Study on the Performance of Aniline Electrodeposited on MnO(2) Nanowire as an Anode for Sodium-Ion Batteries

研究苯胺电沉积在MnO(2)纳米线上作为钠离子电池负极的性能

阅读:1

Abstract

Manganese dioxide is an ideal anode for sodium-ion batteries due to its rich crystal shapes. However, its low conductivity, low reversible discharge capacity, slow diffusion kinetics, and poor cyclic stability limit its potential for industrial application. The design of manganese dioxide (MnO(2)) with various morphologies, such as nanowires, nanorods, and nanoflowers, has proven effective in enhancing its electrochemical performance. Stacking nanowire structures is of interest as they increase the open space by forming an interconnected network, thus facilitating favorable diffusion pathways for sodium ions. Concurrently, the substantial increase in the electrolyte contact area efficiently mitigates the strain induced by the volume expansion associated with the repetitive migration and insertion of sodium ions. Based on previous research, this work presents the structural design of flexible MnO(2)/polyaniline (MnO(2)/PANI) nanowires assembled on carbon cloth (CC), an innovation in MnO(2) modification. Compared to conventional MnO(2) nanowires, the MnO(2)/PANI nanowires exhibit enhanced structural stability and improved dynamic performance, thereby marking a significant advancement in their material properties. This MnO(2)/PANI composite exhibits a rate capacity of approximately 200 mA h g(-1) after 60 cycles at a current density of 0.1 A g(-1), and maintains a rate capacity of 182 mA h g(-1) even after 200 cycles under the same current density. This study not only provides new insights into the underlying mechanisms governing energy storage in MnO(2)/PANI nanowires but also paves the way for their further development and optimization as anodes for sodium-ion batteries, thereby opening up fresh avenues for research and application.

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。