Fluorine-enriched mesoporous carbon as efficient oxygen reduction catalyst: understanding the defects in porous matrix and fuel cell applications. Issue 12 (20th November 2019)

• Record Type: Journal Article
• Authors: Parthiban, V.; Bhuvaneshwari, Balasubramaniam; Karthikeyan, J.; Murugan, P.; Sahu, A. K.
• Is Part Of: Nanoscale advances. Volume 1:Issue 12(2019)
• Page Start: 4926
• Page End: 4937
• Publication Date: 2019-11-20
• Subjects: 620.5
• DOI: 10.1039/c9na00572b
• Languages: English
• ISSNs: 2516-0230

Abstract

Abstract : Synthesis of fluorine-doped mesoporous carbon as a novel alternative metal-free ORR electrocatalyst. Abstract : Herein, fluorine enrichment in mesoporous carbon (F-MC) was explored to introduce maximum charge polarization in the porous matrix, which is beneficial for the preferential orientation of O2 molecules and their subsequent reduction. Ex situ doping of F to porous carbon derived from phloroglucinol–formaldehyde resin using Pluronic F-127 as a structure-directing agent is standardized. The optimized F-MC catalyst exhibited excellent electrocatalytic activity towards the oxygen reduction reaction (ORR) in alkaline media (0.1 M KOH) with an onset potential of −0.10 V vs. SCE and diffusion-limiting current of 4.87 mA cm −2, while displaying only about 50 mV overpotential in the half-wave region compared to Pt–C (40 wt%). In the stability test, the catalyst showed only 10 mV negative shift in its half-wave potential after 10 000 potential cycles. The rotating ring disk electrode (RRDE) experiments revealed that F-MC follows the most preferable 4 e − pathway ( n = 3.61) with a moderate peroxide (HO2 − ) yield. This was further supported by density functional theory calculations and also deeply explains the existence of defects being beneficial for the ORR. The F-MC catalyst owing to its promising ORR activity and long-term electrochemical stability can be viewed as a potential alternative ORR catalyst for anion exchange membrane fuel cell applications.