Loading…
Tri-(Fe/F/N)-doped porous carbons as electrocatalysts for the oxygen reduction reaction in both alkaline and acidic media
Developing a low cost, sustainable and high-performance precious-metal free catalyst to replace platinum (Pt)-based catalysts for the oxygen reduction reaction (ORR) in fuel cells has recently attracted significant attention. It is crucial to produce more abundant and more uniformly dispersed ORR ac...
Saved in:
Published in: | Nanoscale 2020-09, Vol.12 (36), p.18826-18833 |
---|---|
Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Developing a low cost, sustainable and high-performance precious-metal free catalyst to replace platinum (Pt)-based catalysts for the oxygen reduction reaction (ORR) in fuel cells has recently attracted significant attention. It is crucial to produce more abundant and more uniformly dispersed ORR active sites for improving the ORR performance of the catalyst. Herein, we synthesized tri-(Fe/F/N)-doped porous carbons as high-efficiency electrocatalysts for the ORR by using Fe-zeolitic imidazolate framework-8 (Fe-ZIF-8) and ammonium fluoride as precursors. The results indicate that the as-prepared FeFNC-5 catalysts exhibit superior ORR activity, methanol tolerance, and long-term stability compared to commercial 20 wt% Pt/C in both alkaline and acidic media because of the abundant and dispersed Fe-N
x
and pyridinic-N active sites, high specific surface area, and hierarchical porous structure. This work provides a new method and insights into the synthesis of Fe, F, and N triple-doped porous carbons as high-efficiency ORR electrocatalysts.
The uniformly dispersed Fe-N
x
and the increased defects after F doping make tri-(Fe/F/N)-doped porous carbons electrocatalysts have superior ORR performance than Pt/C in both alkaline and acidic media. |
---|---|
ISSN: | 2040-3364 2040-3372 |
DOI: | 10.1039/d0nr04920d |