超级电容器
氢氧化钾
水溶液
材料科学
电解质
电化学
比表面积
碳化
碳纤维
介孔材料
乙腈
化学工程
电容
电极
分析化学(期刊)
化学
复合材料
有机化学
工程类
复合数
物理化学
催化作用
扫描电子显微镜
作者
Nan Mao,Huanlei Wang,Sui Yang,Yongpeng Cui,Jesse Pokrzywinski,Jing Shi,Wei Liu,Shougang Chen,Xin Wang,David Mitlin
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2017-03-27
卷期号:10 (5): 1767-1783
被引量:108
标识
DOI:10.1007/s12274-017-1486-6
摘要
Achieving a satisfactory energy–power combination in a supercapacitor that is based on all-carbon electrodes and operates in benign aqueous media instead of conventional organic electrolytes is a major challenge. For this purpose, we fabricated carbon nanoflakes (20–100 nm in thickness, 5-μm in width) containing an unparalleled combination of a large surface area (3,000 m2·g−1 range) and mesoporosity (up to 72%). These huge-surface area functionalized carbons (HSAFCs) also had a substantial oxygen and nitrogen content (~10 wt.% combined), with a significant fraction of redox-active carboxyl/phenol groups in an optimized specimen. Their unique structure and chemistry resulted from a tailored single-step carbonization-activation approach employing (2-benzimidazolyl) acetonitrile combined with potassium hydroxide (KOH). The HSAFCs exhibited specific capacitances of 474 F·g−1 at 0.5 A·g−1 and 285 F·g−1 at 100 A·g−1 (charging time < 3 s) in an aqueous 2 M KOH solution. These values are among the highest reported, especially at high currents. When tested with a stable 1.8-V window in a 1 M Na2SO4 electrolyte, a symmetric supercapacitor device using the fabricated nanoflakes as electrodes yielded a normalized active mass of 24.4 Wh·kg−1 at 223 W·kg−1 and 7.3 Wh·kg−1 at 9,360 W·kg−1. The latter value corresponds to a charge time of <3 s. The cyclability of the devices was excellent, with 93% capacitance retention after 10,000 cycles. All the electrochemical results were achieved by employing electrodes with near-commercial mass loadings of 8 mg·cm−2.
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