Nikiforidis Georgios, Raghibi Mohamed, Sayegh Adnan, Anouti Mérièm
Laboratoire PCM2E, Université de Tours, Parc de Grandmont, 37200 Tours, France.
LE STUDIUM Institute for Advanced Studies, 45000 Orléans, France.
J Phys Chem Lett. 2021 Feb 25;12(7):1911-1917. doi: 10.1021/acs.jpclett.0c03736. Epub 2021 Feb 16.
Current commercial lithium-ion battery (LIB) electrolytes are heavily influenced by the cost, chemical instability, and thermal decomposition of the lithium hexafluorophosphate salt (LiPF). This work studies the use of an unprecedently low Li salt concentration in a novel electrolyte, which shows equivalent capabilities to their commercial counterparts. Herein, the use of 0.1 M LiPF in a ternary solvent mixture of ethylene carbonate (EC), ethyl methyl carbonate (EMC), and 1,1,2,2-tetrafluoroethyl 2,2,2-trifluoroethyl ether (TFE) (3EC/7EMC/20TFE, by weight) is investigated for the first time in LiNiMnCoO (NMC111)/graphite pouch cells. In solution, the Li transport number and diffusion are governed by the Grotthuss mechanism, with transport properties being independent of salt concentration. The proposed electrolyte operates in a wide temperature window (0-40 °C), is nonflammable (self-extinguishing under 2 s), and shows adequately fast wetting (4 s). When incorporated into the NMC/graphite pouch cell, it initially forms a solid electrolyte interphase (SEI) with minimal gas formation followed by a comparable battery performance to standard LiPF electrolytes, validated by a high specific capacity of 165 mAh g, Coulombic efficiencies of 99.3%, and capacity retention of 85% over 700 cycles.
当前的商用锂离子电池(LIB)电解质受六氟磷酸锂盐(LiPF)的成本、化学不稳定性和热分解影响很大。本研究探索了一种新型电解质中前所未有的低锂盐浓度的使用情况,该电解质表现出与商用同类产品相当的性能。在此,首次在锂镍锰钴氧化物(NMC111)/石墨软包电池中研究了在碳酸乙烯酯(EC)、碳酸甲乙酯(EMC)和1,1,2,2-四氟乙基 2,2,2-三氟乙基醚(TFE)(重量比为3EC/7EMC/20TFE)的三元溶剂混合物中使用0.1 M LiPF的情况。在溶液中,锂的迁移数和扩散受格罗特斯机制控制,传输性质与盐浓度无关。所提出的电解质在较宽的温度窗口(0-40°C)内运行,不可燃(在2秒内自熄),并显示出足够快的润湿速度(4秒)。当应用于NMC/石墨软包电池时,它最初形成固体电解质界面(SEI),气体生成量最小,随后电池性能与标准LiPF电解质相当,通过165 mAh g的高比容量、99.3%的库仑效率和700次循环后85%的容量保持率得到验证。