电解质
超级电容器
材料科学
镍
电化学
氢氧化钾
氢氧化物
电极
氧化物
氧化钴
钴
电容
无机化学
化学工程
冶金
化学
物理化学
工程类
作者
Charmaine Lamiel,Van Hoa Nguyen,Iftikhar Hussain,Jae‐Jin Shim
出处
期刊:Energy
[Elsevier]
日期:2017-12-01
卷期号:140: 901-911
被引量:68
标识
DOI:10.1016/j.energy.2017.09.035
摘要
Metal oxide nanostructures have been studied widely to overcome the limitations in the capacitance of the carbon-based supercapacitor electrode materials. An electrode with a very porous 3D structure is preferred to facilitate the mass transfer of large electrolyte ions. In this study, highly nanostructured, binder-free Ni-Co-based pseudocapacitive electrodes were synthesized directly on porous 3D structured nickel foam (NF) current collectors using low-power microwave irradiation. The electrochemical performance of the Ni-Co layered double hydroxide (Ni-Co-LDH) showed better performance than Ni-Co oxide (Ni-Co-O) with the further addition of redox additive/active electrolytes, such as K3Fe(CN)6. The specific capacitances of 4664 F g−1 for Ni-Co-LDH and 1758 F g−1 for Ni-Co-O at 5 mA cm−2 in the KOH/K3Fe(CN)6 electrolyte were improved greatly compared to the values of their corresponding materials in the conventional KOH electrolyte (2875 and 250 F g−1, respectively). Interestingly, the Ni-Co-LDH//AC asymmetric device exhibited a specific capacitance of 108.9 F g−1 and an energy density of 38.7 Wh kg−1 with a stability of 61.9% after 5000 cycles. The facile yet cost-effective synthesis of nanostructured electrodes provides a versatile approach for the design of high-performance pseudocapacitive electrodes for future energy-storage systems.
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