耗散颗粒动力学模拟
电解质
聚合物
膜
化学物理
粒子(生态学)
耗散系统
材料科学
相(物质)
散射
类型(生物学)
化学工程
高分子化学
化学
物理
热力学
光学
物理化学
复合材料
有机化学
工程类
地质学
电极
海洋学
生物
生物化学
生态学
作者
Toshinori Motegi,Masataka Abe,Yue Zhao,Kimio Yoshimura,Akihiro Hiroki,Toshihiro Kawakatsu,Yasunari Maekawa
出处
期刊:Macromolecules
[American Chemical Society]
日期:2025-08-28
卷期号:58 (17): 9249-9258
被引量:1
标识
DOI:10.1021/acs.macromol.5c01257
摘要
This study showed that an optimized structural simulation model for polymer materials using actual measurements as an indicator can enable the expression of ion channel structures as digital values that affect ion conductivity. The hierarchical structure of polymer electrolyte membranes (PEMs) significantly influences their ionic conductivity and durability. Dissipative particle dynamics (DPD) simulations can reproduce the multiscale phase-separated structures in graft-type PEMs by optimizing conservation parameters and coupling force terms in comparison with small-angle neutron scattering (SANS) profiles. The most decisive χ-parameters are evaluated by the appropriate terminal group and charge assignments of coarse-grained particles. Here, the simulated scattering profiles of ion channels and hydrophilic-hydrophobic phase-separated structures were adjusted by tuning the spring constant between the DPD particles to those in the SANS profiles. The Teubner–Strey model analysis of the simulated scattering profile showed the average diameter d of the ion channel and its deviation ε to be 1.9–2.0 nm and ±0.5 nm, respectively.
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