The electrochemical behavior of titanium ion at liquid tin cathode has been investigated by cyclic voltammetry and square wave voltammetry in a NaCl-KCl melt at 1023 K. The resultsshow that the deposition potentials of alkali metals and titanium at liquid tin are more positive than those at a solid tungsten cathode. Meanwhile, the results prove that titanium (III) ions can be reduced at liquid tin with a one-step reduction Ti 3+ + 3e = Ti, which is a quasi-reversible process with diffusion-controlled mass transfer. The diffusion coefficient of titanium (III) ions is 1.05×10 -5 cm 2 s -1 . Additionally, galvanostatic electrolysis has been carried out to clear the effect of current density on the cathodic products. The result demonstrates that a more depth of titanium will be diffused into the liquid tin cathode at the electrolysis with a lower current density.The electrolyte consisted of an equimolar of NaCl-KCl (reagent grade, AladdinIndustrial Corporation) melt. The electrolyte was pre-dried in an alumina crucible under vacuum by heating it from ambient temperature to 573 K, and then maintaining at this temperature for 24 h. Afterwards, the cooled and pre-dried electrolyte was placed and added 45 mM TiCl 3 prepared beforehand in a glove box for electrochemical test. The working temperature was measured by a thermocouple (protected by an alumina tube) inseted into the melt. All experiments were carried out in a sealed vessel under dried argon atmosphere at 1023 K.A three-electrode setup was applied to investigate the electrochemical behavior of titanium ion. The working electrode, as shown in Fig. 1, was liquid tin stored in a quartz U-bent tube with a 4 mm inner diameter. For comparison, the solid tungsten wire and glass carbon with a 1 mm diameter were served as working electrodes as well. The counter electrode was high purity graphite rod (99.9995%, Alfa Aesar) with a 6 mm diameter. The reference electrode was an Ag/AgCl electrode, referring to a silver wire with a 1mm diameter contained in a mullite tube and dipped into a solution of AgCl (4 wt%) in a NaCl-KCl melt.The reference electrode was calibrated with respect to the Cl 2 /Clelectrode and all experiments potentials were recorded versus the Cl 2 /Clelectrode potential.The electroanalytical techniques including linear polarization, cyclic voltammetry and square wave voltammetry were performed under the same conditions (at 1023 K, under dried argon atmosphere) using a PAR Model 263 potentiostat/galvanostat communicated with a