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Leveraging Dipole–Dipole Interactions for Low-Temperature Lithium-Ion Batteries

  • Jianan Peng
  • , Ye Jia
  • , Qiujie He
  • , Pengfei Xia
  • , Changhaoyue Xu
  • , Xuemei Zhang
  • , Xiaobo Zhu
  • , Wen Jun Feng
  • , Yingze Song*
  • , Xue Qiang Zhang*
  • , Wenlong Cai*
  • *此作品的通讯作者
  • Sichuan University
  • Changsha University of Science and Technology
  • Tsinghua University
  • Southwest University of Science and Technology
  • Beijing Institute of Technology

科研成果: 期刊稿件文章同行评审

摘要

Electrolyte engineering represents a highly effective approach to enhancing the low-temperature performance of lithium-ion batteries. While current electrolyte engineering strategies have prioritized optimizing the interactions within solvation structure to enhance low-temperature performance, they have overlooked the temperature-dependent evolution of these interactions and their critical impact on lithium-ion desolvation kinetics. Herein, the impact of the peripheral solvents and temperature variation of ion–solvent and solvent–solvent interactions was investigated. The dipole–dipole interactions between solvents are the most sensitive to temperature drops. The introduction of a diluent into electrolytes serves to enhance dipole–dipole interactions between the solvent and diluent at low temperatures, thereby suppressing the formation of solvent-separated ion pairs and mitigating charge transfer impedance. The solvation structure of lithium ions exhibits much lower sensitivity to temperature decrease in the formulated electrolyte than in the conventional reference electrolyte. The formulated electrolyte enables graphite | LiNi0.8Co0.1Mn0.1O2 batteries to cycle stably for 200 cycles at −20°C. The Ah-level graphite | LiCoO2 pouch cells retain 63.4% and 54.8% of their capacity at −40°C and −50°C, respectively. This work provides valuable insights into the role of dipole–dipole interactions in solvation structures and guides the design of low-temperature electrolytes.

源语言英语
期刊Advanced Functional Materials
DOI
出版状态已接受/待刊 - 2026
已对外发布

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