Cu1‐Fe Dual Sites for Superior Neutral Ammonia Electrosynthesis from Nitrate

Abstract The electrochemical nitrate reduction reaction (NO 3 RR) is able to convert nitrate (NO 3 − ) into reusable ammonia (NH 3 ), offering a green treatment and resource utilization strategy of nitrate wastewater and ammonia synthesis. The conversion of NO 3 − to NH 3 undergoes water dissociation to generate active hydrogen atoms and nitrogen‐containing intermediates hydrogenation tandemly. The two relay processes compete for the same active sites, especially under pH‐neutral condition, resulting in the suboptimal efficiency and selectivity in the electrosynthesis of NH 3 from NO 3 − . Herein, we constructed a Cu 1 ‐Fe dual‐site catalyst by anchoring Cu single atoms on amorphous iron oxide shell of nanoscale zero‐valent iron (nZVI) for the electrochemical NO 3 RR, achieving an impressive NO 3 − removal efficiency of 94.8 % and NH 3 selectivity of 99.2 % under neutral pH and nitrate concentration of 50 mg L −1 NO 3 − −N conditions, greatly surpassing the performance of nZVI counterpart. This superior performance can be attributed to the synergistic effect of enhanced NO 3 − adsorption on Fe sites and strengthened water activation on single‐atom Cu sites, decreasing the energy barrier for the rate‐determining step of *NO‐to‐*NOH. This work develops a novel strategy of fabricating dual‐site catalysts to enhance the electrosynthesis of NH 3 from NO 3 − , and presents an environmentally sustainable approach for neutral nitrate wastewater treatment.