材料科学
柯肯德尔效应
超级电容器
硫化钴
钴
多孔性
电化学
化学工程
电极
胶囊
纳米技术
复合材料
电容
冶金
化学
物理化学
植物
生物
工程类
作者
Yongfu Tang,Shunji Chen,Shichun Mu,Teng Chen,Yuqing Qiao,Shengxue Yu,Faming Gao
标识
DOI:10.1021/acsami.6b01268
摘要
To construct a suitable three-dimensional structure for ionic transport on the surface of the active materials for a supercapacitor, porous hollow nickel cobalt sulfides are successfully synthesized via a facile and efficient cation-exchange reaction in a hydrothermal process involving the Kirkendall effect with γ-MnS nanorods as a sacrificial template. The formation mechanism of the hollow nickel cobalt sulfides is carefully illustrated via the tuning reaction time and reaction temperature during the cation-exchange process. Due to the ingenious porous hollow structure that offers a high surface area for electrochemical reaction and suitable paths for ionic transport, porous hollow nickel cobalt sulfide electrodes exhibit high electrochemical performance. The Ni1.77Co1.23S4 electrode delivers a high specific capacity of 224.5 mAh g–1 at a current density of 0.25 A g–1 and a high capacity retention of 87.0% at 10 A g–1. An all-solid-state asymmetric supercapacitor, assembled with a Ni1.77Co1.23S4 electrode as the positive electrode and a homemade activated carbon electrode as the negative electrode (denoted as NCS//HMC), exhibits a high energy density of 42.7 Wh kg–1 at a power density of 190.8 W kg–1 and even 29.4 Wh kg–1 at 3.6 kW kg–1. The fully charged as-prepared asymmetric supercapacitor can light up a light emitting diode (LED) indicator for more than 1 h, indicating promising practical applications of the hollow nickel cobalt sulfides and the NCS//HMC asymmetric supercapacitor.
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