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Single-atom oxygen reduction reaction electrocatalysts of Fe, Si, and N co-doped carbon with 3D interconnected mesoporosity

Authors
Kim, Hee SooLee, Chi HoJang, Jue-HyukKang, Min SeokJin, HaneulLee, Kug-SeungLee, Sang UckYoo, Sung JongYoo, Won Cheol
Issue Date
Feb-2021
Publisher
ROYAL SOC CHEMISTRY
Citation
JOURNAL OF MATERIALS CHEMISTRY A, v.9, no.7, pp 4297 - 4309
Pages
13
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF MATERIALS CHEMISTRY A
Volume
9
Number
7
Start Page
4297
End Page
4309
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/449
DOI
10.1039/d0ta11208a
ISSN
2050-7488
2050-7496
Abstract
The development of non Pt-based catalysts (non-PBCs) that show excellent oxygen reduction reaction (ORR) activity for high-performance Zn-air battery (ZAB) and anion exchange membrane fuel cell (AEMFC) is highly necessitated. Here, the unprecedented single-atom ORR activity of Fe, Si, and N co-doped carbon (FeSiNC) supported on 3D interconnected mesoporous carbons (25 and 50 nm) derived from silica templates is reported. Si moieties connected to a carbon surface were involved in the formation of an atomically distributed FeSixN4-x site through substitution of Si at the N position in the Fe-N-4 site, which is the ORR active site of the conventional FeNC. FeSiNC with its larger mesopore (50 nm) exhibits outstanding ORR activity comparable to the most efficient non-Pt-based catalysts and enhanced single-cell performances due to its enhanced mass-transport property. According to theoretical calculations, the ORR activity is originated from not only FeSixN4-x sites located at the basal plane and inter-edge sites, but also C sites adjacent to the Si dopant in both edge and basal regions. Therefore, this study provides a facile strategy toward the rational design of inexpensive and highly active ORR catalysts applicable to single-cell devices.
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