The conductivity of a poly(3,4-ethylene dioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) film is enhanced by more than 100-folds on adding some organic compounds into PEDOT:PSS aqueous solutions or by treating the PEDOT:PSS film with organic solvents, such as ethylene glycol (EG), 2-nitroethanol, methyl sulfoxide or 1-methyl-2-pyrrolidinone. The mechanism for this conductivity enhancement was studied through various chemical and physical characterizations. The PEDOT:PSS film which is soluble in water becomes insoluble after treatment with EG. This strongly suggests an increased interchain interaction among the PEDOT chains. Raman spectroscopy indicates that this increased interchain interaction results from conformational changes of the PEDOT chains, which change from a coil to linear or expanded-coil structure. The increased interchain interaction and conformation changes are further confirmed by the temperature dependence of conductivity and the electron spin resonance (ESR). It is found that EG treatment lowers the energy barrier for charge hopping among the PEDOT chains, lowers the polaron concentration in the PEDOT:PSS film by similar to50%, and increases the electrochemical activity of the PEDOT:PSS film in NaCl aqueous solution by similar to100%. Atomic force microscopy (AFM) and contact angle measurements show that the surface morphology of the PEDOT:PSS film changes as well after the EG treatment. Conductivity enhancement was also observed when other organic compounds were used, but it was strongly dependent on the chemical structure of the organic compounds, and observed only with organic compound with two or more polar groups. These experimental results support our proposal that the conductivity enhancement is due to the conformational change of the PEDOT chains and the driving force is the interaction between the dipoles of the organic compound and dipoles or charges on the PEDOT chains. (C) 2004 Elsevier Ltd. All rights reserved.
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Univ Alabama, Dept Chem & Biol Engn, Tuscaloosa, AL 35487 USA
Univ Alabama, Ctr Mat Informat Technol, Tuscaloosa, AL 35487 USA
Changzhou Inst Mechatron Technol, Dept Elect Engn, Changzhou, Jiangsu, Peoples R ChinaUniv Alabama, Dept Chem & Biol Engn, Tuscaloosa, AL 35487 USA
Ma, S.
Anderson, K.
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Univ Alabama, Ctr Mat Informat Technol, Tuscaloosa, AL 35487 USA
Univ Alabama, Dept Chem, Tuscaloosa, AL 35487 USAUniv Alabama, Dept Chem & Biol Engn, Tuscaloosa, AL 35487 USA
Anderson, K.
Guo, L.
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Univ Alabama, Dept Chem & Biol Engn, Tuscaloosa, AL 35487 USA
Univ Alabama, Ctr Mat Informat Technol, Tuscaloosa, AL 35487 USAUniv Alabama, Dept Chem & Biol Engn, Tuscaloosa, AL 35487 USA
Guo, L.
Yousuf, A.
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Univ Alabama, Dept Chem, Tuscaloosa, AL 35487 USAUniv Alabama, Dept Chem & Biol Engn, Tuscaloosa, AL 35487 USA
Yousuf, A.
Ellingsworth, E. C.
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Univ Alabama, Ctr Mat Informat Technol, Tuscaloosa, AL 35487 USA
Univ Alabama, Dept Chem, Tuscaloosa, AL 35487 USAUniv Alabama, Dept Chem & Biol Engn, Tuscaloosa, AL 35487 USA
Ellingsworth, E. C.
Vajner, C.
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Univ Alabama, Dept Chem & Biol Engn, Tuscaloosa, AL 35487 USA
Univ Alabama, Ctr Mat Informat Technol, Tuscaloosa, AL 35487 USAUniv Alabama, Dept Chem & Biol Engn, Tuscaloosa, AL 35487 USA
Vajner, C.
Wang, H-T
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Univ Alabama, Dept Chem & Biol Engn, Tuscaloosa, AL 35487 USA
Univ Alabama, Ctr Mat Informat Technol, Tuscaloosa, AL 35487 USAUniv Alabama, Dept Chem & Biol Engn, Tuscaloosa, AL 35487 USA
Wang, H-T
Szulczewski, G.
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Laboratory for the Physics and Chemistry of Nanodevices and Department of Electronics, Peking UniversityLaboratory for the Physics and Chemistry of Nanodevices and Department of Electronics, Peking University
XING YingJie
QIAN MinFang
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QIAN MinFang
WANG GuiWei
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ZHANG GengMin
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GUO DengZhu
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WU JinLei
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