摘要
The electrochemical behaviour of samarium was investigated in LiF-BeF2 system on an inert （Mo） electrode by cyclic voltammetry and chronopotentiometry at 804, 833, 847 and 872 K. Redox process Sm3＋＋e–→Sm2＋ was recognized and analysed. Cyclic voltammetry data suggested that at potential sweep rates lower than 0.25 V/s, the reduction was limited by the diffusion of Sm3＋ ions. It was not possible to observe reduction process of Sm2＋＋2e–→Sm0 due to insufficient electrochemical stability of LiF-BeF2. Diffusion coefficients of Sm3＋ ions in LiF-BeF2 were calculated from voltammetric and chronopotentiometric data in the temperature range 804–872 K. Diffusion coefficient values obeyed Arrhenius law. Activation energy was calculated to be 102.5 kJ/mol.
The electrochemical behaviour of samarium was investigated in LiF-BeF2 system on an inert （Mo） electrode by cyclic voltammetry and chronopotentiometry at 804, 833, 847 and 872 K. Redox process Sm3＋＋e–→Sm2＋ was recognized and analysed. Cyclic voltammetry data suggested that at potential sweep rates lower than 0.25 V/s, the reduction was limited by the diffusion of Sm3＋ ions. It was not possible to observe reduction process of Sm2＋＋2e–→Sm0 due to insufficient electrochemical stability of LiF-BeF2. Diffusion coefficients of Sm3＋ ions in LiF-BeF2 were calculated from voltammetric and chronopotentiometric data in the temperature range 804–872 K. Diffusion coefficient values obeyed Arrhenius law. Activation energy was calculated to be 102.5 kJ/mol.
基金
Project supported by Ministry of Industry and Trade of the Czech Republic
