电解质
纳米颗粒
材料科学
原位
盐(化学)
化学工程
准固态
纳米技术
固态
无机化学
电极
工程物理
化学
物理化学
物理
有机化学
工程类
色素敏化染料
作者
Jingwen Wang,Shanshan Lv,Yutong Wu,Jiarui Yang,Guojiang Wen,Shan Wang,Wei Yang,Yu Wang,Xuewei Fu
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-09-30
标识
DOI:10.1021/acsnano.5c09201
摘要
Transforming liquid electrolytes into solids by lithium salt-triggered in situ polymerization-based solidification has been of great interest for the manufacturing of solid-state batteries. However, this strategy faces a tricky obstacle in simultaneously achieving high ionic conductivity and mechanical properties due to the poor controllability of the reaction process and electrolyte microstructures. Here, to overcome this challenge, we propose a neuron-like in situ polysol electrolyte (Neu-iPE) by salt-in-sol cross-linking that realizes a lithium-salt-regulated physical cross-linking of poly(vinylidene fluoride) (PVDF) sol nanoparticles. It is found that lithium salt can effectively regulate the sol-gel transition of PVDF sol, as well as the sol-cross-linking via a salt-in-sol microphase reorganization. Benefiting from the well-controlled neuron-like microstructures, the Neu-iPE integrates the advantages of separator and liquid electrolytes and simultaneously achieves a high room-temperature ion-conductivity of 0.42 mS/cm, mechanical strength of 15.7 MPa, and puncture toughness of 34.4 MJ/m3. Enabled by this Neu-iPE, a component-integrated quasi-solid-state battery is successfully fabricated to achieve structural flexibility and interface stability as compared with conventional batteries. This study on Neu-iPE presents not only a promising alternative to conventional in situ polymerization-based electrolyte solidification but also a salt-in-sol cross-linking strategy for the fabrication of biomimetic functional materials and devices.
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