Self-assembly induced metal ionic-polymer derived Fe-N-x/C nanowire as oxygen reduction reaction electrocatalyst
Metal/nitrogen co-doped carbon (M-N-x/C) materials have shown their good catalytic activity for electrochemical/chemical reactions in energy conversion devices and organics synthesis. However, the preparation of M-N-x/C materials usually involves a high-temperature pyrolysis step, it generates not o...
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Veröffentlicht in: | Journal of catalysis 2020-11, Vol.391, p.1-10 |
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Hauptverfasser: | , , , , , , |
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Sprache: | eng |
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Zusammenfassung: | Metal/nitrogen co-doped carbon (M-N-x/C) materials have shown their good catalytic activity for electrochemical/chemical reactions in energy conversion devices and organics synthesis. However, the preparation of M-N-x/C materials usually involves a high-temperature pyrolysis step, it generates not only active M-N-x sites but also inactive metal-based aggregates that restrict their activity. How to prepare the M-N-x/ C materials with high density of M-N-x sites and specific nanostructure remains a challenge. Herein, we report a general method of "self-assembly induced metal ionic polymer" for preparing M-N-x/C precursors, which can not only preferentially generate M-N-x sites by inhibiting metal aggregation during pyrolysis, but also produce advanced nanostructure for catalysis. Taking the preparation of Fe-N-x/C as an example, the self-assembled nanosheets of [Fe(CN)(6)](4)center dot{[C6H4-(NH3)(2)](2)}(4+) compounds are used as prefabricated materials, which effectively induce the formation of metal ionic-polymer nanowires and nanoparticles. They are applied to synthesize the Fe-N-x/C nanowires and nanoparticles with single metal atoms, respectively. The Fe-N-x/C nanowires exhibit the excellent oxygen reduction reaction activity with the half-wave potentials of 0.82 and 0.92 V under acidic and alkaline conditions, respectively. The proposed strategy can be a general method to prepare the M-N-x/C catalyst precursors with the special morphology and high thermal stability. (C) 2020 Elsevier Inc. All rights reserved. |
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ISSN: | 0021-9517 1090-2694 |
DOI: | 10.1016/j.jcat.2020.08.016 |