分离器(采油)
材料科学
过电位
纳米纤维
电解质
静电纺丝
复合数
集电器
纳米技术
化学工程
聚丙烯
聚丙烯腈
储能
金属
金属锂
膜
聚酰亚胺
离子电导率
电极
枝晶(数学)
锂(药物)
复合材料
超级电容器
电导率
化学气相沉积
作者
Dian Anggreini,Aldan Hadziq Haidar,Naufal Hanif Hawari,Chung‐Yul Yoo,Xiaohui Song,Febri Baskoro,Afriyanti Sumboja
标识
DOI:10.1021/acsaem.5c03533
摘要
Anode-free lithium metal batteries (AFLMBs) are considered promising technologies for future storage applications, capable of achieving superior energy density in a streamlined cell design. Yet, their practical realization remains clouded by persistent challenges, including formation of lithium dendrites and limited cycling durability. Herein, we introduce a composite nanofiber separator composed of polyimide (PI) interwoven with garnet-type Li 6.75 La 3 Zr 1.75 Ta 0.25 O 12 (LLZTO) fillers, fabricated via a one-step electrospinning method and subsequently underwent thermal imidization. The fabricated PI/LLZTO membrane forms a robust, three-dimensional fibrous network with well-distributed LLZTO particles. This architecture significantly improves both electrolyte uptake and mechanical strength, while forming a channel for continuous ion conduction that encourages uniform Li + flux, one of the key factors in suppressing dendrite formation. The separator delivers high ionic conductivity, reaching 3.16 mS cm –1 with a measured Li + transference number of 0.76. In Li symmetric cells, it enables remarkably stable cycling over 2900 h with an ultralow overpotential (∼0.007 V). When deployed in Cu||NMC622 AFLMB full cells, it delivers smooth and dendrite-suppressed lithium deposition behavior, with a first-cycle discharge capacity of 181 mAh g –1 and retaining 40% capacity after completing 100 charge–discharge cycles. In comparison, the commercial polypropylene separator retains 10% only. This work demonstrates how functional separator design, particularly anchored ceramic–polymer synergy, can unlock pathways toward stable, high-performance AFLMBs.
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