The practical deployment of the electrochemical nitrate reduction reaction (eNO 3 RR) for wastewater remediation is primarily hindered by the difficulty of achieving high N 2 selectivity due to the complex multi‐electron transfer pathways and the formation of competing by‐products. Herein, we develop an N‐doped CuO catalyst supported on nickel foam (N‐CuO/NF) through a facile molten‐salt route followed by controlled annealing. The optimized catalyst exhibits enhanced kinetics for eNO 3 RR, reduced charge‐transfer resistance, and an increased electrochemically active surface area. Remarkably, Cl − incorporation into the electrolyte establishes a synergistic interaction between Cl − ‐mediated anodic oxidation and the coexisting Cu 0 /Cu 2+ sites on the optimal N‐CuO/NF‐3h. This synergy enables simultaneous achievement of high nitrate‐removal efficiency (>90%) and high N 2 selectivity (~90%) in an undivided cell. Mechanistic investigations indicate that anodically generated hypochlorous acid (HOCl) oxidizes cathodically produced NH 4 + to N 2 , effectively suppressing ammonia accumulation. Moreover, N‐CuO/NF‐3h demonstrates outstanding cycling stability over four consecutive cycles, with minimal activity loss (<8%) and maintained structural integrity. This work underscores the dual role of N‐doping in modulating the electronic structure of CuO and the pivotal role of Cl − in steering the reaction pathway toward N 2 formation. The findings offer a practical strategy for selective nitrate‐to‐N 2 conversion in wastewater treatment.
Li et al. (Sun,) studied this question.