Effect of solvation shell structure on thermopower of liquid redox pairs

Abstract Developing redox electrolytes with high thermopower is the key to making efficient thermogalvanic batteries for harvesting low‐grade heat. This work applies molecular dynamics simulations to predict the thermopower (i.e. thermogalvanic temperature coefficient) of the redox pairs Fe(CN) 6 3− /Fe(CN) 6 4− and Fe 3+ /Fe 2+ , showing excellent agreement with experimental values. We showed that of the Fe 3+ /Fe 2+ redox pair can be increased from 1.70.4 mV/K to 3.80.5 mV/K with the increased acetone to water fraction. We discovered a significant change in the variance of solvent dipole orientation between Fe 3+ and Fe 2+ , which can serve as a microscopic indicator for large . In mixed acetone‐water solvent, of Fe 3+ /Fe 2+ showed a rapid increase at high acetone fractions, due to the intercalation of acetone molecules into the first solvation shell of the Fe 2+ at high acetone fractions. Our discovery provides insights into how solvation shell order can be engineered to develop electrolytes with high . image