超级电容器
电容
材料科学
石墨
介孔材料
碳纤维
电解质
纳米技术
水平扫描速率
多孔性
比表面积
化学工程
活性炭
电极
电化学
复合材料
化学
循环伏安法
吸附
有机化学
催化作用
工程类
复合数
物理化学
作者
Xi Wang,Jiang Xu,Bingqing Hu,Ningyi Yuan,Xiaoting Cao,Fujian Zhang,Ruijun Zhang,Jianning Ding
标识
DOI:10.1016/j.diamond.2022.109466
摘要
Pore structure in activated carbons (ACs) is critical for supercapacitors with both high capacitance and rate performance. To obtain ACs with suitable pore structures, many efforts in the exploration of technology have been made. In this work, we found that it is easier to form a developed pore structure when precursor carbon is composed of disordered graphite-like micro-crystals. The gas produced during the activation process could provide the force to separate the neighboring graphite layers. Based on this, we propose a controllable adjustment of the pore structure strategy. A sub-micron scale carbon sphere composed of randomly arranged graphite micro-crystals is chosen as the precursor carbon. After CO2 activation, a high specific surface area (SSA, ∼3300 m2 g−1) AC dominated by micropores is obtained. For KOH activation, a hierarchical porous AC possessing ultra-high SSA (∼3400 m2 g−1) is achieved. Benefited from the cross-linked mesopores with the size range of 3 to 5 nm, the fabricated symmetric supercapacitors exhibit high specific capacitances in organic electrolyte (192 F g−1 at 0.01 V s−1) and excellent rate performance (110 F g−1 at 30 V s−1) that is comparable with the CNTs electrode with the similar areal capacitance (∼25 mF cm−2). This provides a route to fabricate ACs with both high specific capacitance and rate performance.
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