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用于高压锂金属电池的原位聚合多氟交联聚醚电解质

In Situ Polymerized Polyfluorinated Crosslinked Polyether Electrolytes for High-Voltage Lithium Metal Batteries.

作者信息

Li Shimei, Hong Hu, Yang Xinru, Li Dedi, Xiong Qi, Zhang Dechao, Wang Shixun, Huang Zhaodong, Lv Haiming, Zhi Chunyi

机构信息

Department of Materials Science and Engineering, City University of Hong Kong, 83 Tat Chee Avenue, Hong Kong SAR, 999077, P. R. China.

Hong Kong Centre for Cerebro-Cardiovascular Health Engineering (COCHE), Shatin, NT, Hong Kong SAR, 999077, P. R. China.

出版信息

Adv Mater. 2025 Jul;37(29):e2504333. doi: 10.1002/adma.202504333. Epub 2025 May 2.

Abstract

In situ polymerized polyether electrolytes are promising for solid-state Li metal batteries due to their high ionic conductivity and excellent interfacial contact. However, their practical application is hindered by Li dendrite formation, interfacial degradation, and limited oxidative stability. Herein, we propose an in situ polymerized polyfluorinated crosslinked polyether electrolyte (PDOL-OFHDBO), synthesized by copolymerizing 1,3-dioxolane (DOL) with 2,2'-(2,2,3,3,4,4,5,5-octafluorohexane-1,6-diyl)bis(oxirane) (OFHDBO) as a polyfluorinated crosslinker. The electron-withdrawing polyfluorinated groups endow PDOL-OFHDBO with enhanced oxidative stability and interfacial compatibility, while reducing the solvation power of the polymer matrix to promote an anion-derived inorganic-rich solid electrolyte interphase for uniform Li deposition. Consequently, PDOL-OFHDBO exhibits a wide electrochemical stability window (>5.6 V) and enables long-term stable Li plating/stripping for over 1100 h. Furthermore, Li||LiNiCoMnO (NCM811) full cells utilizing PDOL-OFHDBO demonstrate outstanding cycling stability with high-loading cathodes (≈3.8 mAh cm) and thin Li anodes (50 µm), achieving capacity retention of 95.5% and 89.1% over 100 cycles at cut-off voltages of 4.3 and 4.5 V, respectively. Remarkably, Ah-level Li||NCM811 pouch cells deliver an impressive specific energy of 401.8 Wh kg, highlighting their potential for practical solid-state Li metal batteries.

摘要

原位聚合聚醚电解质因其高离子电导率和优异的界面接触性能,在固态锂金属电池领域具有广阔前景。然而,锂枝晶的形成、界面降解以及有限的氧化稳定性阻碍了它们的实际应用。在此,我们提出了一种原位聚合的多氟交联聚醚电解质(PDOL-OFHDBO),它是通过将1,3-二氧戊环(DOL)与作为多氟交联剂的2,2'-(2,2,3,3,4,4,5,5-八氟己烷-1,6-二基)双(环氧乙烷)(OFHDBO)共聚合成的。吸电子的多氟基团赋予PDOL-OFHDBO增强的氧化稳定性和界面相容性,同时降低聚合物基体的溶剂化能力,以促进阴离子衍生的富含无机物的固体电解质界面层的形成,从而实现均匀的锂沉积。因此,PDOL-OFHDBO展现出较宽的电化学稳定窗口(>5.6 V),并能实现超过1100小时的长期稳定锂电镀/剥离。此外,使用PDOL-OFHDBO的锂||锂镍钴锰氧化物(NCM811)全电池在高负载阴极(≈3.8 mAh cm)和薄锂阳极(50 µm)的情况下表现出出色的循环稳定性,在4.3和4.5 V的截止电压下,100次循环后的容量保持率分别为95.5%和89.1%。值得注意的是,Ah级锂||NCM811软包电池具有令人印象深刻的401.8 Wh kg的比能量,凸显了它们在实际固态锂金属电池中的应用潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e71/12288804/d4010ede350f/ADMA-37-2504333-g004.jpg

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