Improved efficiency of polymer light-emitting diodes by inserting a hole transport layer formed without thermal treatment above glass transition temperature

We have demonstrated a significant improvement in the performance of polymer light-emitting diodes (PLEDs) by inserting the fluorene-triatylamine copolymer as hole transport layer (HTL) without a thermal treatment above the glass transition temperature (T_g). A thin HTL insolubilized by a thermal treatment above T_g is often inserted as an interlayer between an anode buffer layer and a light-emitting polymer (LEP) in PLEDs fabricated by using a conventional solution process. The evaporative spray deposition using ultradiluted solution (ESDUS) method has enabled fabricating polymer bilayer structure without an insolublizing procedure. The bilayer PLEDs fabricated by ESDUS without the thermal treatment showed significantly higher and more stable external quantum efficiency than PLEDs having the conventional interlayer. Thermal treatment above T_g of the copolymer would induce degradation of its hole injection property. Furthermore, ESDUS bilayer devices showed much higher power efficiency than interlayer devices when calcium was used for cathode. The improvements would be caused by the enhancement of hole injection and the effective electron blocking at the copolymer/LEP interface in the ESDUS bilayer devices.     

A carrier injection type optical switch in GaAs using free carrierplasma dispersion with wavelength range from 1.06 to 1.55 μm

The switching current for the device is about 90 mA at all in-range wavelengths. Its broad wavelength range is suitable for optical signal-processing applications in wavelength-division multiplexing transmission systems. High coupling efficiency to a single-mode fiber is achieved by using a small-Δ waveguide structure with carrier blocking layers. The effective refractive index change in the waveguide per unit of the injected current density is doubled by the carrier blocking layers without reducing coupling efficiency     

EFFECT OF NONSOLVENT ADDITIVES ON THE PORE SIZE AND THE PORE SIZE DISTRIBUTION OF AROMATIC POLYAMIDE RO MEMBRANES

In this paper discussions are made on the effect of nonsolvent swelling agents on the average pore size and pore size distributions at the surface of polyamide membranes which result from casting solutions involving above nonsolvent swelling agents.

The size of the polymer aggregate in the film casting solution and the size of polymer network pores are correlated to physicochemical data of ions which constitute the electrolytes used as nonsolvent swelling agents. As such ionic properties the charge density and the free energy of transition of ions from polyamide phase to water phase were considered. The validity of the correlation is limited in a range of casting solution composition where the polymer concentration in the casting solution is close to the limiting concentration of polymer at the phase boundary and the molar ratio of the nonsolvent swelling agent to the amide group involved in the polyamide polymer is equal to or slightly more than 0.7.     

Study on chemical structures of poly (tetrafluoroethylene-co-perfluoroalkylvinylether) by soft-EB irradiation in solid and molten state

Poly (tetrafluoroethylene-co-perfluoroalkylvinylether) (PFA) was irradiated by soft electron beam (soft-EB) under nitrogen gas atmosphere in solid-state and its molten state, respectively. The changes of thermal property and chemical structures of irradiated PFA in solid-state and molten state were studied by differential scanning calorimetric analysis (DSC) and solid-state ¹⁹F magic angle spinning (MAS) nuclear magnetic resonance (NMR) spectroscopy. By DSC analysis, the melting temperature shifted to lower temperatures, and crystallinity decreased with increasing soft-EB dose. By solid-state ¹⁹F MAS NMR spectroscopy, the new signals was observed and the detected new signals in irradiated PFA at 315 °C and at 30 °C were due to the tertiary carbon group with branching site (Y-type crosslinking site), perfluoro-propylene site and chain end methylene groups, respectively.Moreover, the molar ratio of perfluoroalkylvinylether (FAVE) structure to -CF₂- units decreased with increasing dose.     

An application of the 2-nitrobenzenesulfenyl method to proteomic profiling of human colorectal carcinoma: A novel approach for biomarker discovery

In the development of novel biomarkers, the proteomic approach is advantageous because using it the cancer-associated proteins can be directly identified. We previously developed a 2-nitrobenzenesulfenyl (NBS) method to improve quantitative proteome analysis. Here, we applied this method to proteomic profiling of colorectal carcinoma (CRC) to identify novel proteins with altered expression in CRC. Each pair of tumor and normal tissue specimens from 12 CRC patients was analyzed, and approximately 5000 NBS-labeled paired peaks were quantified. Peaks with altered signal intensities (>1.5-fold) and occurring frequently in the samples (>70%) were selected, and 128 proteins were identified by MS/MS analyses as differentially expressed proteins in CRC tissues. Many proteins were newly revealed to be CRC related; 30 were reported in earlier studies of CRC. Six proteins that were up-regulated in CRC (ZYX, RAN, RCN1, AHCY, LGALS1, and VIM) were further characterized and validated by Western blot and immunohistochemistry. All six were found to be CRC-localized, either in cancer cells or in stroma cells near the cancer cells. These results indicate that the proteins identified in this study are novel candidates for CRC markers, and that the NBS method is useful in proteome mining to discover novel biomarkers.     

Inhibition of resistance to hemopoietic allo-grafts in granulocyte colony-stimulating factor transgenic mice

The measurements of diphenylhexatriene (DPH) and trimethylammonium diphenylhexatriene (TMA-DPH) fluorescence anisotropy in egg yolk lecithin (EYL) and of DPH anisotropy in dipalmitoylphosphatidylcholine (DPPC) liposomes containing different concentrations of oxidized and reduced ubiquinone (UQ) and plastoquinone (PQ) homologues have been performed. All the oxidized UQ homologues strongly induced ordering of EYL membrane structure, whereas in DPPC liposomes, above the phase transition temperature, the most pronounced effect showed UQ-4. PQ-2 and PQ-9 were less effective than the corresponding ubiquinones in this respect. The reduced forms of UQ and PQ homologues increased the order of membrane lipids to a smaller extent than the corresponding quinones both in the interior of the membrane and closer to its surface. Nevertheless, the investigated prenylquinols showed stronger increase in the membrane order than alpha-tocopherol or alpha-tocopherol acetate, which could be connected with binding of prenylquinol head groups to phospholipid molecules by hydrogen bonds. The strong ordering influence of ubiquinones on the membrane structure was attributed to methoxyl groups of the UQ quinone rings.