This study demonstrates an innovative Cu-molybdenum phosphide catalyst for nitrate reduction, achieving high Faradaic efficiency while enhancing Zn-nitrate battery power.
The electrochemical nitrate reduction reaction (NITRR) offers a sustainable route for ammonia synthesis and environmental remediation but faces challenges such as sluggish kinetics and competing hydrogen evolution. This study aims to address these limitations by designing a Cu/molybdenum phosphide (MoP) heterostructure catalyst through one-pot calcination, which integrates Cu nanoparticles with MoP nanograins. Structural and electronic analyses confirm the formation of intimate Cu-MoP interfaces, where charge redistribution polarizes Cu to an electron-deficient state (Cuδ+) and enriches MoP with electrons. This configuration enhances nitrate adsorption on Cuδ+, while MoP efficiently supplies protons via accelerated water dissociation. The Cu/MoP catalyst achieves a record-high NH3 Faradaic efficiency (FE) of 98.93% and a yield rate of 30.72 mmol h-1 cm-2 at -0.5 V (vs. RHE), outperforming isolated Cu or MoP. When deployed in a Zn-nitrate battery, the composite cathode delivers a peak power density of 12.97 mW cm-2. This work provides a promising solution to the insufficient active hydrogen supply and poor NH3 conversion efficiency of Cu-based nitrate reduction catalysts.
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Yang et al. (2025) studied this question.
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