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Carbon Supported Engineering NiCo(2)O(4) Hybrid Nanofibers with Enhanced Electrocatalytic Activity for Oxygen Reduction Reaction

The design of cheap and efficient oxygen reduction reaction (ORR) electrocatalysts is of a significant importance in sustainable and renewable energy technologies. Therefore, ORR catalysts with superb electrocatalytic activity and durability are becoming a necessity but still remain challenging. Her...

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Detalles Bibliográficos
Autores principales: Hassan, Diab, El-safty, Sherif, Khalil, Khalil Abdelrazek, Dewidar, Montasser, Abu El-magd, Gamal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5457091/
https://www.ncbi.nlm.nih.gov/pubmed/28773878
http://dx.doi.org/10.3390/ma9090759
Descripción
Sumario:The design of cheap and efficient oxygen reduction reaction (ORR) electrocatalysts is of a significant importance in sustainable and renewable energy technologies. Therefore, ORR catalysts with superb electrocatalytic activity and durability are becoming a necessity but still remain challenging. Herein, we report C/NiCo(2)O(4) nanocomposite fibers fabricated by a straightforward electrospinning technique followed by a simple sintering process as a promising ORR electrocatalyst in alkaline condition. The mixed-valence oxide can offer numerous accessible active sites. In addition, the as-obtained C/NiCo(2)O(4) hybrid reveals significantly remarkable electrocatalytic performance with a highly positive onset potential of 0.65 V, which is only 50 mV lower than that of commercially available Pt/C catalysts. The analyses indicate that C/NiCo(2)O(4) catalyst can catalyze O(2)-molecules via direct four electron pathway in a similar behavior as commercial Pt/C catalysts dose. Compared to single NiCo(2)O(4) and carbon free NiCo(2)O(4), the C/NiCo(2)O(4) hybrid displays higher ORR current and more positive half-wave potential. The incorporated carbon matrices are beneficial for fast electron transfer and can significantly impose an outstanding contribution to the electrocatalytic activity. Results indicate that the synthetic strategy hold a potential as efficient route to fabricate highly active nanostructures for practical use in energy technologies.