TY - JOUR
T1 - Boosting High-Rate Lithium Metal Batteries by Using Ether-Based Gel Polymer Electrolyte
AU - Zhang, Chenchen
AU - Li, Zuohang
AU - Wang, Su
AU - Li, Chen
AU - Si, Yuchang
AU - Ma, Yue
AU - Song, Dawei
AU - Zhang, Hongzhou
AU - Shi, Xixi
AU - Zhang, Lianqi
N1 - Publisher Copyright:
Copyright © 2025 Chenchen Zhang et al.
PY - 2025
Y1 - 2025
N2 - Ether-based electrolytes are widely used in lithium metal batteries owing to their higher compatibility with Li anodes compared to that of carbonate-based electrolytes. Compared to the concern with high voltage resistance characteristics, little attention has been paid to Li-ion transportation in ether-based systems. Hence, a 1,2-dimethoxyethane-based poly(methyl methacrylate-ethoxylated trimethylolpropane triacrylate) gel polymer electrolyte (named ME-GPE) was developed to realize rapid Li-ion transfer and construct compatible interfaces. The LiFePO4/ME-GPE/Li battery presents a high-rate (10 C) capacity retention of 85.6% after 200 cycles, while sluggish Li-ion transfer is exhibited in the liquid counterpart and a low capacity retention of 47.2% is presented after cycling. Density functional theory calculations show that the binding energies of Li+/DFOB− with a polymer matrix are much higher than those of the liquid electrolyte, which is conducive to the release and the rapid transfer of more Li ions. 7Li solid-state nuclear magnetic resonance exhibits a similar result the higher frequency observed after cycling indicates a larger electron density variation and greater mobility of Li ions. Moreover, the interfacial characteristics were investigated, and Li-ion plating/stripping behaviors are regulated by abundant polar groups on polymers. Therefore, rapid Li-ion transfer capability and outstanding interface stability were simultaneously achieved for ether-based systems for the first time.
AB - Ether-based electrolytes are widely used in lithium metal batteries owing to their higher compatibility with Li anodes compared to that of carbonate-based electrolytes. Compared to the concern with high voltage resistance characteristics, little attention has been paid to Li-ion transportation in ether-based systems. Hence, a 1,2-dimethoxyethane-based poly(methyl methacrylate-ethoxylated trimethylolpropane triacrylate) gel polymer electrolyte (named ME-GPE) was developed to realize rapid Li-ion transfer and construct compatible interfaces. The LiFePO4/ME-GPE/Li battery presents a high-rate (10 C) capacity retention of 85.6% after 200 cycles, while sluggish Li-ion transfer is exhibited in the liquid counterpart and a low capacity retention of 47.2% is presented after cycling. Density functional theory calculations show that the binding energies of Li+/DFOB− with a polymer matrix are much higher than those of the liquid electrolyte, which is conducive to the release and the rapid transfer of more Li ions. 7Li solid-state nuclear magnetic resonance exhibits a similar result the higher frequency observed after cycling indicates a larger electron density variation and greater mobility of Li ions. Moreover, the interfacial characteristics were investigated, and Li-ion plating/stripping behaviors are regulated by abundant polar groups on polymers. Therefore, rapid Li-ion transfer capability and outstanding interface stability were simultaneously achieved for ether-based systems for the first time.
UR - http://www.scopus.com/inward/record.url?scp=105004007626&partnerID=8YFLogxK
U2 - 10.34133/energymatadv.0188
DO - 10.34133/energymatadv.0188
M3 - 文章
AN - SCOPUS:105004007626
SN - 2692-7640
VL - 6
JO - Energy Material Advances
JF - Energy Material Advances
M1 - 188
ER -