LiH is a highly stable light metal hydride with a hydrogen capacity of 12.5 wt%. However, having a dehydrogenation enthalpy, ΔH(dehy), of 181.2 kJ mol(-1)(H2) and a resultant T(1 bar) of 944 °C, it is not a practical hydride for most hydrogen storage applications. In the work presented here, germanium has been found to dramatically reduce the dehydrogenation temperature for LiH down to just 270 °C. The enthalpy of dehydrogenation was reduced through the formation of lithium germanides. The reaction pathway was identified in this study using in situ powder neutron diffraction, showing the successive formation of more Li-rich germanides, following the series: LiGe, Li4Ge2H, Li9Ge4, and Li7Ge2. The enthalpy of formation for these germanides provides the thermodynamic tuning to reduce the ΔH(dehy) for the system. The 3LiH-Ge system investigated is found to be reversible with a maximum capacity of 3.0 ± 0.1 wt%.