超级电容器
聚苯胺
双金属片
化学
电化学
化学工程
金属有机骨架
复合数
电解质
电容
金属氢氧化物
氢氧化物
电极
复合材料
材料科学
金属
无机化学
聚合物
有机化学
吸附
物理化学
聚合
工程类
作者
Jinyue Yang,Jianxin Wang,Chunhua Lou,Yuhan Cui,Xin Huang,Haixia Yu,Liming Bai,Wendi Wang,Xinyou Zhang,Hong Pan
标识
DOI:10.1016/j.molstruc.2024.138392
摘要
Metal-organic framework materials (MOFs) are widely used in electrochemical energy storage due to their abundant active sites and high redox activity. Especially in the field of supercapacitors, the porous structure of MOFs makes them the most promising candidates for composite electrode materials due to their vast specific surface area. However, the poor chemical stability of MOFs in alkaline electrolytes limits their application. Constructing and improving the stability of metal-organic backbone materials through rational structural design is the key to enhancing the electrochemical performance of capacitors. In this paper, the stability of ZIF-67 was enhanced by the complexing with bimetallic hydroxide (CoMn-LDH), and the conductivity is further enhanced by the mixing of polyaniline (PANI) to form a "network structure" morphology. As a result, the composite electrode material has a specific capacity of 1048 F g−1 at 1 A g−1 with a good cycle life (80.5% capacity retention for 5000 cycles). The specific capacity of the CoMn-LDH/ZIF-67/PANI//AC asymmetric supercapacitor (ASC) was 164 F g−1 at 1 A g−1 in the voltage range of 0 ∼ 1.5 V. The maximum energy density of the ASC was 51.25 Wh kg−1 at a power density of 2250 W kg−1. In addition, excellent cycling stability (71.2% capacitance retention after 5000 cycles) was delivered.
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