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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.
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页码:4244 / 4255
页数:12
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