4.7 Article

Ion-compensation regime between electrolyte and cathode to prepare advanced lithium metal batteries

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

  1. National Natural Science Foundation of China [51973073]
  2. Fellowship of China Postdoctoral Science Foundation [2021M701303]
  3. Innova-tion and Talent Recruitment Base of New Energy Chemistry and Device [B21003]
  4. Analysis and Testing Center of HUST

向作者/读者索取更多资源

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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据