Electron Redistribution Enables Redox-Resistible Li6PS5Cl towards High-Performance All-Solid-State Lithium Batteries

被引:45
|
作者
Liu, Chong [1 ]
Chen, Butian [1 ]
Zhang, Tianran [1 ]
Zhang, Jicheng [1 ]
Wang, Ruoyu [1 ]
Zheng, Jian [1 ]
Mao, Qianjiang [1 ]
Liu, Xiangfeng [1 ]
机构
[1] Univ Chinese Acad Sci, Coll Mat Sci & Optoelect Technol, Dept Ctr Mat Sci & Optoelect Engn, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
All-Solid-State Li Metal Battery; Element Doping; Interface Stability; Redox Reaction; Sulfide Solid Electrolyte; INTERPHASE FORMATION; INTERFACE STABILITY; CONDUCTIVITY; ORIGIN; INSIGHTS; GROWTH; BR; CL;
D O I
10.1002/anie.202302655
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Sulfide electrolytes with high ionic conductivity hold great promise for all-solid-state lithium batteries. However, the parasitic redox reactions between sulfide electrolyte and Li metal result in interfacial instability and rapid decline of the battery performance. Herein, a redox-resistible Li6PS5Cl (LPSC) electrolyte is created by regulating the electron distribution in LPSC with Mg and F incorporation. The introduction of Mg triggers the electron agglomeration around S atom, inhibiting the electron acceptance from Li, and F generates the self-limiting interface, which hinders the redox reactions between LPSC and Li metal. This redox-resistible Li6PS5Cl-MgF2 electrolyte therefore presents a high critical current density (2.3 times that of pristine electrolyte). The LiCoO2/Li6PS5Cl-MgF2/Li cell shows an outstanding cycling stability (93.3% @100 cycles at 0.2 C). This study highlights the electronic structure modulation to address redox issues on sulfide-based lithium batteries.
引用
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页数:11
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