Long Functional Graft Polymer Induced Multiscale Morphological Inversion and Enhanced Anion Transport Efficiency in Radiation-Grafted Anion Exchange Membranes
{"title":"Long Functional Graft Polymer Induced Multiscale Morphological Inversion and Enhanced Anion Transport Efficiency in Radiation-Grafted Anion Exchange Membranes","authors":"Yue Zhao, Kimio Yoshimura, Aurel Radulescu, Yasunari Maekawa","doi":"10.1021/acs.macromol.4c02454","DOIUrl":null,"url":null,"abstract":"We comprehensively investigate the hierarchical structures of the previously reported radiation-grafted anion-exchange membranes (AEMs), consisting of <i>p</i>-(2-imidazoliumyl) styrene graft-polymers onto poly(ethylene-<i>co</i>-tetrafluoroethylene) (ETFE) films with different grafting degrees (GD), using the partial scattering function (PSF) analysis. We first confirm the existence of a characteristic GD (GD<sub>c</sub>) of 20–25%, over which AEMs show enhanced anion transport efficiency. To clarify the structure features in correlation with GD<sub>c</sub>, two AEMs with GD of 14% and 42% (AEM14 and AEM42) are selected for PSF analysis, where AEMs are treated as a 3-component system, containing EFTE base polymer (BP), graft polymer (GP), and water (W). Our results reveal the two different microphase inversions across GD<sub>c</sub> in tens of nanometers and a few nanometers ranges, respectively. In the large scale (>10 nm), at GD < GD<sub>c</sub> (i.e., AEM14), the hydrophilic GP/W domains and dry GP domains coexist together, which are spherically shaped with an average radius of ∼11.5 nm, dispersing in the BP matrix. At GD > GD<sub>c</sub> (i.e., AEM42), a network structure is formed by irregularly shaped BP domains with a radius of gyration of ∼9.5 nm dispersed in GP/W matrix (hydrophilic/hydrophobic phase-inversion compared to AEM14). In the small scale (<10 nm), ion-channel inversion from water-in-polymer to polymer-in-water in the hydrophilic region is confirmed by the bicontinuous local structures shown in AEM14 and AEM42, with GP or W being the rich phase, respectively. The extraction of these unique structure factors enables the prediction of scattering intensity profiles of AEMs with GD > 42%.","PeriodicalId":51,"journal":{"name":"Macromolecules","volume":"14 1","pages":""},"PeriodicalIF":5.1000,"publicationDate":"2025-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Macromolecules","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.macromol.4c02454","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
We comprehensively investigate the hierarchical structures of the previously reported radiation-grafted anion-exchange membranes (AEMs), consisting of p-(2-imidazoliumyl) styrene graft-polymers onto poly(ethylene-co-tetrafluoroethylene) (ETFE) films with different grafting degrees (GD), using the partial scattering function (PSF) analysis. We first confirm the existence of a characteristic GD (GDc) of 20–25%, over which AEMs show enhanced anion transport efficiency. To clarify the structure features in correlation with GDc, two AEMs with GD of 14% and 42% (AEM14 and AEM42) are selected for PSF analysis, where AEMs are treated as a 3-component system, containing EFTE base polymer (BP), graft polymer (GP), and water (W). Our results reveal the two different microphase inversions across GDc in tens of nanometers and a few nanometers ranges, respectively. In the large scale (>10 nm), at GD < GDc (i.e., AEM14), the hydrophilic GP/W domains and dry GP domains coexist together, which are spherically shaped with an average radius of ∼11.5 nm, dispersing in the BP matrix. At GD > GDc (i.e., AEM42), a network structure is formed by irregularly shaped BP domains with a radius of gyration of ∼9.5 nm dispersed in GP/W matrix (hydrophilic/hydrophobic phase-inversion compared to AEM14). In the small scale (<10 nm), ion-channel inversion from water-in-polymer to polymer-in-water in the hydrophilic region is confirmed by the bicontinuous local structures shown in AEM14 and AEM42, with GP or W being the rich phase, respectively. The extraction of these unique structure factors enables the prediction of scattering intensity profiles of AEMs with GD > 42%.
期刊介绍:
Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.