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A cobalt–pyrrole coordination compound as high performance cathode catalyst for direct borohydride fuel cells
Pyrrole and cobalt nitrate were used as nitrogen and metal sources respectively to synthesize a dinitratobis(polypyrrole)cobalt(ii) (Co(polypyrrole)(2)(NO(3))(2)) adduct as the precursor of a Co–pyrrole/MPC catalyst. Pyrrole has the capability of polymerization and coordination with Co(ii). Taking t...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9055929/ https://www.ncbi.nlm.nih.gov/pubmed/35521132 http://dx.doi.org/10.1039/d0ra05143h |
Sumario: | Pyrrole and cobalt nitrate were used as nitrogen and metal sources respectively to synthesize a dinitratobis(polypyrrole)cobalt(ii) (Co(polypyrrole)(2)(NO(3))(2)) adduct as the precursor of a Co–pyrrole/MPC catalyst. Pyrrole has the capability of polymerization and coordination with Co(ii). Taking this advantage, the Co(polypyrrole)(2)(NO(3))(2) coordination can form a long-chain structure with abundant and robust Co–N bonds, contributing to significantly increased catalytic sites in the product catalyst. As a result, the obtained Co–pyrrole/MPC (MPC = macroporous carbon) catalyst exhibited high ORR catalytic activity in alkaline media and excellent performance in direct borohydride fuel cell (DBFC). A peak power density up to 325 mW cm(−2) was achieved at ambient condition, outperforming the commercialized Pt/XC-72 benchmark containing 28.6 wt% Pt. The construction of long-chain coordination precursor was verified playing a key role in the electrochemical improvement of Co–pyrrole/MPC catalyst in DBFC. |
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