Electrical and optical properties of white organic light‐emitting devices using blue and orange phosphorescent materials

Abstract— Highly efficient white organic light‐emitting devices have been fabricated by doping phosphorescent orange and blue emitters into the separate layers of a single host. The efficiency and electroluminescence spectrum were strongly affected by the sequence of doped layers. The phosphorescent white devices exhibiting high efficiency and reasonable white balances are obtained when the recombination region is overlapped by the blue doped region. By using this principle, a simple structured phosphorescent white device with a peak power efficiency of 40.7 lm/W and Commission International de L'Eclairage coordinates of (0.43, 0.42) have been demonstrated.     

Double melting behavior of cyclic tris(ethylene terephthalate)

Summary Cyclic tris(ethylene terephthalate) (CTET) was separated from oligomeric extract of poly(ethylene terephthalate) by the conventional solvent separation method. The structure of CTET was characterized by differential scanning calorimetry, X-ray diffraction, and scanning electron microscopy. It is shown that the double melting behavior of meltcrystallized CTET is attributed to the morphological change created by heat-treatment. The effect of the morphological change on the crystal structure of CTET was also examined.     

The Effect of Aluminum Ions on the DC Etching of Aluminum Foil

A study has been made of the electrochemical etching of 99.99% aluminum foils at a current density of 50 mA cm^–2in AlCl₃–HCl solutions (1 m Cl^–) at 80 °C. The solutions were made by dissolving metallic aluminum into 1m HCl solution, to give a Cl^– concentration of 1 m. The number density of etch tunnels and the homogeneity of tunnel length decreased, and the mean pit size and its standard deviation increased with increasing Al³⁺ concentration. The results were discussed based on potential transients at a current density of 50 mA cm^–2, current–potential curves at a scan rate of 10 m Vs^–1 and electrochemical impedance spectra.     

Lonsdaleite diamond growth on reconstructed Si (100) by hot-filament chemical vapor deposition (HFCVD)

In this paper, the growth of Lonsdaleite diamond using hot-filament chemical vapor deposition (HFCVD) on flashed and reconstructed Si (100) is reported. Surface morphology studies using scanning electron microscopy (SEM) show that the film is composed of decahedron and icosahedron diamond particles. The X-ray diffraction (XRD) pattern has a strongest peak at 47° and a peak at 41°, which is indicative of Lonsdaleite nature of the grown diamond film. The Raman spectrum of the film shows a broadened diamond peak at wave number of 1,329 cm⁻¹, which has shifted towards the peak position corresponding to Lonsdaleite nature of the diamond (1,326 cm⁻¹).     

Surface characteristics of fluorine-modified PAN-based carbon fibers

Different fluorination methods were applied to modify the surface properties of carbon fibers. The relationship between the degree of fluorination and the physicochemical properties of carbon fibers was studied using a combination of mechanical tests, elemental analysis (EA), X-ray photoelectron spectrometry (XPS), and X-ray diffraction (XRD). EA and XPS analyses of fluorinated carbon fibers showed that treatment with mixtures of F₂/O₂ introduced a much higher fluorine concentration than that with F₂ only. However, XRD analysis showed that there was no increase in the interlayer distance, due to the mild fluorination condition applied. Consequently, the oxyfluorination was one of the more effective methods to increase surface polarity of carbon fibers, which probably played an important role in improving the tensile properties of the fibers in the epoxy resin system.     

Effect of hydrophobic hexafluoroisopropylidene group on the water sorption behaviors of rigid poly(p‐phenylene pyromellitimide) polyimide thin films

We prepared poly(p‐phenylene pyromellitimide) (PMDA–PDA), poly(p‐phenylene 4,4′‐hexafluoroisopropylidene diphthalimide), and their copolyimides with various compositions to explore the relationship between the water sorption and structure. The water sorption behaviors were gravimetrically investigated as a function of composition and temperature and interpreted with a Fickian diffusion model in films. Overall, the water sorption behaviors were strongly dependent on the changes in morphological structure, which originated from the variations in composition. When the content of the bulky hexafluoroisopropylidene group (6FDA) was increased, the water uptake decreased from 5.80 to 3.18 wt %, whereas the diffusion coefficient increased from 3.6 × 10^?10 to 11.3 × 10^?10 cm²/s. The relatively high water uptake in the PMDA–PDA polyimide film was successfully healed by the incorporation of 6FDA, which may have resulted from the increases in the intermolecular packing order and hydrophobicity. The degree of orientation and crystallinity, which are in‐plane characteristics, were directly correlated to the diffusion coefficient and activation energy in the polyimide film. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 3442–3446, 2003     

