TY - JOUR
T1 - Metal-organic ionogel nanocomposite electrolytes for efficient and stable solid-state lithium batteries
AU - Yang, Ningning
AU - Cao, Wenze
AU - Cui, Mokai
AU - Zhao, Zenan
AU - Guo, Penghui
AU - Wang, Hao
AU - Wang, Jing
AU - Chen, Pan
AU - Xiang, Jin
AU - Mu, Daobin
AU - Yu, Huigen
AU - Wu, Feng
AU - Tan, Guoqiang
N1 - Publisher Copyright:
© 2026 Elsevier B.V.
PY - 2026/5
Y1 - 2026/5
N2 - High-quality solid-state electrolytes with excellent ionic conductivity and interface compatibility are essential for high-performance solid-state batteries. However, at present, all-solid-state electrolytes severely suffer from low intrinsic ionic conductivity and high interface impedance, while quasi-solid-state electrolytes face great challenges of structural metastability due to the heterogeneity. Here, we propose a new metal-organic ionogel concept for extending solid-state electrolytes and investigate their electrochemical properties in Li metal batteries. A simple sol-gel method is used for metal-organic ionogel self-assembly, in which ferric nitrate trimer reacts with trimeric acid to form ordered mesoporous metal-organic frameworks, while ionic liquid electrolyte is in-situ confined within mesoporous channels. The resulting metal-organic ionogel exhibits a glassy homogeneous structure with fast room-temperature Li-ion conduction (1.02 × 10−3 S cm−1), high electrochemical oxidation potential (4.8 V vs Li/Li+), and excellent thermal stability (300 °C), accordingly demonstrating great potential for Li batteries, where both LiFePO4//Li and LiNi0.8Co0.1Mn0.1O2//Li cells display high initial capacities (160 and 202 mAh g−1) and excellent capacity retention (98.6% and 85.4%) after 200 cycles.
AB - High-quality solid-state electrolytes with excellent ionic conductivity and interface compatibility are essential for high-performance solid-state batteries. However, at present, all-solid-state electrolytes severely suffer from low intrinsic ionic conductivity and high interface impedance, while quasi-solid-state electrolytes face great challenges of structural metastability due to the heterogeneity. Here, we propose a new metal-organic ionogel concept for extending solid-state electrolytes and investigate their electrochemical properties in Li metal batteries. A simple sol-gel method is used for metal-organic ionogel self-assembly, in which ferric nitrate trimer reacts with trimeric acid to form ordered mesoporous metal-organic frameworks, while ionic liquid electrolyte is in-situ confined within mesoporous channels. The resulting metal-organic ionogel exhibits a glassy homogeneous structure with fast room-temperature Li-ion conduction (1.02 × 10−3 S cm−1), high electrochemical oxidation potential (4.8 V vs Li/Li+), and excellent thermal stability (300 °C), accordingly demonstrating great potential for Li batteries, where both LiFePO4//Li and LiNi0.8Co0.1Mn0.1O2//Li cells display high initial capacities (160 and 202 mAh g−1) and excellent capacity retention (98.6% and 85.4%) after 200 cycles.
KW - Metal-organic ionogel
KW - Nanocomposite electrolyte
KW - Quasi-solid electrolyte
KW - Sol-gel self-assembly
KW - Solid-state battery
UR - https://www.scopus.com/pages/publications/105033572641
U2 - 10.1016/j.ensm.2026.105052
DO - 10.1016/j.ensm.2026.105052
M3 - Article
AN - SCOPUS:105033572641
SN - 2405-8297
VL - 88
JO - Energy Storage Materials
JF - Energy Storage Materials
M1 - 105052
ER -