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Electronic, chemical and structural change induced by organic solvents in tosylate-doped poly(3,4-ethylenedioxythiophene) (PEDOT-OTs)
The effects of organic solvent on the electronic, structural and chemical properties of tosylate-doped poly(3,4-ethylenedioxythiophene) (PEDOT-OTs) are investigated. The use of different organic solvents during the oxidative chemical polymerization of 3,4-ethylenedioxythiophene (EDOT) with iron(III)...
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Published in: | Synthetic metals 2005-03, Vol.149 (2), p.169-174 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The effects of organic solvent on the electronic, structural and chemical properties of tosylate-doped poly(3,4-ethylenedioxythiophene) (PEDOT-OTs) are investigated. The use of different organic solvents during the oxidative chemical polymerization of 3,4-ethylenedioxythiophene (EDOT) with iron(III)-tosylate can greatly vary the electrical conductivity of PEDOT-OTs along with molecular structure and doping concentration. For example, PEDOT-OTs prepared from methanol shows the conductivity of 20.1
S/cm, which is an increase by a factor of 10
7 compared to PEDOT-OTs prepared from acetone. From the X-ray diffraction (XRD) experiments, it was found that PEDOT-OTs samples prepared from ketone solvents are amorphous state, whereas PEDOT-OTs samples prepared from alcoholic solvents show the better defined crystalline structure in which the charge transport along and between the PEDOT chains are promoted. Chemical analysis employing X-ray photoelectron spectroscopy (XPS) revealed that the doping concentration of PEDOT-OTs with alcoholic solvents is much higher than that of PEDOT-OTs with ketones. It is proposed that the interactions between the organic solvent and iron(III)-tosylate can cause the variation in doping concentration and, therefore, result in the PEDOT-OTs of different conductivities and chain structures. |
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ISSN: | 0379-6779 1879-3290 |
DOI: | 10.1016/j.synthmet.2004.12.011 |