Structural and electrical characteristics of high-κ Er2O3 and Er2TiO5 gate dielectrics for a-IGZO thin-film transistors

In this letter, we investigated the structural and electrical characteristics of high-κ Er₂O₃ and Er₂TiO₅ gate dielectrics on the amorphous indium-gallium-zinc-oxide (a-IGZO) thin-film transistor (TFT) devices. Compared with the Er₂O₃ dielectric, the a-IGZO TFT device incorporating an Er₂TiO₅ gate dielectric exhibited a low threshold voltage of 0.39 V, a high field-effect mobility of 8.8 cm²/Vs, a small subthreshold swing of 143 mV/decade, and a high I_on/I_off current ratio of 4.23 × 10⁷, presumably because of the reduction in the oxygen vacancies and the formation of the smooth surface roughness as a result of the incorporation of Ti into the Er₂TiO₅ film. Furthermore, the reliability of voltage stress can be improved using an Er₂TiO₅ gate dielectric.     

Temperature- and pH-responsive photosensitization activity of polymeric sensitizers based on poly-N-isopropylacrylamide

We previously reported that a copolymer consisting of N-isopropylacrylamide (NIPAM) and benzophenone (BP) units, behaves as a photosensitizer showing temperature-controlled oxygenation activity in water (J. Am. Chem. Soc.2006, 128, 8751). This polymer shows a heat-induced oxygenation enhancement at low temperature region (5-20 °C), while showing a heat-induced oxygenation suppression at high temperature region (20-60 °C), resulting in an off-on-off activity profile against the temperature window. This is driven by a heat-induced phase transition of the polymer from coil to micelle and then to globule states. In the present work, effects of adding an amine component (N-[3-(dimethylamino)propyl]acrylamide: DMAPAM) to the polymer on the sensitization activity were studied, where the relationship between the phase transition behavior and the activity was clarified by several spectroscopic analyses. The polymers, poly(NIPAM_x-co-BP_y-co-DMAPAM_z), show activity controlled by temperature and pH. The off-on-off activity profile shifts to higher temperature with a pH decrease. This is because protonation of the DMAPAM units leads to an increase in the polymer polarity and, hence, the polymer aggregates at higher temperature. In addition, increase in the DMAPAM content of the polymer leads to further shift of the activity profile. In contrast, at pH < 8, no activity enhancement is observed because complete protonation of the DMAPAM units suppresses polymer aggregation.     

添加钛、铌、锰、硫及镁对亚共晶灰铸铁初生奥氏体形核及生长的影响

共晶铸铁在共晶凝固时,熔体中碳的状态,即“C的微小集合体”已经被深入研究.然而时于与初生奥氏体密切相关的铁原子的状态,即“铁的微小集合体”却缺乏研究.本文作者提出,在亚共晶灰铸铁熔体中,初晶γ的形核受“Fe的富集部”的影响,而“Fe的富集部”的形成及消失与“C的微小集合体”有关.研究表明,初生奥氏体的形核过冷度、形核数和晶核生长形貌随工艺条件如过热度、保温时间和冷却速率而变化.本文讨论了在熔体的过热度、保温时间和冷却速率固定的条件下,钛、铌、锰、硫和镁这五种添加元素对亚共晶灰铸铁初晶γ的凝固过程的影响.     

Effects of processing and cooking on the levels of pesticide residues in soybean samples

The effects of processing and cooking on the levels of pesticide residues in soybean samples were investigated for 14 pesticides in pre-harvest samples. On soaking, the transfer ratios (%, total pesticide residue amount in product/that in soybean) of soaked soybean were greater than 60% for most of the pesticides investigated. The transfer ratio of soymilk ranged from 37% to 92%, and that of tofu ranged from 7% to 63%. The processing factor (Pf, the concentration (mg/kg) of pesticide in product/that in soybean) of tofu ranged from 0.026 to 0.28. These values varied among pesticides. There was a high correlation between the log P(ow) and the transfer ratio of tofu. The test described here should be useful to obtain the transfer ratios of pesticide residues in processing and/or cooking steps.     

A Hybrid Decoupled Power Flow Method for Balanced Power Distribution Systems

This paper proposes a hybrid decoupled power flow method for balanced power distribution systems with distributed generation sources.The method formulates the power flow equations in active power and reactive power decoupled form with polar coordinates.Second-order terms are included in the active power mismatch iteration,and constant Jacobian and Hessian matrices are used.A hybrid direct and indirect solution technique is used to achieve efficiency and robustness of the algorithm.Active power correction is solved by means of a sparse lower triangular and upper triangular(LU) decomposition algorithm with partial pivoting,and the reactive power correction is solved by means of restarted generalized minimal residual algorithm with an incomplete LU pre-conditioner.Typical distribution generation models and distribution load models are included.The impact of zero-impedance branches is explicitly modeled through reconfiguring of the adjacent branches with impedances.Numerical examples on a sample distribution system with widespread photovoltaic installations are given to demonstrate the effectiveness of the proposed method.     

