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The Effect of Temperature on Kinetics and Diffusion Coefficients of Metallocene Derivatives in Polyol-Based Deep Eutectic Solvents

机译:温度对多元醇基深共溶剂中茂金属衍生物动力学和扩散系数的影响

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摘要

The temperature dependence of the density, dynamic viscosity and ionic conductivity of several deep eutectic solvents (DESs) containing ammonium-based salts and hydrogen bond donvnors (polyol type) are investigated. The temperature-dependent electrolyte viscosity as a function of molar conductivity is correlated by means of Walden’s rule. The oxidation of ferrocene (Fc/Fc+) and reduction of cobaltocenium (Cc+/Cc) at different temperatures are studied by cyclic voltammetry and potential-step chronoamperometry in DESs. For most DESs, chronoamperometric transients are demonstrated to fit an Arrhenius-type relation to give activation energies for the diffusion of redox couples at different temperatures. The temperature dependence of the measured conductivities of DES1 and DES2 are better correlated with the Vogel-Tamman-Fulcher equation. The kinetics of the Fc/Fc+ and Cc+/Cc electrochemical systems have been investigated over a temperature range from 298 to 338 K. The heterogeneous electron transfer rate constant is then calculated at different temperatures by means of a logarithmic analysis. The glycerol-based DES (DES5) appears suitable for further testing in electrochemical energy storage devices.
机译:研究了几种含铵盐和氢键donvnors(多元醇型)的深共熔溶剂(DES)的密度,动态粘度和离子电导率与温度的关系。随温度变化的电解质粘度与摩尔电导率的关系通过沃尔登定律进行关联。通过循环伏安法和电位步长计时电流法研究了DES中二茂铁的氧化(Fc / Fc + )和钴ce的还原(Cc + / Cc)。对于大多数DES,已证明计时电流瞬变符合Arrhenius型关系,从而为不同温度下的氧化还原对的扩散提供激活能。测得的DES1和DES2电导率的温度依赖性与Vogel-Tamman-Fulcher方程更好地相关。在298至338 K的温度范围内研究了Fc / Fc + 和Cc + / Cc电化学系统的动力学。然后,异质电子传递速率常数为通过对数分析在不同温度下计算得到。基于甘油的DES(DES5)似乎适合在电化学储能装置中进行进一步测试。

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