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Neste trabalho as propriedades ópticas do poli[2-metóxi,5-(2’etil-hexiloxi)-p-fenilenovinileno] - MEH-PPV foram estudadas sob efeito de luz azul proveniente de super LEDs utilizada no tratamento da hiperbilirrubinemia neonatal (ou icterícia). Os resultados mostraram que o MEH-PPV apresenta uma mudança de cor do vermelho-alaranjado para o incolor, passando por diversas tonalidades de amarelo, bem como uma diminuição da intensidade dos espectros de absorção e de fotoluminescência (PL) em função do tempo de exposição à radiação. Essas mudanças foram usadas para projetar um sensor de acúmulo de dose de radiação azul, tipo indicador de cores, para avaliar a dose de radiação recebida por recém-nascidos durante o tratamento da icterícia neonatal. In this work we investigated the optical behavior of poly[2-methoxy-5(2’-ethylhexyloxy)-p-phenylenevinylene] (MEH-PPV) under the effect of blue-light LED source applied in neonatal hyperbilirubinemia treatment. There is a visible response that covers the electronic absorption of bilirubin (350-500 nm), and hence this material is applicable for controlling the radiation doses in the treatment of jaundice of neonates, which is one of the most common reasons for hospital readmission of newborn infants. The results show that the material presents a gradation of color from orange-red to yellow and quenching on the absorption and photoluminescent (PL) spectra with the radiation exposure time. The rate of these changes can be altered by manipulations of organic solution concentration, suggesting these color and emission/absorption changes can be used to design an indicator-dosimeter that is readily associated with the radiation exposure time used in treating neonatal jaundice.

In this work, a new type of WO3 and V2O5 photovoltaic cell were fabricated. The oxides were obtained by sol-gel route. Both V2O5 and WO3 presented a lamellar structure with d = 1.17 nm and 0.69 nm, respectively. From SEM of V2O5 was observed ribbons and for WO3 noted a presence of platelets. For WO3, increasing the distance of lamp was observed a decreasing of light intensity: 164 mV in 44000 lux to 42 mV in 60 lux. For V2O5, in 1700 lux it was observed a voltage of 1418 mV and in 15000 lux a value of 1572 mV.

The properties of a commercial indium-tin-oxide (ITO) layer deposited on glass substrates were evaluated as a function of the treatment time in diluted aqua regia solution. The samples were characterized by atomic force microscopy (AFM), bulk conductivity, ellipsometry, energy-dispersive X-ray analysis (EDX), contact angle/surface energy, and work function measurements. The results show that shorter times of treatment do not affect significantly the ITO properties but decrease the ITO thickness. For longer times (more than 30 min), although the work function and In/Sn ratio are not affected by the treatment, conductivity, roughness, UV–VIS absorption spectra, and refraction index values are greatly affected. Contact angle and surface energy data indicated that the dispersive component of the surface energy was not affected by the treatments. However, a strong decrease in the polar contribution occurred, indicating that ITO surface becomes more hydrophobic as the chemical treatment proceeds. These treated surfaces can interact more strongly with nonpolar materials, such as poly-(p-phenylene-vinylene) derivatives, resulting in a strong polymer ITO adhesion that can improve the efficiency of polymer light-emitting diodes (PLEDs).

In this work, the electrical properties of polymeric light-emitting diodes (LEDs) based on poly(2-methoxy-5-(2′-ethyl-hexyloxy)-1,4-phenylene vinylene), MEH-PPV, were studied by dc current–voltage (I–V) curves and impedance/admittance spectroscopy, at different temperatures. ITO/polymer/metal (Al and Au) structures were used to study the effect of the barrier height on the charge injection at the polymer/metal interfaces. For ITO/MEH-PPV/Al devices, strong temperature influence on the dc conductivity was observed in the forward direction whereas, in the reverse direction, the conductivity was almost temperature independent. On the other hand, ITO/MEH-PPV/Au devices presented temperature dependent conductivities for both polarities. This indicates that, for low barrier height at the interfaces (

