超级电容器
材料科学
生物量(生态学)
复合数
脚手架
纳米技术
化学工程
多孔性
电极
碳纤维
复合材料
电化学
化学
生物医学工程
海洋学
地质学
工程类
物理化学
作者
Xiaomin Yuan,Yue Zhang,Yushan Yan,Bingqing Wei,Kun Qiao,Bo Zhu,Xun Cai,Tsu‐Wei Chou
标识
DOI:10.1016/j.cej.2019.03.090
摘要
Electrodeposition based on 3D scaffold-templates is a unique and facile method to tune the microstructure of composite electrode materials for energy storage devices. In this work, we developed a green process to fabricate 3D hierarchical porous carbon scaffold-MnO2 ([email protected]2) nanohybrids with colony-like microstructures. Acting as conductive template and pyrolysis accelerant, the 3D-HPCS enables microstructural control of MnO2 electrodeposits and facilitates valence conversion from Mn2+ to Mn4+. Comparing with depositing on nickel foam, the morphology of MnO2 changed from nanospheres to nanowrinkles when depositing on the 3D-HPCS templates. Benefiting from abundant forest-like micro/mesopores, the resultant 3D-HPCS possesses high specific surface area (1627 m2 g−1) and rich heteroatom dopants (6.94 wt%), affording a high gravimetric specific capacitance (231.5 F g−1) with outstanding cycling performance (95% capacitance retention after 10,000 cycles). The assembled asymmetric supercapacitor based on HPCS//[email protected]2 exhibits an energy density of 60.8 Wh kg−1 and a maximum power density of 20.7 kW kg−1. Our investigation has quantitatively proved that mesopores contribute more than micropores in increasing capacitance of HPCS and both surface capacitive and diffusion-controlled processes play roles in capacitive performance of [email protected]2. Moreover, the influence of the morphology and surface functionality on the electrochemical performances of composite electrodes have been analyzed.
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