Construction of α-MnO2 on Carbon Fibers Modified with Carbon Nanotubes for Ultrafast Flexible Supercapacitors in Ionic Liquid Electrolytes with Wide Voltage Windows

用碳纳米管改性的碳纤维上构建 α-MnO2,用于具有宽电压窗口的离子液体电解质中的超快柔性超级电容器

阅读:4
作者:Mai Li, Kailan Zhu, Hanxue Zhao, Zheyi Meng, Chunrui Wang, Paul K Chu

Abstract

In this study, α-MnO2 and Fe2O3 nanomaterials are prepared on a carbon fiber modified with carbon nanotubes to produce the nonbinder core-shell positive (α-MnO2@CNTs/CC) and negative (Fe2O3@CNTs/CC) electrodes that can be operated in a wide voltage window in ultrafast asymmetrical flexible supercapacitors. MnO2 and Fe2O3 have attracted wide research interests as electrode materials in energy storage applications because of the abundant natural resources, high theoretical specific capacities, environmental friendliness, and low cost. The electrochemical performance of each electrode is assessed in 1 M Na2SO4 and the energy storage properties of the supercapacitors consisting of the two composite electrodes are determined in Na2SO4 and EMImBF4 electrolytes in the 2 V and 4 V windows. The 2 V supercapacitor can withstand a large scanning rate of 5000 mV S-1 without obvious changes in the cyclic voltammetry (CV) curves, besides showing a maximum energy density of 57.29 Wh kg-1 at a power density of 833.35 W kg-1. Furthermore, the supercapacitor retains 87.06% of the capacity after 20,000 galvanostatic charging and discharging (GCD) cycles. The 4 V flexible supercapacitor shows a discharging time of 1260 s and specific capacitance of 124.8 F g-1 at a current of 0.5 mA and retains 87.77% of the initial specific capacitance after 5000 GCD cycles. The mechanical robustness and practicality are demonstrated by physical bending and the powering of LED arrays. In addition, the contributions of the active materials to the capacitive properties and the underlying mechanisms are explored and discussed.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。