Fabrication of Asymmetric Supercapacitors Based on Coordination Polymer Derived Nanoporous Materials

被引:22
|
作者
Salunkhe, Rahul R. [1 ]
Zakaria, Mohamed B. [1 ,2 ]
Kamachi, Yuichiro [1 ]
Alshehri, Saad M. [3 ]
Ahamad, Tansir [3 ]
Torad, Nagy L. [1 ,2 ]
Dou, Shi Xue [4 ]
Kim, Jung Ho [4 ]
Yamauchi, Yusuke [1 ,2 ]
机构
[1] Natl Inst Mat Sci, World Premier Int WPI Res Ctr Mat Nanoarchitecton, 1-1 Namiki, Tsukuba, Ibaraki 3050044, Japan
[2] Waseda Univ, Fac Sci & Engn, Shinjuku Ku, Tokyo 1698555, Japan
[3] King Saud Univ, Dept Chem, Coll Sci, Riyadh 11451, Saudi Arabia
[4] Univ Wollongong, Australian Inst Innovat Mat, Inst Superconducting & Elect Mat, North Wollongong, NSW 2500, Australia
基金
日本科学技术振兴机构; 日本学术振兴会; 澳大利亚研究理事会;
关键词
coordination polymers; nanoporous carbons; nickel oxides; asymmetric supercapacitors; PRUSSIAN BLUE; ELECTRODE MATERIALS; ACTIVATED CARBON; POROUS CARBON; FRAMEWORK; TEMPERATURE; STORAGE; SODIUM; OXIDE; NIO;
D O I
10.1016/j.electacta.2015.05.034
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Considerable efforts have been devoted to the synthesis and characterization of novel nanoporous materials because of their versatile applications, such as gas storage, catalysis, and energy storage applications. Controllable synthesis of coordination polymers (CPs) with two-and three-dimensional architectures has given impetus to the development of nanomaterials with many exciting properties and applications. Here, we focus on CP-derived nanoporous materials and study their electrochemical performance as electrode materials in supercapacitors. Nanoporous carbon is prepared by simple carbonization of zinc-containing zeolitic imidazolate framework (ZIF-8). On the other hand, nanoporous nickel oxide (NiO) is prepared by thermal treatment of cyano-bridged CPs. By using the above two electrodes, we fabricate a novel asymmetric supercapacitor. These CP-derived nanoporous materials exhibit excellent electrochemical performance with high specific energy and specific power, and excellent cycling stability. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:94 / 99
页数:6
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