4.8 Article

In Situ Formed Li-Ag Alloy Interface Enables Li10GeP2S12-Based All-Solid-State Lithium Batteries

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 13, 期 42, 页码 50076-50082

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c16356

关键词

lithium anode; Li10GeP2S12; Li-Ag alloy; surface modification; radio frequency magnetron sputtering; all-solid-state lithium-metal batteries

资金

  1. National Key R&D Program of China [2018YFB0905400]
  2. National Natural Science Foundation of China [U1964205, 51872303, 51902321]
  3. Zhejiang Provincial Natural Science Foundation of China [LD18E020004]
  4. Ningbo S&T Innovation 2025 Major Special Programme [2018B10061, 2018B10087, 2019B10044]
  5. Youth Innovation Promotion Association CAS [2017342]
  6. Postdoctoral International Exchange Program [YJ20180234]

向作者/读者索取更多资源

Introducing a thin Ag layer between Li and Li10GeP2S12 for in situ formation of a Li-Ag alloy interface can improve the interfacial stability and electrochemical properties of all-solid-state lithium-metal batteries. Optimizing the Ag thicknesses can achieve a steady voltage evolution and high reversible capacity, demonstrating the validity of the Ag layer in improving the cycle life of ASSLMBs. This work highlights the importance of re-engineering the Li/SE interface and provides a new strategy for enhancing the performance of ASSLMBs.
All-solid-state lithium-metal batteries (ASSLMBs) have received great interest due to their high potential to display both high energy density and safety performance. However, the poor compatibility at the Li/solid electrolyte (SE) interface and penetration of lithium dendrites during cycling strongly impede their successful commercialization. Herein, a thin Ag layer was introduced between Li and Li10GeP2S12 for the in situ formation of a Li-Ag alloy interface, thus tuning the interfacial chemistry and lithium deposition/dissolution behavior. Superior electrochemical properties and improved interfacial stability were achieved by optimizing the Ag thicknesses. The assembled symmetric cell with Li@Ag 1 mu m showed a steady voltage evolution up to 1000 h with an areal capacity of 1 mAh cm(-2). Moreover, a high reversible capacity of 106.5 mAh g(-1) was achieved in an all-solid-state cell after 100 cycles, demonstrating the validity of the Ag layer. This work highlights the importance of the Li/SE interface re-engineering and provides a new strategy for improving the cycle life of ASSLMBs.

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