期刊
MATERIALS TODAY ENERGY
卷 29, 期 -, 页码 -出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.mtener.2022.101107
关键词
Gel polymer electrolyte; Gradient design; LLithium batteries; Radical polymerization; Polyacrylic complexes
资金
- National Natural Science Foundation of China [51973073]
- Fellowship of China Postdoctoral Science Foundation [2021M701303]
- Innova-tion and Talent Recruitment Base of New Energy Chemistry and Device [B21003]
- Analysis and Testing Center of HUST
By using a gradient design of polymer electrolyte with polyacrylic salt-catalyzed radical polymerization, gel polymer electrolytes with excellent thermal and electrochemical stability are prepared to improve the ion conduction ability and interfacial issues between electrolyte and electrode in polymer electrolyte-based lithium metal batteries. The resulting gel polymer electrolytes show high performance in lithium plating-stripping property and long-term cycling stability, and the manual ion-compensation between the bulk electrolyte and the cathode enhances the diffusion of lithium ions and slows down the capacity decay, providing a direction for improving the electrolyte-electrode compatibility and designing advanced lithium metal batteries.
To improve the ion conduction ability and interfacial issues between electrolyte and electrode and provide a high safety and long lifespan for polymer electrolyte-based lithium metal batteries, gel polymer electrolytes with excellent thermal and electrochemical stability are prepared via polyacrylic salt -catalyzed radical polymerization. The gradient design of polyacrylic complex impels the in-situ formation of gel polymer electrolytes, robust solid electrolyte interphase and cathode electrolyte interface layer, delivering an excellent lithium platting-stripping property (1000 h, 0.1 mA cm(-2)) and a long-term cycling with 80.1% capacity retention (600 cycles, 1C) for the as-assembled lithium symmetric and Li/LiFePO4 cells, respectively. Moreover, the manual ion-compensation between the bulk electrolyte and the cathode enhances the diffusion of lithium ion with a high diffusion coefficient of 3.47 x 10(-13) cm(2) s(-1), and slows down the capacity decay with a high discharge capacity of 121.0 mA h/g at 5C. This method provides a direction for improving the electrolyte-electrode compatibility and designing advanced lithium metal batteries. (C) 2022 Elsevier Ltd. All rights reserved.
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