Browsing by Subject "Electric conductivity of solids"

Now showing 1 - 8 of 8

Open Access
Conducting polymer composites of polypyrrole and a poly(arylene ether ketone)
(1998) Selampinar F.; Akbulut, U.; Toppare L.
Electrically conducting composites of polypyrrole and a poly(arylene ether ketone) were synthesized by electroinitiated polymerization of pyrrole on a poly(arylene ether ketone)-coated platinum electrode. The electrolysis medium was water and p-toluene sulfonic acid. The conductivities of the composites were in the range 1-10 S/cm. The composites were characterized by scanning electron microscopy, Fourier transform infrared, and thermal analyses. The composites were found to be composed of bilayers which can be peeled into two free-standing polymer films. The solution side of the polypyrrole layer of the alloy film contains globular structures, whereas the other side is smoother.
Open Access
Conducting polymer composites of polypyrrole and polyindene
(Elsevier, 1996) Bozkurt, A.; Akbulut, U.; Toppare, L.
Polypyrrole-polyindene composites were prepared via electrochemical methods. Two different approaches were utilized. In the first, the electro-initiated polymerization of indene on a platinum electrode was achieved at 2.0 V versus Ag/Ag+ in acetonitrile. Then the polyindene-coated electrode was used for the electrochemical polymerization of pyrrole at 1.0 V versus Ag/Ag+. In the second case, electrochemical coating of platinum electrode with polypyrrole at 1.0 V versus Ag/Ag+ was carried out and indene was polymerized on the conducting polymer at 2.0 V versus Ag/Ag+ in acetonitrile medium. The characterizations of these composites were done by FT-IR, scanning electron microscopy (SEM) and thermal gravimetric analysis (TGA). Electrical conductivities were evaluated by two-probe and four-probe methods.
Open Access
Conducting polymer composites: polypyrrole and poly (vinyl chloride-vinyl acetate) copolymer
(John Wiley & Sons, Inc., 1997) Balci, N.; Bayramli, E.; Toppare, L.
Composites of a polypyrrole (PPy) and poly (vinyl chloride-vinyl acetate) copolymer (PVC-PVA) were prepared both chemically and electrochemically. An insulating polymer was retained in the blend and the thermal stability of the polymer was enhanced by polymerizing pyrrole into the host matrix in both cases. The composites prepared electrochemically gave the best results in terms of conductivity and air stability. © 1997 John Wiley * Sons, Inc.
Open Access
Doping of 2-Cl-PANI/PVC films by exposure to UV, γ-rays and e-beams
(Elsevier Sequoia SA, Lausanne, Switzerland, 2000) Sevil, U. A.; Güven, O.; Birer, Ö.; Süzer, Ş.
2-Chloro-polyaniline (2-Cl-PANI) is chemically prepared in its non-conducting (Emeraldine Base, EB) form and dissolved together with polyvinylchloride (PVC) in THF for casting into thin (10-50 μm) composite films. The electrical conductivity of these films increases by more than four orders of magnitude (from 10-6 to 10-2 S/cm) when they are exposed to UV, γ-rays and e-beams. This is attributed to the dehydrochlorination (loss of HCl) of PVC by exposure to energetic particles and subsequent doping of the 2-Cl-PANI (i.e., conversion to Emeraldine Salt, ES) by the in-situ-created HCl. The doped films can also be returned to their undoped form by further exposure to NH3 vapours. The UV (or other particles)-induced doping/NH3 undoping cycles can be repeated several times until almost total dehydrochlorination of the PVC matrix. UV-Vis-NIR, Fourier transform infrared (FTIR) and X-ray photoelectron spectroscopic (XPS) techniques are employed to follow the changes in the composite films upon doping by exposure to these energetic particles.
Open Access
Electronic properties of polypyrrole/polyindene composite/metal junctions
(Elsevier, 1997) Bozkurt, A.; Ercelebi, C.; Toppare, L.
Junction properties between conducting polymer composites of polypyrrole/polyindene (PPy/PIn) with different conductivities and metals like Pt, Au, Al and In have been investigated. Rectifying junctions were observed for low work function metals, In and Al; however, high work function metals, Pt and Au, were observed to form ohmic contacts to PPy/PIn composite in the sandwich geometry. The rectifying behavior of the metal/composite/Pt junctions improved when the conductivity of the composite was decreased from 1 to 0.01 S/cm. Using the ideal Schottky theory various junction parameters have been determined. All planar junctions were ohmic regardless of the conductivities of the samples.
Open Access
Investigation of the effect of donor-acceptor substitution on band gap, band width, and conductivity
(Elsevier, 2001) Salzner, U.
Polymers of two donor-acceptor systems, 3-cyano,3′-hydroxybithiophene 1 and 4-dicyanomethylene-4H-cyclopenta[2,1-b:3,4-b′],3,4-ethylenedioxythiophene (CDM-EDOT) 2, were analyzed with density functional theory. As predicted by perturbation theory, interactions between donors and acceptors with very different energy levels are greatly reduced compared to those between fragments with similar energy levels. This leads to localized states and bands with little dispersion. For poly-1 these localized states lie below the valence band and above the conduction band. For 2 localized unoccupied levels lie within the band gap. These acceptor levels account for the high electron affinity of poly-2 and allow for self-doping. Self doping explains the increased intrinsic conductivity of poly-2, the localized nature of the low lying MOs rationalizes the low mobility of n-type carriers in poly-2.
Open Access
Theoretical analysis of poly(difluoroacetylene)
(American Chemical Society, 2003) Salzner, U.
The electronic structure of poly(difluoroacetylene) was investigated with the aim of determining whether it is a good candidate for a conducting polymer with high n-type conductivity. Positions of valence and conduction bands and bandwidths indicate that planar all-trans poly(difluoroacetylene) is p- and n-dopable and that on-chain mobility of electrons and holes is high. Various geometries of oligomers with eight carbon atoms were optimized and compared to those of decacyanooctatetraene and octatetraene. Decafluorooctatetraene has a tendency to adopt nonplanar structures, but the planar trans form lies only 5.44 kcal/mol above the helical minimum. Since the energy for planarization is small, poly(difluoroacetylene) might be planar in the solid state. This is in contrast to the cyano analogue for which the planar trans structure lies 23.26 kcal/mol above the helical minimum. Alternating acetylene and difluoroacetylene units give rise to planar polymers with reduced band gap. Bandwidths, ionization potential, and electron affinity are average between those of the homopolymers.
Open Access
UV-induced acid-base chemistry within the PVC matrix: Wavelength selectivity
(ACS, Washington, DC, United States, 2000) Süzer, Şefik; Birer O.
The dehydrochlorination of polyvinyl chlorides (PVC) is investigated by using it as an in-situ Bronsted acid source, in blends with pH indicators for optical changes, and with basic forms of conducting polymers to determine the electrical conductivity changes. The in-situ created HCl was responsible for the optical and electrical conductivity changes in pH indicator+PVC and nonconducting electroactive polymer (PANI) or PANI+PVC systems. It was possible to sensitized PVC and trigger polyene formation at higher wavelengths. The nature of polyene formation was strongly dependent on the wavelength of irradiation as well as the amount of energy transferred to the matrix from the sensitizer.