Ionomer solution to film solidification dependence upon solvent type and its impact upon morphology and ion transport. (December 2017)

• Record Type: Journal Article
• Authors: Wang, Donghui; Fan, YanFang; Zhang, Mingqiang; Moore, Robert B.; Cornelius, Chris J.
• Is Part Of: European polymer journal. Volume 97(2017)
• Page Start: 169
• Page End: 177
• Publication Date: 2017-12
• Subjects: Ionomer -- Morphology -- Film solution-casting method and processing temperature -- SAXS -- FTIR -- Proton conductivity; Polymers -- Periodicals; Polymerization -- Periodicals; Polymères -- Périodiques; Polymérisation -- Périodiques; Polymerization; Polymers; Periodicals; Electronic journals; 547.705
• DOI: 10.1016/j.eurpolymj.2017.10.011
• Languages: English
• ISSNs: 0014-3057

Abstract

Graphical abstract: Highlights: PBC morphology, transport, and physical properties were casting-solvent dependent. ΔGmix and χ were predicted for PBC dissolved in THF, CHCl3, and C:H. Ionomer morphology transitioned from random to non-random due to solvent. PBC with a lamella-like morphology had stable conductivity vs. a random structure. Abstract: Ionomer chain and solvent molecule interactions during solution-casting, solvent evaporation, and solidification impacts chain entanglements, spatial arrangement of functional groups, microstructure development, morphology, and physical properties. These concepts were investigated using poly( t -butylstyrene- b -ethylene- alt -propylene- b -sulfonatedstyrene- b -ethylene- alt -propylene- b - t -butylstyrene) with a fixed ion-exchange capacity of 1.0, and estimated solubility parameter of 21.8 (J/cm 3 ) 1/2 . Films were solution-cast using an equal volume cyclohexane:heptane mixture (C:H), chloroform (CHCl3 ), and tetrahydrofuran (THF). Subsequent film structures were evaluated using transmission electron microscopy (TEM), small-angle X-ray scattering (SAXS), FT-IR, and electrochemical impedance spectroscopy. A commercially supplied film had sulfonated domains randomly distributed throughout it, and its initial proton conductivity was 11.8 mS/cm. A film created by solution-casting from C:H had a morphology containing randomly distributed sulfonated domains. This random morphology became more ordered with a lamella-like morphology when solution-cast using THF. The film produced from CHCl3 had a morphology that was between random and ordered. Film morphology differences were attributed to a poorer solvent system that inhibited chain solvation. The solution-cast film's proton conductivity was 1.0 mS/cm for a random morphology, and 15.3 mS/cm with a lamella-like structure. Increasing the ionomer-THF solution-casting temperature to 40 °C produced a film with a 103% increase in conductivity (31.2 mS/cm). This led to a water uptake change from 29 wt% to 80 wt%. Cycling a THF solution-cast film from its dry to a wet state revealed that a lamella-like morphology would maintain its conductivity, but the commercial film's conductivity decreased from 11.8 mS/cm to 0.98 mS/cm. Ionomer film properties were found to be dependent upon solvent quality and processing.