Polypyrrole Films (polypyrrole + film)

Distribution by Scientific Domains


Selected Abstracts


Multistep filling of porous silicon with conductive polymer by electropolymerization

PHYSICA STATUS SOLIDI (A) APPLICATIONS AND MATERIALS SCIENCE, Issue 6 2009
Kazuhiro Fukami
Abstract The filling of porous silicon with polypyrrole by electropolymerization was investigated. The filling with polypyrrole proceeded preferentially along the porous silicon wall, leading to the formation of tubular structures. By repeating the porosification, the pore filling and the additional porosification, through-tubes of polypyrrole were formed in macropores. The technique to form through-tube was also applied to medium-sized pores. A double layer with polypyrrole was produced by the repetition of porosification and pore filling twice. The immobilization of glucose oxidase was performed by electropolymerization in an aqueous solution containing glucose oxidase and pyrrole. Glucose oxidase was immobilized physically in the polypyrrole film. In the double layer, the sensitivity of glucose oxidase was measured by electrochemical oxidation of hydrogen peroxide, which was produced by the enzymatic reaction of glucose oxidase to gluconolactone. When glucose oxidase was immobilized in the upper layer, glucose was detected sensitively. On the other hand, when glucose oxidase was immobilized in the lower layer, the sensing current showed a slow and a low response. (© 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source]


Fabrication and Properties of Conducting Polypyrrole/SWNT-PABS Composite Films and Nanotubes

ELECTROANALYSIS, Issue 11 2006

Abstract We report the electropolymerization and characterization of polypyrrole films doped with poly(m-aminobenzene sulfonic acid (PABS) functionalized single-walled nanotubes (SWNT) (PPy/SWNT-PABS). The negatively charged water-soluble SWNT-PABS served as anionic dopant during the electropolymerization to synthesize PPy/SWNT-PABS composite films. The synthetic, morphological and electrical properties of PPy/SWNT-PABS films and chloride doped polypyrrole (PPy/Cl) films were compared. Characterization was performed by cyclic voltammetry, atomic force microscopy (AFM), scanning electron microscopy (SEM) and Raman spectroscopy. SEM and AFM images revealed that the incorporation of SWNT-PABS significantly altered the morphology of the PPy. Cyclic voltammetry showed improved electrochemical properties of PPy/SWNT-PABS films as compared to PPy/Cl films. Raman Spectroscopy confirmed the presence of SWNT-PABS within composite films. Field effect transistor (FET) and electrical characterization studies show that the incorporation of the SWNT-PABS increased the electronic performance of PPy/SWNT-PABS films when compared to PPy/Cl films. Finally, we fabricated PPy/SWNT-PABS nanotubes which may lead to potential applications to sensors and other electronic devices. [source]


Oxidative Inorganic Multilayers for Polypyrrole Film Generation

ADVANCED FUNCTIONAL MATERIALS, Issue 13 2010
Mikko Salomäki
Abstract A controlled nanoscale fabrication of conducting polymer films sets severe requirements for the preparation method and substrate. A new and versatile approach for producing thin polypyrrole films on a variety of surfaces is presented. Purely inorganic thin films are first prepared from poly(metaphosphate) and tetravalent metal ions using a sequential layer-by-layer technique. Redox-active cerium(IV) polyphosphate multilayer and redox-inactive zirconium(IV) and hafnium(IV) polyphosphate multilayers are prepared. Cerium-based polyphosphate films grow exponentially with the number of layers but multilayers containing zirconium or hafnium exhibit a linear buildup process. All the studied systems produce relatively smooth films with initial bilayer thickness less than 2,nm. The cerium(IV) containing film is redox-active, which is shown by its capability to form a polypyrrole layer on its surface by oxidation of pyrrole monomers in the adjacent aqueous solution. This is a general method to produce thin oxidative films of arbitrary size and form on a wide variety of surfaces. [source]


Electrochemical polymerization of chiral pyrrole derivatives in electrolytes containing chiral camphor sulfonic acid

POLYMER INTERNATIONAL, Issue 10 2004
GY Han
Abstract N -Substituted pyrrole derivatives with chiral side groups have been synthesized and electrochemically polymerized in acetonitrile containing tetrabutylammonium perchlorate (TBAClO4) and (S)-(+)-camphor-10-sulfonic acid ((S)-(+)-CSA) or (R)-(,)-camphor-10-sulfonic acid ((R)-(,)-CSA). The resulting N -substituted polypyrrole films were characterized by cyclic voltammetry, infrared, Raman and X-ray photoelectron (XPS) spectroscopies. XPS results demonstrated that the as-grown polymer films are preferably doped by CSA anions when the monomer and the CSA anion have the same optical rotation dispersion (ORD). Furthermore, the conductivities of the polymers synthesized in the media containing CSA with the same ORD of the corresponding monomers were measured to be about 2,10 times higher than those of polymers obtained from electrolytes without CSA. Copyright © 2004 Society of Chemical Industry [source]