锂(药物)
金属锂
材料科学
电解质
硫化物
金属
涂层
无机化学
固态
快离子导体
化学工程
纳米技术
化学
冶金
电极
物理化学
内分泌学
工程类
医学
作者
Zhiying He,Yiwen Liu,Yuankai Liu,Haiyan Xiao,Zhengkun Xie,Chan Kok Sheng,Aoyuan Chen,Ping He,Haoshen Zhou
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-09-11
卷期号:19 (37): 33523-33533
被引量:2
标识
DOI:10.1021/acsnano.5c10768
摘要
All-solid-state batteries (ASSBs) are regarded as a promising route to enhanced safety and energy density through the use of lithium metal anodes. However, lithium dendrite growth and interfacial instability between Li and the solid electrolyte (SE) remain critical bottlenecks. To address these issues, a spontaneously preformed solid electrolyte interphase (PSEI) on the surface of the SE strategy was devised. By incorporating lithium difluoro(oxalato)borate (LiODFB) as a tailored SE additive into Li5.5PS4.5Cl1.5, an in situ SEI is engineered that synergistically suppresses dendrite formation, stabilizes the Li/SE interface, and mitigates mechanical degradation. The resulting multifunctional PSEI, which consists of a hybrid organic-inorganic outer layer and an inorganic-rich inner layer, is found to both reduce the electronic conductivity of the SE (thus preventing Li nucleation within SEs) and accommodate mechanical degradation arising from Li plating/stripping to avoid contact loss. Consequently, Li-Li symmetric cells incorporating LPSC with PSEI achieved a critical current density (CCD) of 2.4 mA cm-2 and ultrastable cycling for over 3500 h at 0.2 mA cm-2. The Li-LiNi0.8Co0.1Mn0.1O2 full cells retained 80% capacity after 310 cycles at 0.5 C and can also operate stably under 4.5 V. This work establishes a rational interface design for SEs that integrates electronic and mechanical modulation with electrochemical stability to unlock the potential of lithium metal anodes in ASSBs.
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