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Surface light emitting diodes SLEDs , in which previously microfabricated electrodes were coated with a conjugated polymer, were made with greatly different electrode spacings 250 nm and 10 or 20 mm and with different electrode material combinations. The fabrication process allowed us to compare several electrode materials. The SLED structures also enabled imaging of the light emission zone with fluorescence video microscopy. Conventional sandwich structures were also made for comparison electrode separation 50 nm. In this study, the emitting layer was poly[3- (2',5'-bis(1'',4'',7''trioxaoctyl)phenyl)-2,2'-bithiophene] (EO-PT), a conjugated polymer based on polythiophene with oligo ethyleneoxide side chains. The current-voltage (I(V)) and light-voltage (L(V)) characteristics of the SLEDs were largely insensitive to electrode separation except at high voltages, at which the current in the devices with the largest separations was limited. Sandwich structures had the same light output at a given current. Light could be obtained in forward and reverse bias from indium tin oxide ITO -aluminum, gold silicide-aluminum, and gold silicide-gold SLEDs, but the turn-on voltages were lowest with the ITO-aluminum devices, and these were also the brightest and most reliable. Adding salt to the EO-PT increased the current and brightness, decreased the turn-on voltages, and made the I(V) characteristics symmetric; thus, a device with an electrode separation of 10 mm had the extraordinarily low turn-on voltage of 6 V. The location of the light emission was at the electron-injecting contact.
New substituted 2,5-diphenyl-1,3,4-oxadiazoles are reported as luminescent materials in light emitting diodes LEDs . The investigated new oxadiazoles show efficient blue and green emission in single layer devices. The combination with a hole transporting and red emitting polythiophene led to a white emission with higher quantum efficiency (QE).
Lead island films were obtained via vacuum vapor deposition on glass and ceramic substrates at 80 K. Electrical conductance was measured during vapor condensation and further annealing of the film up to room temperature. The resistance behavior during film formation and atomic force microscopy of annealed films were used as information sources about their structure. A model for the quenched growth, based on ballistic aggregation theory, was proposed. The nanostructure, responsible for chemiresistive properties of thin lead films and the mechanism of sensor response are discussed. (C) 2003 Elsevier B.V. All rights reserved
The photoalignment ability of poly[methyl(phenyl)silylene] (PMPSi) films makes it possible to use them as hole- transporting substrates for the preparation of organic oriented films. A PMPSi layer prepared by spin coating was irradiated, after drying, with linearly polarized UV light. Then, water-soluble hydroxyaluminium phthalocyaninesulfonate [Al(OH)Pc(SO3Na)(1-2)] was deposited by casting. The cell ITO/PMPSi/AI(OH)Pc(SO3Na)(1-2)/Al showed non-linear current- voltage characteristics. For applied voltages higher than 10 V, polarized electroluminescence was observed. Its spectral characteristic consisted of two peaks with maxima at about 320 and 700 nm; their polarized anisotropies R-EL = Phi(parallel to) / Phi(perpendicular to) were ca. 15 and 0.5, respectively
Films of emeraldine base of polyaniline (PAni) doped by various transition metal salts have been prepared, and current-voltage characteristics of the indium-tin oxide (ITO)/PAni film/metal electrode heterostructures were investigated. It was found that the electrical characteristics of the heterostructures are greatly affected by the dopant used and the metal electrode used. Different dopants resulted in different current anomalies with asymmetric current-voltage characteristics. Depending on the dopant used, the exponential and power law of the current behavior can be distinguished. Depending on the metal electrode used, two different regimes of current passing have been found at low applied voltages, namely, a nearly ohmic regime for the indium electrode, and a diode regime for the aluminum electrode. The diode regime was found to accompany by a positive charge accumulation in the film near the film/metal interface, which creates a built-in potential in the film. The amount of positive charges accumulated at the interface and therefore the value of the built-in potential can be reversibly increased or reduced by successive runs of the applied voltage in the forward or reverse direction, respectively. (C) 2004 Elsevier B.V. All rights reserved
Dielectric properties of zinc phthalocyanine thin films : effects of annealing in air and in N-2
(2005)
