Jana, Milan and Saha, Sanjit and Khanra, Partha and Samanta, Pranab and Koo, Hyeyoung and Murmu, Naresh Chandra and Kuila, Tapas (2015) Non-covalent functionalization of reduced graphene oxide using sulfanilic acid azocromotrop and its application as a supercapacitor electrode material. Journal of Materials Chemistry A, 3. pp. 7323-7331.
Full text not available from this repository.Abstract
Sulfanilic acid azocromotrop (SAC) modified reduced graphene oxide (SAC-RGO) was prepared by simple non-covalent functionalization of graphene oxide (GO) followed by post reduction using hydrazine monohydrate. Spectral analysis (Fourier transform infrared, Raman and X-ray photoelectron spectroscopy) revealed that successful modification had occurred of GO with SAC through π–π interaction. The electrical conductivity of SAC-RGO was found to be ∼551 S m−1. The capacitive performance of SAC-RGO was recorded using a three electrode set up with 1 (M) aqueous H2SO4 as the electrolyte. The –SO3H functionalities of SAC contributed pseudocapacitance as evidenced from the redox peaks (at ∼0.43 and 0.27 V) present in the cyclic voltammetric (CV) curves measured for SAC-RGO. The contribution of electrical double layer capacitance was evidenced from the near rectangular shaped CV curves and resulted in a high specific capacitance of 366 F g−1 at a current density of 1.2 A g−1 for SAC-RGO electrode. An asymmetric device (SAC-RGO//RGO) was designed with SAC-RGO as the positive electrode and RGO as the negative electrode. The device showed an energy density of ∼25.8 W h kg−1 at a power density of ∼980 W kg−1. The asymmetric device showed retention in specific capacitance of ∼72% after 5000 charge–discharge cycles. The Nyquist data of the device was fitted with Z-view and different components (solution resistance, charge-transfer resistance and Warburg elements) were calculated from the fitted curves.
Item Type: | Article |
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Subjects: | Chemistry |
Depositing User: | Dr. Sarita Ghosh |
Date Deposited: | 14 Sep 2016 12:00 |
Last Modified: | 14 Sep 2016 12:00 |
URI: | http://cmeri.csircentral.net/id/eprint/251 |
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