A polymeric artificial solid electrolyte interface dramatically enhances lithium-ion transport

被引:0
|
作者
Li, Chun [1 ]
Hu, Bin [1 ]
Wang, Yujuan [1 ]
Bi, Kedong [1 ]
机构
[1] Southeast Univ, Sch Mech Engn, Jiangsu Key Lab Design & Manufacture Micronano Bio, Nanjing 211189, Peoples R China
关键词
MOLECULAR-DYNAMICS; MECHANICAL-PROPERTIES; ANODE MATERIAL; BATTERY; GRAPHITE; POLYTHIOPHENE; CONDUCTIVITY; INTERPHASES;
D O I
10.1039/d4cc03688c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Coulombic efficiency and cycle life require further improvement in an ever-growing practical demand for lithium-ion batteries (LIBs), which are one of the most prevalent electrochemical energy storage systems. In this work, a more stable and highly lithium-ion (Li-ion) conductive artificial solid electrolyte interface (A-SEI) is constructed by coating polythiophene (PTh) on the surface of a graphite anode based on molecular dynamic simulations. Our findings reveal that PTh chains effectively prevent direct contact between the electrolyte and the negative electrode while providing a rapid transport channel for lithium ions (Li-ions), resulting in significantly shorter trapping times for Li-ions-at least two orders of magnitude shorter than those in the predominant component of traditional SEI layers. Schematic diagram of polythiophene as artificial solid electrolyte interfaces enhancing lithium-ion transport in batteries.
引用
收藏
页码:11124 / 11127
页数:4
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