The effect of low-temperature conditions on the electrochemical polymerization of polypyrrole films with high density, high electrical conductivity and high stability

Citation
Co. Yoon et al., The effect of low-temperature conditions on the electrochemical polymerization of polypyrrole films with high density, high electrical conductivity and high stability, SYNTH METAL, 99(3), 1999, pp. 201-212
Citations number
31
Categorie Soggetti
Apllied Physucs/Condensed Matter/Materiales Science
Journal title
SYNTHETIC METALS
ISSN journal
03796779 → ACNP
Volume
99
Issue
3
Year of publication
1999
Pages
201 - 212
Database
ISI
SICI code
0379-6779(19990226)99:3<201:TEOLCO>2.0.ZU;2-0
Abstract
High-quality polypyrrole-hexafluorophosphate (PPy-PF6) films with high dens ity ( similar to 1.4 g/cm(3)), high conductivity ( > 300 S/ cm for unstretc hed film) and high electrochemical stability are obtained reproducibly by g alvanostatic polymerization at low-temperature conditions. The optimal poly merization current density of J(p) = 0.02-0.05 mA/cm(2) was obtained at the polymerization temperature of T-p= -40 degrees C. The surface morphology o f the film sensitively varies depending upon the properties of electrode an d its surface conditions. The transport measurements characterize the high- density PPy-PF6 film as a disordered metal close to the boundary of disorde r induced metal-insulator (M-I) transition. The X-ray diffraction measureme nts suggest that partially crystalline structure of PPy-PF6 film is related to the transport properties. The uniaxial stretching induces an increase o f the conductivity up to similar to 930 S/cm in a direction parallel to str etching as well as the anisotropy of conductivity. The comparative studies of thermogravimetric analysis (TGA), cyclic voltammetry (CV) and electroche mical impedance spectroscopy (EIS) for PPy-PF6 films prepared at room-tempe rature and low-temperature conditions show that the latter exhibit better t hermal stability as well as electrochemical stability under long oxidative polarization. (C) 1999 Elsevier Science S.A. All rights reserved.