The sulfide solid electrolyte Li 4 SnS 4 has gained attention owing to its high moisture durability. In this study, we quantitatively investigated the changes in the electrochemical properties and chemical/physical states of Li 4 SnS 4 resulted from moisture exposure using the XRD, Raman spectroscopy, and high-frequency electrochemical impedance spectroscopy (HF-EIS). Li 4 SnS 4 was subjected to Ar gas flow at a dew point ranging from −20 °C to 0 °C for 1 h, and sulfide hydrolysis generated only a minute amount of H 2 S. The XRD patterns and Raman spectra revealed the formation of Li 4 SnS 4 •4H 2 O with increasing dew point. The HF-EIS analysis, which was conducted to clarify the spatial distribution of the hydrate within the particle, revealed a significant decrease in the ionic conductivity of Li 4 SnS 4 .; this result can be attributed to the increased grain-boundary (SE/SE particle contact) resistance due to the formation of Li 4 SnS 4 •4H 2 O at the particle surface, despite the generation of a minute amount of H 2 S. By combining these multifaceted analytical methods, we demonstrated that the thermodynamically stable surface hydrate Li 4 SnS 4 •4H 2 O reduced the lithium-ion conductivity without H 2 S generation owing to the hydrolysis of sulfide. Thus, we chemically, spatially, and quantitatively verified the mechanism underlying the observed decrease in the ionic conductivity.