Poly(p-phenylenevinylene) (PPV) and its derivatives exhibit strong luminescence, being serious candidates to be used as active layers in organic light-emitting diodes. However, the structural degradation caused by photo-oxidation is an obstacle for commercial applications of such materials. Here, we show that spectroscopy ellipsometry is a useful technique to investigate the photo-oxidation of poly[(2-methoxy-5-hexyloxy)-p-phenylenevinylene] (MH-PPV), a PPV derivative, which emits a red color light. Spectroscopy ellipsometry enables determination of the complex dielectric function ∈ * (E) of MH-PPV thin-layer films exposed to air, in the 2.1-4.2 eV energy range, as a function of the light exposure time (t e ). By using the Lorentz model to fit the experimental ∈*(E) curves, it was inferred that the interactions among polymeric chains increase with t e . From ∈*(E), it is also possible to obtain the complex refractive index, N*(E) = n + ik. At higher energies (where k << n), n increases from 1.32 to 1.40 with the photo-oxidation progress. The behavior of n was investigated by using the Lorenz-Lorentz equation, taking into account the contribution for n by the chromophores of MH-PPV. The effect of photo-oxidation, mainly due to the replacement of vinyl C=C by the ketone C=O bonds, is confirmed by Fourier transform infrared measurements, an effect that reduces the average effective polymer conjugation length.

In this paper we present the photoconduction effect of the poly( p -phenylenevinylene) (PPV) and its derivative, the poly[(2-methoxy-5-hexyloxy)-p-phenylenevinylene] (MH-PPV). The structures used to study photoconductivity were prepared using solutions of either PPV-precursor in methanol or MH-PPV in chloroform, both spin-coated on an interdigitated chromium-gold line array previously deposited onto glass substrate. Currents vs. voltage curves were carried out as well as of the films optical characteristics have been studied by UV-Vis, and photoluminescence and eletroluminescent spectroscopies.

In this paper we study the photo-oxidation phenomenon in the structure of a PPV derivative, the poly[(2-methoxy-5-hexyloxy)- p -phenylenevinylene] - (MH-PPV), using ellipsometry and infrared spectroscopy techniques. Ellipsometric measurements were carried out in MH-PPV films previously exposed to light irradiation in air. It was observed a variation of both real and imaginary components of the refractive index. These variations are related with the replacement of the vinyl C=C bounds by the carbonyl C=O bounds, as confirmed by the infrared absorption measurements.

The ac complex conductivity σ*(f) of polyaniline (PAN) films at different doping levels and different temperatures, in the 1–100 KHz frequency range, are reported. The results are typical of a disordered medium where the real component of ac conductivity is frequency independent at low frequencies, rising for higher values of frequencies. In order to interpret both the real and the imaginary components of σ*(f), we developed a model which considers the doped PAN as a disordered insulating matrix, sprinkled with conductive islands generated by doping, as indicated by energy dispersed x-ray microanalysis. The conduction through the insulating matrix obeys the random free energy barrier model, while in the conductive islands a metallic frequency-independent conductivity is considered. From the fittings we obtained the activation energy value of the maximum energy barrier of the doping mechanism and estimated the concentration of hopping sites.

This paper presents a methodology for the preparation of a-HgI2 by Physical Vapor Transport and of PbI2 crystals using the Bridgman technique. The results of the growth of HgI2 diluted in PbI2 by the Bridgman technique are shown for the first time, its limit of solubility having been determined at 600 ppm of HgI2 in the PbI2 matrix. Optical absorption, photoluminescence and electrical conductivity measurements show that the crystals prepared are of good crystalline quality.

In this work we investigate the radio-degradation of MEH-PPV polymer film as a tool for measuring high doses of gamma radiation. In order to produce film samples with thickness in the micron range, we have mixed the photoluminescent poly(2-methoxy-5(2'-ethylhexyloxy)-p-phenylenevinylene) copolymer (MEH-PPV) with a biodegradable poly(butylene adipate-co-terephthalate) copolymers (PBAT). The system was irradiated with a Co-60 source with doses ranging from 1 to 1,000 kGy. Ultraviolet-visible (UV-Vis) and photoluminescence (PL) spectroscopy have been used to investigate the radiation induced changes in the absorption and photon-emission spectra of the irradiated samples. Results indicate that the PL emission intensity varies exponentially with the applied gamma radiation dose for doses ranging from 30 to 500 kGy. The unambiguous relationship between PL & Dose together with the good flexibility of the copolymer films indicate that MEH-PPV/PBAT blends have great potential for applications in high gamma dose dosimetry.

