Study of poly (organic palygorskite-methyl methacrylate)/poly(vinylidene fluoride-co-hexafluoropropylene) blended gel polymer electrolyte for lithium-ion batteries

被引:2
|
作者
Yuan, Ge [1 ,2 ,3 ,4 ]
Guo, Haijun [1 ,2 ,3 ]
Bo, Li [1 ,2 ,3 ,4 ]
Wang, Mengkun [1 ,2 ,3 ]
Zhang, Hairong [1 ,2 ,3 ]
Chen, Xinde [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Guangzhou Inst Energy Convers, Guangzhou 510640, Peoples R China
[2] Chinese Acad Sci, Key Lab Renewable Energy, Guangzhou 510640, Peoples R China
[3] R&D Ctr Xuyi Attapulgite Energy & Environm Mat, Xuyi 211700, Peoples R China
[4] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
关键词
Gel polymer electrolyte; Lithium ion battery; Poly(vinylidene fluoride-co-hexafluoropropylene); ELECTROCHEMICAL PERFORMANCE; PHASE INVERSION; HIGH-SAFETY; COMPOSITE; CONDUCTIVITY; SEPARATOR; MEMBRANE; NANOPARTICLES; MATRIX;
D O I
10.1007/s10008-022-05339-z
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The composite membrane (PDFP-POPM) based on the blending of poly(vinylidene fluoride-co-hexafluoropropylene) (PDFP) and POPM (the copolymer of organic palygorskite and methyl methacrylate) was prepared by the phase-inversion method, and a gel polymer electrolyte (GPE) was obtained when the PDFP-POPM was activated by absorbing liquid electrolyte (LE). The SEM morphologies showed that the PDFP-POPM had a porous structure. The XRD results indicated that PDFP-POPM was an amorphous polymer and that the POPM could effectively suppress the crystallization of PDFP. The lithium ion transference number of GPE was higher than that of pristine POPM- and PDFP-based GPE. When the mass concentration of PDFP was 40%, the uptake of the PDFP-POPM and ionic conductivity of GPE reached the maximum values of 164% and 2.37 mS/cm, respectively. The electrochemical stability window of Li/GPE/SS batteries was over 4.7 V (vs. Li+/Li), and the Li/40PDFP-POPM GPE/LiFePO4 battery exhibited good cycling performance. The discharge capacity of the battery was 145mAh g(-1) after 100 cycles and the columbic efficiency was over 95%.
引用
收藏
页码:455 / 465
页数:11
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