期刊
SCIENCE CHINA-TECHNOLOGICAL SCIENCES
卷 65, 期 10, 页码 2369-2379出版社
SCIENCE PRESS
DOI: 10.1007/s11431-022-2075-8
关键词
quasi-solid-state electrolyte; ionic conductivity; electrochemical window; photopolymerization; lithium-ion batteries
资金
- Recruitment Program of Global Experts
- Hundred-Talent Project of Fujian
- Fuzhou University
This research successfully prepared a quasi-solid-state electrolyte based on ethoxylated trimethylolpropane triacrylate through a one-step in-situ photopolymerization method. The electrolyte has a three-dimensional network structure, overcoming the contradiction between the plasticizer-related conductivity and the thickness-dependent mechanical performance of traditional solid-state electrolytes. The electrolyte demonstrates excellent ionic conductivity, high lithium ion transference number, and a wide electrochemical window. When applied in lithium-ion batteries, it significantly reduces interface resistance and enhances electrode/electrolyte interface stability, leading to improved initial discharge capacity and Coulombic efficiency.
The practical applications of solid-state electrolytes in lithium-ion batteries (LIBs) are hindered by their low ionic conductivity and high interfacial resistance. Herein, an ethoxylated trimethylolpropane triacrylate based quasi-solid-state electrolyte (ETPTA-QSSE) with a three-dimensional (3D) network is prepared by a one-step in-situ photopolymerization method. The 3D network is designed to overcome the contradiction between the plasticizer-related ionic conductivity and the thickness-dependent mechanical property of quasi-solid-state electrolytes. The ETPTA-QSSE achieves superb room-temperature ionic conductivity up to 4.55x10(-3) S cm(-1), a high lithium ion transference number of 0.57, along with a wide electrochemical window of 5.3 V (vs. Li+/Li), which outperforms most ever of the reported solid-state electrolytes. Owing to the robust network structure and the cathode-electrolyte integrated electrode design, Li metal symmetrical cells show reduced interface resistance and reinforced electrode/ electrolyte interface stability. When applying the ETPTA-QSSE in LiFePO4 parallel to Li cells, the quasi-solid-state cell demonstrates an enhanced initial discharge capacity (155.5 mAh g(-1) at 0.2 C) accompanied by a high average Coulombic efficiency of greater than 99.3%, offering capacity retention of 92% after 200 cycles. Accordingly, this work sheds light on the strategy of enhancing ionic conductivity and reducing interfacial resistance of quasi-solid-state electrolytes, which is promising for high-voltage LIBs.
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