超级电容器
纳米片
材料科学
化学工程
电极
电容
原位聚合
沥青质
离子液体
碳纤维
比表面积
电解质
聚合
纳米技术
有机化学
复合材料
化学
聚合物
复合数
催化作用
工程类
物理化学
作者
Fangfang Qin,Xiaodong Tian,Zhongya Guo,Wenzhong Shen
标识
DOI:10.1021/acssuschemeng.8b04227
摘要
Asphaltene with high aromaticity derived from coal direct liquefaction residue is a favorable precursor to prepare new carbon materials because it is easy to polymerize or cross link. Here, asphaltene was used as a carbon precursor for synthesis of porous carbon nanosheets via an in situ sheet-structure-directing agent from urea thermal polymerization. The porous carbon nanosheet with controllable thickness and a graphitized-like ribbon structure was obtained after KOH activation. As supercapacitor electrode materials, the as-prepared porous carbon nanosheets demonstrated a specific capacitance of 282.9 F/g even at 100 A/g in a three-electrode test and 186.7 F/g at 20 A/g in a two-electrode test. The electrolyte was a KOH aqueous solution in both tests; the specific capacitance of the device retained 89.6% after 10,000 cycles showing a good lifetime and durability. The specific capacitance of the device was 135.4 and 119.1F/g at 1 A/g, respectively, in ionic liquid and organic electrolyte; its highest energy density reached 53.5 Wh/kg (at 159.9 W/kg) and 35.9 Wh/kg (at 134.9 W/kg), respectively. The synergism of high specific surface area to volume ratio developed micromesoporous structure, graphitized-like conduction paths, resulting in excellent specific capacitance and outstanding cycle life and rate performance capability of the prepared porous carbon nanosheets as supercapacitor electrodes.
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