低温锂离子电池中多功能离子液体添加剂的共晶转变和界面调制

IF 26 1区 材料科学 Q1 CHEMISTRY, PHYSICAL
Jun Su Kim, Uddhav Kulkarni, Jeong Hee Park, Won‐Jang Cho, Won Il Kim, Jin Suk Byun, You Kyung Jeong, Kyungho Ahn, Chul Haeng Lee, Gi‐Ra Yi, Ho Seok Park
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引用次数: 0

摘要

商用锂离子电池(lib)在零度以下的温度下,由于碳酸乙烯(EC)基电解质的粘度增加,以及石墨阳极界面上锂离子(Li +)脱溶的高能量垒,会导致性能大幅下降,这对在寒冷气候和极端环境下的应用提出了严峻的挑战。为了克服这一问题,引入了一种基于磷的离子液体——烯丙基三甲基磷二(三氟甲烷)磺酰亚胺(APT)作为多功能电解质添加剂。APT与EC形成共晶混合物,有效降低凝固点和粘度,同时在低温下提高离子电导率。此外,APT削弱了Li + -EC的相互作用,促进了Li +在石墨界面上更有效的脱溶,并促进了石墨阳极上薄、均匀、富liff的固体电解质界面相的形成,从而实现了Li +快速的界面转移动力学。具有高质量负载电极(NCM811||石墨,4.9 mAh cm - 2)和含有1 wt.% APT的稀薄电解质(3g Ah - 1)的袋状电池在- 20°C下进行100次循环后保留了87.56%的容量,显著优于未添加添加剂的电池(保留率为64.60%)。因此,这项工作为多功能电解质添加剂提供了一种合理的设计策略,该策略可以同时优化整体输运性能和界面稳定性,从而在零下条件下可靠地运行LIB。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Eutectic Transition and Interfacial Modulation of Multifunctional Ionic Liquid Additives for Subzero‐Temperature Lithium‐Ion Batteries
Commercial lithium‐ion batteries (LIBs) suffer substantial performance degradation at subzero temperatures due to the increased viscosity of ethylene carbonate (EC)‐based electrolytes and a high energy barrier for lithium‐ion (Li⁺) desolvation at the graphite anode interface, posing critical challenges for applications in cold climates and extreme environments. To overcome this, a phosphonium‐based ionic liquid, allyl trimethyl phosphonium bis(trifluoromethane)sulfonimide (APT), is introduced as a multifunctional electrolyte additive. APT forms a eutectic mixture with EC, effectively lowering the freezing point and viscosity while enhancing ionic conductivity at low temperatures. Furthermore, APT weakens the Li⁺–EC interaction, facilitating more efficient Li⁺ desolvation at the graphite interface, and promotes the formation of a thin, uniform, LiF‐rich solid electrolyte interphase on the graphite anode, leading to the fast interfacial Li⁺ transfer kinetics. Pouch cells with high‐mass‐loading electrodes (NCM811||graphite, 4.9 mAh cm−2) and lean electrolyte (3 g Ah−1) containing 1 wt.% of APT retained 87.56% of their capacity after 100 cycles at −20 °C, significantly outperforming cells without the additive (64.60% retention). Therefore, this work provides a rational design strategy for multifunctional electrolyte additives that simultaneously optimize bulk transport properties and interfacial stability for reliable LIB operation under subzero conditions.
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来源期刊
Advanced Energy Materials
Advanced Energy Materials CHEMISTRY, PHYSICAL-ENERGY & FUELS
CiteScore
41.90
自引率
4.00%
发文量
889
审稿时长
1.4 months
期刊介绍: Established in 2011, Advanced Energy Materials is an international, interdisciplinary, English-language journal that focuses on materials used in energy harvesting, conversion, and storage. It is regarded as a top-quality journal alongside Advanced Materials, Advanced Functional Materials, and Small. With a 2022 Impact Factor of 27.8, Advanced Energy Materials is considered a prime source for the best energy-related research. The journal covers a wide range of topics in energy-related research, including organic and inorganic photovoltaics, batteries and supercapacitors, fuel cells, hydrogen generation and storage, thermoelectrics, water splitting and photocatalysis, solar fuels and thermosolar power, magnetocalorics, and piezoelectronics. The readership of Advanced Energy Materials includes materials scientists, chemists, physicists, and engineers in both academia and industry. The journal is indexed in various databases and collections, such as Advanced Technologies & Aerospace Database, FIZ Karlsruhe, INSPEC (IET), Science Citation Index Expanded, Technology Collection, and Web of Science, among others.
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