Immobilizing single atom catalytic sites onto highly reduced carbon hosts: Fe–N4/CNT as a durable oxygen reduction catalyst for Na–air batteries

Immobilizing metal ions on a carbon support usually involves severe aggregation (sintering) and loose attachment of metal ions owing to a weak metal–support interaction. Here, we propose an alternative synthetic strategy termed ‘selective microwave annealing’ (SMA) to stabilize abundant single atom...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2020-01, Vol.8 (36), p.18891-18902
Hauptverfasser: Woo Yeong Noh, Kim, Eun Mi, Kwang Young Kim, Kim, Jin Hyun, Hu Young Jeong, Sharma, Pankaj, Lee, Geunsik, Ji-Wook Jang, Joo, Sang Hoon, Jae Sung Lee
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Immobilizing metal ions on a carbon support usually involves severe aggregation (sintering) and loose attachment of metal ions owing to a weak metal–support interaction. Here, we propose an alternative synthetic strategy termed ‘selective microwave annealing’ (SMA) to stabilize abundant single atom catalytic sites onto a highly reduced form of carbon host with only a few minutes of microwave irradiation. Thus, nitrogen-coordinated single atom iron sites on a carbon nanotube (Fe–N4/CNT) synthesized via SMA show unprecedented oxygen reduction reaction (ORR) activity and pH-universal durability superior to those of thermally annealed Fe–N4/CNT and expensive Pt/C catalysts. Furthermore, an aqueous Na–air battery with our Fe–N4/CNT catalyst operates as effectively as the device with the Pt/C catalyst. The method provides a new concept for the design of various strongly coupled and highly dispersed carbon-supported catalysts, which could open up new avenues for use in a wide range of electrochemical and catalytic applications.
ISSN:2050-7488
2050-7496
DOI:10.1039/d0ta06489k