Metal organic framework reinforced polymer electrolyte with high cation transference number to enable dendrite-free solid state Li metal conversion batteries

电解质 材料科学 离子电导率 聚合物 电池(电) 氧化物 阴极 化学工程 锂(药物) 化学 电极 冶金 复合材料 物理化学 工程类 功率(物理) 量子力学 医学 物理 内分泌学
作者
Xiaoxue Wu,Keyi Chen,Zhenguo Yao,Jiulin Hu,Minsong Huang,Junwei Meng,Shiping Ma,Tao Wu,Yanhua Cui,Chilin Li
出处
期刊:Journal of Power Sources [Elsevier]
卷期号:501: 229946-229946 被引量:139
标识
DOI:10.1016/j.jpowsour.2021.229946
摘要

Solid polymer electrolytes are intrinsically advantageous over rigid inorganic ones in terms of their easy processability and scalability by film-based battery technology. Here, a three-dimensional (3D) structured Ce-based metal organic framework (Ce-MOF) nano-filler with plentiful catalytic active sites is introduced into polyethylene oxide (PEO) based electrolyte. This unusual filler with abundant cavities enables the strong Lewis acid-base interactions with both ether oxygen in PEO and anion in Li salt, leading to significantly improved ionic conductivity and Li+ transference number as high as 0.75. Such an electrolyte compositing can remarkably improve the mechanical (stretching) and thermal stabilities and effectively suppress Li dendrites, and the Li/Li symmetrical cells can continuously cycle without short circuit even under long-term 1800 h or relatively high current density of 0.4 mA cm−2. The polymer electrolyte composited with 10 wt% Ce-MOF can endow the integrated all-solid-state batteries with superior cycling stability and rate performance (e.g. with capacities as high as 120 mAh g−1 after 3800 cycles for Li/LiFePO4 and 300 mAh g−1 after 240 cycles for Li/FeF3). The electrolyte modification by MOF planting is expected to well alleviate the volume extrusion and species dissolution from the cathode side and promote its interface confinement especially during conversion reaction.
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