Evolution of morphology, segmental dynamics, and conductivity in ionic liquid swollen short side chain perfluorosulfonate ionomer membranes

被引:7
作者
Lin, Jun-Hong [1 ]
Colby, Ralph H. [2 ,3 ]
机构
[1] Natl Kaohsiung Univ Appl Sci, Dept Mold & Die Engn, Kaohsiung 807, Taiwan
[2] Penn State Univ, Dept Mat Sci & Engn, University Pk, PA 16802 USA
[3] Penn State Univ, Dept Chem Engn, University Pk, PA 16802 USA
关键词
glass transition; ionomers; relaxation; SAXS; swelling; DIELECTRIC-RELAXATION; GLASS-TRANSITION; ELECTROLYTE; TEMPERATURE; PERFORMANCE; COPOLYMERS; DILUENTS; BEHAVIOR; MODEL;
D O I
10.1002/polb.23770
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
We investigate the morphology, segmental dynamics, and conductivity of 1-ethyl-3-methylimidazolium trifluoromethanesulfonate (EMI-Tf) swollen short side chain perfluorosulfonate ionomer (Aquivion) over a broad uptake range using small angle X-ray scattering (SAXS), dielectric relaxation spectroscopy, and transient current measurement. The SAXS data indicate that the absorbed EMI-Tf is mainly bounded in the ionic region of Aquivion. At low uptakes, EMI-Tf acts as an effective plasticizer lowering the cluster T-g and markedly shifting the segmental relaxation to a high frequency; however, at high uptakes, the additional EMI-Tf acts like a filler instead. A time-domain model was employed to quantify the conductivity of these membranes containing two mobile ion species, that is, cations and anions. The conductivity of both neat EMI-Tf and EMI-Tf swollen membranes exhibits Vogel-Fulcher-Tamman relation, revealing different activation parameters for ionic conduction. Furthermore, membranes containing different EMI-Tf uptakes have similar conductivity over the reduced T-g/T axis and also follow Debye-Stokes-Einstein relation. Therefore, despite the abrupt change in conductivity near the critical uptake (29 wt %), both cluster T-g and segmental motion remain the key factors for the ionic conduction in these EMI-Tf swollen membranes. (c) 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2015, 53, 1273-1280
引用
收藏
页码:1273 / 1280
页数:8
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