电解质
杰纳斯
材料科学
阴极
锂(药物)
电池(电)
容量损失
枝晶(数学)
纳米技术
相间
氧化还原
电流密度
能量密度
化学工程
储能
耐久性
聚合物电解质
电极
电化学
溶解
金属锂
表面能
工作(物理)
准固态
降级(电信)
化学稳定性
电池容量
热容
锂离子电池
聚合物
作者
Hanbing Yan,Qi Liu,Weiqian Guo,Cheng Jiang,Yang Song,Fu Zhou,Chenguang Bao,Baohua Li
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-10-25
卷期号:19 (43): 37983-37993
被引量:11
标识
DOI:10.1021/acsnano.5c12885
摘要
The practical application of poly(ethylene oxide) (PEO)-based polymer electrolytes in all-solid-state lithium–metal batteries (ASSLMBs) is severely restricted by their low energy density and uncontrolled lithium dendrite growth. Herein, we introduced a trace amount of MgI 2 as a dual-functional Janus additive that simultaneously addresses limited capacity and interfacial stability in PEO electrolytes. The Mg 2+ competitively coordinates with both PEO chains and TFSI – anions, effectively weakening the Li + -TFSI – interaction and promoting Li + dissociation, thereby increasing the free Li + concentration and enhancing interfacial lithium-ion transport. Simultaneously, iodine species (I – /I 3 – ) participate in cathode redox reactions to enhance reversible capacity while facilitating the formation of a robust, inorganic-rich solid electrolyte interphase (SEI) at the anode, which effectively suppresses dendrite formation. As a result, the modified electrolyte delivers a recorded critical current density of 1.7 mA/cm 2, and Li||Li symmetric cells achieve ultralong cycling stability for over 10,000 h at 60 °C. A Li||LiFePO 4 full battery exhibits exceptional durability of 10 times that of the blank system, with 93.28% capacity retention at 1 C after 2000 cycles. More impressively, as-fabricated pouch cells demonstrate the capacity retention of 95.80% after 250 cycles at 60 °C. This work presents a facile and economically viable strategy to synergistically regulate additionally reversible capacity and interfacial chemistry for next-generation, high-performance ASSLMBs.
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