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Size Matters! On the way to ionic liquid systems without ion pairing

 
: Rupp, A.; Roznyatovskaya, N.; Scherer, H.; Beichel, W.; Klose, P.; Sturm, C.; Hoffmann, A.; Tübke, J.; Koslowski, T.; Krossing, I.

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Chemistry. A European journal 20 (2014), Nr.31, S.9794-9804
ISSN: 0947-6539
ISSN: 1521-3765
Deutsche Forschungsgemeinschaft DFG
SPP1191
Englisch
Zeitschriftenaufsatz
Fraunhofer ICT ()

Abstract
Several, partly new, ionic liquids (ILs) containing imidazolium and ammonium cations as well as the medium-sized [NTf2](-) (0.230 nm(3); Tf=CF3SO3-) and the large [Al-(hfip)(4)](-) (0.581 nm(3); hfip=OC(H)(CF3)(2)) anions were synthesized and characterized. Their temperature-dependent viscosities and conductivities between 25 and 80 degrees C showed typical Vogel-Fulcher-Tammann (VFT) behavior. Ion-specific self-diffusion constants were measured at room temperature by pulsed-gradient stimulated-echo (PGSTE) NMR experiments. In general, self-diffusion constants of both cations and anions in [Al(hfip)(4)](-)-based ILs were higher than in [NTf2](-)-based ILs. Ionicities were calculated from self-diffusion constants and measured bulk conductivities, and showed that [Al(hfip)(4)](-)-based ILs yield higher ionicities than their [NTf2](-) analogues, the former of which reach values of virtually 100% in some cases. From these observations it was concluded that [Al(hfip)(4)](-)-based ILs come close to systems without any interactions, and this hypothesis is underlined with a Hirshfeld analysis. Additionally, a robust, modified Marcus theory quantitatively accounted for the differences between the two anions and yielded a minimum of the activation energy for ion movement at an anion diameter of slightly greater than 1 nm, which fits almost perfectly the size of [Al(hfip)(4)](-). Shallow Coulomb potential wells are responsible for the high mobility of ILs with such anions.

: http://publica.fraunhofer.de/dokumente/N-307131.html