材料科学
共聚物
原子转移自由基聚合
聚合物
三氟氯乙烯
化学工程
高分子化学
聚合
嫁接
复合材料
四氟乙烯
工程类
作者
Tong Liu,Rohan Parekh,Piotr Mocny,Brian P. Bloom,Yuqi Zhao,So Young An,Bonian Pan,Rongguan Yin,David H. Waldeck,Jay Whitacre,Krzysztof Matyjaszewski
出处
期刊:ACS materials letters
[American Chemical Society]
日期:2023-08-25
卷期号:5 (10): 2594-2603
被引量:10
标识
DOI:10.1021/acsmaterialslett.3c00485
摘要
High-nickel layered oxides, e.g., LiNi0.8Co0.1Mn0.1O2 (NCM811), are promising candidates for cathode materials in high-energy-density lithium-ion batteries (LIBs). Complementing the notable developments of modification of active materials, this study focused on the polymer binder materials, and a new synthetic route was developed to engineer PVDF binders by covalently grafting copolymers from poly(vinylidene fluoride-co-chlorotrifluoroethylene) (PVDF-CTFE) with multiple functionalities using atom transfer radical polymerization (ATRP). The grafted random copolymer binder provided excellent flexibility (319% elongation), adhesion strength (50 times higher than PVDF), transition metal chelation capability, and efficient ionic conductivity pathways. The NCM811 half-cells using the designed binders exhibited a remarkable rate capability of 143.4 mA h g–1 at 4C and cycling stability with 70.1% capacity retention after 230 cycles at 0.5 C, which is much higher than the 52.3% capacity retention of nonmodified PVDF. The well-retained structure of NCM811 with the designed binder was systematically studied and confirmed by post-mortem analysis.
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