Decoupling of ionic conductivity from structural dynamics in polymerized ionic liquids.

Charge transport and structural dynamics in low molecular weight and polymerized 1-vinyl-3-pentylimidazolium bis(trifluoromethylsulfonyl)imide ionic liquids (ILs) are investigated by a combination of broadband dielectric spectroscopy, dynamic mechanical spectroscopy and differential scanning calorimetry. While the dc conductivity and fluidity exhibit practically identical temperature dependence for the non-polymerized IL, a significant decoupling of ionic conduction from structural dynamics is observed for the polymerized IL. In addition, the dc conductivity of the polymerized IL exceeds that of its molecular counterpart by four orders of magnitude at their respective calorimetric glass transition temperatures. This is attributed to the unusually high mobility of the anions especially at lower temperatures when the structural dynamics is significantly slowed down. A simple physical explanation of the possible origin of the remarkable decoupling of ionic conductivity from structural dynamics is proposed.

The behavior and origin of the excess wing in DEET (N,N-diethyl-3-methylbenzamide).

Broadband dielectric spectroscopy along with a high pressure technique and quantum-mechanical calculations are employed to study in detail the behavior and to reveal the origin of the excess wing (EW) in neat N,N-diethyl-3-methylbenzamide (DEET). Our analysis of dielectric spectra again corroborates the idea that the EW is a hidden ß-relaxation peak. Moreover, we found that the position frequency of the ß peak corresponds to the position of the primitive relaxation of the Coupling Model. We also studied the possible intramolecular rotations in DEET by means of DFT calculation. On that basis we were able to describe the EW as the JG ß-relaxation and find the possible origin of the γ-relaxation visible in DEET dielectric spectra at very low temperatures.

Charge transport and dipolar relaxations in imidazolium-based ionic liquids.

Charge transport and dipolar relaxations in a series of imidazolium-based ionic liquids are studied by means of broadband dielectric spectroscopy. Despite the shift of more than 5 decades in the dielectric spectra upon systematic variation of the anion, scaling with respect to the dc conductivities and the characteristic rates yields a collapsing plot. The dielectric spectra are described at higher frequencies in terms of dipolar relaxations whereas hopping conduction in a random spatially varying energy landscape is quantitatively shown to dominate the spectra at lower frequencies. The beta-relaxations observed for both the precursor and the ionic liquids are assigned to librational motion of the imidazolium ring. The corresponding dielectric strength exhibits a strong dependence on the anion.

Universal scaling of charge transport in glass-forming ionic liquids.

Charge transport and glassy dynamics of a variety of glass-forming ionic liquids (ILs) are investigated in a wide frequency and temperature range by means of broadband dielectric spectroscopy, differential scanning calorimetry and rheology. While the absolute values of dc conductivity and viscosity vary over more than 11 decades with temperature and upon systematic structural variation of the ILs, quantitative agreement is found between the characteristic frequency of charge transport and the structural alpha-relaxation. This is traced back to dynamic glass transition assisted hopping as the underlying mechanism of charge transport.

Charge transport and glassy dynamics in imidazole-based liquids.

Broadband dielectric spectroscopy, differential scanning calorimetry, rheology, and pulsed field gradient-nuclear magnetic resonance (PFG NMR) are combined to study glassy dynamics and charge transport in a homologous series of imidazole-based liquids with systematic variation of the alkyl chain length. The dielectric spectra are interpreted in terms of dipolar relaxation and a conductivity contribution. By applying the Einstein, Einstein-Smoluchowski, and Stokes-Einstein relations, translational diffusion coefficients--in quantitative agreement with PFG NMR measurements--are obtained. With increasing alkyl chain length, it is observed that the viscosity increases, whereas the structural alpha-relaxation rate decreases, in accordance with Maxwell's relation. Between the rate omega(e) of electrical relaxation and the rate omega(alpha) of the structural alpha-relaxation, scaling is observed over more than six decades with a decoupling index of about 2.

Charge transport and mass transport in imidazolium-based ionic liquids.

The mechanism of charge transport in the imidazolium-based ionic liquid 1,3-dimethylimidazolium dimethylphosphate is analyzed by combining broadband dielectric spectroscopy (BDS) and pulsed field gradient nuclear magnetic resonance (PFG NMR). The dielectric spectra are dominated-on the low-frequency side-by electrode polarization effects while, for higher frequencies, charge transport in a disordered matrix is the underlying physical mechanism. Using the Einstein and Einstein-Smoluchowski equations enables one to determine-in excellent agreement with direct measurements by PFG NMR-the diffusion coefficient of the charge carriers. By that, it becomes possible to extract from the dielectric spectra separately the number density and the mobilities of the charge carriers and the type of their thermal activation. It is shown that the observed Vogel-Fulcher-Tammann (VFT) dependence of the dc conductivity can be traced back to a similar temperature dependence of the mobility while for the number density an Arrhenius-type thermal activation is found. Extrapolating the latter to room temperature indicates that nearly all charge carriers are participating in the conduction process.