Redox Couple Stability Studies for Thermodynamic Reference Electrodes and Fluoroacidity Investigation

Thursday, 13 October 2022: 09:40
Room 303 (The Hilton Atlanta)
H. Williams (University of California - Berkeley) and R. O. Scarlat (University of California, Berkeley)
A stable reference electrode is essential for electrochemical studies in molten fluoride salts, yet reference electrode design is hindered by challenges such as materials compatibility and high temperature operation. Electroanalytical studies are relevant to sensor development for molten fluoride salt systems as well as fundamental chemistry studies of salt structure and speciation. Dynamic reference electrode techniques have been used to find benchmark reference potentials, but the application of a constant current for the technique may not be feasible for sensing or high throughput studies. A thermodynamic reference electrode which is durable, stable, and reproduceable is urgently needed for both scientific studies and engineering applications of molten fluoride salts.

Fluoroacidity studies are of particular interest for a fundamental understanding of molten salt speciation. The more dissociated fluoride anions present in a melt, the more of a fluorodonor it is. Thus, it is considered to have a higher fluorobasicity due to its Lewis base behavior. Fluoroacidity is related to the coordination of solvent and solute ions and, therefore, solute diffusion coefficients and viscosity. Ion solvation differs in fluoride salts of various fluoroacidities, so solvated ions have different activity coefficients in different fluoride solvents. The relationship between activity coefficients of solvated ions and a melt’s fluoroacidity is not fully understood. The electrochemical determination of these activity coefficients benefits from a stable reference electrode. In addition, quantification of fluoroacidity requires the measurement of the activity of dissociated fluoride, which can be done electrochemically. The measurement of redox potential of a given couple in various fluoride melts can lead to a classification of the solvent melts based on the Nernst equation. Therefore, the study of redox couple behavior in various fluoride melts is relevant to both the development of a robust thermodynamic reference electrode & the quantification and theory of fluoroacidity.

The Ni/NiF2 and Ag/AgF redox couples have been previously investigated for use in thermodynamic reference electrodes for molten fluoride salt. Ni/NiF2 has been characterized for its stability in molten fluorides. The Ag/AgCl redox couple has commonly been used for chloride mixtures but literature on the fluoride couple is marginal. Our preliminary studies have shown the stability of the Ag/AgF redox couple in a FLiNaK melt by OCP measurement. Polarization studies will be carried out to test for reversibility, and other redox couples may be investigated. In this presentation, we present results from the Ag/AgF redox couple studies in FLiNaK, as well as their impact on current understandings of fluoroacidity.