Decoding the Entropy‐Performance Relationship in Aqueous Electrolytes for Lithium‐Ion Batteries
Advanced Energy Materials, EarlyView.

An electrolyte design strategy is proposed for enhanced aqueous lithium-ion batteries by introducing EA to the LiTFSI-H2O electrolyte, which essentially leads to entropy-driven electrolytes. The preferential hydrogen-bonding effect between EA and H2O effectively reduces the water activity and hinders the decomposition of the electrolyte. Furthermore, this solvation structure leads to the formation of a more robust solid−electrolyte interphase and enhances the anodic stability.
Abstract
Developing aqueous low-temperature electrolytes aligns with the societal demand for lithium batteries in extreme climates and environments. However, the main challenges include high thermodynamic freezing points, slow ion diffusion, and instability at the interface under low temperatures, resulting in low energy density and poor cycle performance. Here, the role of mixing entropy ΔSmix, hydrogen bonding, and electrostatic interactions in achieving an optimal electrolyte composition is explored. By systematically varying the ethyl acetate (EA)/H2O ratio, a critical “mixing entropy optimal point” at a molar ratio of 3.91, where the electrolyte exhibits the best balance between molecular disorder and interfacial stability is identified. At this optimal point, EA molecules with polar ester group (-COO-) effectively break the hydrogen-bond network of water, enhancing the ΔSmix and lowering the freezing point to −106.95 °C. Furthermore, the stable interfacial chemistry derived from entropy-driven solvation structure effectively suppress hydrogen evolution and expand the electrochemical window to 6.2 V. Full aqueous Li-ion batteries with LiMn2O4-Li4Ti5O12 full cell delivered an initial discharge specific capacity of 135.1 mAh g−1 for 1000 cycles under rapid 10 C rate. The results provide a promising thermodynamic foundation for designing high-performance aqueous electrolytes, with implications for next-generation low-temperature aqueous lithium-ion batteries.