26 research outputs found

    Recent Advances in Conjugated Polymers for Light Emitting Devices

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    A recent advance in the field of light emitting polymers has been the discovery of electroluminescent conjugated polymers, that is, kind of fluorescent polymers that emit light when excited by the flow of an electric current. These new generation fluorescent materials may now challenge the domination by inorganic semiconductor materials of the commercial market in light-emitting devices such as light-emitting diodes (LED) and polymer laser devices. This review provides information on unique properties of conjugated polymers and how they have been optimized to generate these properties. The review is organized in three sections focusing on the major advances in light emitting materials, recent literature survey and understanding the desirable properties as well as modern solid state lighting and displays. Recently, developed conjugated polymers are also functioning as roll-up displays for computers and mobile phones, flexible solar panels for power portable equipment as well as organic light emitting diodes in displays, in which television screens, luminous traffic, information signs, and light-emitting wallpaper in homes are also expected to broaden the use of conjugated polymers as light emitting polymers. The purpose of this review paper is to examine conjugated polymers in light emitting diodes (LEDs) in addition to organic solid state laser. Furthermore, since conjugated polymers have been approved as light-emitting organic materials similar to inorganic semiconductors, it is clear to motivate these organic light-emitting devices (OLEDs) and organic lasers for modern lighting in terms of energy saving ability. In addition, future aspects of conjugated polymers in LEDs were also highlighted in this review

    Optical properties of poly(9,9’-di-n-octylfluorenyl-2.7-diyl)/amorphous SiO2 nanocomposite thin films

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    Identified as potential materials for optoelectronic applications, the polymer/inorganic nanocomposites are actively studied. In this work, the effect of amorphous silica nanoparticles (NPs) content on the optical properties of Poly (9,9’-di-n-octylfluorenyl- 2.7-diyl) (PFO) thin films has been investigated. Different ratios of PFO/SiO2 NPs composites have been prepared using solution blending method. Then, the blends were spin-coated onto glass substrates at 2000 rpm for 30 s and subsequently dried at room temperature. XRD and TEM were used to determine the structural properties, while UV-Vis and PL spectrophotometers were employed to investigate the optical properties of the films. XRD confirms that there was no variation on structure of both PFO and SiO2 NPs resulted from the blending process. TEM micrographs display that majority of amorphous SiO2 NPs were well coated with PFO. The absorption spectra of the composite thin films were red-shifted, indicating the increment in conjugation length of the PFO/SiO2 composite. In addition, the calculated values of the optical energy gap, the width of the energy tails and vibronic spacing of the composite films exhibited SiO2 content dependence

    Optical Properties and Amplified Spontaneous Emission of Novel MDMO-PPV/C500 Hybrid

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    The influence of the solvent nature on optical properties of poly[2-methoxy-5-3,7-dimethyloctyloxy-1,4-phenylenevinylene] (MDMO-PPV)/Coumarine 500 (C500) have been investigated. In addition, the amplified spontaneous emission (ASE) from MDMO-PPV and efficient energy transfer between the MDMO-PPV and C500 has been verified. The MDMO-PPV was dissolved in aromatic and nonaromatic solvents, while the solution blending method was employed to prepare the MDMO-PPV:C500 hybrid. The quantum yield of the MDMO-PPV was found to increase with the reduction of a few factors such as polarity index of the solvent, absorption cross section (σa), emission cross section (σe), and extinction coefficient (εmax). The fluorescence spectra of the MDMO-PPV appears from two vibronic band transitions (0-0, 0-1) and the ASE occurs at 0-1 transition, which was verified by the ASE from MDMO-PPV. The MDMO-PPV in toluene exhibited the best ASE efficiency due to its high quantum yield compared with other solvents. Strong overlap between the absorption spectrum of MDMO-PPV and emission spectrum of C500 confirmed the efficient energy transfer between them. Moreover, the ASE for energy transfer of the MDMO-PPV:C500 hybrid was proved

    Time Evolution of the Excimer State of a Conjugated Polymer Laser

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    An excited dimer is an important complex formed in nano- or pico-second time scales in many photophysics and photochemistry applications. The spectral and temporal profile of the excimer state of a laser from a new conjugated polymer, namely, poly (9,9-dioctylfluorenyl-2,7-diyl) (PFO), under several concentrations in benzene were investigated. These solutions were optically pumped by intense pulsed third-harmonic Nd:YAG laser (355-nm) to obtain the amplified spontaneous emission (ASE) spectra of a monomer and an excimer with bandwidths of 6 and 7 nm, respectively. The monomer and excimer ASEs were dependent on the PFO concentration, pump power, and temperature. Employing a sophisticated picosecond spectrometer, the time evolution of the excimer state of this polymer, which is over 400 ps, can be monitored

