首页  课题组概况  研究方向  研究成果  成员介绍  实验设备  组内活动  合作交流  联系我们 
新闻动态

祝贺王思佳等同学的文章被 J. Collo...
祝贺樊杰等同学的文章被Journal of ...
祝贺牛文莎等同学的文章被 ACS Ener...
祝贺赵梦琦、李添翼、李传彬等同学...
祝贺李成龙等同学的文章被ChemCatCh...
祝贺董灵玉等同学的文章被Angew. Ch...
祝贺乔一凡等同学的文章被Applied C...

首页
您的位置: 首页>>正文

祝贺张蒙蒙等同学的文章被 Journal of Power Source 接受发表!

2022年02月24日 18:26  点击:[]

祝贺张蒙蒙等同学的文章

Regulation of Dual-Ion Batteries via the Defects Design in Carbon Electrode Based on the Different Storage Behaviors of PF6- and Li+

Journal of Power Source 接受发表!



Meng-Meng Zhang, Dong Yan, and Wen-Cui Li*.Regulation of Dual-Ion Batteries via the Defects Design in Carbon Electrode Based on the Different Storage Behaviors of PF6- and Li+, Journal of Power Source, 2022, 231169.  [DOWNLOAD]


Abstract


Dual-ion batteries (DIBs) have aroused much attention due to their high energy density, low cost, and environmental friendliness compared to conventional alkali metal-ion batteries. However, there are still two severe challenges to confront, including structural collapse for the graphitic carbon cathode due to the intercalation of anions with large size and limited specific capacity of cations intercalation for the graphitic carbon anode, rendering poor rate performance, unsatisfactory cyclability, and insufficient energy density. Herein, a simple design is proposed to prepare cathode and anode materials for PF6- and Li+ intercalation in one synthesis system by regulating boron content in the complex of amino acid with iron (III). The graphitic mesoporous carbon cathode with minimal defect sites shows a superior rate performance and cycling stability for PF6- intercalation. The boron-doped porous carbon anode shows a high capacity of up to 606 mAh g-1 for Li+ storage by introducing abundant defects. The DIB assembled by the above cathode and anode can exhibit a maximum energy density of 130 Wh kg-1 at a power density of 580 W kg-1 and an energy density of 74 Wh kg-1 at an ultrahigh power density of 29000 W kg-1.




上一条:祝贺邱彬等同学的文章被 J. Catal. 接受发表! 下一条:祝贺郭行等同学的文章被 化工学报 接受发表!

关闭

先进能源材料与催化团队 版权所有

本站部分内容来源于网络,版权归原作者或来源机构所有,如果涉及任何版权方面的问题请及时和我们联系,我们将尽快妥善处理!

推荐使用 Internet Explorer 浏览器浏览本站