Water, not salt, causes most of the Seebeck effect of nonisothermal aqueous electrolytes

Abstract

When two electrolyte-immersed electrodes have different temperatures, a voltage $\Delta \psi$ can be measured between them. This electrolyte Seebeck effect is usually explained by cations and anions flowing differently in thermal gradients. However, our molecular dynamics simulations of aqueous electrolytes reveal a large temperature-dependent potential drop $\chi$ near blocking electrodes caused by water layering and orientation. The difference in surface potentials at hot and cold electrodes is more important to the Seebeck effect than ionic thermodiffusion, $\Delta \psi \sim {\chi }_{\mathrm{hot}}-{\chi }_{\mathrm{cold}}$.

Main text: 6 pages with 3 figures. Supplemental material: 5 pages with 5 figures