Electrocatalytic nitrate reduction sustainably produces ammonia and alleviates water pollution, yet is still challenging due to the kinetic mismatch and hydrogen evolution competition. Cu/Cu 2 O heterojunction is proven effective to break the rate‐determining NO 3 − ‐to‐NO 2 − step for efficient NH 3 conversion, while it is unstable due to electrochemical reconstruction. Here we report a programmable pulsed electrolysis strategy to achieve reliable Cu/Cu 2 O structure, where Cu is oxidized to CuO during oxidation pulse, then regenerating Cu/Cu 2 O upon reduction. Alloying with Ni further modulates hydrogen adsorption, which transfers from Ni/Ni(OH) 2 to N‐containing intermediates on Cu/Cu 2 O, promoting NH 3 formation with a high NO 3 − ‐to‐NH 3 Faraday efficiency (88.0±1.6 %, pH 12) and NH 3 yield rate (583.6±2.4 μmol cm −2 h −1 ) under optimal pulsed conditions. This work provides new insights to in situ electrochemically regulate catalysts for NO 3 − ‐to‐NH 3 conversion.
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Bu et al. (2023) studied this question.
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