TY - JOUR
T1 - Interface-Compatible Deep Eutectic Polymer Electrolytes for High-Voltage Solid-State Lithium Metal Batteries
AU - Zhang, Dashan
AU - Tian, Ting
AU - Guo, Yu
AU - Zhang, Jikai
AU - An, Junwei
AU - Hui, Jia
AU - Shi, Yongzheng
AU - Müller-Buschbaum, Peter
AU - Yang, Shubin
AU - Li, Bin
N1 - Publisher Copyright:
© 2025 Wiley-VCH GmbH.
PY - 2026/3/19
Y1 - 2026/3/19
N2 - Polymer electrolytes (PEs) are attractive due to their lightweight, flexibility, facile processability, and intimate solid–solid contact with electrodes for solid-state lithium-metal batteries (LMBs). Unfortunately, their practical application is impeded by insufficient ionic conductivity and an unstable electrolyte/electrode interface. Herein, by integrating a butadiene sulfone-based deep-eutectic solvent with a fluorinated polymer matrix (PVDF-HFP), a deep eutectic polymer electrolyte (DEPE) is developed. It is demonstrated that the butadiene sulfone not only liberates lithium ions from the C-F dipoles in polymer chains, but also establishes a contact-ion-pair-dominated solvation structure, resulting in the DEPE with a high ionic conductivity of 2.1 × 10−4 S cm−1 at room-temperature and a lithium-ion transference number of 0.64. More importantly, the DEPE exhibits outstanding interface compatibility with both the lithium anode and high-voltage cathode. Benefiting from the weak adsorption of butadiene sulfone on lithium metal, a robust, LiF-rich solid electrolyte interface is formed at the anode. In addition, its higher HOMO energy level facilitates the formation of a uniform, -SOx-rich cathode electrolyte interface on the high-voltage cathode. As a result, a symmetrical Li||Li cell operates stably for over 1200 h, and full batteries of Li||NCM811 exhibit long-term cycling stability even at 4.5 V. This study proposes an effective strategy for designing high-performance PEs, paving the way for the development of high-voltage, long-life LMBs.
AB - Polymer electrolytes (PEs) are attractive due to their lightweight, flexibility, facile processability, and intimate solid–solid contact with electrodes for solid-state lithium-metal batteries (LMBs). Unfortunately, their practical application is impeded by insufficient ionic conductivity and an unstable electrolyte/electrode interface. Herein, by integrating a butadiene sulfone-based deep-eutectic solvent with a fluorinated polymer matrix (PVDF-HFP), a deep eutectic polymer electrolyte (DEPE) is developed. It is demonstrated that the butadiene sulfone not only liberates lithium ions from the C-F dipoles in polymer chains, but also establishes a contact-ion-pair-dominated solvation structure, resulting in the DEPE with a high ionic conductivity of 2.1 × 10−4 S cm−1 at room-temperature and a lithium-ion transference number of 0.64. More importantly, the DEPE exhibits outstanding interface compatibility with both the lithium anode and high-voltage cathode. Benefiting from the weak adsorption of butadiene sulfone on lithium metal, a robust, LiF-rich solid electrolyte interface is formed at the anode. In addition, its higher HOMO energy level facilitates the formation of a uniform, -SOx-rich cathode electrolyte interface on the high-voltage cathode. As a result, a symmetrical Li||Li cell operates stably for over 1200 h, and full batteries of Li||NCM811 exhibit long-term cycling stability even at 4.5 V. This study proposes an effective strategy for designing high-performance PEs, paving the way for the development of high-voltage, long-life LMBs.
KW - PVDF-HFP
KW - compatible interface
KW - deep eutectic solvent
KW - high-voltage lithium metal battery
KW - polymer electrolyte
UR - https://www.scopus.com/pages/publications/105020770453
U2 - 10.1002/adfm.202524041
DO - 10.1002/adfm.202524041
M3 - 文章
AN - SCOPUS:105020770453
SN - 1616-301X
VL - 36
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 23
M1 - e24041
ER -