Long Functional Graft Polymer Induced Multiscale Morphological Inversion and Enhanced Anion Transport Efficiency in Radiation-Grafted Anion Exchange Membranes

IF 5.1 1区 化学 Q1 POLYMER SCIENCE Macromolecules Pub Date : 2025-01-03 DOI:10.1021/acs.macromol.4c02454
Yue Zhao, Kimio Yoshimura, Aurel Radulescu, Yasunari Maekawa
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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%.

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长功能接枝聚合物在辐射接枝阴离子交换膜中诱导多尺度形态反转和增强阴离子传输效率
我们利用部分散射函数(PSF)分析全面研究了先前报道的辐射接枝阴离子交换膜(AEMs)的层次结构,该膜由对-(2-咪唑酰基)苯乙烯接枝聚合物组成,具有不同接枝度(GD)的聚乙烯-共四氟乙烯(ETFE)薄膜。我们首先证实了在20-25%的GD (GDc)的存在,在此范围内AEMs表现出增强的阴离子传输效率。为了明确与GDc相关的结构特征,我们选择了两种GD分别为14%和42%的AEM14和AEM42进行PSF分析,其中AEM14被视为含有EFTE基聚合物(BP)、接枝聚合物(GP)和水(W)的3组分体系。我们的结果揭示了两种不同的微相转化在GDc范围内分别在几十纳米和几纳米范围内。在大尺度下(>10 nm),在GD <;GDc(即AEM14)、亲水性GP/W结构域和干性GP结构域共存,它们呈球形,平均半径为~ 11.5 nm,分散在BP矩阵中。在GD >;GDc(即AEM42),由分布在GP/W基体中的旋转半径为~ 9.5 nm的不规则形状BP域形成的网络结构(与AEM14相比亲水/疏水相反转)。在小尺度(<10 nm)下,AEM14和AEM42所示的双连续局部结构证实了离子通道在亲水性区域从水-聚合物向水-聚合物的转变,其中GP或W分别为富相。这些独特结构因子的提取使得利用GD >预测AEMs的散射强度曲线成为可能;42%。
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来源期刊
Macromolecules
Macromolecules 工程技术-高分子科学
CiteScore
9.30
自引率
16.40%
发文量
942
审稿时长
2 months
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.
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