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Facile synthesis of sandwich-like polyaniline/boron-doped graphene nano hybrid for supercapacitors
The physicochemical property of chemically prepared graphene can be significantly changed due to the incorporating of heteroatoms into graphene. In this article, boron-doped graphene sheets are used as carbon substrates instead of graphene for loading polyaniline by in situ polymerization. Compared...
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Published in: | Carbon (New York) 2015-01, Vol.81, p.552-563 |
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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: | The physicochemical property of chemically prepared graphene can be significantly changed due to the incorporating of heteroatoms into graphene. In this article, boron-doped graphene sheets are used as carbon substrates instead of graphene for loading polyaniline by in situ polymerization. Compared with the individual component and polyaniline/non-doped graphene, the sandwich-like polyaniline/boron-doped graphene exhibits remarkably enhanced electrochemical specific capacitance in both acid and alkaline electrolytes. In a three-electrode configuration, the hybrid has a specific capacitance about 406Fg−1 in 1M H2SO4 and 318Fg−1 in 6M KOH at 1mVs−1. In the two-electrode system of a symmetric supercapacitor, this hybrid achieves a specific capacitance about 241 and 189Fg−1 at 0.5Ag−1 with a specific energy density around 19.9 and 30.1Whkg−1, in the acid and alkaline electrolytes, respectively. The as-obtained polyaniline/boron-doped graphene hybrid shows good rate performance. Notably, the obtained electrode materials exhibit long cycle stability in both acid and alkaline electrolytes (∼100% and 83% after 5000 cycles, respectively). The improved electrochemical performance of the hybrid is mainly attributed to the introduction of additional p-type carriers in carbon systems by boron-doping and the well combination of pseudocapacitive conducting polyaniline. |
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ISSN: | 0008-6223 1873-3891 |
DOI: | 10.1016/j.carbon.2014.09.090 |