Chevrel phases, CPs (Mo 6 T 8 ; T = S, Se) can accommodate cations (Li + , Mg 2+ etc.) within the Mo 6 T 8 open framework at room temperature due to its unusually high electronic conductivity and ionic mobility and proposed as positive electrodes for secondary batteries. However, cations insertion into Mo 6 T 8 generate strong repulsion between cation-cation or cation-Mo atoms leads to partial charge trapping within the Mo 6 T 8 structure. The present work examine CPs as positive electrodes for sodium-ion batteries. In this regard, ternary CPs of Cu x Mo 6 S 8 and Cu x Mo 6 Se 8 phase were prepared by solution chemistry and high energy mechanical milling (HEMM) routes, respectively, followed by acid leaching of copper. X-rays diffraction and scanning electron micrographs revealed the formation of 1-1.5 µm size cuboidal Cu 1.8 Mo 6 S 8 particles, whereas, HEMM of CuSe, MoSe 2 and Mo powder followed by heating leads to the formation of Cu 2 Mo 6 Se 8 phase. Results from cyclic voltammetry and galvanostatic cycling of Na/Mo 6 S 8 and Na/Mo 6 Se 8 cells within 1.2-2.2V versus sodium revealed that two-step sodiation/de-sodiation reaction occurs with a gradual capacity fade due to Na-ion trapping within two terminal compositions, Na x Mo 6 T 8 (T = S, Se; x ~1 and 3). Electrochemical impedance spectroscopy at ~0.1V intervals during sodiation/de-sodiation process illustrates that partial Na-ion trapping resulted an increase in charge transfer resistance, R e due to the formation of stable Na~1Mo 6 S 8 phase after 1 st charge cycle. However, charge trapping continues to occur during 1 st and 2 nd cycle in the case of Mo 6 Se 8 phase. Nevertheless, the ease of fabrication, stable capacity, and high Coulombic efficiency render Mo 6 T 8 (T=S, Se) as promising Na-ion positive electrodes for stationary electrical energy storage (EES) applications.