A novel approach for studying the thermal conversion of poly-p-xylylidene tetrahydrothiophenium chloride (PTHT) into poly(p-phenylenevinylene) (PPV) films has been proposed on the basis of calculated optical parameters. Spin-cast PTHT films were thermally converted into partially conjugated PPV films over conversion temperatures ranging from 22 °C to 200 °C. A strong correlation between refractive index (n) and damping constant extinction coefficient (k) was verified by spectroscopic ellipsometry (SE) for the films studied in the visible range of energy. The conversion temperature has a strong influence on the values of n and k, which were theoretically modeled using a Lorentz harmonic oscillator analysis. The films were also studied by spectroscopic techniques (photoluminescence, FTIR, and UV–VIS), and it was verified that the values of n decrease with increasing the amount of C C groups present along the polymer chains, as a strong evidence that both structure and optical properties of thermally converted PPV films can be directly compared. The optical properties of the PPV films were also compared with those of two electroluminescent derivatives in which side chains are introduced into the phenyl ring of PPV, poly(2-methoxy-5-hexyloxy)-p-phenylenevinylene) (MH-PPV) and poly(3-methoxy-5-dodecyloxy-p-phenylene–vinylene) (MD-PPV).

Neste trabalho são apresentadas a fabricação e a caracterização óptica de um novo detector de raios X para monitoramento da dose nos processos de radioterapia empregando fótons de alta energia (6,0 MV). O dispositivo foi fabricado a partir de materiais orgânicos luminescentes consolidados como elemento ativo de displays eletroluminescentes nanoestrurados, mas que, até esse momento, têm sido pouco investigados como detectores de radiação ionizante. Para tanto, foram preparadas soluções à base de tris(8-hidroxiquinolato) de alumínio - Alq3 e poli(2-metóxi-5-(2-etilhexiloxi)-pfenilenovinileno) – MEH-PPV, cujo espectro de emissão do primeiro material se sobrepõe ao de absorção do segundo. Os resultados obtidos mostram que os espectros de emissão do sistema MEH-PPV/Alq3 desloca-se do vermelho-laranja (λmax = 598 nm) para o verde (λmax = 545 nm) quando a dose de radiação vai de 0 a 100 Gy. Essa mudança, consequência da degradação induzida pela radiação do MEH-PPV, foi usada no desenvolvimento de dosímetros para possível futura aplicação no controle do tratamento de pacientes oncológicos. In this work it is presented the characterization and fabrication of a novel ionizing radiation detector for high energy photon beam (6.0 MV). It is used organic luminescent materials usually applied in light-emitting and nanostructure device, but still few explored in radiation dosimetry. Organic solutions of tris(8-hydroxyquinolinato) aluminum - Alq3 and poly[2-methoxy-5-(2’-ethylhexyloxy)-p-phenylene vinylene] - MEH-PPV were prepared to better study the impact of spectral overlap between the Alq3 emission and MEH-PPV absorption. It is observed a blue-shift on the photoluminescence of the MEH-PPV/Alq3 solution system from red-orange (λmax = 598 nm) to green (λmax = 545 nm) when the radiation dose changes from 0 to 100 Gy. This effect is attributed to the photoxidation process of MEH-PPV and was employed to design dose accumulation detector in order to represent easily the radiation dose for cancer treatment.

The alternating conductivity, σ *( f ) = σ ′( f ) + iσ ″( f ), of in situ polymerized polyaniline thin films doped with hydrochloric acid, deposited on top of an interdigitated gold line array previously deposited on glass substrates, were measured in the frequency ( f ) range between 0.1 Hz to 10 MHz and in the temperature range from 100 to 430 K. The results for σ ′( f ) are typical of a disordered solid material: for frequencies lower than a certain hopping frequency γ hop , log[ σ ′( f )] is frequency-independent rising almost linearly for in log f > γ hop . A master curve was thus obtained by plotting the real component of the conductivity using normalized scales σ ′( f )/ σ dc and f / γ hop , which is indicative of a single process operating in the whole frequency range. An expression encompassing the conduction through a disordered structure taken from previous random free energy barrier model for hopping carriers, as well a dielectric function to represent the capacitive behavior of the PAni was employed to fit the experimental results. The dielectric constant and activation energy for hopping carriers were obtained as function of the polymer doping level.

