Microphase Separation of Linear-Comb Block Copolymer Electrolyte: Electrostatic Effect and Conformational Asymmetry

IF 5.1 1区 化学 Q1 POLYMER SCIENCE Macromolecules Pub Date : 2024-05-31 DOI:10.1021/acs.macromol.4c00444
Lei Shen, Rui Liu, Yue Zhou, Tiantian Song, Yu Guan, Xiaoxue Wu, Zizhen Wei, Xiaotong Chen, Wangqing Zhang and Weichao Shi*, 
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Abstract

In this work, we synthesize a series of linear-comb block copolymers, polystyrene-b-poly(polyethylene glycol methyl ether acrylate) (PS–PPEGMEA), and study the microphase separation mechanism by LiTFSI-doping. The increasing salt concentration promotes the microphase separation of PS–PPEGMEA and also deflects the phase transition boundaries to the lower PPEGMEA volume fraction. We reveal that the effective interaction parameter exhibits a linear to nonlinear dependence on increasing salt concentration and is eventually weakened by the formation of ion clusters at high salt concentration. We further quantify the conformational asymmetry of PS–PPEGMEA by theoretical analysis and point out that the limit of the order–order transition boundaries is defined by strong segregation theory. Therefore, electrostatic interaction and conformational asymmetry jointly determine the microphase separation of PS–PPEGMEA block copolymer electrolytes. This study provides a fundamental understanding of the phase behaviors of salt-doped linear-comb block copolymers and suggests experimental strategies to modulate their nanostructures, which could be very useful for developing novel solid polymer electrolytes.

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线性-组合嵌段共聚物电解质的微相分离:静电效应与构象不对称
在这项研究中,我们合成了一系列线性梳状嵌段共聚物--聚苯乙烯-b-聚(聚乙二醇甲基醚丙烯酸酯)(PS-PPEGMEA),并研究了掺杂 LiTFSI 的微相分离机理。盐浓度的增加促进了 PS-PPEGMEA 的微相分离,同时也使相变边界向较低的 PPEGMEA 体积分数偏移。我们发现,有效相互作用参数随盐浓度的增加呈现出从线性到非线性的依赖关系,并最终因高浓度盐形成离子簇而减弱。我们通过理论分析进一步量化了 PS-PPEGMEA 的构象不对称性,并指出阶-阶转变边界的极限是由强偏析理论定义的。因此,静电作用和构象不对称共同决定了 PS-PPEGMEA 嵌段共聚物电解质的微相分离。这项研究从根本上理解了盐掺杂线性嵌段共聚物的相行为,并提出了调节其纳米结构的实验策略,这对开发新型固体聚合物电解质非常有用。
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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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