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

被引:7
|
作者
Shi, Senhao [1 ]
Zhang, Daoxin [2 ]
Lv, Junwei [1 ]
Luo, Junhui [1 ]
Yang, Fan [2 ]
Wu, Tong [2 ]
Liu, Xiangyang [1 ,2 ]
机构
[1] Sichuan Univ, Coll Polymer Sci & Engn, Chengdu 610065, Peoples R China
[2] Sichuan Univ, State Key Lab Polymer Mat Engn, Chengdu 610065, Peoples R China
基金
中国国家自然科学基金;
关键词
Lithium-ion batteries; Separator; Direct fluorination; Oxygen groups; Wettability; POLYPROPYLENE SEPARATOR; PERFORMANCE; FILM;
D O I
10.1021/acsapm.3c00495
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Due to the intrinsic inertness of polyethylene (PE),it is difficultto induce polar oxygen-containing groups onto the PE separator surfaceunder mild conditions on a large scale and further enhance their wettability.Herein, utilizing the ultrastrong oxidation of elemental fluorine(F-2), it was found that F-2 could easily reactwith the PE separator surface via radical-related routes, and thusoxygen would be naturally captured onto the separator surface forits radical affinity. The fluorinated PE separator exhibited significantlyimproved wettability as the water contact angle decreased from 117 & DEG;to 62 & DEG; at the minimum. Therefore, electrolyte uptake of the fluorinatedseparator reached 803.9% (of which the PE electrolyte uptake was 246.2%),and the ionic conductivity increased from 0.29 to 0.52mS/cm. Capacityretention of LiCoCO2/graphite cells assembled by a fluorinatedPE 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 79.07mAh/g to 109.77 mAh/g) at 1.2 C. Besides, due to the spontaneous couplingbetween direct fluorination induced radicals, micro-cross-linkingspots 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-treatmentstrategy for high-performance PE separators.
引用
收藏
页码:5857 / 5866
页数:10
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