ABSTRACT
Molten salt electrolysis is a vital technique to produce high-purity lanthanide metals and alloys. However, the coordination environments of lanthanides in molten salts, which heavily affect the related redox potential and electrochemical properties, have not been well elucidated. Here, the competitive coordination of chloride and fluoride anions towards lanthanide cations (La3+ and Nd3+ ) is explored in molten LiCl-KCl-LiF-LnCl3 salts using electrochemical, spectroscopic, and computational approaches. Electrochemical analyses show that significant negative shifts in the reduction potential of Ln3+ occur when F- concentration increases, indicating that the F- anions interact with Ln3+ via substituting the coordinated Cl- anions, and confirm [LnClx Fy ]3-x-y (ymax =3) complexes are prevailing in molten salts. Spectroscopic and computational results on solution structures further reveal the competition between Cl- and F- anions, which leads to the formation of four distinct Ln(III) species: [LnCl6 ]3- , [LnCl5 F]3- , [LnCl4 F2 ]3- and [LnCl4 F3 ]4- . Among them, the seven-coordinated [LnCl4 F3 ]4- complex possesses a low-symmetry structure evidenced by the pattern change of Raman spectra. After comparing the polarizing power (Z/r) among different metal cations, it was concluded that Ln-F interaction is weaker than that between transition metal and F- ions.
