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Order of Activity of Nitrogen, Iron Oxide, and FeNx Complexes towards Oxygen Reduction in Alkaline Medium

机译:氮气,氧化铁和FENx复合物的活性顺序氧化碱性介质的氧气减少

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摘要

In alkaline medium, it seems that both metal-free and iron-containing carbon-based catalysts, such as nitrogen-doped nanocarbon materials, FeOx-doped carbon, and Fe/N/C catalysts, are active for the oxygen reduction reaction (ORR). However, the order of activity of these different active compositions has not been clearly determined. Herein, we synthesized nitrogen-doped carbon black (NCB), Fe3O4/CB, Fe3O4/NCB, and FeN4/CB. Through the systematic study of the ORR catalytic activity of these four catalysts in alkaline solution, we confirmed the difference in the catalytic activity and catalytic mechanism for nitrogen, iron oxides, and Fe-N complexes, respectively. In metal-free NCB, nitrogen can improve the ORR catalytic activity with a four-electron pathway. Fe3O4/CB catalyst did not exhibit improved activity over that of NCB owing to the poor conductivity and spinel structure of Fe3O4. However, FeN4 coordination compounds as the active sites showed excellent ORR catalytic activity.
机译:在碱性培养基中,似乎既有金属和含铁的碳基催化剂,如氮掺杂的纳米碳材料,飞掺杂碳和Fe / N / C催化剂,对氧还原反应有效(ORR )。 然而,这些不同活性组合物的活性顺序尚未明确确定。 在此,我们合成氮掺杂炭黑(NCB),Fe3O4 / Cb,Fe3O4 / NCb和Fen4 / Cb。 通过对碱溶液中这四种催化剂的ORR催化活性的系统研究,我们确认了氮,氧化铁和Fe-N复合物的催化活性和催化机制的差异。 在无金属NCB中,氮气可以通过四电子通路改善ORR催化活性。 由于Fe3O4的导电性差和尖晶石结构,Fe 3 O 4 / Cb催化剂未在NCB的情况下表现出改善的活性。 然而,Fen4配位化合物作为活性位点显示出优异的ORR催化活性。

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