Electrochemical nitrate reduction demonstrates efficient ammonia production in a dual-process system, suggesting improved sustainability in chemical synthesis.
Electrochemical nitrate reduction represents a promising route for sustainable ammonia (NH 3 ) production, yet its practical deployment is constrained by the limited efficiency of state‐of‐the‐art electrocatalysts and immature system architectures. Here, we report a generalist copper–nickel–tungsten tri‐component tandem electrocatalyst via a sequential microwave‐hydrothermal deposition route. Under pulsed electrolysis conditions, the catalyst delivers a remarkable Faradaic efficiency of 97.1% and a record‐high ammonia yield rate of 43.87 mg h −1 cm −2 . Online differential electrochemical mass spectrometry (DEMS) identifies key intermediates and associated pathways, while density functional theory (DFT) calculations elucidate the cooperative roles of each component: the copper component facilitates nitrate adsorption and deoxygenation, the nickel component promotes water dissociation for steady *H supply, and the tungsten component serves as a dynamic *H reservoir. This synergy efficiently suppresses hydrogen evolution and enhances ammonia selectivity. Furthermore, coupling with glycerol valorization (to formic acid) as the anodic reaction demonstrates the potential for energy‐efficient ammonia electrosynthesis. Collectively, this work offers both design strategies and mechanistic understanding for next‐generation multi‐component tandem electrocatalysts targeting advanced nitrogen‐based chemical synthesis.
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Nickel et al. (2026) studied this question.
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