4.6 Article

Usefulness of uselessness: Teamwork of wide temperature electrolyte enables LFP/Li cells from-40 °C to 140 °C

期刊

ELECTROCHIMICA ACTA
卷 425, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2022.140698

关键词

Lithium-metal battery; Wide-temperature electrolytes; Glutaronitrile; Lithium difluoro(oxalate)borate

资金

  1. National Natural Science Foundation of China [21773279, 22075305, 52061135110]
  2. Zhejiang Provincial Natural Science Foundation of China [LD22E020003]
  3. Key Research Program of the Chinese Academy of Sciences [ZDRW_CN_2020-1]
  4. Ningbo Science & Technology Innovation 2025 Major Project [2019B10050, 2019B10113, 2020Z024, 2020Z101, 2020Z025]
  5. Key Laboratory of Bio-based Polymeric Materials of Zhejiang Province

向作者/读者索取更多资源

This paper presents an effective strategy for constructing a wide-temperature range electrode-electrolyte interface layer for lithium secondary batteries. By using electrolyte formulation and the synergy of propylene carbonate and glutaronitrile, stable electrochemical performance in the range of -40℃ to 140℃ is achieved.
Lithium secondary battery with a wide working temperature range is crucial to boost its increasing applications in harsh circumstances. Suppressing excessive electrolyte decomposition at high temperatures while maintaining reasonable electrochemical kinetics at low temperatures is critical for wide-temperature electrochemical performance. Construction of high temperature stable electrode-electrolyte interface layer by electrolyte formulation is an effective strategy to prevent electrolyte from uncontrollable decomposition. On the contrary to conventional thinking, propylene carbonate (PC) bearing poor filming ability to suppress electrolyte decomposition is used in this work to promote decomposition of the single lithium difluoro(oxalate)borate (LiODFB) salt in the electrolyte, producing inorganic-rich interface layer with good structure stability over a wide temperature range. Glutaronitrile (GLN) is further utilized to minimize the decomposition of PC by expelling PC out of the solvation sheath of lithium-ion. The teamwork of LiODFB, PC, and GLN makes a synergistic contribution to building a high-temperature stable electrode-electrolyte interface layer at both LFP and MCMB electrodes. Based on the approach developed in this work, the temperature window is successfully expanded to the range of from -40 degrees C to 140 degrees C. Excellent electrochemical performance is exhibited by both LFP/Li and MCMB/Li cells from -20 degrees C to 100 degrees C in terms of reversible capacity and cyclic stability.

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