Electronic Structure Optimization and Proton-Transfer Enhancement on Titanium Oxide-Supported Copper Nanoparticles for Enhanced Nitrogen Recycling from Nitrate-Contaminated Water

Abstract

Electrocatalytic reduction of nitrate to NH₃ (NO3RR) on Cu offers sustainable NH₃ production and nitrogen recycling from nitrate-contaminated water. However, Cu affords limited NO3RR activity owing to its unfavorable electronic state and the slow proton transfer on its surface, especially in neutral/alkaline media. Furthermore, although a synchronous "NO3RR and NH₃ collection" system has been developed for nitrogen recycling from nitrate-laden water, no system is designed for natural water that generally contains low-concentration nitrate. Herein, we demonstrate that depositing Cu nanoparticles on a TiO₂ support enables the formation of electron-deficient Cu^δ+ species (0 < δ ≤ 2), which are more active than Cu⁰ in NO3RR. Furthermore, TiO₂-Cu coupling induces local electric-field enhancement that intensifies water adsorption/dissociation at the interface, accelerating proton transfer for NO3RR on Cu. With the dual enhancements, TiO₂-Cu delivers an NH₃-N selectivity of 90.5%, mass activity of 41.4 mg-N h g_Cu^-1, specific activity of 377.8 mg-N h^-1 m^-2, and minimal Cu leaching (<25.4 μg L^-1) when treating 22.5 mg L^-1 of NO₃^--N at -0.40 V, outperforming most of the reported Cu-based catalysts. A sequential NO3RR and NH₃ collection system based on TiO₂-Cu was then proposed, which could recycle nitrogen from nitrate-contaminated water under a wide concentration window of 22.5-112.5 mg L^-1 at a rate of 209-630 mg_N m^-2 h^-1. We also demonstrated this system could collect 83.9% of nitrogen from NO₃^--N (19.3 mg L^-1) in natural lake water.