Li Shenyuan, Wang Liying, Liu Chengzhe, Liu Yuhan, Li Zhangnan, Liu Baijun, Sun Zhaoyan, Hu Wei
Faculty of Chemistry, Northeast Normal University, 5268 Renmin Street, Changchun 130024, P. R. China.
Faculty of Chemistry, Jilin University, 2699 Qianjin Street, Changchun 130012, P. R. China.
ACS Appl Mater Interfaces. 2024 Sep 11;16(36):47590-47598. doi: 10.1021/acsami.4c09287. Epub 2024 Aug 27.
Lithium-ion batteries (LIBs) have revolutionized the energy storage landscape and are the preferred power source for various applications, ranging from portable electronics to electric vehicles. The constant drive and growth in battery research and development aim to enhance their performance, energy density, and safety. Advanced lithium batteries (LIBs) are considered to be the most promising electrochemical storage devices, which can provide high specific energy, volumetric energy density, and power density. However, the trade-off between ionic conductivity and cycling stability is still a major contradiction for SPEs. In this work, a novel hydroxylated PAF-1 was designed and synthesized through post-modification, and the lithium-rich single-ion porous aromatic framework PAF-1-OLi was thereafter prepared by lithiation, achieved with a specific surface area to be 155 m g and a lithium content of 2.01 mmol g. PAF-1-OLi, lithium bis(trifluoromethanesulfony)limine (LiTFSI), and poly(vinylidene fluoride-hexafluoropropylene) (PVDF-HFP) were compounded to obtain PAF-1-OLi/PVDF by solution casting, which had good mechanical, thermodynamic, and electrochemical properties. The ion conductivity of PAF-1-OLi/PVDF infiltrated with plasticizer was 2.93 × 10 S cm at 25 °C. The was 0.77, which was much higher than that of the traditional dual-ion polymer electrolytes. The electrochemical window of PAF-1-OLi/PVDF can reach 4.9 V. The Li//PAF-1-OLi/PVDF//LiFePO battery initial discharge specific capacity was 147 mAh g and reached 134.9 mAh g after 600 cycles with a capacity retention rate of 91.2%, demonstrating its good cycling stability. The anionic part of lithium salt was fixed on the framework of PAF-1 to increase the Li transfer number of PAF-1-OLi/PVDF. The lithium-rich PAF-1-OLi and the LiTFSI provided abundant Li sources to transfer, while PAF-1-OLi helped to form a continuous Li transport channel, effectively promoting the migration of Li in the PAF-1-OLi/PVDF and effectively improving the Li conductivity. This study afforded a novel polymer electrolyte based on lithium-rich PAF-1-OLi, which has excellent electrochemical performance, providing a new choice for the polymer electrolyte of lithium batteries.
锂离子电池(LIBs)彻底改变了储能格局,是从便携式电子设备到电动汽车等各种应用的首选电源。电池研发的持续推动和发展旨在提高其性能、能量密度和安全性。先进的锂电池(LIBs)被认为是最有前途的电化学储能装置,能够提供高比能量、体积能量密度和功率密度。然而,离子电导率和循环稳定性之间的权衡仍然是固态电解质的一个主要矛盾。在这项工作中,通过后修饰设计并合成了一种新型羟基化PAF-1,随后通过锂化制备了富锂单离子多孔芳香骨架PAF-1-OLi,其比表面积为155 m²/g,锂含量为2.01 mmol/g。将PAF-1-OLi、双(三氟甲磺酰)亚胺锂(LiTFSI)和聚(偏二氟乙烯-六氟丙烯)(PVDF-HFP)通过溶液浇铸复合得到PAF-1-OLi/PVDF,其具有良好的机械、热力学和电化学性能。在25℃下,增塑剂渗透的PAF-1-OLi/PVDF的离子电导率为2.93×10⁻³ S/cm。迁移数为0.77,远高于传统双离子聚合物电解质。PAF-1-OLi/PVDF的电化学窗口可达4.9 V。Li//PAF-1-OLi/PVDF//LiFePO₄电池的初始放电比容量为147 mAh/g,600次循环后达到134.9 mAh/g,容量保持率为91.2%,表明其具有良好的循环稳定性。锂盐的阴离子部分固定在PAF-1的骨架上,以增加PAF-1-OLi/PVDF的锂转移数。富锂的PAF-1-OLi和LiTFSI提供了丰富的锂源用于传输,而PAF-1-OLi有助于形成连续的锂传输通道,有效促进锂在PAF-1-OLi/PVDF中的迁移,有效提高锂电导率。本研究提供了一种基于富锂PAF-1-OLi的新型聚合物电解质,其具有优异的电化学性能,为锂电池的聚合物电解质提供了新的选择。