    Fabrication of Cost-Effective Dye-Sensitized Solar Cells Using Sheet-Like CoS2 Films and Phthaloylchitosan-Based Gel-Polymer Electrolyte

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    Platinum-free counter electrodes (CE) were developed for use in efficient and cost-effective energy conversion devices, such as dye-sensitized solar cells (DSSCs). Electrochemical deposition of CoS2 on fluorine-doped tin oxide (FTO) formed a hierarchical sheet-like structured CoS2 thin film. This film was engaged as a cost-effective platinum-free and high-efficiency CE for DSSCs. High stability was achieved using a phthaloychitosan-based gel-polymer electrolyte as the redox electrolyte. The electrocatalytic performance of the sheet-like CoS2 film was analyzed by electrochemical impedance spectroscopy and cyclic voltammetry. The film displayed improved electrocatalytic behavior that can be credited to a low charge-transfer resistance at the CE/electrolyte boundary and improved exchange between triiodide and iodide ions. The fabricated DSSCs with a phthaloychitosan-based gel-polymer electrolyte and sheet-like CoS2 CE had a power conversion efficiency (PCE, η) of 7.29% with a fill factor (FF) of 0.64, Jsc of 17.51 mA/cm2, and a Voc of 0.65 V, which was analogous to that of Pt CE (η = 7.82%). The high PCE of the sheet-like CoS2 CE arises from the enhanced FF and Jsc, which can be attributed to the abundant active electrocatalytic sites and enhanced interfacial charge-transfer by the well-organized surface structure

    An Efficient Violet Amplified Spontaneous Emission (ASE) from a Conjugated Polymer (PFO-co-pX) in Solution

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    The optical of conjugated polymer poly[(9,9-dioctylfluorenyl-2,7-diyl)-co-(2,5-p-xylene)] also known as [(PFO-co-pX), ADS145UV], dissolved in a few solvents, has been measured. The absorption, emission spectra, and quantum yield have been investigated by using a spectrophotometer and spectrofluorometer, respectively. The properties of Amplified Spontaneous Emission (ASE) of conjugated PFO-co-pX polymer under different conditions such as solvent type, concentration, and pumping energy have been examined by using the tripled frequency of a Nd:YAG laser as a source of pumping. The relation between output energy and pumping energy for the samples with different concentrations in three solvents has been studied. In addition, efficiency and optical gain from the ASE were measured. Additionally, the stability of this polymer as a laser material was investigated. Among the host of conjugated polymer lasers obtained by optical pumping, this conjugated polymer has exhibited only one ASE band under a wide range of concentrations and pump power values. This is most likely due to the steric hindrance by the copolymer segment pX (2,5-p-xylene). This investigation has provided new insights into the excited state dynamics of conjugated polymer materials and has shown that this new conjugated polymer is quite efficient in the violet region

    Hydrothermal synthesis of titanium dioxide nanoparticles: mosquitocidal potential and anticancer activity on human breast cancer cells (MCF-7)

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    Mosquito vectors (Diptera: Culicidae) are responsible for transmission of serious diseases worldwide. Mosquito control is being enhanced in many areas, but there are significant challenges, including increasing resistance to insecticides and lack of alternative, cost-effective, and eco-friendly products. To deal with these crucial issues, recent emphasis has been placed on plant materials with mosquitocidal properties. Furthermore, cancers figure among the leading causes of morbidity and mortality worldwide, with approximately 14 million new cases and 8.2 million cancer-related deaths in 2012. It is expected that annual cancer cases will rise from 14 million in 2012 to 22 million within the next two decades. Nanotechnology is a promising field of research and is expected to give major innovation impulses in a variety of industrial sectors. In this study, we synthesized titanium dioxide (TiO2) nanoparticles using the hydrothermal method. Nanoparticles were subjected to different analysis including UV–Vis spectrophotometry, Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), zeta potential, and energy-dispersive spectrometric (EDX). The synthesized TiO2 nanoparticles exhibited dose-dependent cytotoxicity against human breast cancer cells (MCF-7) and normal breast epithelial cells (HBL-100). After 24-h incubation, the inhibitory concentrations (IC50) were found to be 60 and 80 μg/mL on MCF-7 and normal HBL-100 cells, respectively. Induction of apoptosis was evidenced by Acridine Orange (AO)/ethidium bromide (EtBr) and 4′,6-diamidino-2-phenylindole dihydrochloride (DAPI) staining. In larvicidal and pupicidal experiments conducted against the primary dengue mosquito Aedes aegypti, LC50 values of nanoparticles were 4.02 ppm (larva I), 4.962 ppm (larva II), 5.671 ppm (larva III), 6.485 ppm (larva IV), and 7.527 ppm (pupa). Overall, our results suggested that TiO2 nanoparticles may be considered as a safe tool to build newer and safer mosquitocides and chemotherapeutic agents with little systemic toxicity
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