4.8 Article

Long-Life and High-Rate-Charging Lithium Metal Batteries Enabled by a Flexible Active Solid Electrolyte Interphase Layer

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 13, 期 50, 页码 60678-60688

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c19952

关键词

anode electrolyte interphases; solid electrolyte interphases; lithium metal batteries; fast charging; click chemistry

资金

  1. National Natural Science Foundation of China [22075174, 21671133]
  2. Technology Commission of Shanghai Municipality [18020500800, 18JC1412900, 19DZ2271100, 19160712900]
  3. International Joint Laboratory on Resource Chemistry

向作者/读者索取更多资源

This study introduces a simple method of adding multifunctional fluorosulfonate to commercial electrolytes to increase inorganic LiF content in the SEI of lithium metal batteries. The formation of a flexible interface layer inhibits the growth of lithium dendrites, leading to stable fast charge cycles. This innovative approach provides insights into the practical application of the new electrolyte and offers a new idea for building a stable SEI in commercial lithium metal batteries.
Commercially, lithium metal batteries are still limited by the growth of lithium dendrites and excessive consumption of the electrolyte. A stable multifunctional solid electrolyte interface is the development strategy of lithium metal batteries in the future. However, most of the artificial solid electrolyte interphases (SEIs) cannot meet the original intention of multifunctional design and cannot form an SEI film with a high conductivity and low nucleation potential. In this work, we report a universal and simple method of adding multifunctional fluorosulfonate to a commercial electrolyte, so increasing the inorganic LiF in the SEI. In addition, the imidazole ring in the fluorosulfonate combines with the alkyl group in the electrolyte to form a flexible interface layer, which inhibits the growth of lithium dendrites and makes lithium deposition more uniform, thereby realizing a stable fast charge cycle. With an ultralow capacity of 2 mAh/cm(2) deposited, the symmetrical battery can be deposited stably for nearly 300 h at a high current density of 20 mA/cm(2). The capacity retention rate of the Li-LiFePO4 (LFP) full cell was still at 90.6% after 1000 cycles at 5 C. Even with 5 C high-rate fast charging, the capacity was maintained at 76.56% after 200 cycles, which is four times that of commercial electrolytes. This simple addition strategy gives insights into the practical application of the new electrolyte and provides a new idea for the construction of a stable SEI for commercial lithium metal batteries.

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