Impact of Ion Pairs on the Properties of Dynamic Ion Gels Formed by Complex Coacervation of Oppositely Charged Poly(Ionic Liquids)

IF 6.7 Q1 POLYMER SCIENCE
ACS polymers Au Pub Date : 2026-06-10 Epub Date: 2026-03-25 DOI:10.1021/acspolymersau.6c00013
Malak Alaa Eddine, Daniil R. Nosov, Luiz Fernando Lepre, Anatoli Serghei, Daniel F. Schmidt, Damien Montarnal, Alexander S. Shaplov, Eric Drockenmuller
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引用次数: 0

Abstract

Dynamic ion gels (DIGs) obtained via complex coacervation of oppositely charged poly(ionic liquid)s (PILs) address the inherent trade-off between ionic conductivity (σDC) and mechanical strength (G′) of PILs by providing both enhanced ion transport and robust viscoelastic properties. In order to tune the strength of ionic cross-links through charge delocalization of ion pairs, we study a series of four DIGs obtained from the combination of a cationic PIL (PIL+) containing pendant imidazolium groups and free bis(trifluoromethylsulfonyl)imide (TFSI) counteranions with four anionic PILs (PIL–) bearing pendant sulfonate anions and various free counter cations (i.e., 1-methyl-3-butylimidazolium, trimethylpropylammonium, tetrabutylammonium, and tetrabutylphosphonium). These new DIGs are produced via the formation of ionic cross-links with ion pairs having more localized charges (i.e., cations paired with sulfonate instead of TFSI). This results in stronger electrostatic interactions with counterions, reducing their mobility and significantly increasing the enthalpic driving force for ion exchange-induced coacervation. As a consequence, the four resulting DIGs release different free ionic liquids (ILs) consisting of TFSI anions associated with imidazolium, ammonium or phosphonium cations. The physical, ion-conducting, and viscoelastic properties of the resulting DIGs are systematically investigated by differential scanning calorimetry, broadband dielectric spectroscopy and rheology. The DIG having sulfonate-imidazolium ionic cross-links and releasing EMIM-TFSI ILs exhibits the best compromise between G′ = 62 kPa (at 25 °C, 1 rad s–1) and σDC = 6.5 × 10–6 S cm–1 (at 25 °C), significantly outperforming the parent PILs. These results highlight DIGs as a highly promising class of materials with enhanced processability and mechanical integrity, making them ideal candidates for electrochemical applications such as supercapacitors, soft robotics, electrochromic devices, sensors, and solar cells.

Abstract Image

Abstract Image

离子对极性聚离子液体复凝聚形成的动态离子凝胶性质的影响。
动态离子凝胶(DIGs)是通过反向带电的多离子液体-s (PILs)的复杂凝聚得到的,通过提供增强的离子传输和强大的粘弹性性能,解决了PILs的离子电导率(σDC)和机械强度(G’)之间的内在权衡。为了优化离子交叉连接的强度通过电荷离域的离子对,我们研究一系列的四个挖掘所得阳离子公益诉讼(公益诉讼+)的组合包含吊坠imidazolium组和自由双(trifluoromethylsulfonyl)酰亚胺(TFSI) counteranions四阴离子得利(公益诉讼)轴承吊坠磺酸盐阴离子和各种免费计数器阳离子(例如,1-methyl-3-butylimidazolium, trimethylpropylammonium、四丁铵和tetrabutylphosphonium)。这些新的DIGs是通过与具有更多局域电荷的离子对形成离子交联而产生的(即,阳离子与磺酸盐而不是TFSI配对)。这导致了与反离子更强的静电相互作用,降低了它们的迁移率,并显著增加了离子交换诱导的凝聚的焓驱动力。结果,四种DIGs释放出不同的自由离子液体(ILs),由TFSI阴离子与咪唑、铵离子或磷离子结合而成。通过差示扫描量热法、宽带介电光谱和流变学等方法系统地研究了所得DIGs的物理性质、离子导电性和粘弹性。在G′= 62 kPa(25℃,1 rad S -1)和σDC = 6.5 × 10-6 S cm-1(25℃)之间,具有磺酸-咪唑离子交联并释放EMIM-TFSI il的DIG表现出最佳折衷,显著优于亲本il。这些结果突出了DIGs作为一种非常有前途的材料,具有增强的可加工性和机械完整性,使其成为超级电容器、软机器人、电致变色器件、传感器和太阳能电池等电化学应用的理想候选者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
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