Raman Ashwin Sankara, Johnson Billy R, Jhulki Samik, Chandra Vismay, Leisen Johannes, Avis Morgan, Dong Sam, Butcher Riley, Narla Aashray, Lee Haewon, Fu Wenbin, Yushin Gleb
School of Materials Science and Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332, United States.
Sila Nanotechnologies Inc (Sila), Alameda, California 94501, United States.
ACS Appl Mater Interfaces. 2024 Oct 30;16(43):58506-58519. doi: 10.1021/acsami.4c09655. Epub 2024 Oct 21.
Solid polymer electrolytes (SPEs) typically consist of salts with mobile anions that could cause instabilities and parasitic side reactions in solid-state lithium (Li) batteries. To address this challenge, single-Li-ion conducting (SLIC) SPEs, where anions of Li salts are covalently attached to the polymer backbone, have been utilized to reduce the number of mobile anions. This approach improves the cationic transference number but is accompanied by a loss of ionic conductivity. In this work, we investigate a synergetic approach of using both a polymerizable SLIC salt and a conventional Li salt in a polymer matrix by in situ polymerization of the poly(propylene glycol) acrylate (PPGA) monomer. The synthesized hybrid SPEs show a high ionic conductivity of up to ∼2 × 10 S cm and a relatively high Li-ion transference number of ∼0.4. With a significantly reduced fraction of mobile anions in the combined salt SPE, in situ polymerized SPE cells with a LiFePO (LFP) cathode achieve a stable performance for over 100 cycles at temperatures as high as 100 °C, which is unattainable with conventional Li salts or electrolytes. Furthermore, solid-state nuclear magnetic resonance spectra provide additional insights into differences in Li nucleus environments and emphasize a reduction in activation energy for hybrid SPEs due to their more open structure. This study opens the path for the fabrication of high-performance solid polymer Li batteries capable of operating at high temperatures using commercial battery fabrication equipment, as in situ polymerized acrylate-based polymers provide drop-in compatibility with conventional battery production, ease of acrylate polymerization, and inexpensive, facile SPE chemistry. We expect that further tuning of the acrylate-based SPE composition may allow further increases in its conductivity without sacrificing its electrochemical stability or mechanical properties.
固态聚合物电解质(SPEs)通常由带有可移动阴离子的盐组成,这些阴离子会在固态锂(Li)电池中导致不稳定性和寄生副反应。为应对这一挑战,已采用单锂离子传导(SLIC)SPEs,其中锂盐的阴离子共价连接到聚合物主链上,以减少可移动阴离子的数量。这种方法提高了阳离子迁移数,但伴随着离子电导率的损失。在这项工作中,我们研究了一种协同方法,即在聚丙烯二醇丙烯酸酯(PPGA)单体的原位聚合过程中,在聚合物基质中同时使用可聚合的SLIC盐和传统锂盐。合成的混合SPEs显示出高达约2×10 S cm的高离子电导率和约0.4的相对较高的锂离子迁移数。在组合盐SPE中可移动阴离子的比例显著降低的情况下,具有磷酸铁锂(LFP)阴极的原位聚合SPE电池在高达100°C的温度下可实现超过100次循环的稳定性能,这是传统锂盐或电解质无法实现的。此外,固态核磁共振光谱提供了关于锂核环境差异的更多见解,并强调了混合SPEs由于其更开放的结构而降低了活化能。这项研究为使用商业电池制造设备制造能够在高温下运行的高性能固态聚合物锂电池开辟了道路,因为原位聚合的丙烯酸酯基聚合物与传统电池生产具有直接兼容性、丙烯酸酯聚合容易,且SPE化学方法廉价、简便。我们预计,进一步调整丙烯酸酯基SPE的组成可能会在不牺牲其电化学稳定性或机械性能的情况下进一步提高其电导率。