Study on the exchange current density of lanthanide chlorides in LiCl-KCl molten salt

被引:37
作者
Lim, Keun Hong [1 ]
Yun, Jong-Il [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Nucl & Quantum Engn, Daejeon 34141, South Korea
基金
新加坡国家研究基金会;
关键词
Lanthanides; Exchange current density; Transfer coefficient; Tafel plot; Activation energy; Pyroprocessing; ELECTROCHEMICAL-BEHAVIOR; MO SUBSTRATE; AL ALLOYS; GADOLINIUM; ELECTRODE; ELECTROCRYSTALLIZATION; MORPHOLOGY; REDUCTION; NEODYMIUM; CORROSION;
D O I
10.1016/j.electacta.2018.10.104
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
In this study, the exchange current density, transfer coefficient, and reaction activation energy of Ln(III)/Ln(0) and Ln(III)/Ln(II) reactions in LiCl-KCl molten salt at 500 degrees C were precisely obtained using electrochemical techniques, especially Tafel measurement. The number of redox couples and the redox potential of lanthanides in the LiCl-KCl redox range were investigated through cyclic voltammetry (CV). With the exception of NdCl3, which has a two-step reaction (Nd(III)/Nd(II) and Nd(II)/Nd(0)) within a significantly narrow potential range, all lanthanides have a single redox couple in the measured potential window. Each redox couple has distinctive exchange current densities and transfer coefficients. Ln(III)/Ln(0) reactions exhibited exchange current densities ranging from 7.77 to 25.48mA/cm(2), which are greater values compared to the exchange current densities of Ln(III)/Ln(II) reactions that range from 1.16 to 5.52 mA/cm(2) when taking the number of transferred electrons into account. The number of transferred electrons of Sm, Eu, Tm, and Yb were determined to be 1.02, 1.01, 0.98, and 1.01, respectively, through square wave voltammetry (SWV). In addition, the reaction activation energy was determined using the temperature dependency of exchange current density according to Arrhenius' law. The activation energy tendency of the Ln(III)/Ln(0) reactions was mechanistically elucidated by considering the atomization energy of lanthanides. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:577 / 583
页数:7
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