Ferrocene-based porous organic polymer derived high-performance electrocatalysts for oxygen reduction
Two nitrogen-rich porous organic polymers (POPs) were prepared via facile and low-cost Schiff base chemistry with ferrocene (Fc) and melamine/melem as building blocks. Carbonization of these POP precursors results in porous carbon nanohybrids with carbon composites containing crystalline Fe 3 C/Fe....
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Veröffentlicht in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2017, Vol.5 (42), p.22163-22169 |
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Sprache: | eng |
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Zusammenfassung: | Two nitrogen-rich porous organic polymers (POPs) were prepared
via
facile and low-cost Schiff base chemistry with ferrocene (Fc) and melamine/melem as building blocks. Carbonization of these POP precursors results in porous carbon nanohybrids with carbon composites containing crystalline Fe
3
C/Fe. Characterization based on a variety of techniques demonstrates that the porous carbon nanohybrids feature rich-nitrogen doping, good conductivity and high BET surface area with unique porous structure, endowing them with an excellent catalytic activity toward the oxygen reduction reaction (ORR) in alkaline electrolytes. The catalysts obtained by carbonization at 800 °C (N-Fc-800) exhibit favorable activity with a rather high onset potential and half wave potential of 0.96 and 0.82 V, respectively. Furthermore, a rechargeable zinc-air battery was assembled using the N-Fc-800 as the cathode catalyst. Compared with the commercial Pt/C, the N-Fc-800 based battery displays a considerably high power density of 178 mW cm
−2
with a smaller charge-discharge voltage gap of 0.94 V, and holds excellent stability with a less activity decay (1.0%) over long charge-discharge cycles (200 cycles).
Two nitrogen-rich porous organic polymers (POPs) were prepared
via
Schiff base chemistry. Carbonization of these POPs results in porous carbon nanohybrids which exhibit excellent catalytic activity toward the oxygen reduction reaction (ORR). |
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ISSN: | 2050-7488 2050-7496 2050-7496 |
DOI: | 10.1039/c7ta06515a |