Temperature Effects on the Kinetics of Ferrocene and Cobaltocenium in Methyltriphenylphosphonium Bromide Based Deep Eutectic Solvents

被引:6
|
作者
Bahadori, L. [1 ]
Chakrabarti, M. H. [2 ]
Hashim, M. A. [1 ]
Manan, N. S. A. [3 ]
Mjalli, F. S. [4 ]
AlNashef, I. M. [5 ]
Brandon, N. P. [2 ]
机构
[1] Univ Malaya, Fac Engn, Dept Chem Engn, Kuala Lumpur 50603, Malaysia
[2] Univ London Imperial Coll Sci Technol & Med, Dept Earth Sci & Engn, London SW7 2AZ, England
[3] Univ Malaya, Dept Chem, Fac Sci, Kuala Lumpur 50603, Malaysia
[4] Sultan Qaboos Univ, Petr & Chem Engn Dept, Muscat 123, Oman
[5] Masdar Inst Sci & Technol, Dept Chem & Environm Engn, Abu Dhabi, U Arab Emirates
基金
英国工程与自然科学研究理事会;
关键词
IONIC LIQUIDS; QUATERNARY AMMONIUM; CYCLIC VOLTAMMETRY; PHYSICOCHEMICAL PROPERTIES; REDOX COUPLES; DIFFUSION; ACETYLACETONATE; ELECTRODES; REDUCTION; PROSPECTS;
D O I
10.1149/2.0381509jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The oxidation of ferrocene (Fc/Fc(+)) and reduction of cobaltocenium (Cc(+)/Cc) under different temperatures has been studied by cyclic voltammetry and double potential step chronoamperometry in deep eutectic solvents (DESs) consisting of methyltriphenylphosphonium bromide salt with tri-ethylene glycol, glycerol or ethylene glycol as hydrogen bond donors. The temperature dependence of the measured physical properties of DESs (such as viscosity and conductivity) is discussed in detail. The kinetics of the redox couples are studied using cyclic voltammetry, and the standard heterogeneous electron transfer rate constant, k(0) is found to be of the order of 10(-5) to 10(-4) cms(-1) at different temperatures. The diffusion coefficient, D, of Fc and Cc(+) is determined to lie between 8.28 x 10(-10) to 6.65 x 10(-9) cm(2) s(-1). These results show that both k(0) and D increase with temperature in the studied DESs. In addition, better kinetic parameters for the DES with ethylene glycol as hydrogen bond donor means that this could be evaluated favorably as both solvents and electrolytes for redox flow cells. (C) The Author(s) 2015. Published by ECS. All rights reserved.
引用
收藏
页码:H617 / H624
页数:8
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