Molecular dynamics and charge transport in highly conductive Polymeric Ionic Liquids
Falk Frenzel, Ryan Guterman, A. Markus Anton, Jiayin Yuan, and, Friedrich Kremer

TL;DR
This study investigates the glassy dynamics and charge transport in highly conductive polymeric ionic liquids using broadband dielectric spectroscopy, revealing a glass transition assisted hopping mechanism and the impact of polymerization degree on conductivity.
Contribution
It provides the first evidence of increased conductivity with higher polymerization degree in PILs and models charge transport as glass transition assisted hopping.
Findings
Highest dc-conductivity observed below 100°C for this class of PILs
Conductivity increases with rising degree of polymerization
Charge transport follows the random free-energy barrier model
Abstract
Glassy dynamics and charge transport are studied for the polymeric Ionic Liquid (PIL) poly(tris(2-(2-methoxyethoxy)ethyl)ammonium acryloxypropylsulfonate) (PAAPS) with varying molecular weight (9700, 44200, 51600 and 99500 g per mol) by Broadband Dielectric Spectroscopy (BDS) in a wide frequency (0.01 - 10E7 Hz) and temperature range (100 - 400 K) and by DSC- and AC-chip calorimetry. The dielectric spectra are characterized by a superposition of (i) relaxation processes, (ii) charge transport and (iii) electrode polarization. The relaxation processes (i) are assigned to the dynamic glass transition and a secondary relaxation. Charge transport (ii) can be described by the random free-energy barrier model as worked out by Dyre et al.; the Barton-Namikawa-Nakajima (BNN) relationship is well fulfilled over more than 8 decades. Electrode polarization (iii) follows the characteristics as…
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Taxonomy
TopicsIonic liquids properties and applications · Electrochemical Analysis and Applications · Material Dynamics and Properties
