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Large Decrease in the Melting Point of Benzoquinones via High-n Eutectic Mixing Predicted by a Regular Solution Model

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JOURNAL OF PHYSICAL CHEMISTRY B
卷 127, 期 27, 页码 6102-6112

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AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcb.3c01125

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Decreasing the melting point of mixtures is important in various applications. The traditional approach is to mix components with negative enthalpic interactions, while a complementary strategy is to mix components with neutral or slightly positive enthalpic interactions, using the number of components to increase the entropy of mixing. This approach can achieve a low melting point and has potential applications in high energy density flow battery electrolytes. The study investigates the eutectic composition of benzoquinone derivatives and demonstrates a large decrease in melting point by tuning the entropy of melting. The regular solution model shows better prediction accuracy for this type of mixture compared to the ideal solution model.
Decreasing the melting point (T (m)) ofa mixture is of interest in cryopreservatives, molten salts, and batteryelectrolytes. One general strategy to decrease T (m), exemplified by deep eutectic solvents, is to mix componentswith favorable (negative) enthalpic interactions. We demonstrate acomplementary strategy to decrease T (m) bymixing many components with neutral or slightly positive enthalpicinteractions, using the number of components (n)to increase the entropy of mixing and decrease T (m). In theory, under certain conditions this approach couldachieve an arbitrarily low T (m). Furthermore,if the components are small redox-active molecules, such as the benzoquinonesstudied here, this approach could lead to high energy density flowbattery electrolytes. Finding the eutectic composition of a high-n mixture can be challenging due to the large compositionalspace yet is essential for ensuring the existence of a purely liquidphase. We reformulate and apply fundamental thermodynamic equationsto describe high-n eutectic mixtures of small redox-activemolecules (benzoquinones and hydroquinones). We illustrate a novelapplication of this theory by tuning the entropy of melting, ratherthan the enthalpy, in systems highly relevant to energy storage. Wedemonstrate with differential scanning calorimetry measurements that1,4-benzoquinone derivatives exhibit eutectic mixing that decreasestheir T (m), despite slightly positive enthalpiesof mixing (0-5 kJ/mol). By rigorously investigating all 21binary mixtures of a set of seven 1,4-benzoquinone derivatives withalkyl substituents (T (m)'s between44 and 120 & DEG;C), we find that the eutectic melting point of amixture of all seven achieves a large decrease in T (m) to -6 & DEG;C. We further determine that theregular solution model shows improvement over an ideal solution modelin predicting the eutectic properties for this newly investigatedtype of mixture composed of many small redox-active organic molecules.

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