二硫化钼
超级电容器
材料科学
二硫化钨
马来酰亚胺
电导率
电容
表面改性
电化学
纳米技术
储能
电极
钨
膜
化学工程
共价键
表面工程
电阻率和电导率
钼
过渡金属
电化学能量转换
表面能
无机化学
相(物质)
金属
作者
Yue Zhang,Mingzi Sun,WeiKang Zheng,Bintong Yang,Ting Ying,Liang Mei,Ruixin Yan,Honglu Hu,Guozhao Fang,Dongliang Chao,Bolong Huang,Zhong‐Shuai Wu,Zhiyuan Zeng
出处
期刊:Small
[Wiley]
日期:2025-09-30
卷期号:: e06741-e06741
标识
DOI:10.1002/smll.202506741
摘要
The rising need for efficient energy storage has sparked interest in high-performance supercapacitors. However, their low energy density is a significant drawback. 2D transition metal dichalcogenides (TMDs) like molybdenum disulfide (MoS2) and tungsten disulfide (WS2) are promising for electrodes due to their adjustable surface chemistry and electronic properties. However, MoS2 and WS2 are still facing challenges, including phase instability, limited interlayer accessibility, and poor conductivity in ambient conditions. Here, a rapid and controllable strategy is presented for the covalent functionalization of MoS2 and WS2 nanosheets via a "click"-type Michael addition reaction with maleimide derivatives. This approach increases interlayer spacing by more than 1.5 times and enhances electrical conductivity by over threefold, thereby exceptionally improving charge transport and ion diffusion. The functionalized membranes deliver outstanding electrochemical performance, including a volumetric capacitance of up to 164 F cm-3 and capacitance retention exceeding 92% after 10 000 cycles, which are 30-fold increase when comparing with their pristine counterparts. This work offers a robust platform for engineering high-performance TMD-based electrodes and provides a viable route toward next-generation high-performance flexible energy storage devices.
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