Direct involvement of acid centers of polyaniline in charge transfer on organic acceptor

被引:21
作者
Matveeva, ES [1 ]
HernandezFuentes, I [1 ]
Parkhutik, V [1 ]
DiazCalleja, R [1 ]
机构
[1] UNIV POLITECN VALENCIA,DEPT APPL THERMODYNAM,VALENCIA 46071,SPAIN
关键词
FT-IR; doping; charge transfer; quinone; hydroquinone;
D O I
10.1016/S0379-6779(97)80075-6
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Electrochemical behavior of hydroquinone and 4F-hydroquinone has been studied on Pt/polyaniline (PANI) electrodes in 1 M H2SO4 solution. Redox transformation of quinone/hydroquinone systems takes place on PANI practically without overpotential and, probably, the two-electron charge transfer processes are realized in such systems. Reaction currents depend un PANI quantities deposited on the Pt electrode and the molecular complex is formed. There exists a great electronic exchange between acid centers of PANI and quinone/hydroquinone molecules, resulting in electronic conjugation of this surface state (adsorbed molecule) with the polymer. Existence of such complexes was confirmed by FT-IR analysis which has been carried out on free-standing polymer films. Based on these findings we have assumed that the charge transfer complexes form along the polymer chain and the acceptor molecules participate in the doping and conductivity processes.
引用
收藏
页码:181 / 184
页数:4
相关论文
共 19 条