An electrochemical quartz crystal microbalance (EQCM) was used to examine the sodium plating-stripping reactions in two room-temperature molten salts: (i) buffered-neutral 1-methyl-3-propylimidazolium chloride and (ii) methanesulfonyl-aluminum chloride. In cyclic voltammetry scans on melt (i), slightly more mass was plated on the electrode than required by the charge passed for sodium reduction. The excess mass deposition suggests coreduction of either electrolytes or impurities and formation of protective layers; this results in irreversible deposition and less than 100% coulombic efficiency. In chronoamperometry scans, the mass deposition rate was lower than the equivalent charge passed for pure sodium. This indicates possible reaction between sodium metal and the electrolytes or impurities at the electrode surface after depletion of sodium ions. The inorganic molten salt melts, (ii), were made of aluminum chloride, methanesulfonyl chloride, and sodium chloride. The amount of sodium chloride added to melts was critical to the stability of the sodium deposited. The highest coulombic efficiency for the sodium couple in these melts was 97%, and the self-discharge rate was 3 muA/cm(2). The EQCM results showed reduction of the electrolyte or reaction with sodium metal forming irreversible products.