锌酸盐溶液中锌在钨电极上恒流成核的阶段

Iurii G. Krishtop, T. N. Kalyuzhna, V. Trofimenko
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引用次数: 0

摘要

根据经典的恒流成核理论和Vetter动力学概念,研究了锌酸盐电解质(0.5 М ZnO, 6 M NaOH)在钨电极上形成锌核的过程。在电流密度200 ~ 600 mАсm -2范围内,测定了电荷转移过电位(100 ~ 200 mV)、结晶过电位(50 ~ 60 mV)、成核功((2 ~ 12)×10 ~ 20 J)、核内原子数(2 ~ 10)。结果表明,氧化钨表面的还原位发生了成核。在所研究的电流密度介子范围内,原子核在能量相似的电极中心上形成。电荷转移系数较低(α = 0.26)表明双层电场对电荷转移活化能的影响较弱。
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The stages of galvanostatic nucleation of zinc on the tungsten electrode from a zincate solution
On the basis of the classical theory of galvanostatic nucleation and Vetter’s kinetic conception, formation of zinc nuclei on the tungsten electrode from the zincate electrolyte (0.5 М ZnO, 6 M NaOH) has been investigated. In the region of the current density 200 - 600 mАсm -2 the charge transfer overpotential (100 - 200 mV), the crystallization overpotential (50 - 60 mV), the nucleation work ((2 - 12)×10 -20 J), the number of atoms in the nuclei (2 - 10) were determined. It was proved that nucleation take place on reduced sites of the oxidized tungsten surface. Within the range of studied diapason of current densities nucleis are forming on energetically similar electrode centers. The low value of the charge transfer coefficient (α = 0.26) indicates a weak effect of the double layer electrical field on the activation energy of charge transfer.
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