Complex impedance measurements were used to analyze the influence of ultraviolet and ozone gas on the electronic behaviour of ZnO films grown by rf magnetron sputtering. The data show that UV exposure strongly increases the ac conductivity of the film at very low frequencies, and that after ozone exposure it recovers the original value. At high frequencies, however, UV-light exposure it does not change the conductivity but the ozone acts in the sense to decrease it. Two distinct mechanisms, related to two relaxation time distributions are clearly observed: they are superimposed in the virgin sample, but they split forming two semicircles in the z ″( f ) − z ′( f ) diagrams when the samples are treated with UV and/or ozone gas. A combination of the bruggeman effective medium approximation (BEMA) with the random free energy barrier model is used to fit the data and to explain the ac conductivity variation phenomena observed.

In this work, we study the influence of organic solvents on the absorption and emission spectra of solutions and films of a soluble poly-(p-phenylenevinylene)- PPV derivative, the poly(3-methoxy-5-dodecoxy-p-phenylene-vinylene)- MD-PPV. We carried out absorption in the UV-Vis range, photoluminescence (PL) and photoluminescence excitation (PLE) measurements of MD-PPV solutions and cast films from five different solvents at room temperature. UV-Vis measurements show a solvatochromic effect, presenting a blue shift of the lowest-energy edge of the φ-φ* transition band for different solvents. PL spectra, on the other hand, show a multi-peak behavior, which is fitted considering an excitonic transition model followed by vibronic structure replica. It is observed that the first vibronic peak intensity tends to increase in comparison to the excitonic peak as δH increases, indicating that the solubility parameter of the solvent has a direct influence on the electron-phonon coupling. In addition, deviations from the intrachain model were observed for aromatic solvents, suggesting that aggregate formation can take place in the emission spectrum. Excitation spectra show that a new excitation peak comes out around 550 nm for poorer solvent solutions at higher PLE detection wavelengths, which is consistent with aggregate states emission.

This paper describes a new approach to improve the analysis of surface modification of free-standing semiconducting polymer films emerged from the interfacial interaction between aluminium electrode and HCl-doped polyaniline (PANI) films. The Al–PANI–Al structure was prepared by casting PANI/N-methyl-2-pirrolidone onto a glass substrate and then being sandwiched between Al electrodes after immersion in HCl aqueous solutions and then dried. The Al–polymer interface was investigated by means of complex impedance spectroscopy in the frequency domain on HCl-doped PANI films. The dc conductivity of the interfacial layer between the Al and PANI surface exposed to air during the film processing is higher than those obtained with Al and PANI surface exposed to glass. Raman spectroscopy data confirm this evidence. Here, it is speculated that some dissociated chlorine and aluminium-salt-containing species have contributed as ionic carriers increasing the electrical conductivity of the polymer bulk, and by the formation of an Al2O3 thin layer between the Al and PANI films. An equivalent circuit model considering the influence of Al–PANI reactions on the electrical behaviour of the Al–PANI–Al structure was proposed. Additionally, it was demonstrated that the impedance spectroscopy facilitates the identification of interface modification in the Al–PANI–Al films.

Alternating conductivity measurements of polyaniline, in the 1–10 5 Hz range, were carried out in samples under different temperatures. It was observed that for low frequencies the real component, σ'(ƒ), of ac conductivity is frequency-independent, however obeying the relation σ'(ƒ) ∝ ƒ s , beyond a critical value; the imaginary component increases with frequency in the whole measurements frequency range. The Random Free Energy Barrier Model approach was used to explain the experimental results, and from the theoretical-experimental fittings, it was concluded that the temperature acts in the sense of increasing the carrier mobility.