Enhanced Nitrate‐to‐Ammonia Activity on Fe/ZnO Nanoparticles via Tuning Intermediate Adsorption in Alkaline Electrolyte

Abstract The electrocatalytic recycling of waste nitrate (NO 3 RR) is a promising decentralized route for green ammonia synthesis. Nonetheless, it suffers from the competing hydrogen evolution reaction and the insufficient proton supply in high pH conditions. Herein, iron oxide nanoparticles anchored on ZnO is introduced as a strategy to enhance the water dissociation ability and proton transfer rate, advancing NH 4 + production from alkaline NO 3 RR. Supported by a set of ex situ and in situ characterization, the findings reveal the reduction of iron oxides, along with improvements in charge transfer properties and proton generation from H 2 O. Theoretical calculations show that iron oxides reduce the kinetic barrier of the rate‐limiting step (*NO 2 ‐to‐*NO 2 H) and result in a thermodynamically favorable process to hydrogenation steps, which in turn reduce the overall energy barrier of alkaline NO 3 RR. Optimal catalytic activity is realized with a Fe loading of 0.5 wt.%, delivering a Faradaic efficiency of ≈83% for ammonium with a NH 4 + yield rate of 31 nmol s −1 cm −2 at −0.7 V versus RHE. The results pave the way for the utilization of bi‐metal interaction to tune the reaction pathway for achieving sustainable ammonium synthesis in alkaline, contributing to ongoing efforts to achieve a sustainable nitrogen cycle via N‐based electrochemistry.