摘要
Electrochemical nitrite reduction reaction (NO 2 − RR) is a potential sustainable route for regulating the nitrogen cycle and ambient ammonia (NH 3 ) synthesis. However, it remains a challenge to precisely regulate the reaction pathways and inhibit competing reactions (e.g. hydrogenolysis) for efficient and selective NH 3 production in an aqueous solution environment. Here, we utilize the Schottky barrier-induced surface electric field to construct high-density electron-deficient Pd nanoparticles by modulating the N content in the carbon carrier to promote the enrichment and immobilization of NO 2 − on the electrode surface, which ensures the ultimate selectivity for NH 3 . With these properties, Pd@N 0.14 C with the highest N content achieved excellent catalytic performance for the reduction of NO 2 − to NH 3 with the 100% Faraday efficiency at −0.5 and −0.6 V vs. reversible hydrogen electrode (RHE) for NH 3 production, which was significantly better than Pd/C and Pd@N x C samples with lower N content. This study opens new avenues for rational construction of efficient electrocatalysts for nitrite removal and NH 3 electrosynthesis.
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