TY - JOUR
T1 - Dual-anion ionic liquid electrolytes
T2 - a strategy for achieving high stability and conductivity in lithium metal batteries
AU - Lee, Jemin
AU - Choi, Wonwoo
AU - Jang, Eunbin
AU - Kim, Hyunjin
AU - Yoo, Jeeyoung
N1 - Publisher Copyright:
© 2025 The Royal Society of Chemistry.
PY - 2025/3/13
Y1 - 2025/3/13
N2 - Ionic liquid electrolytes (ILEs) provide promising thermal and electrochemical stability characteristics for safer lithium metal batteries (LMBs). However, their development faces challenges due to their low ionic conductivity and poor wettability on separators. In this study, we introduce a dual-anion locally concentrated ionic-liquid electrolyte (D-LCILE), designed with a diluent and two distinct anions to significantly improve the ionic conductivity and wettability. These improvements were confirmed through electrochemical impedance spectroscopy (EIS) measurements on stainless steel symmetric cells, contact angle tests, and rate capability assessments on a 300 μm thick lithium metal half-cell. Notably, the dual-anion design enhances the interfacial stability, as density functional theory (DFT) calculations revealed a more stable solvation shell structure, further supported by molecular dynamics (MD) simulations. Additionally, scanning electron microscopy (SEM) experiments confirmed the deposition of a thin and, dense lithium layer, while X-ray photoelectron spectroscopy (XPS) depth profile analysis showed a stable solid electrolyte interphase (SEI) with increased LiF content. Performance tests on a 20 μm-thick Li‖LiFePO4 full cell revealed an average Coulombic efficiency exceeding 99.90% and capacity retention >99.93% after 200 cycles at 1C, making D-LCILE a highly promising candidate for next-generation, high-performance LMBs.
AB - Ionic liquid electrolytes (ILEs) provide promising thermal and electrochemical stability characteristics for safer lithium metal batteries (LMBs). However, their development faces challenges due to their low ionic conductivity and poor wettability on separators. In this study, we introduce a dual-anion locally concentrated ionic-liquid electrolyte (D-LCILE), designed with a diluent and two distinct anions to significantly improve the ionic conductivity and wettability. These improvements were confirmed through electrochemical impedance spectroscopy (EIS) measurements on stainless steel symmetric cells, contact angle tests, and rate capability assessments on a 300 μm thick lithium metal half-cell. Notably, the dual-anion design enhances the interfacial stability, as density functional theory (DFT) calculations revealed a more stable solvation shell structure, further supported by molecular dynamics (MD) simulations. Additionally, scanning electron microscopy (SEM) experiments confirmed the deposition of a thin and, dense lithium layer, while X-ray photoelectron spectroscopy (XPS) depth profile analysis showed a stable solid electrolyte interphase (SEI) with increased LiF content. Performance tests on a 20 μm-thick Li‖LiFePO4 full cell revealed an average Coulombic efficiency exceeding 99.90% and capacity retention >99.93% after 200 cycles at 1C, making D-LCILE a highly promising candidate for next-generation, high-performance LMBs.
UR - https://www.scopus.com/pages/publications/105000416704
U2 - 10.1039/d5ee00119f
DO - 10.1039/d5ee00119f
M3 - Article
AN - SCOPUS:105000416704
SN - 1754-5692
VL - 18
SP - 5277
EP - 5286
JO - Energy and Environmental Science
JF - Energy and Environmental Science
IS - 11
ER -