A new approach of structural and chemical modification on graphene electrodes for high-performance supercapacitors

被引:54
作者
Hwang, Yun-Hwa [1 ]
Lee, Sun Min [1 ]
Kim, Yong Jae [1 ]
Kahng, Yung Ho [1 ,2 ]
Lee, Kwanghee [1 ,3 ,4 ]
机构
[1] Gwangju Inst Sci & Technol, Res Inst Solar & Sustainable Energies RISE, Gwangju 500712, South Korea
[2] Chonnam Natl Univ, Dept Phys Educ, Gwangju 500757, South Korea
[3] Gwangju Inst Sci & Technol, Sch Mat Sci & Engn, Gwangju 500712, South Korea
[4] Gwangju Inst Sci & Technol, HCAM, Gwangju 500712, South Korea
关键词
HIGH-ENERGY; FUNCTIONALIZED GRAPHENE; COMPOSITE ELECTRODES; CARBON; OXIDE; REDUCTION; ACTIVATION; FRAMEWORKS; NANOSHEETS; NETWORKS;
D O I
10.1016/j.carbon.2015.12.079
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The low energy density of graphene-based supercapacitors has been a critical bottleneck for their commercialization. In particular, the poor capacitance due to the lack of electrically porous channels and insufficient Faradaic reactions in reduced graphene oxide (RGO) electrodes has been a major limiting factor for their successful application. Herein, we demonstrate an innovative process for modifying the electrode properties with well-interconnected porous channels and oxygen-functional groups (denoted as the PRGO-O electrode) achieved via a ZnO-template assisted by alkaline treatment at room temperature. The PRGO-O electrodes are dominated by hierarchical mesoporous structures located between the isolated macroporous RGO interlayers and arranged sequentially by oxygen-functional groups anchored on the surface of interconnected porous structures. Those synergetic effects of interconnected porous structures and oxygen-functionalization resulted in a specific capacitance of 322.1 F g(-1) with a high energy density of 38.8 Wh kg(-1) in two-electrode supercapacitor cells. This result provides a promising solution for designing high-capacitive and high-rate electrodes for high-performance energy storage devices. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7 / 15
页数:9
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