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Porous Organic Polymer-Derived Fe(2)P@N,P-Codoped Porous Carbon as Efficient Electrocatalysts for pH Universal ORR
[Image: see text] A new porous organic polymer (CP-CMP) was designed and synthesized via the direct polymerization of pyrrole and hexakis(4-formyl-phenoxy)cyclotriphosphazene, skipping the tedious synthetic procedure of porphyrin-monomers containing special groups. This special porous organic polyme...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7143406/ https://www.ncbi.nlm.nih.gov/pubmed/32280863 http://dx.doi.org/10.1021/acsomega.9b03851 |
Sumario: | [Image: see text] A new porous organic polymer (CP-CMP) was designed and synthesized via the direct polymerization of pyrrole and hexakis(4-formyl-phenoxy)cyclotriphosphazene, skipping the tedious synthetic procedure of porphyrin-monomers containing special groups. This special porous organic polymer (POP) serves as an “all in one” precursor for C, N, P, and Fe. Direct carbonization of this special POP afforded Fe(2)P@N,P-codoped porous carbons with hierarchical pore structure and high graphitization. Finally, the optimal catalyst (CP-CMP-900) prepared by carbonization of CP-CMP at 900 °C exhibited high efficiency for oxygen electroreduction. Typically, CP-CMP-900 presented an oxygen reduction reaction half-wave potential (E(1/2)) of 0.85, 0.73, and 0.65 V, respectively, in alkaline, neutral, and acidic media, close to those of commercial Pt/C in the same electrolyte (0.843, 0.71, and 0.74 V). Furthermore, it also displayed excellent methanol immunity and long-time stability in various electrolytes better than commercial Pt/C (20%). |
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