TY - JOUR
T1 - Anion-Dominated Conventional-Concentrations Electrolyte to Improve Low-Temperature Performance of Lithium-Ion Batteries
AU - Chen, Nan
AU - Feng, Mai
AU - Li, Chengjie
AU - Shang, Yanxin
AU - Ma, Yue
AU - Zhang, Jinxiang
AU - Li, Yifan
AU - Chen, Guoshuai
AU - Wu, Feng
AU - Chen, Renjie
N1 - Publisher Copyright:
© 2024 Wiley-VCH GmbH.
PY - 2024
Y1 - 2024
N2 - Low temperatures (< −20 °C) significantly diminish lithium-ion battery performance due to freezing issues within commercial electrolytes and the high energy barrier for Li+ desolvation at the interface. Although high-concentration electrolytes and localized high-concentration electrolytes enhance Li+ desolvation kinetics featuring anion-participated solvation structures, their high viscosity and propensity for Li salt precipitation render them unsuitable for low-temperature environments. This study introduces an anion-dominated conventional-concentrations electrolyte (ACCE) created by incorporating Lithium difluorophosphate(LiPO2F2)into a 1 M Lithium bis((trifluoromethyl)sulfonyl)azanide(LiTFSI) Dimethyl carbonate(DMC)/Fluoroethylene carbonate(FEC)/Methyl acetate(MA) electrolyte solution. LiPO2F2, characterized by its poor solubility and strong binding with Li+, demonstrates a pronounced tendency to integrate into the primary solvation sheath of Li+. Moreover, the synergy between LiTFSI and LiPO2F2 establishes a dual anion configuration, unveiling a dual anion-driven mechanism. This mechanism significantly diminishes the interaction between Li+ and solvent molecules, resulting in reduced desolvation energy under low temperatures. The ACCE exhibits high ionic conductivity of 1.3 mS cm−1 at −50 °C, enabling stable cycling of Li/NCM811 cells at −50 °C, and further allows 0.75 Ah graphite(Gr)/LiNi0.8Co0.1Mn0.1O2(NCM811) batteries dischargeable at −40 °C. This study presents a practical application potential for poorly soluble lithium salts and provides a new avenue for designing electrolytes suitable for low-temperature applications.
AB - Low temperatures (< −20 °C) significantly diminish lithium-ion battery performance due to freezing issues within commercial electrolytes and the high energy barrier for Li+ desolvation at the interface. Although high-concentration electrolytes and localized high-concentration electrolytes enhance Li+ desolvation kinetics featuring anion-participated solvation structures, their high viscosity and propensity for Li salt precipitation render them unsuitable for low-temperature environments. This study introduces an anion-dominated conventional-concentrations electrolyte (ACCE) created by incorporating Lithium difluorophosphate(LiPO2F2)into a 1 M Lithium bis((trifluoromethyl)sulfonyl)azanide(LiTFSI) Dimethyl carbonate(DMC)/Fluoroethylene carbonate(FEC)/Methyl acetate(MA) electrolyte solution. LiPO2F2, characterized by its poor solubility and strong binding with Li+, demonstrates a pronounced tendency to integrate into the primary solvation sheath of Li+. Moreover, the synergy between LiTFSI and LiPO2F2 establishes a dual anion configuration, unveiling a dual anion-driven mechanism. This mechanism significantly diminishes the interaction between Li+ and solvent molecules, resulting in reduced desolvation energy under low temperatures. The ACCE exhibits high ionic conductivity of 1.3 mS cm−1 at −50 °C, enabling stable cycling of Li/NCM811 cells at −50 °C, and further allows 0.75 Ah graphite(Gr)/LiNi0.8Co0.1Mn0.1O2(NCM811) batteries dischargeable at −40 °C. This study presents a practical application potential for poorly soluble lithium salts and provides a new avenue for designing electrolytes suitable for low-temperature applications.
KW - electrolyte
KW - lithium difluorophosphate
KW - lithium-ion batteries
KW - low temperature
KW - solvation structure
UR - http://www.scopus.com/inward/record.url?scp=85188569737&partnerID=8YFLogxK
U2 - 10.1002/adfm.202400337
DO - 10.1002/adfm.202400337
M3 - Article
AN - SCOPUS:85188569737
SN - 1616-301X
JO - Advanced Functional Materials
JF - Advanced Functional Materials
ER -