| Literature DB >> 27976867 |
Haitao Wang1, Wei Wang1, Mengxi Gui1, Muhammad Asif1, Zhengyun Wang1, Yang Yu1, Junwu Xiao1, Hongfang Liu1.
Abstract
Developing a facile strategy to synthesize an efficient and inexpensive catalyst for the oxygen reduction reaction (ORR) is critical to the commercialization of many sustainable energy storage and conversion techniques. Herein, a novel and convenient strategy was presented to prepare Fe3O4 embedded into nitrogen-doped mesoporous carbon spheres (Fe3O4/N-MCS) by the polycondensation between methylolmelamines and ammonium ferric citrate (AFC) and subsequent pyrolysis process. In particular, the polycondensation reaction was completely finished within a very short time (6.5 min), and the iron contents can be adjusted and had a great influence on the microstructure. Moreover, the Fe3O4/N-MCS can be used as a robust catalyst for the ORR in alkaline media, and the catalyst with the iron content of 3.35 wt % exhibited excellent electrochemical performance in terms of more positive onset potential (E0 = 1.036 V vs RHE) and half-wave potential (E1/2 = 0.861 V) and much better methanol tolerance and long-term durability, in comparison with that of 20% Pt/C. The remarkable performance was ascribed to the characteristics of large specific surface area, mesoporous structure, high contents of pyridinic N and graphitic N, as well as strong electronic interaction between Fe3O4 and protective N-doped graphitic layers.Entities:
Keywords: ammonium ferric citrate; iron oxides; mesoporous structure; nitrogen-doped carbon matrices; oxygen reduction reaction
Year: 2016 PMID: 27976867 DOI: 10.1021/acsami.6b11608
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229