Uniform Fe3O4/Nitrogen-Doped Mesoporous Carbon Spheres Derived from Ferric Citrate-Bonded Melamine Resin as an Efficient Synergistic Catalyst for Oxygen Reduction
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...
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Veröffentlicht in: | ACS applied materials & interfaces 2017-01, Vol.9 (1), p.335-344 |
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creator | Wang, Haitao Wang, Wei Gui, Mengxi Asif, Muhammad Wang, Zhengyun Yu, Yang Xiao, Junwu Liu, Hongfang |
description | 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 (E 0 = 1.036 V vs RHE) and half-wave potential (E 1/2 = 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. |
doi_str_mv | 10.1021/acsami.6b11608 |
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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 (E 0 = 1.036 V vs RHE) and half-wave potential (E 1/2 = 0.861 V) and much better methanol tolerance and long-term durability, in comparison with that of 20% Pt/C. 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Mater. Interfaces</addtitle><description>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 (E 0 = 1.036 V vs RHE) and half-wave potential (E 1/2 = 0.861 V) and much better methanol tolerance and long-term durability, in comparison with that of 20% Pt/C. 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Mater. Interfaces</addtitle><date>2017-01-11</date><risdate>2017</risdate><volume>9</volume><issue>1</issue><spage>335</spage><epage>344</epage><pages>335-344</pages><issn>1944-8244</issn><eissn>1944-8252</eissn><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 (E 0 = 1.036 V vs RHE) and half-wave potential (E 1/2 = 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.</abstract><pub>American Chemical Society</pub><doi>10.1021/acsami.6b11608</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-9180-6629</orcidid></addata></record> |
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title | Uniform Fe3O4/Nitrogen-Doped Mesoporous Carbon Spheres Derived from Ferric Citrate-Bonded Melamine Resin as an Efficient Synergistic Catalyst for Oxygen Reduction |
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