超级电容器
假电容
材料科学
碳化
电容
化学工程
电解质
介孔材料
比表面积
电极
纳米技术
化学
扫描电子显微镜
复合材料
有机化学
物理化学
工程类
催化作用
作者
Danfeng Xue,Dazhang Zhu,Wei Xiong,Tongcheng Cao,Zhiwei Wang,Yaokang Lv,Liangchun Li,Mingxian Liu,Lihua Gan
标识
DOI:10.1021/acssuschemeng.8b06774
摘要
A template-free and self-doping approach is developed for fabricating N,O-enriched porous carbon spheres (PCSs) via direct carbonization/activation of melamine-glyoxal polymer. The interconnected spherical morphology of PCSs generates stacking porosities as ion reservoirs for rapid ion diffusion and affords conductive networks to shorten the transport lengths for electron transfer. Besides, PCSs exhibit a large surface area (1302 m2 g–1), ample ultramicropores (0.54 nm), and developed supermicro- and mesopores. This unique pore architecture provides optimized ion-accessible pore size to enhance double layer capacitance, and serves as ion-highways for rapid diffusion of electrolyte ions. Furthermore, high N/O elements (7.97/10.16 wt %) incorporated into PCSs improve surface wettability and supply additional pseudocapacitance. Therefore, the resultant PCS electrodes exhibit superior electrochemical performances, such as a high specific capacitance up to 344 F g–1 at 1.0 A g–1, remarkable rate capability, and long-term stability in a three-electrode. Notably, the PCS-based supercapacitor exhibits an impressive energy density of 33.37 Wh kg–1 and power density of 9000 W kg–1 in Na2SO4 electrolyte. This result provides a simple and efficient fabrication of PCSs for high-performance supercapacitors.
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