AlCl 3 -NaCl was utilized as an electrolyte in this work due to its low melting point and Lewis acidity, in which samarium exists in two oxidation states, Sm(III) and Sm(II), resulting in unique electrochemical behaviours. Sm metal dissolves in AlCl 3 -NaCl melt to form SmCl 2 , which is verified by electrochemical and spectroscopic techniques. As the Lewis acidity of the melt increases, the diffusion coefficient of Sm(II) gradually increases, and the activation energy of diffusion decreases. Moreover, an additional co-reduction peak of Sm 3 + and AlCl 4À is observed to be more positive than that of Al(0)/Al(III) in Lewis basic melt, which may be tightly correlated with the variation of Sm(II) coordination in AlCl 3 -NaCl melt and ligand variation from Cl À to AlCl 4 À and Al 2 Cl 7 À as the Lewis acidity of the AlCl 3 -NaCl melt increases, according to the in situ electronic absorption spectra of Sm in this melt.