点接触水合五氧化二钒薄膜电致变色的圆柱形模型

P. Boriskov, S. V. Burdyukh, O. Berezina
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引用次数: 1

摘要

本文对点接触水合五氧化二钒干凝胶(微米)薄膜内部电致变色动力学进行了实验分析。它描述了一个圆柱形的电致变色模型,该模型用于评估初始膜和通过等离子体离子注入对该膜进行额外氢化后的色心浓度。当我们将色心浓度的计算值与静电凝胶中质子的平衡浓度进行比较时,我们看到质子从薄膜深处迁移到阴极区域的迁移率,这与电化学反应有关,并不是电致变色动力学的决定因素。电致变色的速率可以通过基于水合五氧化二钒的层状膜结构的形成来提高,这增加了整体的电子导电性,因此,电致变色阴极反应的法拉第电阻很低。
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Cylindrical model of electrochromic colouration of hydrated vanadium pentoxide thin films with point contacts
This article analyses experiments on the kinetics of the internal electrochromism of thin (micron) films of hydrated vanadium pentoxide xerogel with point contacts. It describes a cylindrical model of electrochromic colouration, which was used to evaluate the concentration of the colour centres in the initial film and after additional hydrogenation of this film by plasmaimmersion ion implantation.When we compared the calculated values of the concentration of colour centres with the equilibrium concentration of protons in the xerogel, we saw that the mobility of the protons migrating from the depth of the film to the cathode region, which are involved in the electrochemical reaction, was not a determinant of the electrochromism kinetics.The rate of electrochromic colouration could be increased by the formation of layered film structures based on hydrated vanadium pentoxide, which have increased overall electron conductivity and, as a consequence, low faradaic resistance of the electrochromic cathodic reaction.
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