The electrochemical behavior of tantalum in the form of K2TaF7 in an LiF-NaF-KF eutectic melt has been studied by linear voltammetry in the temperature range of 560 to 815~ with and without additions of Na20. An amperometric titration has been performed by measuring the heights of the cathodic and the anodic peaks. It was shown that at a molar ratio Na20/K2TaF7 = 1 the predominating complex in the melt is TaOF~ , whereas with an Na20/K2TaF7 molar ratio of 2 it is TaO2F(= =-I)-, probably in the form of TaO2F~-. Increase in the Na20/K2TaF7 molar ratio in excess of two leads to a decrease of tantalum concentration in the melt, and precipitation of KTaQ occurs. Both the fluoro complex and the monooxefluoro complex were reduced to metal in a single five-electron step. The fluoro complexes, in the temperature range 625 to 815~ with potential scan rates <0.5 V 9 s i, discharge quasi-reversibly, but at potential scan rates >0.5 V 9 s -I they discharge irreversibly. Monooxofluore complexes discharge irreversibly at all temperatures and scan rates studied. The diffusion coefficient of the tantalum fluoro complex depends on the temperature as log D = -2.55 -2044/Twith an activation energy of 39.1 kJ 9 mol -~. For the tantalum monooxofluoro complex the dependence is log D = -2.35 -2293/T with an activation energy of 43.9 kJ 9 mol -I.