Enhanced electrochemical nitrate reduction to ammonia with nanostructured Mo2C on carbon nanotube-reduced graphene oxide hybrid support

The electrochemical nitrate reduction reaction (NO3−RR) is emerging as a promising method for ammonia production under ambient conditions while simultaneously addressing nitrate pollution. Due to the complexity of NO3−RR, which involves multi-electron/proton transfer and competes with the hydrogen e...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Dalton transactions : an international journal of inorganic chemistry 2024-11, Vol.53 (45), p.18141-18147
Hauptverfasser: Jang, So Eun, Jae Young Kim, Youn, Duck Hyun
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The electrochemical nitrate reduction reaction (NO3−RR) is emerging as a promising method for ammonia production under ambient conditions while simultaneously addressing nitrate pollution. Due to the complexity of NO3−RR, which involves multi-electron/proton transfer and competes with the hydrogen evolution reaction (HER), the development of efficient electrocatalysts with high activity and stability is crucial. In this study, we report the use of Mo2C nanoparticles homogeneously dispersed on a carbon nanotube-reduced graphene oxide hybrid support (Mo2C/CNT-RGO) as an effective electrocatalyst for NO3−RR. The three-dimensional CNT-RGO hybrid provides a large surface area for electrolyte contact, enhanced electrical conductivity, and prevents the aggregation of Mo2C nanoparticles. Consequently, the Mo2C/CNT-RGO electrocatalyst demonstrated high NO3−RR performance, achieving a maximum NH3 production rate of 5.23 mg h−1 cm−2 with a faradaic efficiency of 95.9%. Mo2C/CNT-RGO also exhibited excellent long-term stability during consecutive cycling tests. This work presents a promising strategy for developing high-performance and durable NO3−RR electrocatalysts.
ISSN:1477-9226
1477-9234
1477-9234
DOI:10.1039/d4dt02817a