Abstract
Charge storage in concentrated electrolytes gives redox flow batteries (RFBs) a unique edge in grid-scale energy storage. It also creates a unique challenge in the design of organic molecules as alternatives to expensive vanadium salts. Molecules often come in the form of organic salts, and dissolve by ionic bond breakingand ion solvation, which can hardly be interpreted by “like dissolves like.” Here we use anthraquinone sulfonate salts as a model system to investigate factors underlying their aqueous solubility. We synthesize fifteen salts, measure their solubilities with UV–vis spectroscopy, and find that the solubility of the same quinone could change by three orders of magnitude with a change in its counter-cation. The same impact can come from the position and number of the sulfonate groups. We explain the results with the differences in the ion solvation energy and the lattice energy, the latter of which is corroborated by single-crystal X-ray diffraction. We also derive a simple method to semi-quantitatively predict the solubility of a quinone sulfonate salt based on that of a common sulfate salt. The work provides a physical-chemical base for understanding the solubilities of organic salts for the design of high capacity electrolytes for aqueous flow batteries.
Funder
Research grant council, Hong Kong
Science and Technology Innovation Committee, Shenzhen
Publisher
The Electrochemical Society
Subject
Materials Chemistry,Electrochemistry,Surfaces, Coatings and Films,Condensed Matter Physics,Renewable Energy, Sustainability and the Environment,Electronic, Optical and Magnetic Materials
Cited by
20 articles.
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