Pulse-Engineered Ion Redistribution Suppresses Cation Interference in Electrocatalytic Nitrate Reduction

Electrocatalytic nitrate reduction (eNO 3 RR) to ammonia offers a sustainable route for nitrate remediation and nitrogen resource recovery. However, its implementation in real wastewater remains challenging, with limited strategies to address interference from coexisting ions. Here, we identify Mg 2+ as a representative precipitation-prone impurity and demonstrate that pulsed electrolysis effectively alleviated its inhibitory effects. Under optimized pulsed conditions, the nitrate removal and ammonia yield rate reached 98.0% and 3544.7 μg h –1 cm –2, respectively, restoring the lost performance under static operation with Mg 2+ (85.3% and 2821.5 μg h –1 cm –2 ) and matching the Mg 2+ -free baseline (96.1% and 3449.0 μg h –1 cm –2 ). Mechanistic studies revealed three key functions of pulsing: (i) suppression of local pH elevation, which limits Mg 2+ precipitation and particle growth on the catalyst surface; (ii) dynamic modulation of interfacial ion distributions, reducing Mg 2+ accumulation via electric-field-induced repulsion; and (iii) K + enrichment at the interface, which increases the energy barrier (1.15 eV) for Mg 2+ adsorption and enhances NO 3 – conversion. The pulsed strategy also effectively mitigated cationic interference in complex multi-ion wastewater analogs, demonstrating its broad applicability. Our findings uncover the mechanistic basis of pulsed electrolysis-induced ion redistribution in complex water matrices, establishing a generalizable framework to enhance the eNO 3 RR and other electrocatalytic water treatment processes under realistic conditions.