The versatile behaviour of poly-vinylbutyral (PVB) and its ability to form quasi-solid polymer electrolytes (SPE) with reliable ionic mobility, has been investigated over the temperature range from 120 K to 350 K, by mechanical and dielectric spectroscopic measurements. Enhancements in the polymer chain flexibility, due to the addition of low molar mass organic liquid plasticizers (acetonitrile, AcN, and methoxy-propionitrile, MPN) favouring the long-range motion of charge carriers, give rise to a room temperature ionic conductivity which in the hybrid PVB/MPN/LiI system increases of about 3 and 9 orders of magnitude with respect to the counterparts PVB/LiI and pure dry-PVB system, respectively. This result proves the existence of coupling between cooperative segmental motion and ion dynamics in such kind of materials.

Rising the molecular mobility of polyvinyl butyral by plasticizers: Towards energy storage applications

Federico M.
Penultimo
Investigation
;
Carini G.
Ultimo
Investigation
2020-01-01

Abstract

The versatile behaviour of poly-vinylbutyral (PVB) and its ability to form quasi-solid polymer electrolytes (SPE) with reliable ionic mobility, has been investigated over the temperature range from 120 K to 350 K, by mechanical and dielectric spectroscopic measurements. Enhancements in the polymer chain flexibility, due to the addition of low molar mass organic liquid plasticizers (acetonitrile, AcN, and methoxy-propionitrile, MPN) favouring the long-range motion of charge carriers, give rise to a room temperature ionic conductivity which in the hybrid PVB/MPN/LiI system increases of about 3 and 9 orders of magnitude with respect to the counterparts PVB/LiI and pure dry-PVB system, respectively. This result proves the existence of coupling between cooperative segmental motion and ion dynamics in such kind of materials.
2020
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11570/3205928
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