TY - JOUR
T1 - Anion-Modulated Solvation Sheath and Electric Double Layer Enabling Lithium-Ion Storage From −60 to 80 °C
AU - Yuan, Song
AU - Cao, Shengkai
AU - Chen, Xi
AU - Wei, Jiaqi
AU - Lv, Zhisheng
AU - Xia, Huarong
AU - Chen, Lixun
AU - Ng, Rayner Bao Feng
AU - Tan, Fu Lun
AU - Li, Haicheng
AU - Loh, Xian Jun
AU - Li, Shuzhou
AU - Feng, Xue
AU - Chen, Xiaodong
N1 - Publisher Copyright:
© 2025 American Chemical Society.
PY - 2025/2/5
Y1 - 2025/2/5
N2 - Current lithium batteries experience significant performance degradation under extreme temperature conditions, both high and low. Traditional wide-temperature electrolyte designs typically addressed these challenges by manipulating the solvation sheath and selecting solvents with extreme melting/boiling points. However, these solvent-mediated solutions, while effective at one temperature extreme, invariably fail at the opposite end due to the inherent difficulties in maintaining solvent stability across wide temperatures. Herein, we report the use of the main lithium salt to simultaneously address interfacial challenges at both extremely high and low temperatures. This approach is different from the conventional solvent-mediated strategies. As a proof of concept, we utilized lithium nitrate (LiNO3) to establish an anion-controlled solvation structure and electric double layer. The formulated electrolytes exhibited remarkable performance across temperature extremes, retaining 56.1% capacity at −60 °C and sustaining 400 stable cycles at 80 °C. In contrast, electrolytes based on current solvent-mediated strategies failed to operate at −60 °C and could not exceed 50 cycles at 80 °C. By shifting the focus to the main salt rather than the solvent, our work offers the possibility of addressing the enduring challenges of electrolyte stability across a broad temperature range.
AB - Current lithium batteries experience significant performance degradation under extreme temperature conditions, both high and low. Traditional wide-temperature electrolyte designs typically addressed these challenges by manipulating the solvation sheath and selecting solvents with extreme melting/boiling points. However, these solvent-mediated solutions, while effective at one temperature extreme, invariably fail at the opposite end due to the inherent difficulties in maintaining solvent stability across wide temperatures. Herein, we report the use of the main lithium salt to simultaneously address interfacial challenges at both extremely high and low temperatures. This approach is different from the conventional solvent-mediated strategies. As a proof of concept, we utilized lithium nitrate (LiNO3) to establish an anion-controlled solvation structure and electric double layer. The formulated electrolytes exhibited remarkable performance across temperature extremes, retaining 56.1% capacity at −60 °C and sustaining 400 stable cycles at 80 °C. In contrast, electrolytes based on current solvent-mediated strategies failed to operate at −60 °C and could not exceed 50 cycles at 80 °C. By shifting the focus to the main salt rather than the solvent, our work offers the possibility of addressing the enduring challenges of electrolyte stability across a broad temperature range.
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U2 - 10.1021/jacs.4c13011
DO - 10.1021/jacs.4c13011
M3 - Article
C2 - 39871466
AN - SCOPUS:85217537989
SN - 0002-7863
VL - 147
SP - 4089
EP - 4099
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 5
ER -