Redox reactions of polyaniline films doped with d,l-camphor sulfonic acid

被引:12
作者
Kocherginsky, N. M. [1 ]
Wang, Zheng [1 ]
机构
[1] Natl Univ Singapore, Div Bioengn, Dept Chem & Biomol Engn, Singapore 119260, Singapore
关键词
polyaniline; camphor sulfonic acid; redox reaction;
D O I
10.1016/j.reactfunctpolym.2006.04.002
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Simplified comparison of standard redox potentials demonstrates that redox reactions of d,l-camphor sulfonic acid (CSA) doped polyaniline (PANI) films with aqueous solutions of FeCl3 and K3Fe(CN)(6) should not take place. Nevertheless the reactions are possible and described here. The initial rate of 0.01M Fe3+ reduction is higher than that obtained with HCl doped PANI film at similar conditions. Films doped with CSA stay active at neutral pH with K3Fe(CN)6 as the oxidizing agent, which is different from depressed electroactivity of PANI-HCl films in these conditions. The redox processes are not limited by simple surface reaction and have two kinetically different steps (the initial, fast and the second, slower). A new mechanism is suggested according to which two redox half reactions (oxidation of the polymer fragments and reduction of ions in the solution) are separated in space and are coupled by counter transport of electrons and Cl- anions into the opposite direction. A new phenomenon is demonstrated where the gradient of Cl- activity in the film changes the equilibrium state of the redox process in aqueous solution. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:1384 / 1393
页数:10
相关论文
共 40 条
[1]   The inductive behavior derived from hydrolysis of polyaniline [J].
Chen, WC ;
Wen, TC ;
Gopalan, A .
ELECTROCHIMICA ACTA, 2002, 47 (26) :4195-4206
[2]   A STUDY OF THE REDOX REACTION-MECHANISMS OF POLYANILINE USING A QUARTZ CRYSTAL MICROBALANCE [J].
DAIFUKU, H ;
KAWAGOE, T ;
YAMAMOTO, N ;
OHSAKA, T ;
OYAMA, N .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1989, 274 (1-2) :313-318
[3]  
DONG YH, 1991, ELECTROCHIM ACTA, V36, P2015
[4]   INSULATOR-TO-METAL TRANSITION IN POLYANILINE [J].
EPSTEIN, AJ ;
GINDER, JM ;
ZUO, F ;
BIGELOW, RW ;
WOO, HS ;
TANNER, DB ;
RICHTER, AF ;
HUANG, WS ;
MACDIARMID, AG .
SYNTHETIC METALS, 1987, 18 (1-3) :303-309
[5]   Reduction of Cr(VI) at a polyaniline film: Influence of film thickness and oxidation state [J].
Farrell, ST ;
Breslin, CB .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2004, 38 (17) :4671-4676
[6]   REDOX MECHANISM AND ELECTROCHEMICAL-BEHAVIOR OF POLYANILINE DEPOSITS [J].
GENIES, EM ;
TSINTAVIS, C .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1985, 195 (01) :109-128
[7]   SPECTROELECTROCHEMICAL STUDY OF POLYANILINE VERSUS POTENTIAL IN THE EQUILIBRIUM STATE [J].
GENIES, EM ;
LAPKOWSKI, M .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1987, 220 (01) :67-82
[8]   POLYANILINE - A HISTORICAL SURVEY [J].
GENIES, EM ;
BOYLE, A ;
LAPKOWSKI, M ;
TSINTAVIS, C .
SYNTHETIC METALS, 1990, 36 (02) :139-182
[9]   ESR linewidth and polaron mobility in conducting polymers [J].
Houze, E ;
Nechtschein, M ;
Pron, A .
SYNTHETIC METALS, 1997, 84 (1-3) :981-982
[10]   POLYANILINE, A NOVEL CONDUCTING POLYMER - MORPHOLOGY AND CHEMISTRY OF ITS OXIDATION AND REDUCTION IN AQUEOUS-ELECTROLYTES [J].
HUANG, WS ;
HUMPHREY, BD ;
MACDIARMID, AG .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1986, 82 :2385-&