Hydration structure of strongly bound water on the sulfonic acid group in a Nafion membrane studied by infrared spectroscopy and quantum chemical calculation.

The hydration structure of the 'strongly bound water' around the sulfonic acid (SA) groups in Nafion, which has recently been revealed by (1)H NMR spectroscopy (Anal. Chem., 2013, 85, 7581), is studied using infrared spectroscopy with the aid of quantum chemical (QC) calculations. During a heated drying process, bulky water is firstly dehydrated, which is followed by the disappearance of the hydronium ion and the appearance of bands that have been assigned to the fully dehydrated species at 140 °C. However, a spectral simulation based on QC reveals that the spectrum at 140 °C comes from the SA group associated with a single-water molecule via two H-bonds. This implies that a thoroughly dried membrane is unavailable even at 140 °C, and the involved water corresponds to the 'strongly bound water.' The QC-analytical results are experimentally confirmed by evolved gas analysis mass spectrometry (EGA-MS). At ca. 300 °C, which is the temperature where the SA group is selectively decomposed, the molecular fragment of SO2 is observed accompanying water molecules as expected. This confirms that the last single-water molecule can remain on the SA group until the thermal decomposition.

Collective rotational dynamics in ionic liquids: a computational and experimental study of 1-butyl-3-methyl-imidazolium tetrafluoroborate.

The aim of this study is the analysis of the rotational motion in ionic liquids, in particular, 1-butyl-3-methyl-imidazolium tetrafluoroborate. By comparing single-particle and collective motion it is found that the Madden-Kivelson relation is fairly fulfilled in long-term simulation studies (>100 ns), i.e., the collective reorientation can be predicted by the corresponding single-particle property and the static dipolar correlation factor, GK. Furthermore, simulated reorientation is in accordance with hydrodynamic theories yielding hydrodynamic radii comparable to van der Waals radii. Since viscosity is the central quantity entering hydrodynamic formulas, we calculated and measured the viscosity of our system in order to have two independent cycles of hydrodynamic evaluation, a computational and an experimental one. While the static dielectric constant agrees with dielectric reflectance experiment, the hydrodynamic radii derived from the experiments are much lower as a consequence of enhanced rotational motion. Even more, a considerable dynamic broadening is observed in the experiments.