherent kinetic complexity and energy-intensive multi-electron steps. Most literature has reported that the first step of N2 adsorption and activation is the bottleneck of electrochemistry N2 reduction reaction (NRR). However, it is a considerable challenge to understand the design rule of catalysts with perfect performances for NRR. Here, as a proof-of-concept experiment, we apply the theoretical calculations with the experimental studies to reveal the influence of the high spin related to the size effect and the charge density related to the substrate effect on the catalytic activity of NRR catalysts. The desired ultrafine Rh nanoparticles anchored on CNT exhibit excellent NRR performances, especially high NH3 yield (26.91 μg h−1 mgcat.−1), Faradaic efficiency (23.48 %) and energy efficiency (20.50 %), outperforming most reported NRR electrocatalysts under ambient conditions, which can be attributed to excellent synergism of the high-spin polarization of Rh NPs and the charge exchange between Rh NPs and the substrate that can promote N2 adsorption and activate its intrinsic N N triple bond.