Papers by Keyword: PPV

Abstract: The physical and chemical characterize of quantum dots (QDs) extensively depend upon the optical and morphological factors such as size and shape. The zinc selenide (ZnSe) quantum dots (QDs) have been prepared by chemical method and used to fabricate quantum dot hybrid junction devices with different types of organics polymers. The optical studies illustrate that the band gap value from the photoluminescence (PL) with high intensity of these QDs is found about 3.1 eV. The electroluminescence's (EL) hybrid devices were demonstrated by room temperature PL and electroluminescence (EL). Current-voltage (I–V) characteristics indicate that the output current is good compared to the few voltages (5.5 V) used which gives good results to get a generation of white light. The EL spectrum reveals a broad emission band covering the range from 350 - 700 nm. The emissions producing this white luminescence were recognized depending on the chromaticity coordinates (CIE 1931). The correlated color temperature (CCT) was found to be about 5759, 3500 and 3498 K for ITO/TPD/ZnSe, ITO/PPV/ZnSe and ITO/PEDOT/ZnSe QDs respectively. Fabrication of EL- hybrid devices from semiconductors materials (ZnSe QDs) with holes injection organic polymer (TPD, PPV and PEDOT) was effective in white light generation.

Abstract: In the article we present a unique analytical tool for the characterization of conjugated polymers – SEC-DAD (Size Exclusion Chromatography – Diode Array Detector). The chromatographic separation is performed in a conventional SEC mode which provides narrow molecular-weight fractions of the analyzed polymer. The uniqueness of the SEC-DAD combination comes out with the utilization of DAD for the monitoring the absorption characteristics of particular fractions along the molecular weight distribution. If applied in the characterization of the conjugated polymers, SEC-DAD helps to reveal the dependencies of (i) the extent of conjugation and (ii) covalent and configuration structure of the polymer on the molecular weight.

Abstract: The influence of the solvent temperature and the solvent quality on the chain conformation and the aggregation of semiconducting block copolymers is described in this paper. In selective solvents for the polystyrene block, aggregation is detected by means of optical spectroscopy. The author thinks that the research is useful for the development of material engineering.

Abstract: Beijing East Road No.1 tunnel in Guiyang city has the most complexity in arround, so prediction and control the blasting vibration is the most important task. In order to improve the accuracy of the prediction of the blasting vibration to mitigate the possible hazard in tunnel construction, studied on method of predicting peak particle velocity (PPV) using support vector machine (SVM) and established regression prediction model based on SVM. Comparisons between the predicted PPV using the empirical equation regression and SVM was made, find that the SVM gives much better prediction of PPV than does the empirical equation regression.

Abstract: Semiconductor polymers are successfully implemented in a broad range of applications such as light emitting diodes, field effect transistors and photovoltaic devices. Most of the achievements reached in the development of these devices were obtained at experimental level, being difficult to identify individually the influence of each factor that limits and controls these devices efficiency. One of the factors that strongly influence the performance of polymer-based devices is the presence of chemical defects in the polymer strands that change their molecular properties. As a result, these polymer strands can work like traps or deep energetic states for charge transport, leading, for instance, to a decrease on charge mobility. At experimental level it is a difficult task to isolate the influence of each type of chemical defects individually on the molecular properties of the polymer strands. It is in this context that theoretical modelling seems to be the most suitable approach to get a deep understanding of the influence of chemical defects on the molecular properties of semiconductor polymers. By performing quantum molecular dynamics calculations we study the influence of chemical defects on the molecular properties of poly(para-phenylenevinylene) (PPV). Our results show clearly a significant difference on the electronic properties of defective polymer strands (e.g. charge carrier localization, ionization potential, electron affinity and electric-field threshold for charge carrier mobility along the polymer backbone) as compared with defect-free strands.

