Abstract
The electrochemical reduction of nitrate (NO3−) presents a sustainable approach for mitigating NO3− contamination while generating value-added ammonia (NH3). However, achieving high efficiency and selectivity under ambient conditions remains a significant challenge. Here, we develop an enzyme-like CuO-Co3O4 heterojunction catalyst that efficiently facilitates NO3− reduction to NH3 under neutral conditions, mimicking enzymatic active sites to boost activity. The enzyme-like catalyst exhibits an exceptional NO3− conversion rate of 99.6 % and 100 % NH3 selectivity, achieved through the optimization of interfacial electronic interactions. In-situ Raman spectroscopy and density functional theory analyses reveal that cascade reactions facilitated by the CuO-Co3O4 interface significantly enhance the rate-determining step and lower the energy barrier, thereby improving NO3− electroreduction efficiency. Furthermore, a continuous supply system suppling NH4+-N demonstrates its potential to promote plant growth and fruit production, highlighting its practical applicability. This study offers targeted strategies for addressing NO3− contamination, synthesizing value-added NH3, and advancing sustainable agriculture practices.
| Original language | English |
|---|---|
| Article number | 169087 |
| Journal | Chemical Engineering Journal |
| Volume | 524 |
| DOIs | |
| State | Published - 15 Nov 2025 |
Keywords
- Ammonium
- Cascade
- CuO-CoO heterojunctions
- Nitrate electrochemical reduction