TY - JOUR
T1 - Response mechanism of potentiometric Ag+ sensor based on poly(3,4-ethylenedioxythiophene) doped with silver hexabromocarborane
AU - Mousavi, Zekra
AU - Bobacka, Johan
AU - Lewenstam, Andrzej
AU - Ivaska, Ari
PY - 2006
Y1 - 2006
N2 - Potentiometric Ag+ sensors were prepared by galvanostatic electropolymerization of 3,4-ethylenedioxythiophene (EDOT) on glassy carbon electrodes by using silver 7,8,9,10,11,12-hexabromocarborane (Ag+CB11H6Br6-) as supporting electrolyte. The analytical performance of the resulting GC/PEDOT(CB11H6Br6-) sensors was studied by potentiometric measurements. The electrodes showed a selective response to Ag+ compared to several alkali, alkaline-earth, and transition-metal cations. Pretreatment of the electrodes by cyclic voltammetry was found to enhance their analytical performance. In order to elucidate the response mechanism, PEDOT(CB11H6Br6-) films were studied using scanning electron microscopy (SEM)/energy dispersive analysis of X-rays (EDAX), X-ray photoelectron spectroscopy (XPS), and atomic force microscopy (AFM). Results from SEM/EDAX and AFM measurements showed that PEDOT(CB11H6Br6-) films accumulate silver after being conditioned in silver solution. XPS measurements show that the accumulated silver is mainly in the elemental form, in the outermost surface of the conducting polymer. CV shows two redox peaks from Ag+, which can be attributed to the presence of Ag+ complexes in the polymer film. (c) 2006 Elsevier B.V. All rights reserved.
AB - Potentiometric Ag+ sensors were prepared by galvanostatic electropolymerization of 3,4-ethylenedioxythiophene (EDOT) on glassy carbon electrodes by using silver 7,8,9,10,11,12-hexabromocarborane (Ag+CB11H6Br6-) as supporting electrolyte. The analytical performance of the resulting GC/PEDOT(CB11H6Br6-) sensors was studied by potentiometric measurements. The electrodes showed a selective response to Ag+ compared to several alkali, alkaline-earth, and transition-metal cations. Pretreatment of the electrodes by cyclic voltammetry was found to enhance their analytical performance. In order to elucidate the response mechanism, PEDOT(CB11H6Br6-) films were studied using scanning electron microscopy (SEM)/energy dispersive analysis of X-rays (EDAX), X-ray photoelectron spectroscopy (XPS), and atomic force microscopy (AFM). Results from SEM/EDAX and AFM measurements showed that PEDOT(CB11H6Br6-) films accumulate silver after being conditioned in silver solution. XPS measurements show that the accumulated silver is mainly in the elemental form, in the outermost surface of the conducting polymer. CV shows two redox peaks from Ag+, which can be attributed to the presence of Ag+ complexes in the polymer film. (c) 2006 Elsevier B.V. All rights reserved.
KW - conducting polymers
KW - PEDOT
KW - silver hexabromocarborane
KW - silver ion-selective electrode
KW - conducting polymers
KW - PEDOT
KW - silver hexabromocarborane
KW - silver ion-selective electrode
KW - conducting polymers
KW - PEDOT
KW - silver hexabromocarborane
KW - silver ion-selective electrode
U2 - 10.1016/j.jelchem.2006.04.022
DO - 10.1016/j.jelchem.2006.04.022
M3 - Artikel
SN - 0022-0728
VL - 593
SP - 219
EP - 226
JO - Journal of Electroanalytical Chemistry and Interfacial Electrochemistry
JF - Journal of Electroanalytical Chemistry and Interfacial Electrochemistry
IS - 1-2
ER -