The Ameliorative Effect of Dexamethasone on the Development of Autoimmune Lung Injury and Mediastinal Fat-Associated Lymphoid Clusters in an Autoimmune Disease Mouse Model

In our previous study, we revealed the ameliorative therapeutic effect of dexamethasone (Dex) for Lupus nephritis lesions in the MRL/MpJ-Fas ^lpr/lpr (Lpr) mouse model. The female Lpr mice developed a greater number of mediastinal fat-associated lymphoid clusters (MFALCs) and inflammatory lung lesions compared to the male mice. However, the effect of Dex, an immunosuppressive drug, on both lung lesions and the development of MFALCs in Lpr mice has not been identified yet. Therefore, in this study, we compared the development of lung lesions and MFALCs in female Lpr mice that received either saline (saline group “SG”) or dexamethasone (dexamethasone group “DG”) in drinking water as a daily dose along with weekly intraperitoneal injections for 10 weeks. Compared to the SG group, the DG group showed a significant reduction in the levels of serum anti-dsDNA antibodies, the size of MFALCs, the degree of lung injury, the area of high endothelial venules (HEVs), and the number of proliferating and immune cells in both MFALCs and the lungs. A significant positive correlation was observed between the size of MFALCs and the cellular aggregation in the lungs of Lpr mice. Therefore, this study confirmed the ameliorative effect of Dex on the development of lung injury and MFALCs via their regressive effect on both immune cells’ proliferative activity and the development of HEVs. Furthermore, the reprogramming of MFALCs by targeting immune cells and HEVs may provide a therapeutic strategy for autoimmune-disease-associated lung injury.     

Calcium Chloride (CaCl2) as Catalyst for Asymmetric Organic Reactions

Pybox–CaCl₂ was found to be an efficient chiral catalyst for asymmetric 1,4-addition reactions of 1,3-dicarbonyl compounds with nitroalkenes, affording γ-nitro carbonyl compounds in high yields with high enantioselectivities. The reactions proceeded smoothly even in air, and were successfully applied to a continuous flow system.     

Organofunctionalized catalyst surfaces highly active and selective for carbon–carbon bond-forming reactions

This article illustrates two types of organofunctionalized heterogeneous catalysts for variety of organic carbon–carbon bond-forming reactions, summarizing our previous reports and also presenting new data. Organic amines with an alkoxysilane moiety were immobilized on inorganic silica-alumina surfaces (SA-NR₂) by simple silane-coupling reactions between the silica-alumina surface (SA) and the alkoxysilane. This SA-NR₂ acted as acid–base bifunctional heterogeneous catalysts for carbon–carbon bond-forming reactions, such as cyano-ethoxycarbonylation, Michael reaction of nitriles, and nitro-aldol reaction. These reactions did not occur with either SA or homogeneous amine compounds. In addition, the mixture of SA and homogeneous amine showed low catalytic activity due to undesirable acid–base neutralization reaction. Achiral organic silane-coupling reagents with a variety of functional groups were also immobilized on a SiO₂ surface that had been immobilized with chiral bis(oxazoline) (BOX), to which Cu ions were coordinated to make chiral Cu–BOX complexes on the SiO₂ surface. The SiO₂-supported Cu–BOX complex catalyst functionalized with achiral 3-methacryloxypropyltrimethoxysilane dramatically increased enantioselectivity in the asymmetric Diels–Alder reaction of cyclopentadiene and 3-acryloyl-2-oxazolidinone. The organofunctionalized catalysts showed much better performances for the C–C bond-forming reactions compared to the corresponding homogeneous systems. The heterogeneous catalysts thus obtained were characterized by solid-state ¹³C and ²⁹Si MAS NMR, FT-IR, UV/vis, XAFS, ESR, XRF, and elemental analysis.     

Phthalocyanine molecular nanowires that were prepared using porous alumina as a template: Development in the sample preparation procedure to evaluate electronic properties

We have proposed the synthesis of organic molecular nanowires using porous alumina as a template. We also proposed the use of a magnetic field to control the molecular packing structure in the nanowires. In this paper, we developed the method to evaluate the electronic properties of the nanowire of a phthalocyanine derivative that was synthesized using porous alumina as a template. The developed method facilitates the study in the organic molecular nanowires that were synthesized using templates and helps their use in future electronic devices.     

Depression of melting point of eutectic metal alloy by the interaction with polyacrylates in metal-polymer composites

The composites of polyacrylates and eutectic metal alloy composed by Bi, In, and Sn were prepared by mixing the metal and polymer above the melting point of the metal alloy (80 °C) with a homogenizer. Two melting peaks, which were assigned as the melting peak of the original metal alloy and that of the interfacial phase of the metal alloy interacting with polyacrylates (70 °C) by differential scanning calorimetry. Metal particles with the diameter of about 100 nm which were stabilized by the interfacial interaction with polyacrylates were observed by transmission electron microscopy. The melting peak at 70 °C was assigned as the melting peak of these small particles.