Study on the relation between pore size and supercapacitance in mesoporous carbon electrodes with silica-supported carbon nanomembranes

被引:48
作者
Zhi, Jian [1 ]
Wang, Youfu [1 ]
Deng, Sheng [1 ]
Hu, Aiguo [1 ]
机构
[1] E China Univ Sci & Technol, Sch Mat Sci & Engn, Shanghai Key Lab Adv Polymer Mat, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
SELF-ASSEMBLED MONOLAYERS; BERGMAN CYCLIZATION; ION SIZE; CAPACITANCE; PERFORMANCE; NANOSHEETS;
D O I
10.1039/c4ra06260d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electrochemical capacitors (ECs) have traditionally been considered as standing at the opposite end against batteries in energy-power diagram. They charge and discharge faster than batteries but are limited by much lower energy density. By optimizing the pore structure of porous electrode materials, the performance of ECs could overcome this limitation. However to date, no study has addressed the complex relationship between the texture parameters of the electrode materials and the supercapacitance of ECs. Using silica-supported carbon nanomembranes, four electrode materials with similar pore geometry are generated. The electrodes with a pore size of 4.14 nm shows the highest capacitance of 305 F g(-1) in aqueous electrolytes. A new model is developed to simulate the accommodation of the solvated ions at the electrode surface. The simulation reveals that the optimal capacitance of ECs can be achieved using porous carbon electrode materials with open pores of 3.0-5.0 nm.
引用
收藏
页码:40296 / 40300
页数:5
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