Stabilizing Polymer-Lithium Interface in a Rechargeable Solid Battery

被引:87
作者
Yan, Min [1 ]
Liang, Jia-Yan [1 ,2 ]
Zuo, Tong-Tong [2 ]
Yin, Ya-Xia [1 ,2 ]
Xin, Sen [1 ,2 ]
Tan, Shuang-Jie [1 ,2 ]
Guo, Yu-Guo [1 ,2 ]
Wan, Li-Jun [1 ,2 ]
机构
[1] Chinese Acad Sci, CAS Key Lab Mol Nanostruct & Nanotechnol, CAS Res Educ Ctr Excellence Mol Sci, BNLMS,Inst Chem, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Sch Chem Sci, Beijing 100049, Peoples R China
基金
国家重点研发计划; 北京市自然科学基金; 中国博士后科学基金; 中国国家自然科学基金;
关键词
interface modifications; Li anodes; mixed conducting interlayers; polymer electrolytes; solid batteries; ELECTROLYTE; CONDUCTIVITY; CHEMISTRY;
D O I
10.1002/adfm.201908047
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Solid polymer electrolytes (SPEs) are promising candidates for developing high-energy-density Li metal batteries due to their flexible processability. However, the low mechanical strength as well as the inferior interfacial regulation of ions between SPEs and Li metal anode limit the suppress ion of Li dendrites and destabilize the Li anode. To meet these challenges, interfacial engineering aiming to homogenize the distribution of Li+/electron accompanied with enhanced mechanical strength by Mg3N2 layer decorating polyethylene oxide is demonstrated. The intermediary Mg3N2 in situ transforms to a mixed ion/electron conducting interlayer consisting of a fast ionic conductor Li3N and a benign electronic conductor Mg metal, which can buffer the Li+ concentration gradient and level the nonuniform electric current distribution during cycling, as demonstrated by a COMSOL Multiphysics simulation. These characteristics endow the solid full cell with a dendrite-free Li anode and enhanced cycling stability and kinetics. The innovative interface design will accelerate the commercial application of high-energy-density solid batteries.
引用
收藏
页数:6
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