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掌握用于锂金属电池应用的氰基丙烯酸乙酯作为凝胶聚合物电解质的共聚行为。

Mastering the Copolymerization Behavior of Ethyl Cyanoacrylate as Gel Polymer Electrolyte for Lithium-metal Battery Application.

作者信息

Min Weixing, Li Lengwan, Wang Mingli, Ma Shuaijiang, Feng Hao, Wang Weirong, Ding Hang, Cheng Tianhui, Li Zhenxi, Saito Tomonori, Yang Huabin, Cao Peng-Fei

机构信息

Institute of New Energy Material Chemistry, School of Materials Science and Engineering, Nankai University, Tianjin, 300350, China.

State Key Laboratory of Organic-Inorganic Composites, School of Materials Science and Engineering, Beijing University of Chemical Technology, Beijing, 100029, China.

出版信息

Angew Chem Int Ed Engl. 2025 Mar 24;64(13):e202422510. doi: 10.1002/anie.202422510. Epub 2025 Jan 21.

Abstract

Polymers with strong electron-withdrawing groups (e.g., cyano-containing polymers) are attractive for a wide range of applications due to their high dielectric constant and outstanding electrochemical stability. However, the polymerization of such monomers is difficult to control with trace of water affording instant reactions, and copolymerization with other monomers without using strong acid is even more challenging. The present study demonstrates a facile approach enabling efficient and controllable copolymerization of ethyl cyanoacrylate (ECA) without adding undesired additives, achieving mechanically robust and high ion-conduction gel polymer electrolyte (GPE) for safe and long cycle-life lithium-metal batteries (LMBs). The incorporated dual-lithium salts, i.e., lithium difluoro(oxalato)borate (LiDFOB) and lithium bis(trifluoromethanesulphonyl)imide (LiTFSI) not only facilitate radical polymerization of ECA monomers by suppressing their anionic polymerization, but also promote the formation of high-ionic conducting GPE. The incorporated methyl methacrylate (MMA) monomer accelerates the radical polymerization of ECA (confirmed by DFT calculations), achieving controlled copolymerization of ECA-based copolymers. The mechanically robust polymer network made by the ECA copolymer enables LMBs with both LFP cathodes and high-voltage LCO cathodes (4.5 V) operatable at different temperatures with ultra-long cycle life at 1 C (capacity retention of 81.1 % and 83.8 %, respectively, over 1000 cycles).

摘要

带有强吸电子基团的聚合物(如含氰基聚合物)因其高介电常数和出色的电化学稳定性而在广泛的应用中具有吸引力。然而,此类单体的聚合反应难以控制,因为痕量水会引发即时反应,且在不使用强酸的情况下与其他单体进行共聚更具挑战性。本研究展示了一种简便方法,可在不添加不良添加剂的情况下实现氰基丙烯酸乙酯(ECA)的高效可控共聚,从而获得用于安全且长循环寿命锂金属电池(LMBs)的机械坚固且高离子传导的凝胶聚合物电解质(GPE)。所引入的双锂盐,即二氟(草酸根)硼酸锂(LiDFOB)和双(三氟甲磺酰)亚胺锂(LiTFSI),不仅通过抑制ECA单体的阴离子聚合促进其自由基聚合,还促进了高离子传导GPE的形成。所引入的甲基丙烯酸甲酯(MMA)单体加速了ECA的自由基聚合(经密度泛函理论计算证实),实现了基于ECA的共聚物的可控共聚。由ECA共聚物制成的机械坚固的聚合物网络使配备磷酸铁锂(LFP)阴极和高压钴酸锂(LCO)阴极(4.5 V)的LMBs能够在不同温度下运行,在1 C下具有超长循环寿命(1000次循环后容量保持率分别为81.1%和83.8%)。

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