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The remarkable flexibility in structural tunability and designability of poly(ionic liquids) (PILs) has garnered significant attention. Integration of PILs with membranes, novel properties, and functionalities is anticipated for applications in the fields of membrane separation. Here, we develop a facile method to prepare PIL-functionalized membranes in a one-step process by combining selective swelling-induced pore generation and ionic liquid functionalization. The block copolymer of poly(2-dimethylaminoethyl methacrylate)--polystyrene (PDMAEMA--PS, abbreviated as SDMA) films is immersed in a mixture of ethanol and bromopropane. In addition to the formation of nanoporous structures, an interfacial quaternization reaction between the PDMAEMA blocks and bromopropane occurs to generate poly(methacrylatoethyl propyl dimethylammonium bromide), resulting in the PIL-Br-functionalized membrane (SIL-Br) during the swelling process. It is noteworthy that bromopropane acting as a reactant also promotes the process of selective swelling. The water permeability of the resulting SIL-Br membrane is several times higher than that of the SDMA membrane, which is attributed to the increased pore size and significantly higher hydrophilicity of the SIL-Br membrane. In addition, the anion exchange of SIL-Br with l-proline (l-Pro) readily forms SIL-Pro-functionalized membranes (SIL-Pro), which exhibit exceptional electrical neutrality. Antifouling tests demonstrate that both SIL-Br and SIL-Pro have excellent resistance to proteins compared to the non-PIL-functionalization SDMA membrane, implying their great potential as antifouling membranes for water treatment.
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http://dx.doi.org/10.1021/acs.langmuir.4c04240 | DOI Listing |
Soft Matter
September 2025
Transport phenomena, Chemical engineering Department, Faculty of applied sciences, Delft University of Technology, Van der Maasweg 9, 2629HZ Delft, The Netherlands.
Polymer membranes are prime candidates for separation and purification processes, with their functionality enhanced by nanoparticle incorporation and diverse polymer structures. Poly(ionic liquids) (PILs), highly charged electrolyte-like polymers, are gaining interest as membrane polymer matrices. Embedding photocatalytic nanoparticles enables water purification through filtration and degradation reactions.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2025
Key Laboratory of High-Performance Plastics, Ministry of Education, National & Local Joint Engineering Laboratory for Synthesis Technology of High-Performance Polymers, College of Chemistry, Jilin University, Changchun, 130012, China.
Thanks to the unique rigid conformation and designable side-chain structure, helical polymers are starting to be more widely considered as ideal electrode materials in secondary batteries. In this study, a series of helical poly(isocyanide anthraquinones) (PIC-AQs), including PIC-1AQ and PIC-2AQ, were designed and synthesized via living polymerization using a palladium catalyst (Pd-II). The polymers feature a helical polyisocyanide main chain and anthraquinone (AQ) pendants, offer high yields (approximately 90%), controlled number-average molecular weight (M), and a low polymer dispersity index (PDI).
View Article and Find Full Text PDFPolymers (Basel)
August 2025
Department of Chemistry, School of Sciences and Humanities, Nazarbayev University, Astana 010000, Kazakhstan.
Over the past few decades, lithium-ion batteries (LIBs) have gained significant attention due to their inherent potential for environmental sustainability and unparalleled energy storage efficiency. Meanwhile, polymer electrolytes have gained popularity in several fields due to their ability to adapt to various battery geometries, enhanced safety features, greater thermal stability, and effectiveness in reducing dendrite growth on the anode. However, their relatively low ionic conductivity compared to liquid electrolytes has limited their application in high-performance devices.
View Article and Find Full Text PDFNat Commun
August 2025
School of Materials Science and Engineering, Nanyang Technological University, Singapore, Singapore.
Dielectric elastomer actuators (DEAs) exhibit large actuation strains, lightweight, and fast response, making them a promising candidate for soft robotics and soft grippers. Ionogels have been used as the electrodes in DEAs to offer thermostability and self-healability, however, typically the elastic modulus of the self-healing ionogel electrodes is of several tens of kPa (or higher), limiting the actuation strain performance and self-healing speed of the DEA. In this work, a poly(ionic liquid) (PIL) electrode with an ultralow elastic modulus of 3.
View Article and Find Full Text PDFACS Appl Mater Interfaces
August 2025
Laboratoire Charles Coulomb (L2C), Université de Montpellier, CNRS, 34095 Montpellier, France.
Understanding the molecular structure of mesoporous solid ionic systems is essential for optimizing their macroscopic properties, such as enhanced ionic transport for energy applications and improved mechanical flexibility. These systems can be synthesized efficiently using "one-pot" conditions, where mesopores form via the microphase separation of a templating ionic liquid. Furthermore, incorporating poly(ionic liquid)s can improve structural connectivity and tailor the mechanical strength of the material.
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