This work presents the effects of ambient conditions, in particular oxygen and humidity, on the dielectric spectra of thin zinc phthalocyanine (ZnPc) films equipped with interdigitated electrodes and the effect of annealing in dry N-2 or in ambient air. The measurements were performed in the frequency range 10(-2)-10(5) Hz. The results indicate that the electric properties of ZnPc films are not only affected by oxygen but also by water vapour the presence of which always leads to the drop in alternating current conductance (ac-conductance). Moreover, at room temperature, the ac-conductance of ZnPc films previously exposed to air exhibits a reversible change with humidity, which makes these films attractive for humidity sensing applications. (C) 2004 Elsevier B.V. All rights reserved
The formation of a Langmuir monolayer of an amphiphilic derivative of zinc phthalocyanine (Na[(ZnPcSO3)-S-t]) has been studied by means of surface potential technique and Brewster angle microscopy. The experiments were undertaken in order to understand the behaviour of this monolayer with a well-defined surface pressure isotherm. The floating film is described as a truly monomolecular layer formed by very rigid islands in which the phthalocyanine units tend to take on a preferential orientation with their planes perpendicular to the air-water interface, for high values of the surface pressure. (c) 2004 Elsevier B.V. All rights reserved
Two basic morphologies of emeraldine base of polyaniline-transition metal salt complex films cast from N- methylpyrrolidinone solutions are described. The first morphology consists of grains and the other consists of loose aggregates, respectively. The correlation of the film morphology with formation of precipitate in the complex solution, kinetics of solvent evaporation from the cast film, amount of solvent entrapped in the film, film conductivity, and IR absorption spectra is shown. Two different mechanisms of the complex formation as a result of competition in the polymer- inorganic salt-solvent trio interactions are discussed; the first mechanism results in folding of macromolecules into compact coils being then a core of grains in the complex films, and the second mechanism leads to blending of the polymer chains with solvent giving rise to formation of loose aggregates. (c) 2005 Elsevier B.V. All rights reserved
Non-linear optical and electrical properties of polymer films obtained by dipole orientation of active units are reported. Novel polar oligomer with N-(indan-1,3-dion-2-yl)pyridinium betaine (IPB) as a side group is studied. Orientation of polar groups in oligomer thin films causes an increase of the photo-induced change of surface potential on irradiation in the region of photo-induced electron transfer (PIET) where the IPB group exhibits a reversible change of the value and sign of the dipole moment. At longer wavelengths, the value of the surface potential of the oligomer may be determined by transport of photo-generated charge carriers
In this work, we report our investigations on the film-forming properties as well as the optical and electroluminescent characterisations of a series of lateral-substituted soluble oligo(phenylenevinylenes) of various conjugation length. Preliminary investigations show that these materials are potential candidates for use in organic light-emitting devices (OLEDs). Two types of OLEDs were fabricated: single layer (SL) and single heterostructure (SHS), with poly(p-phenylenevinylene) (PPV) as hole transporting layer. Our best results were obtained with single layer device emitting green light with a luminance of 0.18 cd m(-2) and 0.24 cd m(-2) at a driving voltage of 10 V. (c) 2004 Elsevier B.V. All rights reserved
An increase in random molecular vibrations of a solid owing to heating above the melting point leads to a decrease in its long-range order and a loss of structural symmetry. Therefore conventional liquids are isotropic media. Here we report on a light-induced isothermal transition of a polymer film from an isotropic solid to an anisotropic liquid state in which the degree of mechanical anisotropy can be controlled by light. Whereas during irradiation by circular polarized light the film behaves as an isotropic viscoelastic fluid, it shows considerable fluidity only in the direction parallel to the light field vector under linear polarized light. The fluidization phenomenon is related to photoinduced motion of azobenzene-functionalized molecular units, which can be effectively activated only when their transition dipole moments are oriented close to the direction of the light polarization. We also describe here how the photofluidization allows nanoscopic elements of matter to be precisely manipulated
The work presents low signal dielectric spectra of gold/copper phthalocyanine/magnesium and gold/copper phthalocyanine/gold sandwich systems in the 25 Hz-1 MHz frequency range. The performed analysis enables us to distinguish the electrode resistance and the lattice polarization from processes related with electric transport, such as charge carrier relaxation at space charge region of a barrier and charge carrier injection in dielectric response.