Abstract: This work focuses on studying a novel polymer/nanocrystal multilayer for the fabrication of donor and accepter typed photovoltaic device. Highly luminescent anionic CdTe nanocrystals were prepared by aqueous synthesis method using 3-mercaptopropionic acid as stabilizer. The resultant CdTe served as electron acceptor and poly(p-phenylene vinylene) (PPV) was used as electron donor. Through the electrostatic interactions between cationic PPV precursor poly(p-xylene tetrahydrothiophenium chloride) and anionic poly(sodium4-styrenesulfonate) (PSS), PPV/PSS complex was fabricated on the surface of pretreated quartz substrate by layer-by-layer electrostatic self-assembly method. UV-Vis spectrum shows that PSS in the PPV/PSS complex make PPV precursors thermally convert into PPV at a lower temperature and less time. PPV/ PSS/PPV/CdTe multilayer were fabricated on the surface of quartz substrate by electrostatic self-assembly method. The surface of the polymer/CdTe complex is flat, which was characterized by atomic force microscopy (AFM). UV-Vis spectrum of the polymer/CdTe complex shows that the absorbance increases with the increase of the number of deposition cycles. In the same way, PPV/PSS/PPV/CdTe multilayer were fabricated on the surface of ITO substrate disposed by the poly(3,4- ethylenedioxythiophene) poly(styrenesulfonate) (PEDOT:PSS). The resultant polymer/ CdTe complex is measured under AM1.5G simulated solar illumination with 100mW•cm-2 in air. The open circuit current density (VOC) and short circuit current density (JSC) of the polymer/CdTe complex are 0.60 V and 0.305 mA•cm-2 which are better than PPV or CdTe nanocrystal individual. This could be ascribed to interfacial hole-electron converter between the conjugated polymer layer and CdTe nanocrystal layer. Besides, the photovoltaic properties of PPV/CdTe complex can be improved by controlling the layers of PPV/ CdTe nanocrystals complex on the ITO substrate.

Abstract: Polymers have been known for their flexibility and easy processing into coatings and films, which made them suitable to be applied in a variety of areas and in particular the growing area of organic electronics. The electronic properties of semiconducting polymers made them a serious rival in areas where until now inorganic materials were the most used, such as light emitting diodes or solar cells. Typical polymers can be seen as a network of molecular strands of varied lengths and orientations, with a random distribution of physical and chemical defects which makes them an anisotropic material. To further increase their performance, a better understanding of all aspects related to charge transport and space charge distribution in polymeric materials is required. The process associated with charge transport depends on the properties of the polymer molecules as well as connectivity and texture, and so we adopt a mesoscopic approach to build polymer structures. Changing the potential barrier for charge injection we can introduce holes in the polymer network and, by using a generalised Monte-Carlo method, we can simulate the transport of the injected charge through the polymer layer caused by imposing a voltage between two planar electrodes. Our results show that the way that holes distribute within polymer layer and charge localization in these materials is quite different from the inorganic ones.

Abstract: Thin layers of the OLED related polyphenylene-vinylene (PPV) deposited by a precursor on micro-fabricated Si cantilevers were studied by applying the vibrating-reed technique during repeated temperature cycling between 100 and 520 K. By means of the Langmuir-Blodgett method for film production, the dependence of damping and elastic modulus on well defined values of film thickness (16 to 69 nm) was determined. Simultaneous measurements of these quantities showed four damping peaks during heating around 130 K (called γ), 250 K (β), 350 K (β’), and 400 K (called C). Three of them (γ, β’, C) disappeared after heating to the highest temperature (520 K) indicating their presence in the precursor only. The activation parameters of the relaxation peaks (γ, β, β’) were estimated and assigned to specific atomic movements in the molecule. Peak C occurs during the conversion process of precursor to polymer. Earlier results are essentially substantiated, indicating only slight differences to those for layers produced previously by spin coating. The observed thickness dependence of damping for the γ and β peaks suggests a weaker contribution of molecules in the surface region than of those in the bulk, while the β’ peak is supposed to result from molecules in the interface region between layer and substrate.