Soon-Ki Jeong

This study explores the potential of titanium disulfide (TiS2) as an active material for aqueous calcium-ion batteries (CIBs). We investigate the electrochemical redox reactions of calcium ions within TiS2 and assess its suitability for use in aqueous CIBs. Additionally, we examine the impact of varying electrolyte concentrations, ranging from 1.0 to 8.0 mol dm−3, on TiS2 electrode reactions. Our findings reveal that TiS2 exhibits distinct charge–discharge behaviors in various aqueous calcium-ion electrolytes. Notably, at higher electrolyte concentrations, TiS2 effectively suppresses the hydrogen generation reaction caused by water decomposition. In situ X-ray diffraction analysis confirms the intercalation of Ca2+ ions between the TiS2 layers during charging, which is a groundbreaking discovery, signifying TiS2’s applicability in aqueous CIBs. X-ray photoelectron spectroscopy analysis further supports the formation of a solid electrolyte interphase (SEI) on the TiS2 electrode surface, contributing to the suppression of electrolyte decomposition reactions. Furthermore, we investigate the influence of anions in the electrolyte on charge–discharge behavior. Our findings suggest that the choice of anion coordinated with Ca2+ ions affects the SEI formation and cycling performance. Understanding the role of anions in SEI formation is crucial for optimizing aqueous CIBs. In conclusion, this research underscores TiS2’s potential as an active material for aqueous calcium-ion batteries and emphasizes the importance of the electrolyte composition in influencing SEI formation and battery performance, contributing to sustainable and efficient energy storage technologies.