Electrochemistry and Mass Transport of Ytterbium(III) in Bis(trifluoromethylsulfonyl)imide-Based Room-Temperature Ionic Liquids: Effects of Temperature, Viscosity, and Electrode Materials

Cyclic staircase voltammetry, rotating disk electrode voltammetry, controlled potential coulometry, and electrochemical impedance spectroscopy were used to probe the electrochemistry and mass transport of Yb3+ in the six room temperature ionic liquids based on the bis(trifluoromethylsulfonyl)imide (Tf2N-) anion with, 1-(1-butyl)-3-methylimidazolium (BuMeIm(+)), 1-(1-butyl)-1-methylpyrrolidinium (BuMePyro(+)), 1-(1-butyl)pyridinium (BuPy+), 1-butyltrimethylammonium (BuMe3N+), 1-ethyl-3-methylimidazolium (EtMeIm(+)), and tri(1-butyl)methylammonium (Bu3MeN+) cations. These investigations were carried out at glassy carbon as well as polycrystalline gold, platinum, and tungsten electrodes. The heterogeneous electron transfer rate of the quasireversible Yb3+/2+ redox couple was found to depend strongly on the electrode materials with the fastest rate observed at gold and the slowest rate found at tungsten, but was independent of the physicochemical properties of the various ionic liquids, in particular, the absolute viscosity. However, the mass transport of Yb3+ was dependent on the viscosity, and the temperature dependence of the diffusion coefficients was well represented by a Vogel-Tammann-Fulcher type expression for glass-forming ionic liquids. Analysis of the diffusion coefficient data with the Stokes-Einstein equation indicated that the solvodynamic radius of the diffusing Yb3+ was constant and independent of the structure and properties of the ionic liquid cations. The solvodynamic radius of Yb3+ was estimated from the stick model for the Stokes-Einstein equation. Application of the Random Closest Packing (RCP) model for spheres in consideration of the solvodynamic radius of the diffusing Yb3+ and the ionic radii of Yb3+ and Tf2N-, indicated that the former must diffuse in association with similar to 5-6 of the anions.

Automated summary

Cyclic staircase voltammetry, rotating disk electrode voltammetry, controlled potential coulometry, and electrochemical impedance spectroscopy were used to investigate the electrochemistry and mass transport of Yb3+ in six ionic liquids. The rate of heterogeneous electron transfer of the Yb3+/2+ redox couple was dependent on the electrode materials, but independent of the physicochemical properties of the ionic liquids. The mass transport of Yb3+ was found to be dependent on the viscosity of the ionic liquids.