Carbon dots for ultrastable solid-state batteries

被引:33
作者
Xu, Laiqiang [1 ]
Tu, Hanyu [1 ]
Zhu, Fangjun [1 ]
Xiang, Yinger [1 ]
Luo, Zheng [1 ]
Fang, Susu [1 ]
Deng, Wentao [1 ]
Zou, Guoqiang [1 ]
Hou, Hongshuai [1 ]
Ji, Xiaobo [1 ,2 ]
机构
[1] Cent South Univ, Coll Chem & Chem Engn, Changsha 410083, Peoples R China
[2] Zhengzhou Univ, Coll Mat Sci & Engn, Zhengzhou, Peoples R China
来源
SMARTMAT | 2022年 / 3卷 / 02期
基金
中国国家自然科学基金;
关键词
carbon dots; Li+ conductor; LiF; selective ion transport; solid-state batteries; COMPOSITE ELECTROLYTES; POLYMER ELECTROLYTES; TRANSFERENCE NUMBER; QUANTUM DOTS; LITHIUM;
D O I
10.1002/smm2.1097
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Among the solid electrolytes for solid-state Li batteries, polymer electrolytes are actively explored on the basis of the good interfacial contact and easy making, while it is still constrained by slow ionic transport and low lithium ion transference number. Herein, functional carbon dots-based Li+ conductor (CD-Li) is designed to improve the dynamics and selectivity of Li+ transport in polyethylene oxide (PEO) electrolyte. High ionic conductivity (1.0 x 10(-4) S/cm, 25 degrees C) and Li+ transference number (0.60) were successfully achieved within the CD-Li-based PEO composite electrolyte, which could be attributed to the enhanced chain movement and the limited motion of anion. Moreover, the characteristics of big volume of individual anions of CD-Li can provide more free Li+. As well, benefiting from the existence of F atom in the CD-Li, in-situ constructed LiF-containing interfacial layer is in favor of maintaining the interface stability and facilitating the rapid transmission of Li ions. The composite electrolyte with CD-Li can address the ionic conductivity issues accompanied with strengthening the interfacial stability. The distinctive composite electrolyte realizes the stable cycle performance for Li/LiFePO4 and Li/LiNi0.5Co0.2Mn0.3O2 batteries. The exploration of multifunctional carbon dot fillers provides new ideas for the efficient development of composite electrolytes.
引用
收藏
页码:286 / 297
页数:12
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