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Supercapacitive properties of coiled carbon nanotubes directly grown on nickel nanowires
In this paper, Coiled carbon nanotubes (CNTs) have been grown directly on an anodized aluminum oxide (AAO) template by using catalytic chemical vapor deposition (CVD). The nanochannels of the AAO template, which is covered on one side with a conducting Au layer, were filled by using Catalytic Ni nan...
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Published in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2014-11, Vol.2 (41), p.17446-17453 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | In this paper, Coiled carbon nanotubes (CNTs) have been grown directly on an anodized aluminum oxide (AAO) template by using catalytic chemical vapor deposition (CVD). The nanochannels of the AAO template, which is covered on one side with a conducting Au layer, were filled by using Catalytic Ni nanowires (Ni-NWs). Scanning electron microscopy (SEM/EDX) and Raman spectroscopy were used to prove the formation of coiled CNTs on Ni-NWs. Cyclic voltammetry, galvanostatic charge-discharge, and impedance spectroscopy were used to investigate the capacitive behavior of the coiled CNT/Ni-NW. Electrochemical analysis revealed that as electrodes for supercapacitors the coiled CNT/NW porous structured materials exhibit a high specific capacitance (202 F g super(-1) at a current density of 10 A g super(-1)) as well as excellent cycle stability and can retain more than 92% of the initial response after 6000 cycles. On the other hand as prepared coiled CNT/Ni-NW electrode worked over a wide potential window (2.1 V) in 1 M Na sub(2)SO sub(4) aqueous solution at room temperature. Combining the specific capacitance with the large electrochemical window ensures the superior energy and power densities of nanostructure electrodes, which would be useful to improve the performance of new energy storage technologies. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/c4ta03022b |