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Updated: Sep 25, 2025

Solid-state Graft Copolymer Electrolytes for Lithium Battery Applications
Published on: August 12, 2013
Acidity effects of medium fluids on anhydrous proton conductivity of acid-swollen block polymer electrolyte membranes
Takato Kajita1, Atsushi Noro1,2, Takahiro Seki1
1Department of Molecular & Macromolecular Chemistry, Graduate School of Engineering, Nagoya University Furo-cho, Chikusa-ku Nagoya 464-8603 Japan noro@nagoya-u.jp.
Abstract:
Proton-conductive polymer electrolyte membranes (PEMs) were prepared by infiltrating sulfuric acid (Sa) or phosphoric acid (Pa) into a polystyrene-b-poly(4-vinylpyridine)-b-polystyrene (S-P-S) triblock copolymer. When the molar ratio of acid to pyridyl groups in S-P-S, i.e., the acid doping level (ADL), is below unity, the P-block/acid phase in the PEMs exhibited a moderately high glass transition temperature (T g) of ∼140 °C because of consumption of acids for forming the acid-base complexes between the pyridyl groups and the acids, also resulting in almost no free protons in the PEMs; therefore, the PEMs were totally glassy and exhibited almost no anhydrous conductivity. In contrast, when ADL is larger than unity, the T gs of the phase composed of acid and P blocks were lower than room temperature, due to the excessive molar amount of acid serving as a plasticizer. Such swollen PEMs with excessive amounts of acid releasing free protons were soft and exhibited high conductivities even without humidification. In particular, an S-P-S/Sa membrane with ADL of 4.6 exhibited a very high anhydrous conductivity of 1.4 × 10-1 S cm-1 at 95 °C, which is comparable to that of humidified Nafion membranes. Furthermore, S-P-S/Sa membranes with lower T gs exhibited higher conductivities than S-P-S/Pa membranes, whereas the temperature dependence of the conductivities for S-P-S/Pa is stronger than that for S-P-S/Sa, suggesting Pa with a lower acidity would not be effectively dissociated into a dihydrogen phosphate anion and a free proton in the PEMs at lower temperatures.
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