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Advance Aqueous Asymmetric Supercapacitor Based on Large 2D NiCo(2)O(4) Nanostructures and the rGO@Fe(3)O(4) Composite

[Image: see text] NiCo(2)O(4) nanostructure is a widely studied pseudocapacitor material because of its high specific capacitance value. Most of the time, the thickness of the nanostructure inhibits the electrode material from whole-body participation and causes sluggish charge transportation. These...

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Detalles Bibliográficos
Autores principales: Sahoo, Ramkrishna, Acharyya, Paribesh, Singh, Navin Kumar, Pal, Anjali, Negishi, Yuichi, Pal, Tarasankar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6644927/
https://www.ncbi.nlm.nih.gov/pubmed/31457255
http://dx.doi.org/10.1021/acsomega.7b01091
Descripción
Sumario:[Image: see text] NiCo(2)O(4) nanostructure is a widely studied pseudocapacitor material because of its high specific capacitance value. Most of the time, the thickness of the nanostructure inhibits the electrode material from whole-body participation and causes sluggish charge transportation. These phenomena directly interfere with the electrochemical performance of the electrode, such as specific capacitance value, stability, energy density, and so forth. Here, two different thin two-dimensional morphologies (nanosheet and nanoplate) of the NiCo(2)O(4) nanocomposite with a large lateral size are reported using ammonia as a hydrolyzing agent. The large size and flat surface of the as-synthesized materials offer enormous active sites during the electrochemical reaction, and the thin wall makes the ion penetration and transportation very effective and facile. Therefore, the NiCo(2)O(4) nanosheet and nanoplate structures exhibited high specific capacitance values of 1540 and 1333 F/g, respectively, with excellent rate and good cycling stability. Here also, two different advance aqueous asymmetric supercapacitors have been reported utilizing two NiCo(2)O(4) nanostructure materials as positive electrodes and the rGO@Fe(3)O(4) composite as a negative electrode, which exhibited excellent rate and high specific energy without sacrificing the specific power. We also studied the electrochemical activity of the rGO@Fe(3)O(4) composite at different compositions.