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Correlation between segmental dynamics, glass transition, and lithium ion conduction in poly(methyl methacrylate)/ionic liquid mixture

AutorJeddi, Kazem; Taheri Qazvini, Nader; Cangialosi, Daniele ; Chen, Pu
Palabras claveLithium ion mobility
Segmental dynamics
Segmental dynamics
Solid-state electrolytes
Solid-state electrolytes
Glass transition
Glass transition
Fecha de publicación2013
EditorTaylor & Francis
CitaciónJournal of Macromolecular Science Part B Physics 52(4): 590-603 (2013)
ResumenA solid-state membrane of a polymer/ionic liquid miscible mixture, poly(methyl methacrylate) (PMMA) and 1-butyl-3-methylimidazolium hexafluorophosphate (BMIMPF6) doped with lithium perchlorate (LiClO4), was prepared and characterized. Miscibility, segmental dynamics, glass transition and ionic conductivity were investigated. Based on the results from differential scanning calorimetry (DSC) and dynamic mechanical thermal analysis (DMTA), the system is fully miscible and of single phase. Broadening of the glass transition was observed when increasing the amount of ionic liquid, which can be attributed to mobility and flexibility differences between the polymer and ionic liquid. A large dynamical asymmetry and intrinsic mobility difference allow segmental and structural motion/relaxation over a wider temperature range by increasing the amount of ionic liquid. Saturation recovery spin-lattice relaxation time (T1) versus temperature obtained from 7Li nuclear magnetic resonance (NMR) showed high mobility of lithium ions, which was almost temperature independent. Lithium ion conductivity significantly increases with increasing ionic liquid amount. It is concluded that lithium ion mobility and its conduction is positively correlated to segmental dynamics of ion carriers in this model system, which is more noticeable in mixtures with higher amounts of the ionic liquid. © 2013 Copyright Taylor and Francis Group, LLC.
Identificadoresdoi: 10.1080/00222348.2012.716664
issn: 0022-2348
e-issn: 1525-609X
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