Thermo-responsive ionic polymers have the ability to form adaptive and switchable morphologies, which may offer enhanced control in energy storage and catalytic applications. Current thermo-responsive polymers are composed of covalently attached thermo-responsive moieties, restricting their mobility and global dynamic response. Here, we report the synthesis and assembly at the water-air interface of symmetric and asymmetric amphiphilic thermo-responsive branched polymers with weakly ionically bound arms of amine-terminated poly(-isopropylacrylamide) (PNIPAM) macro-cations.
View Article and Find Full Text PDFFlexible and mechanically robust gel-like electrolytes offer enhanced energy storage capabilities, versatility, and safety in batteries and supercapacitors. However, the trade-off between ion conduction and mechanical robustness remains a challenge for these materials. Here, we suggest that the introduction of ionic hyperbranched polymers in structured sustained ionogels will lead to both enhanced ion conduction and mechanical performance because of the hyperbranched polymers' ionically conductive groups and the complementary interfacial interactions with ionic liquids.
View Article and Find Full Text PDFWe synthesized amphiphilic hyperbranched poly(ionic liquid)s (HBPILs) with asymmetrical peripheral composition consisting of hydrophobic -octadecylurethane arms and hydrophilic, ionically linked poly(-isopropylacrylamide) (PNIPAM) macrocations and studied low critical solution temperature (LCST)-induced reorganizations at the air-water interface. We observed that the morphology of HBPIL Langmuir monolayers is controlled by the surface pressure with uniform well-defined disk-like domains formed in a liquid phase. These domains are merged and transformed to uniform monolayers with elevated ridge-like network structures representing coalesced interdomain boundaries in a solid phase because the branched architecture and asymmetrical chemical composition stabilize the disk-like morphology under high compression.
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