Synthesis and Characterization of Reduced Graphene Oxide for Supercapacitor Application with a Biodegradable Electrolyte

被引:20
|
作者
Adarsh Rag, S. [1 ]
Selvakumar, M. [2 ]
Bhat, Somashekara [1 ]
Chidangil, Santhosh [3 ]
De, Shounak [1 ]
机构
[1] Manipal Acad Higher Educ, Manipal Inst Technol, Dept Elect & Commun Engn, Manipal 576104, Karnataka, India
[2] Manipal Acad Higher Educ, Manipal Inst Technol, Dept Chem, Manipal 576104, Karnataka, India
[3] Manipal Acad Higher Educ, Dept Atom & Mol Phys, Manipal 576104, Karnataka, India
关键词
Reduced graphene oxide; modified Hummers' method; bio-polymer electrolyte; supercapacitor; POLYMER ELECTROLYTES; HIGH-PERFORMANCE; CARBON; REDUCTION; GRAPHITE;
D O I
10.1007/s11664-019-07853-9
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
The possibility of synthesizing a proton-conducting biopolymer electrolyte of polyvinyl alcohol (PVA) doped with 1-ethyl-3-methylimidazolium ethyl sulphate ([EMIM][EtSO4]) ionic liquid and ammonium acetate (CH3COONH4) by solvent casting has been investigated. The ionic conductivity of electrolyte membrane increased with addition of IL and fairly good ionic conductivity of 6.56 x 10(-4) S cm(-1) has been attained. The conductivity studies of the biopolymer electrolyte membrane have been carried out in coplanar configuration. Graphene oxide (GO) and reduced graphene oxide (rGO) have been synthesized by a chemical method. The prepared rGO has been characterized using ultraviolet-visible (UV-Vis) absorption spectroscopy, x-ray diffraction, Raman and x-ray photoelectron spectroscopy analysis. The surface area of rGO has been increased from 2.69 m(2) g(-1) to 203.78 m(2) g(-1). In this work, a supercapacitor with a symmetric electrode has been fabricated using PVA-doped ionic liquid as a biopolymer electrolyte and rGO as electrode materials. Its electrochemical performance has been verified, and the device exhibited a good specific capacitance of 138 F g(-1). This combination was found to be very useful to improve the capacitance of supercapacitor.
引用
收藏
页码:985 / 994
页数:10
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