Revisiting the electrochemical and polymeric behavior of a polypyrrole free-standing electrode in aqueous solution

被引:69
|
作者
Otero, TF [1 ]
Ariza, MJ [1 ]
机构
[1] Univ Politecn Cartagena, Grp Electroquim Mat & Disposit Inteligentes, E-30203 Cartagena, Murcia, Spain
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2003年 / 107卷 / 50期
关键词
D O I
10.1021/jp0362842
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A procedure to obtain homogeneous free-standing polypyrrole (ppy) films 10-20 mum thick is described. The resulting films have mechanical characteristics good enough to be used as a working electrode for electrochemical measurements and applications. Structures and uniformity of both film surfaces and the cross section were studied by SEM. Three different procedures were used to determine the film thickness. The free-standing film can be reduced in aqueous solution up to -3.0 V without any presence of hydrogen release or polymer degradation. Voltammetric experiments show the usual voltammograms, but they only involve a partial oxidation and reduction of the film capabilities: voltammetric charges increase for decreasing sweep rates. A deep reduction of the film is achieved by polarization times longer than 300 s at -0.6 V or more cathodic potentials. The second cathodic maximum, appearing on the voltammograms between -0.7 and -0.9 V, is related to slow kinetic and structural processes since the film reduction is completed by long polarization time at -0.6 V; the concomitant equilibrium potential is then more anodic than -0.6 V. All of these results are consistent with the electrochemically stimulated conformational relaxation (ESCR) model. The swelled and oxidized film shrinks progressively along the voltammetric reduction. Around -1.0 V the polymeric structure is closed when still 35% to 60% (depending on the scan rate) of the material remains oxidized. The reduction is then completed by slow migration of the counterions through the increasingly compacted polymeric entanglement by stimulating conformational relaxation processes of the ppy chains. A constant and low cathodic current is observed on the voltammograms up to -3.0 V. Oxidation potentials higher than +0.6 V promote the electrochemical degradation of the ppy. Three potential windows are distinguished for these films in aqueous solutions: from potentials as low as -3.0 to -0.6 V they are a compacted semiconductor electrode without hydrogen release; from -0.6 to +0.5 V they are a progressively more oxidized and swelled conducting polymer electrode; and potentials higher than +0.6 V bring on ppy over-oxidation processes and degradation of the electrochemical activity.
引用
收藏
页码:13954 / 13961
页数:8
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