Zn-triggered critical behavior of the formation of highly coherent domains in a Mg1-xZnxO thin film on Al2O3

A series of Mg1-xZnxO (x=0, 0.05, 0.10, and 0.15) thin films were grown by metal-organic chemical vapor deposition on a (0001) sapphire substrate, and the structural characteristics of Mg1-xZnxO thin films were investigated by synchrotron x-ray diffraction. The increasing amount of Zn was found to gradually enhance the structural coherence of Mg1-xZnxO films. For a sample with 15 at. % of Zn, in particular, the formation of highly coherent domains in Mg1-xZnxO was observed to be triggered, with an accompanying phase separation of ZnO. An integrated intensity analysis predicted that the critical concentration x(c) of Zn at which the phase separation occurred was 0.086+/-0.015, and that the highly coherent domains in Mg1-xZnxO accounted for 12+/-1%.open11910sciescopu

Temperature-driven crystalline ordering and Ohmic contact formation of PdAu layers on p-type GaN

We have investigated the effect of thermal annealing on the electrical characteristics of Pd/Au contact layer to p-GaN and on its crystalline ordering. While an as-deposited Pd/Au layer on p-GaN showed Schottky-contact characteristics. a thermally annealed Pd/Au layer yielded Ohmic characteristics, accompanying single-crystalline ordering with an abrupt interface with GaN. The Ohmic contact characteristics and crystalline ordering of PdAu layer were attributed to the substantial elimination of oxidation layers at the interface during thermal annealing.open116sciescopu

Induction of microglial toll-like receptor 4 by prothrombin kringle-2: a potential pathogenic mechanism in Parkinson's disease

Microglia-mediated neuroinflammation may play an important role in the initiation and progression of dopaminergic (DA) neurodegeneration in Parkinson's disease (PD), and toll-like receptor 4 (TLR4) is essential for the activation of microglia in the adult brain. However, it is still unclear whether patients with PD exhibit an increase in TLR4 expression in the brain, and whether there is a correlation between the levels of prothrombin kringle-2 (pKr-2) and microglial TLR4. In the present study, we first observed that the levels of pKr-2 and microglial TLR4 were increased in the substantia nigra (SN) of patients with PD. In rat and mouse brains, intranigral injection of pKr-2, which is not directly toxic to neurons, led to the disruption of nigrostriatal DA projections. Moreover, microglial TLR4 was upregulated in the rat SN and in cultures of the BV-2 microglial cell line after pKr-2 treatment. In TLR4-deficient mice, pKr-2-induced microglial activation was suppressed compared with wild-type mice, resulting in attenuated neurotoxicity. Therefore, our results suggest that pKr-2 may be a pathogenic factor in PD, and that the inhibition of pKr-2-induced microglial TLR4 may be protective against degeneration of the nigrostriatal DA system in vivo