超级电容器
材料科学
电化学
沸石咪唑盐骨架
电极
咪唑酯
多孔性
纳米技术
化学工程
电容
纳米结构
金属有机骨架
复合材料
吸附
化学
有机化学
工程类
物理化学
作者
Henan Jia,Zhaoyue Wang,Xiaohang Zheng,Yidong Cai,Jinghuang Lin,Haoyan Liang,Junlei Qi,Jian Cao,Jicai Feng,Weidong Fei
标识
DOI:10.1016/j.electacta.2019.04.192
摘要
Hollow nanostructures with high complexity in shell architectures have attracted tremendous interest in electrode materials for energy storage and conversion because of their unique structural features. However, the synthesis of delicate structures for hollow metal sulfides are still difficult. Herein, we demonstrate the designed synthesis of porous quadruple-shelled CoS2 hollow dodecahedrons with the concave surfaces through a template engaged formation process. Uniform yolk-shell Co3O4 dodecahedrons are first synthesized from zeolitic imidazolate framework-67 and then transformed into quadruple-shelled CoS2 hollow dodecahedrons through the reaction with sulfur powder. As the result of the assembly of the advantages from materials and structures, when evaluating as electrodes for supercapacitors, the porous quadruple-shelled CoS2 shows a high specific capacity of 375.2 C g−1 with a good rate performance and excellent stability with 92.1% retention after 10000 cycles. Moreover, the assembling quadruple-shelled CoS2//active carbon asymmetric supercapacitor achieves a high energy density of 52.1 Wh kg−1, excellent specific capacitance (146 F g−1 at 0.5 A g−1), and electrochemical cycling stability (89% retention after 5000 cycles). The improved electrochemical performance of quadruple-shelled CoS2 hollow dodecahedrons demonstrates the importance of design of hollow electrodes materials with higher complexity.
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