Lithium Borate Polycarbonates for High-Capacity Solid-State Composite Cathodes

被引:4
|
作者
Charlesworth, Thomas [1 ]
Yiamsawat, Kanyapat [1 ]
Gao, Hui [1 ,2 ]
Rees, Gregory J. [2 ]
Williams, Charlotte K. [1 ]
Bruce, Peter G. [2 ]
Pasta, Mauro [2 ]
Gregory, Georgina L. [1 ]
机构
[1] Univ Oxford, Chem Res Lab, 12 Mansfield Rd, Oxford OX1 3TA, England
[2] Univ Oxford, Mat Dept, Oxford OX1 3PH, England
基金
英国工程与自然科学研究理事会;
关键词
Polymerization; Materials Science; Batteries; Polymer Electrolytes; Ring-Opening (Co)Polymerization; POLYMER ELECTROLYTES; CYCLIC CARBONATES; PRESSURE; CO2;
D O I
10.1002/anie.202408246
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Improving composite cathode function is key to the success of the solid-state battery. Maximizing attainable cathode capacity and retention requires integrating suitable polymeric binders that retain a sufficiently high ionic conductivity and long-term chemo-mechanical stability of the cathode active material-solid-electrolyte-carbon mixture. Herein, we report block copolymer networks composed of lithium borate polycarbonates and poly(ethylene oxide) that improved the capacity (200 mAh g(-1) at 1.75 mA cm(-2)) and capacity retention (94 % over 300 cycles) of all-solid-state composite cathodes with nickel-rich LiNi0.8Co0.1Mn0.1O2 cathode active material, Li6PS5Cl solid electrolyte, and carbon. Tetrahedral B(OR)(2)(OH)(2)(-) anions immobilized on the polycarbonate segments provide hydrogen-bonding chain crosslinking and selective Li-counterion conductivity, parameterized by Li-ion transference numbers close to unity (t(Li+)similar to 0.94). With 90 wt % polycarbonate content and a flexible low glass transition temperature backbone, the single-ion conductors achieved high Li-ion conductivities of 0.2 mS cm(-1) at 30 degrees C. The work should inform future binder design for improving the processability of cathode composites towards commercializing solid-state batteries, and allow use in other cell configurations, such as lithium-sulphur cathode designs.
引用
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页数:8
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