超级电容器
材料科学
电极
电容
纳米技术
蚀刻(微加工)
制作
碳纤维
电化学
光电子学
化学工程
复合数
复合材料
图层(电子)
化学
医学
替代医学
物理化学
病理
工程类
作者
Yongbin Wang,Ningjun Chen,Bin Zhou,Xuefeng Zhou,Ben Pu,Jia Bai,Qi Tang,Yan Liu,Weiqing Yang
标识
DOI:10.1007/s40820-023-01204-4
摘要
2D MXene (Ti3CNTx) has been considered as the most promising electrode material for flexible supercapacitors owing to its metallic conductivity, ultra-high capacitance, and excellent flexibility. However, it suffers from a severe restacking problem during the electrode fabrication process, limiting the ion transport kinetics and the accessibility of ions in the electrodes, especially in the direction normal to the electrode surface. Herein, we report a NH3-induced in situ etching strategy to fabricate 3D-interconnected porous MXene/carbon dots (p-MC) films for high-performance flexible supercapacitor. The pre-intercalated carbon dots (CDs) first prevent the restacking of MXene to expose more inner electrochemical active sites. The partially decomposed CDs generate NH3 for in situ etching of MXene nanosheets toward 3D-interconnected p-MC films. Benefiting from the structural merits and the 3D-interconnected ionic transmission channels, p-MC film electrodes achieve excellent gravimetric capacitance (688.9 F g-1 at 2 A g-1) and superior rate capability. Moreover, the optimized p-MC electrode is assembled into an asymmetric solid-state flexible supercapacitor with high energy density and superior cycling stability, demonstrating the great promise of p-MC electrode for practical applications.
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