电解质
材料科学
离子电导率
电化学
制作
化学工程
多孔性
电导率
金属锂
电池(电)
锂(药物)
锂离子电池
导电体
纳米技术
快离子导体
金属
电极
离子键合
膜
沸石
离子
聚合物电解质
离子交换
离子液体
作者
Tongtai Ji,Honghao Ge,Nicole Rivera,Luisa Gomes,Ruizhi Dong,Jochem Struppe,Jason J. Guo,Sanjeev Mukerjee,Huidong Dai
出处
期刊:Nano Letters
[American Chemical Society]
日期:2025-10-30
卷期号:25 (45): 16169-16178
被引量:1
标识
DOI:10.1021/acs.nanolett.5c04133
摘要
Solid electrolytes are critical to enabling safe and high-energy-density batteries; yet, their practical deployment is impeded by poor electrochemical stability, inadequate interfacial contact, and challenging manufacturing processes. Here, we introduce a novel "solid-in-solid" electrolyte architecture comprising a porous Li zeolite electrolyte (LiX) infiltrated with a melt-processable plastic crystal electrolyte (PCE). This LiX-PCE electrolyte achieves an ionic conductivity of 0.55 mS/cm at 20 °C, alongside improved electrochemical stability over pure PCE. Solid-state nuclear magnetic resonance reveals three Li+ transport pathways: through LiX, through PCE, and via ion exchange at phase boundaries. Leveraging the melt-processability of the PCE, we proposed a roll-to-roll-compatible melt infiltration strategy for scalable solid-state battery (SSB) fabrication with the LiX-PCE electrolyte. The SSBs demonstrate excellent rate performance (up to 10 C), 93% capacity retention after 200 cycles at 2C, and 4.5 V compatibility. This work elucidates critical design principles for high-performance solid-state electrolytes and presents a viable path toward practical, fast-charging, high-power SSBs.
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