Eliminating Local Electrolyte Failure Induced by Asynchronous Reaction for High-Loading and Long-Lifespan All-Solid-State Batteries

被引:3
|
作者
An, Hanwen [1 ,3 ]
Liu, Qingsong [1 ,3 ]
Deng, Biao [4 ]
Wang, Jian [5 ]
Li, Menglu [1 ]
Li, Xin [2 ]
Lou, Shuaifeng [1 ,3 ]
Wang, Jiajun [1 ,3 ]
机构
[1] Harbin Inst Technol, Sch Chem & Chem Engn, Minist Ind & Informat Technol MIIT Key Lab Crit Ma, Harbin 150001, Peoples R China
[2] Harvard Univ, John A Paulson Sch Engn & Appl Sci, Cambridge, MA 02138 USA
[3] Chongqing Res Inst HIT, Chongqing 401135, Peoples R China
[4] Chinese Acad Sci, Shanghai Inst Appl Phys, 239 Zhangheng Rd, Shanghai 201204, Peoples R China
[5] Univ Saskatchewan, Canadian Light Source Inc, Saskatoon S7N 2V3, SK, Canada
基金
加拿大健康研究院; 中国国家自然科学基金; 加拿大自然科学与工程研究理事会; 加拿大创新基金会;
关键词
asynchronous charge-equilibration; electrochemical stability; high-loading cathodes; solid-state batteries; synchrotron techniques; INSIGHTS;
D O I
10.1002/adfm.202305186
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The design of practical cathodes with high areal capacity in polymer-based all-solid-state batteries remains challenged by the absence of an effective guiding principle that prolongs battery life-span. Unlike liquid batteries, the notorious interface incompatibility between cathodes and electrolytes limited the cycling life of the all-solid-state batteries. Herein, this study proposes a dynamically stable cathode design with a fully covered surface, effectively mitigating interface failure and enabling the cyclic time of batteries with a cathode loading of 12.7 mg cm(-2) over 10 000 h. This study unveils the importance of local state of charge in affecting the interfacial properties of particles through local oxidative-stability of electrolytes on the interface. This study shows that the phenomena can be strongly influenced by the porosity of the cathode through the perspective of discreteness of ion transport. These insights and approach provide a broader promise for solid batteries for long lifetime.
引用
收藏
页数:9
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