Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.polymer.2004.01.047
Title: Embedding poly(styrene sulfonic acid) into PVDF matrix - A new type of proton electrolyte membrane
Authors: Chen, N.
Hong, L. 
Keywords: Amphiphilic polymer blend
Poly(styrene sulfonic acid)
Proton electrolyte membrane
Issue Date: Mar-2004
Citation: Chen, N., Hong, L. (2004-03). Embedding poly(styrene sulfonic acid) into PVDF matrix - A new type of proton electrolyte membrane. Polymer 45 (7) : 2403-2411. ScholarBank@NUS Repository. https://doi.org/10.1016/j.polymer.2004.01.047
Abstract: Hydrophilic polymer segments, consisting of styrene sulfonic acid (SSA) units, were uniformly embedded into hydrophobic poly(vinylidene fluoride) (PVDF) matrix through the mediation of poly(methyl methacrylate) (PMMA) segments, with which SSA segments form a copolymer. Discrete domains (∼100 nm) assembled by the SSA segments have been identified throughout the matrix of the membrane, which was prepared through blending of the copolymer P(MMA-SSA) and the PVDF. The thermal stability of the SSA was largely boosted in such hydrophobic environment. This unique matrix structure offers proton conductivity of as high as 10-3S/cm at a low SSA equivalent (0.6 mmol -SO3H/g of membrane), which is accompanied with a low level of water uptake (26%) at ambient temperature. Using this type of polymer membrane as electrolyte, the electrochemical cell possesses obvious capacitive resistance when the membrane is in the anhydride form according to the impedance analysis. However, the capacitive character vanishes when the membrane is hydrated; this response is attributed to the existence of highly dispersed SSA domains in the membrane. This work also analyzes the impedance spectra of the membranes at different hydrated states or with different SSA contents by using an equivalent electrical circuit. © 2004 Elsevier Ltd. All rights reserved.
Source Title: Polymer
URI: http://scholarbank.nus.edu.sg/handle/10635/88832
ISSN: 00323861
DOI: 10.1016/j.polymer.2004.01.047
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