4.7 Article

Fundamental Limitations of Ionic Conductivity in Polymerized Ionic Liquids

Journal

MACROMOLECULES
Volume 51, Issue 21, Pages 8637-8645

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.macromol.8b01221

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Funding

  1. Laboratory Directed Research and Development program of Oak Ridge National Laboratory
  2. U.S. Department of Energy, Office of Science, Basic Energy Sciences, Materials Sciences and Engineering Division
  3. U.S. Office of Naval Research
  4. National Science Centre [DEC-2014/15/B/ST3/04246]
  5. Deutsche Forschungsgemeinschaft [GA2680/1-1]

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We present detailed studies of ionic conductivity in several polymerized ionic liquids (PolyILs) with different size of mobile ions. Presented analysis revealed that charge diffusion in PolyILs is about 10 times slower than ion diffusion, suggesting strong ion-ion correlations that reduce ionic conductivity. The activation energy for the ion diffusion shows a nonmonotonous dependence on the mobile ion size, indicating a competition between Coulombic and elastic forces controlling ion transport in PolyILs. The former dominates mobility of small ions (e.g., Li), while the latter controls mobility of large ions (e.g., TEST). We propose a simple qualitative model describing the activation energy for the ion diffusion. It suggests that an increase in dielectric constant of PolyILs should lead to a significant enhancement of conductivity of small ions (e.g., Li and Na).

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