Abstract
The electrochemical nitrate reduction reaction (NO3−RR) represents a promising and environmentally friendly approach for both the removal of nitrate (NO3−) pollutants and the production of high-value ammonia (NH3). However, this process faces significant challenges in achieving industrial application due to mismatched reaction kinetics involved in the conversion of NO3− to NO2−, the formation of active hydrogen (H*) via water dissociation, and the stepwise hydrogenation processes. In this study, we developed a trimetallic CuCoRu catalyst with multiple active sites to enhance the selective NH3 synthesis at industrial-scale current density, where Cu primarily catalyzes the reduction of NO3− to NO2−, Co facilitates the deep hydrogenation of NO2− to NH3, and Ru promotes water dissociation to generate H*, effectively bridging the aforementioned processes. The optimized CuCoRu catalyst achieves near-100% NH3 Faradaic efficiency with an NH3 yield rate of 14.6 mmol h−1 cm−2 at a current density of 2.5 A cm−2. The practical application in simulated wastewater with different NO3− concentrations and in the membrane electrode assembly demonstrates great potential for industrial application.
| Original language | English |
|---|---|
| Pages (from-to) | 614-623 |
| Number of pages | 10 |
| Journal | Journal of Energy Chemistry |
| Volume | 108 |
| DOIs | |
| State | Published - Sep 2025 |
Keywords
- Ammonia synthesis
- Industrial-scale current density
- Multi-active sites
- Nitrate reduction reaction
- Tandem catalysis