6,198 research outputs found

    High performance thin film transistor with low temperature atomic layer deposition nitrogen-doped ZnO

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    High performance thin film transistor (TFT) with atomic layer deposition (ALD) nitrogen doped ZnO (ZnO:N) as an active layer is demonstrated. The electrical properties of ZnO thin films were effectively controlled by in situ nitrogen doping using NH4OH as a source for reactants. Especially, the electron concentration in ZnO was lowered to below 10(15) cm(-3). Good device characteristics were obtained from the inverted staggered type TFTs with ZnO:N channel and ALD Al2O3 gate insulator; mu(sat)=6.7 cm(2)/V s, I-off=2.03x10(-12) A, I-on/off=9.46x10(7), and subthreshold swing=0.67 V/decade. The entire TFT fabrication processes were carried out at below 150 degrees C, which is a favorable process for plastic based flexible display. (C) 2007 American Institute of Physics.X11126sciescopu

    Kinetics of the reduction of wüstite by hydrogen and carbon monoxide for the chemical looping production of hydrogen

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    Hydrogen of very high purity can be produced via the steam-iron process, in which steam oxidises metallic Fe in 3/4Fe + H2O→1/4Fe3O4 + H2. It is then advantageous to oxidise Fe3O4 in air to Fe2O3, an oxygen-carrier. This higher oxide of Fe is then reduced to regenerate metallic iron by reacting with synthesis gas, producing metallic Fe and possibly some wüstite (FexO, 0<x<1). In this three-stage process, the reduction of FexO to Fe is the slowest reaction. This paper is concerned with the kinetics of the reduction of wüstite (FexO) by reaction with CO, and, or H2. Starting with pure (99 wt%) wüstite, the intrinsic kinetics of its reduction to metallic iron were measured in fluidised beds at different temperatures. The reaction was found to have 3 distinct stages, (i) the removal of lattice oxygen in wüstite, (ii) rate increasing with conversion of solid and (iii) rate decreasing with conversion of solid. A random pore model was used to simulate the latter stages of the reduction of wüstite by either H2 or CO or a mixture of the two. It was found that the intrinsic rate of reduction in H2 is substantially faster than with CO, whereas the resistances to diffusion of H2 and CO through the product layer of Fe are comparable; these factors account for differences in the overall rates observed with these gases.This is the final published version. It is also available from the publisher at: http://www.sciencedirect.com/science/article/pii/S000925091400428X

    Sphingosine mediates FTY720-induced apoptosis in LLC-PK1 cells

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    FTY720, a synthetic sphingoid base analog, was examined as a new sphingosine kinase inhibitor, which converts endogenous sphingosine into its phosphate form. With 20 ??M of FTY720, sphingosine accumulated in the LLC-PK1 cells in a time- and dose-dependent manner. The FTY720 treated cells showed a high concentration of fragmented DNA, a high caspase-3 like activity and TUNEL staining cells. It was also found that the sphingosine and sphinganine level increased in a time- and dose-dependent manner within 12 h after the FTY720 treatment. The sphingosine kinase activity was reduced by FTY720 as much as other sphingosine kinase inhibitors, N, N-dimethylsphingosine (DMS), dl-threo-dihydrosphingosine (DHS). The fragmented DNA content as a result of the 20 ??M of FTY720 treatment and by 5 ??M of the exogenously added BSA-sphingosine complex indicated typical apoptosis. Under similar conditions, the accumulated sphingosine concentration in all the cells was almost identical even though the sphingosine distribution inside the cells was somewhat different. These results indicate that the FTY720 induced apoptosis is associated with the inhibition of the sphingosine kinase activity and is strongly associated with the successive accumulation of sphingosine.open172

    Crystal Structure of the Rad3/XPD regulatory domain of Ssl1/p44

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    The Ssl1/p44 subunit is a core component of the yeast/mammalian general transcription factor TFIIH, which is involved in transcription and DNA repair. Ssl1/p44 binds to and stimulates the Rad3/XPD helicase activity of TFIIH. To understand the helicase stimulatory mechanism of Ssl1/p44, we determined the crystal structure of the N-terminal regulatory domain of Ssl1 from Saccharomyces cerevisiae. Ssl1 forms a von Willebrand factor A fold in which a central six-stranded beta-sheet is sandwiched between three alpha helices on both sides. Structural and biochemical analyses of Ssl1/p44 revealed that the beta 4-alpha 5 loop, which is frequently found at the interface between von Willebrand factor A family proteins and cellular counterparts, is critical for the stimulation of Rad3/XPD. Yeast genetics analyses showed that double mutation of Leu-239 and Ser-240 in the beta 4-alpha 5 loop of Ssl1 leads to lethality of a yeast strain, demonstrating the importance of the Rad3-Ssl1 interactions to cell viability. Here, we provide a structural model for the Rad3/XPD-Ssl1/p44 complex and insights into how the binding of Ssl1/p44 contributes to the helicase activity of Rad3/XPD and cell viability.X1165Ysciescopu

    Exploring the influence of iron substitution in lithium rich layered oxides Li2Ru1-:XFexO3: Triggering the anionic redox reaction

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    Lithium rich layered materials are an interesting class of materials which exploit both anionic and cationic redox reactions to store energy upwards of 250 mA h g-1. This paper aims to understand the nature of the redox reactions taking place in these compounds. Li2RuO3 was used as the base compound, which is then compared with compounds generated by partially substituting Ru with Ti and Fe respectively. Electrochemical tests indicate that Fe substitution in the sample leads to an improvement in capacity, cycle life and reduction of potential decay. To elucidate the reason for this improvement in operando diffraction experiments were carried out, highlighting the formation of a secondary de-lithiated phase. The distortion of the pristine structure eventually induces frontier orbital reorganization leading to the oxygen redox reaction resulting in extra capacity. Local changes at Fe and Ru ions are recorded using in operando X-ray absorption spectroscopy (XAS). It was noted that while Ru undergoes a reversible redox reaction, Fe undergoes a significant irreversible change in its coordination environment during cycling. The changes in the coordination environment of oxygen and formation of O2n- type species were probed in situ using soft X-rays
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