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Phase transition behavior of two-component viologen adsorption layers on a HOPG electrode surface

机译:双组分紫精吸附层在HOpG电极表面上的相变行为

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摘要

Phase transition behavior of two-component viologen adsorption layers at a HOPG electrode was described using the results of voltammetric measurements. In the coexistence of heptyl viologen (HV) and its bis-carboxylated derivative in the solution phase, a well-mixed condensed monolayer of the radical cations was formed at any molar fraction. In sharp contrast, the binary system of HV and butyl viologen (BV) exhibited phase separation in the molar fraction range where BV is saturated in the predominantly formed condensed phase of HV. It was, however, found that this separation, being opposed to the prediction based on the adsorption free energy, occurs only when the time period enough for full condensation of HV is not given. The significant features of phase transition of two-component viologen adsorption layers on a HOPG electrode surface were highlighted in comparison with the formation and reductive desorption of the self-assembled monolayers of alkanethiols.
机译:使用伏安法测量的结果描述了在HOPG电极上两组分紫精吸附层的相变行为。在溶液相中庚基紫精(HV)及其双羧化衍生物共存的情况下,在任何摩尔分数下均形成了充分混合的自由基基团的稠密单分子层。与之形成鲜明对比的是,HV和丁基紫精(BV)的二元体系在摩尔分数范围内显示出相分离,其中BV在HV的主要冷凝相中饱和。然而,发现这种分离与基于吸附自由能的预测相反,仅在没有给出足以使HV完全冷凝的时间段时才发生。与链烷硫醇的自组装单分子层的形成和还原脱附相比,HOPG电极表面上的两组分紫精吸附层的相变的显着特征得到了强调。

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