Protein Ligation-Assisted Reconstitution of Split HRP Fragments for Facile Production of HRP Fusion Proteins in E. coli

Horseradish peroxidase (HRP) is a pivotal biocatalyst for biosensor development and fine chemical synthesis. HRP proteins are mostly extracted and purified from the roots of horseradish because the solubility and productivity of recombinant HRP in bacteria are significantly low. In this study, we investigate the reconstitution system of split HRP fragments to improve its soluble expression levels in E. coli allowing the cost-effective production of bioactive HRPs. To promote the effective association between two HRP fragments (HRPn and HRPc), we exploit SpyTag-SpyCatcher chemistry, a versatile protein coupling method with high affinity and selectivity. Each HRP fragment was genetically fused with SpyTag and SpyCatcher, respectively, exhibiting soluble expression in the E. coli cytoplasm. The engineered split HRPs were effectively and irreversibly reconstituted into a biologically active and stable assembly that can catalyze intrinsic enzymatic reactions. Compared to the chaperone co-expression system, our approach shows that the production yield of soluble HRP is comparable, but the purity of the final product is relatively high. Therefore, our results can be applied to the high-yield production of recombinant HRP variants and other difficult-to-express proteins in bacteria without complex downstream processes.     

Photoluminescence properties of Eu-activated BaCa2Al8O15 nanophosphors

A new blue-emitting nanophosphor of Eu²⁺-activated BaCa₂Al₈O₁₅ was synthesized by the Pechini method. The phosphors were investigated by X-ray powder diffraction (XRD) measurement and confirmed to be a pure crystalline phase of BaCa₂Al₈O₁₅. The photoluminescence excitation and emission spectra, the luminescence decay and the color coordinates were taken to investigate the luminescence characteristics. The dependence of luminescence intensities BaCa₂Al₈O₁₅:Eu²⁺ on the doping concentrations was investigated. This nanophosphor can be efficiently excited by UV light and presents bright blue luminescence. Under the same conditions, the light yield of BaCa₂Al₈O₁₅:Eu²⁺ is about 1.2 times higher than that of blue-emitting phosphor BaMgAl₁₀O₁₇:Eu²⁺. Eu²⁺-activated BaCa₂Al₈O₁₅ nanophosphor exhibits the long-lasting phosphorescence, which was analyzed by measuring the afterglow decay curves. The co-doped Eu³⁺ ions and some defects were suggested to be the possible trap-centers.     

Enhancement of fibroblastic proliferation from photoreactive starch with immobilized epidermal growth factor

Carboxymethyl starch was modified by the incorporation of an azidophenyl group to prepare photoreactive starch, and characterized by Fourier transform infrared reflectance (FT‐IR), proton nuclear magnetic resonance (¹H‐NMR), and ultraviolet (UV) spectroscopy. Photo‐irradiation immobilized the Az‐starch on a polystyrene plate and it was stably retained on the surface. The protein containing immobilized Az‐starch was also immobilized on a stripe micropatterned plate. UV irradiation time and Az‐starch concentration were used to alter the physical properties of Az‐starch and consequently control the rate of epidermal growth factor (EGF) release. The Az‐starch that released growth factor was not cytotoxic to 3T3‐L1 fibroblast cells, and the immobilized EGF maintained its activity and induced cellular proliferation in vitro. These results suggest that Az‐starch could be useful as a clinical synthetic material for medical applications. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Synthesis of random or tapered solution styrene–butadiene copolymers in the presence of sodium dodecylbenzene sulfonate as a polar modifier

Random or tapered solution styrene–butadiene copolymer (SSBR) is very difficult to prepare in an isothermal batch process without the use of polar modifiers because of the diverse reactivity ratios of the styrene and the butadiene in hydrocarbon solvents. In the presence of polar modifiers, the random SSBR can be synthesized by anionic living polymerization with the variety of microstructures, which results in the change of glass transition temperature (T_g). This article will discuss the use of sodium dodecylbenzene sulfonate as a polar modifier in isothermal batch process that controls the microstructure of the SSBR resulting in a random as well as tapered SSBR with low T_g (?67°C to ?80°C). The T_g of SSBR was controlled by the styrene content rather than the microstructure of polybutadiene. Physical properties of SSBR compounding were discussed for tire tread applications. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013