Iodide/triiodide electrochemistry in ionic liquids: Effect of viscosity on mass transport, voltammetry and scanning electrochemical microscopy

被引:49
作者
Ejigu, Andinet [1 ]
Lovelock, Kevin R. J. [1 ]
Licence, Peter [1 ]
Walsh, Darren A. [1 ]
机构
[1] Univ Nottingham, Sch Chem, Nottingham NG7 2RD, England
基金
英国工程与自然科学研究理事会;
关键词
Ionic liquid; Dye-sensitised solar cell; Ultramicroelectrode; Scanning electrochemical microscopy; TRIIODIDE DIFFUSION-COEFFICIENTS; ELECTRON-TRANSFER KINETICS; SENSITIZED SOLAR-CELLS; CYCLIC VOLTAMMETRY; LOW-COST; MIXTURES; FERROCENE; ELECTROOXIDATION; REACTIVITY; CATALYSIS;
D O I
10.1016/j.electacta.2011.03.108
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The electrochemistry of I(-)/I(3)(-) was studied in ionic liquids using a combination of cyclic voltammetry, chronoamperometry and scanning electrochemical microscopy (SECM). The electrolytes were 1-alkyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide [C(n)C(1)Im][Tf(2)N], ionic liquids (where n = 2,4 and 8) and I(-) was typically added at a concentration of approximately 11 mM. During cyclic voltammetry, two sets of peaks were observed in each ionic liquid due to oxidation and reduction of the I(-)/I(3)(-) redox couple and oxidation/reduction of the I(3)(-)/I(2) redox couple. The diffusion coefficients of I(-) and I(3)(-), as determined using chronoamperometry, increased with increasing temperature and decreased with increasing ionic liquid viscosity. The effect of ionic liquid viscosity on ultramicroelectrode (UME) voltammetry was also determined using the I(-)/I(3)(-) redox couple. Steady-state behaviour was observed at 1.3 mu m UMEs at slow voltammetric scan rates and steady-state SECM feedback approach curves were also obtained at a 1.3 mu m Pt SECM tips, provided that the tip approach speed was sufficiently low. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:10313 / 10320
页数:8
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