Abstract
Electrochemical reduction of nitrate (NO3-RR) to ammonia (NH4+/NH3) offers promising prospects for NO3- treatment. However, this process still suffers from NH4+ causing secondary pollution and catalyst deactivation in high-concentration NO3- wastewater. Herein, a high-performance system comprising a hematite (α-Fe2O3) electrode and a water-resistant membrane achieved 97.6% NO3- removal and 81.6% NH4+ as (NH4)2SO4in situ recovery at wastewater-level NO3-. The system exhibited an energy consumption of 62.2 kWh·KgNH3-1 and a Faradaic efficiency of 85.9%. In-situ spectroscopy and electrochemical measurements revealed that α-Fe2O3 acted as both an electron transfer mediator for reducing NO3- to NO2- and an active center for NH3 formation via NO2-/Fe(Ⅱ) redox. Density functional theory calculations identified *HNO3 to *NO2 as potential-determining step of NO3-RR. Natural hematite-based system exhibited 74.8% total inorganic nitrogen removal and 77.1% NH4+ recovery for actual photovoltaic wastewater. This study provides insights into the development of electrochemical systems for resourcefully treating NO3--containing wastewater.
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