材料科学
陶瓷
金属锂
纳米纤维
导电体
固态
锂(药物)
纳米技术
金属
复合材料
工程物理
阳极
冶金
电极
化学
工程类
物理化学
内分泌学
医学
作者
Yiyuan Yan,Shen Liu,Dezhi Yan,Shichao Zhang,Shuai Yin,Jun Xia,Fangchao Han,Qiang Lü,Wangwei Ren,Xiaomeng Wu,Qianfan Zhang,Yalan Xing,Puheng Yang
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2025-06-04
卷期号:18 (9): 94907651-94907651
被引量:3
标识
DOI:10.26599/nr.2025.94907651
摘要
Composite solid electrolytes hold the promise of merging complementary merits of solid polymer electrolytes and ceramic fillers to achieve solid batteries with comprehensive performance. Especially, three-dimensional inorganic electrolyte frameworks, such as Li7La3Zr2O12, with fast and continuous lithium ion migration channels demonstrates great promise in composite solid electrolytes. Nevertheless, brittle ceramic conductor skeletons are incapable of providing sufficient mechanical adaptability, which restricts their practical application. Herein, a flexible, ion-conducting network which integrates Li7La3Zr2O12 nanoparticles in polyacrylonitrile nanofibers is fabricated through electrospinning method. Subsequently, a composite electrolyte with three-dimensional continuous structure is achieved via in situ polymerizing of 1,3-dioxolane within the ionic conduction framework. The highly conductive Li7La3Zr2O12 reinforced polymer nanofibers are not only available to promote transportation of lithium ion, but also provide structural flexibility and mechanical robustness for composite electrolyte. Accordingly, the obtained composite electrolyte combines enhanced room temperature ionic conductivity (4.38 × 10–4 S cm–1) with structural flexibility and mechanical robustness, supported by exceptional interfacial compatibility with lithium metal, enabling ultra-stable lithium symmetric battery operation (3000 h at 0.1 mA cm–2). Furthermore, as-prepared LiFePO4 and LiCoO2/lithium solid-state batteries deliver high capacity retention of 96% after 350 cycles and capacity retention of 82% after 600 cycles at room temperature. This work provides a new avenue in design of advancing composite solid electrolytes.
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