Fluorine-Initiated Carboxyl Group Enhanced Combination Properties of the Polyethylene Separator for Lithium-Ion Batteries

分离器(采油) 润湿 聚乙烯 接触角 电解质 热稳定性 化学 化学工程 石墨 激进的 离子电导率 材料科学 高分子化学 有机化学 复合材料 电极 物理化学 物理 工程类 热力学
作者
Senhao Shi,Daoxin Zhang,Junwei Lv,Junhui Luo,Fan Yang,Tong Wu,Xiangyang Liu
出处
期刊:ACS applied polymer materials [American Chemical Society]
卷期号:5 (8): 5857-5866 被引量:11
标识
DOI:10.1021/acsapm.3c00495
摘要

Due to the intrinsic inertness of polyethylene (PE), it is difficult to induce polar oxygen-containing groups onto the PE separator surface under mild conditions on a large scale and further enhance their wettability. Herein, utilizing the ultrastrong oxidation of elemental fluorine (F2), it was found that F2 could easily react with the PE separator surface via radical-related routes, and thus oxygen would be naturally captured onto the separator surface for its radical affinity. The fluorinated PE separator exhibited significantly improved wettability as the water contact angle decreased from 117° to 62° at the minimum. Therefore, electrolyte uptake of the fluorinated separator reached 803.9% (of which the PE electrolyte uptake was 246.2%), and the ionic conductivity increased from 0.29 to 0.52mS/cm. Capacity retention of LiCoCO2/graphite cells assembled by a fluorinated PE separator increased to 80.4% from 73.2% after 200 cycles of charge–discharge, and the discharge capacity of it also increased 38.83% (from 79.07 mAh/g to 109.77 mAh/g) at 1.2 C. Besides, due to the spontaneous coupling between direct fluorination induced radicals, micro-cross-linking spots were generated, and thus, modulus and thermal deformability, which meant service stability of the separator, were also improved. Therefore, direct fluorination could be considered an effective post-treatment strategy for high-performance PE separators.
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