<div>This study focuses on the development of in-situ formed solid electrolyte anodes, specifically investigating TiH<sub>2</sub> as a promising candidate due to its high theoretical capacity, electronic conductivity, and low operating potential. Using SEM equipped with windowless Energy Dispersive X-ray Spectroscopy (EDS), the lithiation process and distribution of Ti and LiH were analyzed. Two cells (Cell A and Cell B) with differing lithiation capacities (980 mAh g<sup>−1</sup> and 623 mAh g<sup>−1</sup>, respectively) were compared. Results revealed that the reaction in Cell B progressed uniformly throughout the electrode, while in Cell A, lithiation advanced further, forming a thicker LiH layer (0.5 µm) and fragmenting TiH<sub>2</sub> particles. Unlike MgH<sub>2</sub>, which exhibited planar reaction progression, TiH<sub>2</sub> undergoes lithiation uniformly along the thickness direction of the electrode layer.</div>