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Block Copolymer Electrolytes Synthesized by Atom Transfer Radical Polymerization for Solid-State, Thin-Film Lithium Batteries

机译:通过原子转移自由基聚合合成的固态,薄膜锂电池的嵌段共聚物电解质

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摘要

Block copolymer electrolytes of poly((oxyethylene)_9 methacrylate)-b-poly(butyl methacrylate) (POEM-b-PBMA) (60:40 by mass) synthesized for the first time by atom transfer radical polymerization (ATRP) exhibited mechanical and electrical properties indistinguishable from those of materials made by the more difficult anionic polymerization method. ATRP offers distinct processing advantages as it is easily scalable and almost solvent-free. Solid-state, thin-film batteries comprised of a metallic lithium anode, a binder-free, additive-free, fully dense vanadium oxide cathode, and an electrolyte of ATRP-synthesized POEM-b-PBMA (60:40) doped with LiCF_3SO_3 demonstrate resistance to capacity fade during extended cycling at a discharge rate of C/2, and perform comparably to otherwise identical batteries operated with the liquid electrolyte 1 M LiPF_6 in ethylene carbonate:dimethyl carbonate (1:1 by mass).
机译:通过原子转移自由基聚合(ATRP)首次合成的聚((氧乙烯)_9甲基丙烯酸甲酯)-b-聚甲基丙烯酸丁酯(POEM-b-PBMA)(质量比60:40)的嵌段共聚物电解质表现出机械性能和电性能与通过较困难的阴离子聚合方法制得的材料的电性能没有区别。 ATRP具有明显的加工优势,因为它易于扩展并且几乎没有溶剂。固态薄膜电池,包括金属锂阳极,无粘结剂,无添加剂,完全致密的钒氧化物阴极以及掺杂有LiCF_3SO_3的ATRP合成的POEM-b-PBMA(60:40)电解质展示了在延长的循环中以C / 2的放电速率对容量衰减的抵抗力,并且与在碳酸亚乙酯:碳酸二甲酯(质量比1:1)中使用液体电解质1 M LiPF_6的其他相同电池的性能类似。

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