用于高电压锂金属电池的原位共聚聚(酯-醇-缩醛)电解质:锂盐催化剂决定稳定的固态电解质间相

IF 5.1 Q1 POLYMER SCIENCE
Jiafang Guo, Xiong Liu, Zikai Shen, Yanbing Lv, Xun Zhang, Chengjian Zhang, Xinghong Zhang
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引用次数: 0

摘要

原位形成的聚合物电解质为提高高压锂金属电池的安全性和性能提供了重要的解决方案。本研究报告介绍了通过戊二酸酐和 1,3- 二氧六环原位交替共聚合成的新型聚(酯-盐-缩醛)(PEA)电解质。在 25 wt.% 的双(三氟甲磺酰)亚胺锂(LiTFSI)存在下,采用了三种锂盐:二氟(草酸盐)硼酸锂(LiDFOB)、六氟磷酸锂(LiPF6)和四氟硼酸锂(LiBF4)作为共聚的催化剂。这些锂盐可以调节固体电解质相间层(SEI)的成分。PEA-LiPF6 具有出色的 SEI 化学性质,其 LiF 含量最高,因此临界电流密度高达 2.5 mA cm-2,锂+转移数为 0.81,电化学稳定性窗口为 6.0 V。此外,PEA-LiPF6 的容量保持率分别为 96.6%(0.5 C,在 LiFePO4 ||Li 中的第 200 次/第一周期)、95.6%(0.5 C,在 LiMn0.6Fe0.4PO4||Li)、95.1%(1 C,LiCoO2||Li 中的第 100 次/第一周期)和 87.0%(1 C,LiNi0.6Co0.2Mn0.2O2||Li 全电池中的第 100 次/第一周期)。这项工作展示了一种简便的原位制备聚合物电解质的方法,可用于制备具有均衡综合性能的高压锂金属电池。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Poly(ester-alt-acetal) Electrolyte via In Situ Copolymerization for High-Voltage Lithium Metal Batteries: Lithium Salt Catalysts Deciding Stable Solid-Electrolyte Interphase

Poly(ester-alt-acetal) Electrolyte via In Situ Copolymerization for High-Voltage Lithium Metal Batteries: Lithium Salt Catalysts Deciding Stable Solid-Electrolyte Interphase

Poly(ester-alt-acetal) Electrolyte via In Situ Copolymerization for High-Voltage Lithium Metal Batteries: Lithium Salt Catalysts Deciding Stable Solid-Electrolyte Interphase

The in situ-formed polymer electrolytes provide a vital solution for improving both safety and performance in the high-voltage lithium metal batteries. This study reports new poly(ester-alt-acetal) (PEA) electrolytes, synthesized through in situ alternating copolymerization of glutaric anhydride and 1,3-dioxane. In the presence of 25 wt.% lithium bis(trifluoromethanesulfonyl)imide (LiTFSI), three lithium salts, lithium difluoro(oxalate)borate (LiDFOB), lithium hexafluorophosphate (LiPF6), and lithium tetrafluoroborate (LiBF4) are employed as the catalysts for the copolymerization. These lithium salts can modulate the compositions of the solid-electrolyte interphase (SEI) layer. PEA-LiPF6 exhibits outstanding SEI chemistry, with observing the highest LiF content, thereby achieving a remarkable critical current density of up to 2.5 mA cm−2, a Li+ transference number of 0.81, and an expansive electrochemical stability window of 6.0 V. Furthermore, PEA-LiPF6 demonstrates noteworthy capacity retention rates of 96.6% (0.5 C, 200th/first cycle in LiFePO4||Li), 95.6% (0.5 C, 100th/first cycle in LiMn0.6Fe0.4PO4||Li), 95.1% (1 C, 100th/first cycle in LiCoO2||Li), and 87.0% (1 C, 100th/first cycle in LiNi0.6Co0.2Mn0.2O2||Li full-cells). This work demonstrates a facile in situ route to fabricate polymer electrolytes for high-voltage lithium-metal batteries with balanced and comprehensive performance.

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来源期刊
CiteScore
10.40
自引率
3.40%
发文量
209
审稿时长
1 months
期刊介绍: ACS Macro Letters publishes research in all areas of contemporary soft matter science in which macromolecules play a key role, including nanotechnology, self-assembly, supramolecular chemistry, biomaterials, energy generation and storage, and renewable/sustainable materials. Submissions to ACS Macro Letters should justify clearly the rapid disclosure of the key elements of the study. The scope of the journal includes high-impact research of broad interest in all areas of polymer science and engineering, including cross-disciplinary research that interfaces with polymer science. With the launch of ACS Macro Letters, all Communications that were formerly published in Macromolecules and Biomacromolecules will be published as Letters in ACS Macro Letters.
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