Abstract

Electrochemical reduction of nitrate (NO3−) to ammonia (NH3) in aqueous media is a double-advantage process, which can convert the main pollutant in water to the most useful chemical feedstocks. However, the design and development of highly effective and selective catalyst for NO3− reduction reaction (NO3−RR) is still challenging currently, as the NO3−RR contains multiple pathways and suppresses each other. Here, we demonstrate a highly active and selective Zn single atom supported microporous N-doped carbon catalyst, which was characterized by the atomic resolution high-angle annular dark field-scanning transmission electron microscopy, achieving excellent NO3−RR performance (NO3− conversion: 97.2 %; NH3 selectivity: 94.9 %; NH3 yield rate: ∼39,000 μg h−1 mgcat.−1; Faradaic efficiency: 94.8 %). Density functional theory calculations confirm that the atomically dispersed Zn atom coordinated with four N atoms has moderate interaction with NO3− species due to its positive charge. The reaction mechanism and potential determining step for NO3−RR on single Zn atom were further determined. This research provides an exciting new way for the rational design and development of single atom catalyst for advanced electrochemical applications.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call