TY - JOUR
T1 - All-Solid-State Lithium Metal Batteries with Microdomain-Regulated Polycationic Solid Electrolytes
AU - Ye, Guo
AU - Hong, Xufeng
AU - He, Mengxue
AU - Song, Junjie
AU - Zhu, Lujun
AU - Zheng, Chengxi
AU - Ma, Yue
AU - An, Yun
AU - Shen, Kaier
AU - Shi, Weize
AU - Jia, Yongfeng
AU - Shafqat, Muhammad Burhan
AU - Gao, Peng
AU - Xia, Dingguo
AU - Chen, Fangfang
AU - Pang, Quanquan
N1 - Publisher Copyright:
© 2025 Wiley-VCH GmbH.
PY - 2025/3/26
Y1 - 2025/3/26
N2 - Solid polymer electrolytes (SPEs) are promising for high-energy and high-safety solid-state lithium metal batteries (LMBs). Here, a polycationic solid electrolyte (PCSE) is described that leverages the inherent high thermal/chemical stability of the polycationic domain and the anion trapping (FMAT) effect of another fluorinated microdomain for stable and fast-charging high-voltage LMBs. Specifically, while the polycationic imidazolium backbone ensures high segmental flexibility facilitating the Li+ mobility, the fluorinated microdomain effectively traps the bis(trifluoromethanesulfonyl)imide anions by strong dipole interactions, imparting localized solvation and restricted mobility of the anions, as well as improved oxidation stability. As a result, the PCSE exhibits a high ionic conductivity of 1.4 mS cm−1, a high Li+ transference number of 0.50, and a wide electrochemical window of ∼5.5 V at 25 °C. By way of in situ thermal polymerization of the electrolyte within assembled cells, the PCSE enables ultra-stable cycling of Li|LiNi0.8Co0.1Mn0.1O2 cells with a capacity retention of 98.1% after 500 cycles at 0.2 C at ambient temperatures. The work on the molecular design of PCSEs represents a fundamentally unique perspective for the rational design of SPEs with balanced properties that are historically challenging for high-energy, long-life, ambient-temperature solid-state LMBs.
AB - Solid polymer electrolytes (SPEs) are promising for high-energy and high-safety solid-state lithium metal batteries (LMBs). Here, a polycationic solid electrolyte (PCSE) is described that leverages the inherent high thermal/chemical stability of the polycationic domain and the anion trapping (FMAT) effect of another fluorinated microdomain for stable and fast-charging high-voltage LMBs. Specifically, while the polycationic imidazolium backbone ensures high segmental flexibility facilitating the Li+ mobility, the fluorinated microdomain effectively traps the bis(trifluoromethanesulfonyl)imide anions by strong dipole interactions, imparting localized solvation and restricted mobility of the anions, as well as improved oxidation stability. As a result, the PCSE exhibits a high ionic conductivity of 1.4 mS cm−1, a high Li+ transference number of 0.50, and a wide electrochemical window of ∼5.5 V at 25 °C. By way of in situ thermal polymerization of the electrolyte within assembled cells, the PCSE enables ultra-stable cycling of Li|LiNi0.8Co0.1Mn0.1O2 cells with a capacity retention of 98.1% after 500 cycles at 0.2 C at ambient temperatures. The work on the molecular design of PCSEs represents a fundamentally unique perspective for the rational design of SPEs with balanced properties that are historically challenging for high-energy, long-life, ambient-temperature solid-state LMBs.
KW - aggressive cathodes
KW - anion trapping
KW - Li transference number
KW - lithium metal batteries
KW - polycationic solid electrolytes
UR - http://www.scopus.com/inward/record.url?scp=105001547793&partnerID=8YFLogxK
U2 - 10.1002/adma.202417829
DO - 10.1002/adma.202417829
M3 - 文章
C2 - 39967355
AN - SCOPUS:105001547793
SN - 0935-9648
VL - 37
JO - Advanced Materials
JF - Advanced Materials
IS - 12
M1 - 2417829
ER -