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Sulfuration of an Fe–N–C Catalyst Containing Fe x C/Fe Species to Enhance the Catalysis of Oxygen Reduction in Acidic Media and for Use in Flexible Zn–Air Batteries
Author(s) -
Qiao Yueyang,
Yuan Pengfei,
Hu Yongfeng,
Zhang Jianan,
Mu Shichun,
Zhou Jihang,
Li Hao,
Xia Huicong,
He Jing,
Xu Qun
Publication year - 2018
Publication title -
advanced materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.707
H-Index - 527
eISSN - 1521-4095
pISSN - 0935-9648
DOI - 10.1002/adma.201804504
Subject(s) - catalysis , bifunctional , materials science , oxygen reduction reaction , oxygen , oxygen reduction , chemical engineering , carbon fibers , carbide , chemistry , metallurgy , composite material , organic chemistry , composite number , electrode , engineering , electrochemistry
During the preparation of atomically dispersed Fe–N–C catalysts, it is difficult to avoid the formation of iron‐carbide‐containing iron clusters (“Fe x C/Fe”), along with the desired carbon matrix containing dispersed FeN x sites. As a result, an uncertain amount of the oxygen reduction reaction (ORR) occurs, making it difficult to maximize the catalytic efficiency. Herein, sulfuration is used to boost the activity of Fe x C/Fe, forming an improved system, “FeNC–S–Fe x C/Fe”, for catalysis involving oxygen. Various spectroscopic techniques are used to define the composition of the active sites, which include Fe–S bonds at the interface of the now‐S‐doped carbon matrix and the Fe x C/Fe clusters. In addition to outstanding activity in basic media, FeNC–S–Fe x C/Fe exhibits improved ORR activity and durability in acidic media; its half‐wave potential of 0.821 V outperforms the commercial Pt/C catalyst (20%), and its activity does not decay even after 10 000 cycles. Interestingly, the catalytic activity for the oxygen evolution reaction (OER) simultaneously improves. Thus, FeNC–S–Fe x C/Fe can be used as a high‐performance bifunctional catalyst in Zn–air batteries. Theoretical calculations and control experiments show that the original FeN x active centers are enhanced by the Fe x C/Fe clusters and the Fe–S and C–S–C bonds.