Few-layered Ti3C2Tx MXenes coupled with Fe2O3 nanorod arrays grown on carbon cloth as anodes for flexible asymmetric supercapacitors

被引:100
作者
Li, Fei [1 ]
Liu, Yi-Lin [1 ]
Wang, Gui-Gen [1 ]
Zhang, Hua-Yu [1 ]
Zhang, Bin [1 ]
Li, Gui-Zhong [1 ]
Wu, Zhi-Peng [1 ]
Dang, Le-Yang [1 ]
Han, Jie-Cai [1 ,2 ]
机构
[1] Harbin Inst Technol, Shenzhen Key Lab Adv Mat, Shenzhen 518055, Peoples R China
[2] Harbin Inst Technol, Ctr Composite Mat, Harbin 150080, Heilongjiang, Peoples R China
基金
中国国家自然科学基金;
关键词
HIGH-PERFORMANCE; ACTIVATED CARBON; NEGATIVE ELECTRODES; NANOWIRE ARRAYS; COMPOSITES; NANOARRAYS; ALPHA-FE2O3;
D O I
10.1039/c9ta08144e
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The design of flexible electrodes with high areal capacitance is the key for the application of flexible asymmetric supercapacitors (ASCs) in portable and wearable electronics. In this study, Ti3C2Tx MXene coupled with the Fe2O3/CC flexible negative electrode, with good conductivity, high areal capacitance, and excellent flexibility, was fabricated by a simple dipping method, in which the as-grown Fe2O3 nanorod arrays on carbon cloth were dipped into the few-layered MXene nanosheet solution repeatedly to make the Fe2O3/CC fibers wrapped with MXene completely. The MXene@Fe2O3/CC electrode presents a remarkable areal capacitance of up to 725 mF cm(-2) at a current density of 1 mA cm(-2) which was contributed by both MXene and Fe2O3 nanorods. As to the MXene layer, it not only offers capacitance for the flexible electrode, but also provides fast and efficient ion/electron transport pathways for Fe2O3 to effectively improve electronic conductivity. Besides, the as-constructed ASC devices consisting of MXene@Fe2O3 and MnO2 electrodes achieve a high energy density of 1.61 mW h cm(-3) at a power density of 22.55 mW cm(-3) along with good stability. The work provides a simple effective strategy to load active materials on carbon fibres and to construct hierarchical coating-structured electrodes for high-performance flexible ASC application.
引用
收藏
页码:22631 / 22641
页数:11
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