Mixed-Polarity Copolymers Based on Ethylene Oxide and Cyclic Carbonate: Insights into Li-Ion Solvation and Conductivity

被引:6
|
作者
Bennington, Peter [1 ]
Sanchez-Leija, Regina J. [1 ,2 ]
Deng, Chuting [1 ]
Sharon, Daniel [3 ]
de Pablo, Juan J. J. [1 ,2 ]
Patel, Shrayesh N. N. [1 ]
Nealey, Paul F. F. [1 ,2 ]
机构
[1] Univ Chicago, Pritzker Sch Mol Engn, Chicago, IL 60637 USA
[2] Argonne Natl Lab, Mat Sci Div, Lemont, IL 60439 USA
[3] Hebrew Univ Jerusalem, Inst Chem, IL-91904 Jerusalem, Israel
基金
美国国家科学基金会;
关键词
POLYMER ELECTROLYTES; DIELECTRIC-CONSTANT; SEGMENTAL DYNAMICS; TRANSPORT; ASSOCIATION; TRIFLATE; LITFSI;
D O I
10.1021/acs.macromol.3c00540
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
This study investigates the relationship between polarityand ionicconductivity in random and block copolymer electrolytes comprisinghighly flexible oligo-(ethylene oxide) methyl ether methacrylate (OEM)and highly polar but glassy glycerol carbonate methacrylate (GCMA)monomers, blended with either lithium bis-(trifluoromethanesulfonyl)-imide(LiTFSI) or lithium triflate. Interestingly, the high polarity ofGCMA did not significantly enhance ionic dissociation, and the randomcopolymers (POEM-r-PGCMA) showed similar or lowerionic conductivities than the POEM homopolymer. Further analysis revealedthat Li+ only interacts with OEM and its counterion, notwith GCMA. The less-intermixed and weakly phase-separated block copolymer(POEM-b-PGCMA) exhibited even lower conductivitiesthan the random copolymer. Our results suggest that Li+ solvation occurs only in the POEM-rich phase and that the largerPGCMA regions, depleted of Li+, disrupt long-range iontransport. These findings provide valuable insights into the designof polymer electrolytes and how segmental mobility and functionalgroups with contrasting polarities affect ion transport.
引用
收藏
页码:4244 / 4255
页数:12
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