Redox switching of polyoxometalate-doped polypyrrole films in ionic liquid media

被引:5
作者
Anwar, Nargis [1 ]
Armstrong, Gordon [2 ]
Laffir, Fathima [2 ]
Dickinson, Calum [2 ]
Vagin, Mikhail [3 ,4 ]
McCormac, Timothy [1 ]
机构
[1] Dundalk Inst Technol, Dept Appl Sci, Electrochem Res Grp, Dublin Rd, Dundalk, County Louth, Ireland
[2] Univ Limerick, Bernel Inst, Limerick, Ireland
[3] Linkoping Univ, Dept Phys Chem & Biol, SE-58183 Linkoping, Sweden
[4] Linkoping Univ, Dept Sci & Technol, Lab Organ Elect, SE-60174 Norrkoping, Sweden
关键词
Room temperature ionic liquid; Polyoxometalate; Voltammetry; REDUCTION; IMMOBILIZATION; PHOTOCHROMISM; ELECTRODES; CHEMISTRY; ANIONS; SALTS; ACID;
D O I
10.1016/j.electacta.2017.12.101
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The surface immobilization of the parent Dawson polyoxometalate (POM) as a counter-ion for the electropolymerization of polypyrrole (PPy) or as an electrode-adhered solid was utilized for voltammetric studies of the surface adhered POM in room temperature ionic liquids (RTIL). Illustrating the efficiency of intermediate stabilization, voltammetry at POM-modified electrodes in a PF6-based RTIL revealed richer redox behaviour and higher stabilization in comparison with aqueous electrolytes and with BF4-based RTIL, respectively. High stability of the POM-doped PPy towards continuous charge-discharge voltammetric redox cycles was confirmed by minor changes in film morphology observed after the cycling in RTILs. (c) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:254 / 258
页数:5
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