Double Ionic-Electronic Transfer Interface Layers for All-Solid-State Lithium Batteries

被引:57
|
作者
Zheng, Jingang [1 ]
Sun, Chengguo [1 ,2 ,3 ]
Wang, Zhenxing [2 ]
Liu, Shaojun [1 ]
An, Baigang [1 ]
Sun, Zhenhua [2 ]
Li, Feng [2 ]
机构
[1] Univ Sci & Technol Liaoning, Sch Chem Engn, Anshan 114051, Peoples R China
[2] Chinese Acad Sci, Inst Met Res, Shenyang Natl Lab Mat Sci, Shenyang 110016, Peoples R China
[3] Nanjing Univ Sci & Technol, Sch Chem Engn, Nanjing 210094, Peoples R China
基金
中国国家自然科学基金;
关键词
lithium-metal batteries; mixed ion-electron interface layers; polymer electrolytes; solid electrolyte interphase; solid-state batteries; POLYMER ELECTROLYTES; INTERPHASE LAYER; TRANSPORT; DEPOSITION; RESISTANCE; IMPEDANCE;
D O I
10.1002/anie.202104183
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Large-scale implementation of all-solid-state lithium batteries is impeded by the physical limitations of the interface between the electrode and solid electrolyte; specifically, high resistance and poor stability, as well as poor compatibility with Li+ migration. We report double ionic-electronic transfer interface layers grown at electrode-electrolyte interfaces by in situ polymerization of 2,2 '-bithiophene in polyethylene oxide (PEO) electrolyte. For all-solid-state LiFePO4 parallel to PT-PEO-PT parallel to Li cells, the formation of a conductive polythiophene (PT) layer at the cathode-electrolyte interface resulted in an at least sevenfold decrease in interface resistance, and realized a capacity retention of about 94 % after 1000 cycles along with a lower polarization voltage under a rate of 2 C. The mixed ionic-electronic conductive layers imparted superior interface stability and contact while keeping good compatibility with the Li anode.
引用
收藏
页码:18448 / 18453
页数:6
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