NMR study of photo‐crosslinked solid polymer electrolytes: The influence of monofunctional oligoethers |
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Authors: | Annalisa Chiappone Sebastian Jeremias Roberta Bongiovanni Monika Schönhoff |
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Affiliation: | 1. DISAT Politecnico di Torino, Corso Duca degli Abruzzi, , 24 – 10129 Torino, Italy;2. Institut für Physikalische Chemie, University of Muenster Corrensstr, , 48149 Münster, Germany |
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Abstract: | Solid polymer electrolytes for Lithium batteries applications are commonly prepared by dissolving a lithium salt in poly(ethylene oxide) (PEO)‐based materials. Their performance is strongly related to the structure of the polymer network. In this article, a new salt‐in‐polymer electrolyte prepared by the fast and easy radical photopolymerization of PEO acrylate oligomers is studied. Here, a difunctional monomer used as the polymer backbone is copolymerized with monofunctional monomers of different length and concentration. Thus, the crosslinking density and conductivity are changed. These systems are investigated by a detailed NMR study yielding local dynamics and mass transport by temperature‐dependent spin‐lattice relaxation time and PFG‐NMR diffusion measurements for different nuclei (7Li and 19F). The results indicate that a sufficiently long monofunctional oligoether improves the properties, since it provides a lower crosslinking density as well as more coordinating oxygens for the Li ions. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2013 , 51, 1571–1580 |
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Keywords: | crosslinking density electrochemistry ionic motion NMR photopolymerization polymer electrolytes pulsed field gradient (PFG) |
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