Fu En-De, Zhang Ya-Ting, Zheng Chang-Lu, Hua Yuan-Jun, Hao Shuai, Gao Xue-Ping
Institute of New Energy Material Chemistry, School of Materials Science and Engineering, Nankai University, Tianjin 300350, China.
Tianjin B&M Science and Technology Co. Ltd, Tianjin 300384, China.
ACS Appl Mater Interfaces. 2025 Feb 5;17(5):7811-7820. doi: 10.1021/acsami.4c19766. Epub 2025 Jan 24.
Eutectic-based polymer electrolytes have emerged as promising solid electrolytes because of their ionic liquid-like properties, while modifications are essential to further increase their ionic conductivity at room temperature and solve their compatibility with lithium anode. In this work, an in situ polymerized composite electrolyte is modified by the addition of fluoroethylene carbonate (FEC) whose beneficial effect is systematically investigated in different contents. Poly(ethylene glycol) diacrylate (PEGDA), deep eutectic solvent (LiTFSI:-methylacetamide = 1:3), and alumina fiber work as the monomer, solvent, and three-dimensional skeleton, respectively. In adjusting FEC content, ionic conductivity at room temperature is dramatically raised by three times to 8.93 × 10 S cm, with a 4-fold increase in lithium-ion transference number to 0.405. Meanwhile, the electrochemical window is widened from 3.5 to 4.8 V. The FEC addition also helps in improving the stability with Li anode, which comes from LiF-rich interphases formed at interfaces. The dynamics of LiFePO is significantly enhanced with higher reversibility in full cells, so that fast capacity decay is inhibited with a specific capacity of 124.1 mAh g obtained after 300 cycles at 1 C. These results provide an effective modification for the deep eutectic electrolyte, which will boost its development in solid-state batteries.
基于低共熔物的聚合物电解质因其类似离子液体的性质而成为有前景的固体电解质,然而,进行改性对于进一步提高其室温离子电导率以及解决其与锂负极的兼容性至关重要。在这项工作中,通过添加碳酸氟乙烯酯(FEC)对原位聚合复合电解质进行改性,并系统研究了不同含量FEC的有益效果。聚乙二醇二丙烯酸酯(PEGDA)、深共熔溶剂(LiTFSI: -甲基乙酰胺 = 1:3)和氧化铝纤维分别作为单体、溶剂和三维骨架。在调整FEC含量时,室温离子电导率显著提高了三倍,达到8.93×10 S cm,锂离子迁移数增加了4倍,达到0.405。同时,电化学窗口从3.5 V拓宽到4.8 V。添加FEC还有助于提高与锂负极的稳定性,这源于在界面处形成的富含LiF的界面相。LiFePO的动力学在全电池中得到显著增强,可逆性更高,因此在1 C下循环300次后,抑制了快速容量衰减,获得了124.1 mAh g的比容量。这些结果为深共熔电解质提供了一种有效的改性方法,将推动其在固态电池中的发展。