超级电容器
范德瓦尔斯力
材料科学
异质结
平面(几何)
传输(计算)
纳米技术
复合材料
物理
光电子学
电容
几何学
计算机科学
并行计算
电极
数学
量子力学
分子
作者
Xiaoyang Xu,Zhenni Zhang,Zihao Zhang,Xiaomi Tang,Hong Chen,Li Tian,Zhang Jia,Qingliang Feng,Shanlin Qiao
出处
期刊:eScience
[Elsevier]
日期:2025-04-03
卷期号:5 (6): 100404-100404
被引量:10
标识
DOI:10.1016/j.esci.2025.100404
摘要
Two-dimensional (2D) reticular framework films featuring highly accessible surface areas, tunable active sites, and well-defined channels are promising candidates for flexible in-plane micro-supercapacitor (MSC) electrodes. However, the interlayer Van der Waals forces in 2D heterojunctions can limit mass/charge transport. Herein, we design a non-Van der Waals force bonded heterojunction of covalent organic frameworks (COFs) and metal–organic frameworks (MOFs) linked by metal-ion coordination. A COF@MOF monolithic nanofilm is constructed by growing MOF (M3(HHTP)2) in situ on the COF (COFTD) surface, using nickel (Ni) as the optimal metal to connect the two layers and form a sandwich electrode. We further explore various transition metals in M3(HHTP)2, from manganese (Mn) to zinc (Zn), to adjust the electronic structure and charge redistribution. The optimal MSC-Ni-COFTD@Co3(HHTP)2 device exhibits an impressive specific capacitance (1645.3 F cm−3 at 10 mV s−1), a high energy density (146.3 mWh cm−3), as well as superior cycling and bending stability. This work offers an innovative perspective on overcoming the mass transfer and electron migration limitations of 2D reticular frameworks for miniaturization and wearable energy storage electronics.
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