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用于高性能富镍阴极硫化物固态电池的多功能离子导电聚合物涂层

Multifunctional ion-conductive polymer coatings for high-performance sulfide solid-state batteries with Ni-rich cathodes.

作者信息

Karanth Pranav, Prins Jelle H, Gautam Ajay, Cheng Zhu, Canals-Riclot Jef, Ganapathy Swapna, Ombrini Pierfrancesco, Ladam Alix, Fantini Sebastien, Wagemaker Marnix, Mulder Fokko M

机构信息

Department of Chemical Engineering, Delft University of Technology The Netherlands

Department of Radiation Science and Technology, Delft University of Technology The Netherlands.

出版信息

J Mater Chem A Mater. 2025 May 13. doi: 10.1039/d5ta01827g.

DOI:10.1039/d5ta01827g
PMID:40400779
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12086626/
Abstract

Sulfide-based solid-state batteries (SSBs) are emerging as a top contender for next-generation rechargeable batteries with improved safety and higher energy densities. However, SSBs with Ni-rich cathode materials such as LiNiMnCoO (NMC82) exhibit several chemomechanical challenges at the cathode-electrolyte interface, such as contact loss and solid-electrolyte decomposition, resulting in poor interfacial Li ion transport. To overcome these challenges, we used polymerized ionic liquids (PIL) as coatings at the NMC82 cathode surface, with and without incorporating a lithium salt. The thin Li ion-conductive Li-PIL nanocoating shows excellent compatibility with sulfide solid electrolytes and enables efficient Li transfer over the cathode-solid electrolyte interface, as demonstrated by 2D solid-state exchange NMR. It also improves contact retention between the cathode-solid electrolyte particles and mitigates electrolyte oxidation-induced degradation. This is reflected in the electrochemical performance of coated NMC82 in sulfide SSBs, where both a higher rate performance (190 mA h g 163 mA h g for uncoated at 0.1C) and a remarkable capacity retention of 82.7% after 500 cycles at 0.2C and ambient conditions (20 °C) are observed. These results emphasize the effectiveness of PILs with Li salts as multifunctional coatings that enable high-performance sulfide-based SSBs with Ni-rich cathode materials at ambient temperature.

摘要

硫化物基固态电池(SSB)正成为下一代可充电电池的有力竞争者,具有更高的安全性和能量密度。然而,具有富镍阴极材料(如LiNiMnCoO,NMC82)的SSB在阴极-电解质界面表现出一些化学机械挑战,如接触损失和固体电解质分解,导致界面锂离子传输不良。为了克服这些挑战,我们在NMC82阴极表面使用聚合离子液体(PIL)作为涂层,有无锂盐均可。二维固态交换核磁共振表明,薄的锂离子导电Li-PIL纳米涂层与硫化物固体电解质具有优异的兼容性,并能在阴极-固体电解质界面实现高效的锂转移。它还改善了阴极-固体电解质颗粒之间的接触保持,并减轻了电解质氧化引起的降解。这反映在硫化物SSB中涂覆的NMC82的电化学性能上,在0.1C时,涂覆的NMC82的倍率性能更高(未涂覆的为163 mA h g,涂覆的为190 mA h g),在0.2C和环境条件(20°C)下循环500次后,容量保持率高达82.7%。这些结果强调了含锂盐的PIL作为多功能涂层的有效性,能够在室温下实现具有富镍阴极材料的高性能硫化物基SSB。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8fa/12086626/bb7a2b9c0547/d5ta01827g-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8fa/12086626/417189c05595/d5ta01827g-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8fa/12086626/603063c819a7/d5ta01827g-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8fa/12086626/a145abdf77f5/d5ta01827g-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8fa/12086626/ea566d75178c/d5ta01827g-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8fa/12086626/5d864f026962/d5ta01827g-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8fa/12086626/bb7a2b9c0547/d5ta01827g-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8fa/12086626/417189c05595/d5ta01827g-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8fa/12086626/603063c819a7/d5ta01827g-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8fa/12086626/a145abdf77f5/d5ta01827g-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8fa/12086626/ea566d75178c/d5ta01827g-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8fa/12086626/5d864f026962/d5ta01827g-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8fa/12086626/bb7a2b9c0547/d5ta01827g-f6.jpg

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