Immobilizing single atom catalytic sites onto highly reduced carbon hosts: Fe–N4/CNT as a durable oxygen reduction catalyst for Na–air batteries. Issue 36 (4th September 2020)

• Record Type: Journal Article
• Authors: Noh, Woo Yeong; Kim, Eun Mi; Kim, Kwang Young; Kim, Jin Hyun; Jeong, Hu Young; Sharma, Pankaj; Lee, Geunsik; Jang, Ji-Wook; Joo, Sang Hoon; Lee, Jae Sung
• Is Part Of: Journal of materials chemistry. Volume 8:Issue 36(2020)
• Page Start: 18891
• Page End: 18902
• Publication Date: 2020-09-04
• Subjects: Materials -- Research -- Periodicals; Chemistry, Analytic -- Periodicals; Environmental sciences -- Research -- Periodicals; 543.0284
• DOI: 10.1039/d0ta06489k
• Languages: English
• ISSNs: 2050-7488

Abstract

Abstract : 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. Abstract : 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.