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Metal–organic framework–derived Ni@C and NiO@C as anode catalysts for urea fuel cells
Highly porous self-assembled nanostructured Ni@C and NiO@C were synthesized via calcination of a Ni-based metal–organic framework. The morphology, structure, and composition of as synthesized Ni@C and NiO@C were characterized by SEM, FIB-SEM, TEM, and XRD. The electro-catalytic activity of the Ni@C...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6959365/ https://www.ncbi.nlm.nih.gov/pubmed/31937844 http://dx.doi.org/10.1038/s41598-019-57139-7 |
Sumario: | Highly porous self-assembled nanostructured Ni@C and NiO@C were synthesized via calcination of a Ni-based metal–organic framework. The morphology, structure, and composition of as synthesized Ni@C and NiO@C were characterized by SEM, FIB-SEM, TEM, and XRD. The electro-catalytic activity of the Ni@C and NiO@C catalysts towards urea oxidation was investigated using cyclic voltammetry. It was found that the Ni@C had a higher residual carbon content and a higher specific surface area than NiO@C, thus exhibiting an enhanced electrochemical performance for urea oxidation. A direct urea fuel cell with Ni@C as an anode catalyst featured an excellent maximum power density of 13.8 mW cm(−2) with 0.33 M urea solution in 1 M KOH as fuel and humidified air as oxidant at 50 °C, additionally showing excellent stability during continuous 20-h operation. Thus, this work showed that the highly porous carbon-supported Ni catalysts derived from Ni-based metal–organic framework can be used for urea oxidation and as an efficient anode material for urea fuel cells. |
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