Malak Alaa Eddine, Daniil R. Nosov, Luiz Fernando Lepre, Anatoli Serghei, Daniel F. Schmidt, Damien Montarnal, Alexander S. Shaplov, Eric Drockenmuller
{"title":"Impact of Ion Pairs on the Properties of Dynamic Ion Gels Formed by Complex Coacervation of Oppositely Charged Poly(Ionic Liquids)","authors":"Malak Alaa Eddine, Daniil R. Nosov, Luiz Fernando Lepre, Anatoli Serghei, Daniel F. Schmidt, Damien Montarnal, Alexander S. Shaplov, Eric Drockenmuller","doi":"10.1021/acspolymersau.6c00013","DOIUrl":null,"url":null,"abstract":"<p>Dynamic ion gels (DIGs) obtained via complex coacervation\r\nof oppositely\r\ncharged poly(ionic liquid)s (PILs) address the inherent trade-off\r\nbetween ionic conductivity (σ<sub>DC</sub>) and mechanical strength\r\n(<em>G</em>′) of PILs by providing both enhanced ion\r\ntransport and robust viscoelastic properties. In order to tune the\r\nstrength of ionic cross-links through charge delocalization of ion\r\npairs, we study a series of four DIGs obtained from the combination\r\nof a cationic PIL (<strong>PIL</strong><sup><strong>+</strong></sup>) containing\r\npendant imidazolium groups and free bis(trifluoromethylsulfonyl)imide\r\n(TFSI) counteranions with four anionic PILs (<strong>PIL</strong><sup><strong>–</strong></sup>) bearing pendant sulfonate anions and\r\nvarious free counter cations (i.e., 1-methyl-3-butylimidazolium, trimethylpropylammonium,\r\ntetrabutylammonium, and tetrabutylphosphonium). These new DIGs are\r\nproduced via the formation of ionic cross-links with ion pairs having\r\nmore localized charges (i.e., cations paired with sulfonate instead\r\nof TFSI). This results in stronger electrostatic interactions with\r\ncounterions, reducing their mobility and significantly increasing\r\nthe enthalpic driving force for ion exchange-induced coacervation.\r\nAs a consequence, the four resulting DIGs release different free ionic\r\nliquids (ILs) consisting of TFSI anions associated with imidazolium,\r\nammonium or phosphonium cations. The physical, ion-conducting, and\r\nviscoelastic properties of the resulting DIGs are systematically investigated\r\nby differential scanning calorimetry, broadband dielectric spectroscopy\r\nand rheology. The DIG having sulfonate-imidazolium ionic cross-links\r\nand releasing EMIM-TFSI ILs exhibits the best compromise between <em>G</em>′ = 62 kPa (at 25 °C, 1 rad s<sup>–1</sup>) and σ<sub>DC</sub> = 6.5 × 10<sup>–6</sup> S\r\ncm<sup>–1</sup> (at 25 °C), significantly outperforming\r\nthe parent PILs. These results highlight DIGs as a highly promising\r\nclass of materials with enhanced processability and mechanical integrity,\r\nmaking them ideal candidates for electrochemical applications such\r\nas supercapacitors, soft robotics, electrochromic devices, sensors,\r\nand solar cells.</p>","PeriodicalId":72049,"journal":{"name":"ACS polymers Au","volume":"6 3","pages":"869–880"},"PeriodicalIF":6.7000,"publicationDate":"2026-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS polymers Au","FirstCategoryId":"1085","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acspolymersau.6c00013","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/3/25 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
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.