Li Chenming, Bhandary Rajesh, Marinow Anja, Ivanov Dmitrii, Du Mengxue, Androsch René, Binder Wolfgang H
Macromolecular Chemistry, Institute of Chemistry, Faculty of Natural Science II, Martin Luther University Halle-Wittenberg, Von-Danckelmann-Platz 4, 06120 Halle (Saale), Germany.
Interdisciplinary Center for Transfer-Oriented Research in Natural Sciences, Martin Luther University Halle-Wittenberg, 06099 Halle (Saale), Germany.
Polymers (Basel). 2022 Sep 29;14(19):4090. doi: 10.3390/polym14194090.
Within the era of battery technology, the urgent demand for improved and safer electrolytes is immanent. In this work, novel electrolytes, based on pyrrolidinium-bistrifluoromethanesulfonyl-imide polymeric ionic liquids (POILs), equipped with quadrupolar hydrogen-bonding moieties of ureido-pyrimidinone (UPy) to mediate self-healing properties were synthesized. Reversible addition-fragmentation chain-transfer (RAFT) polymerization was employed using S,S-dibenzyl trithiocarbonate as the chain transfer agent to produce precise POILs with a defined amount of UPy and POIL-moieties. Kinetic studies revealed an excellent control over molecular weight and polydispersity in all polymerizations, with a preferable incorporation of UPy monomers in the copolymerizations together with the ionic monomers. Thermogravimetric analysis proved an excellent thermal stability of the polymeric ionic liquids up to 360 °C. By combining the results from differential scanning calorimetry (DSC), broadband dielectric spectroscopy (BDS), and rheology, a decoupled conductivity of the POILs from glass transition was revealed. While the molecular weight was found to exert the main influence on ionic conductivity, the ultimate strength and the self-healing efficiency (of up to 88%) were also affected, as quantified by tensile tests for both pristine and self-healed samples, evidencing a rational design of self-healing electrolytes bearing both hydrogen bonding moieties and low-molecular-weight polymeric ionic liquids.
在电池技术时代,对改进型和更安全电解质的迫切需求迫在眉睫。在这项工作中,合成了基于吡咯烷鎓-双(三氟甲磺酰)亚胺聚合离子液体(POILs)的新型电解质,其配备有脲嘧啶酮(UPy)的四极氢键部分以介导自修复性能。使用二苄基三硫代碳酸酯作为链转移剂,采用可逆加成-断裂链转移(RAFT)聚合反应,制备具有确定量的UPy和POIL部分的精确POILs。动力学研究表明,在所有聚合反应中对分子量和多分散性具有出色的控制,在与离子单体的共聚反应中,UPy单体具有较好的掺入率。热重分析证明,聚合离子液体在高达360°C时具有出色的热稳定性。通过结合差示扫描量热法(DSC)、宽带介电谱(BDS)和流变学的结果,揭示了POILs的电导率与玻璃化转变的解耦。虽然发现分子量对离子电导率有主要影响,但原始样品和自修复样品的拉伸试验量化结果表明,极限强度和自修复效率(高达88%)也受到影响,这证明了对同时含有氢键部分和低分子量聚合离子液体的自修复电解质进行了合理设计。