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Electrochemical Behavior of Telluride Ions (Te2-) in Molten LiCl-Li2Te Solution at 650 degrees C

机译:650℃熔融LiCL-Li2Te溶液中碲化物离子(TE2-)的电化学行为

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摘要

The electrochemical behavior of Te2- ions was investigated in the LiCl-Li2Te binary on glassy carbon electrodes at 650 degrees C as a means to understand the fundamental thermodynamic and mass transport properties of Te2- ions. Cyclic voltammetry and constant-potential electrolysis confirmed an electrochemically reversible, two-electron soluble-insoluble reaction of Te2-/Te(l). The formal potential for the Te2-/Te(l) reaction was determined to be 1.744 V vs Li+/Li(l), and the diffusivity of Te2- ions was about 0.44-1.25 x 10(5) cm(-2) s(-1). The low value for diffusivity relative to those of other cations in molten salts suggests the possibility of forming complex ions such as [Li8Te](6+) due to strong chemical interactions with Li+ ions in the electrolyte. The anodic polarization of Te(l) indicated that the formation of TeCl2(g) and the cathodic polarization of Te(l) involved the codeposition of Li metal into the Te(l). The results of this work provide essential knowledge in developing electrochemical processes for separation of tellurium as well as in mitigating the degradation reactions with structural materials.
机译:在650℃下在LiCl-Li2Te二进制中研究了TE2-离子的电化学行为,以了解Te2-离子的基本热力学和大规模运输性能的方法。循环伏安法和恒定电位电解证实了TE2- / TE(L)的电化学可逆,双电子可溶性反应。将TE2- / TE(L)反应的正式电位测定为1.744V Vs Li + / Li(L),Te2-离子的扩散率约为0.44-1.25×10(5 )cm(-2) (-1)。相对于熔融盐中其他阳离子的扩散性的低值表明,由于电解质中的Li +离子的强化学相互作用,形成复杂离子如[Li8Te](6+)。 Te(L)的阳极偏振表明TE(G)的形成和TE(L)的阴极偏振涉及LI金属的重质沉积到TE(L)中。该工作的结果提供了开发用于分离碲的电化学过程以及减轻与结构材料的降解反应的基本知识。

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