Strain-tunable optical microlens arrays with deformable wrinkles for spatially coordinated image projection on a security substrate.

As a new concept in materials design, a variety of strategies have been developed to fabricate optical microlens arrays (MLAs) that enable the miniaturization of optical systems on the micro/nanoscale to improve their characteristic performance with unique optical functionality. In this paper, we introduce a cost-effective and facile fabrication process on a large scale up to ~15 inches via sequential lithographic methods to produce thin and deformable hexagonally arranged MLAs consisting of polydimethylsiloxane (PDMS). Simple employment of oxygen plasma treatment on the prestrained MLAs effectively harnessed the spontaneous formation of highly uniform nanowrinkled structures all over the surface of the elastomeric microlenses. With strain-controlled tunability, unexpected optical diffraction patterns were characterized by the interference combination effect of the microlens and deformable nanowrinkles. Consequently, the hierarchically structured MLAs presented here have the potential to produce desirable spatial arrangements, which may provide easily accessible opportunities to realize microlens-based technology by tunable focal lengths for more advanced micro-optical devices and imaging projection elements on unconventional security substrates.

Structural and electrical properties of ZnO films deposited with low-temperature facing targets magnetron sputtering (FTS) system with changes in H2 and O2 flow rate.

ZnO has been studied as a strong candidate for high-quality TCO in accordance with increasing demand to replace ITO. The origin of n-doping in ZnO is not clearly understood, but recently, the H2 effect has received attention due to the role it plays in O-rich and O-poor conditions. In spite of recent rapid developments, controlling the electrical conductivity of ZnO has remained a major challenge. To control the electrical conductivity of ZnO, this study was performed using an FTS system with H2 and O2 addition at low processing temperature. The structural and electrical properties of ZnO thin films deposited at various H2 and O2 flow rates were investigated using XRD and a sheet resistance meter. In response to changes in H2 and O2 flow rates, the crystallization and related grain size of the ZnO films were somewhat changed. The sheet resistance increased from approximately 10(-1) to approximately 10(4) M ohm/sq. when the O2 flow rate was increased, and the resistance decreased from approximately 10(-1) to approximately 10(-4) M ohm/sq. when the H2 flow rate was increased. The increase of sheet resistance with O2 flow rates could be explained by decrease of oxygen vacancies. The decrease of sheet resistance with H2 flow rates could be explained by increase of the electrons from interstitial hydrogen atoms. The plasma characteristics were analyzed using optical emission spectroscopy (OES). But, the overall spectrum did not change with the H2 and O2 gas flow rates. So, the dramatic changes in the electrical properties of ZnO thin films could be considered to be a result of changes in chemical composition of the thin films rather than the plasma status.

Influence of electrolytes (TEABF4 and TEMABF4) on electrochemical performance of graphite oxide derived from needle coke.

The structure of needle coke was changed to graphite oxide structure after oxidation treatment with 70 wt.% of nitric acid and sodium chlorate (NaClO3), and the inter-layer distance of the oxidized needle coke was expanded to 6.9 angstroms. The first charge profile of the oxidized needle coke-cell with 1.2 M TEMABF4/acetonitrile solution displayed that the intercalation of electrolyte ions into the inter-layer occurred at 1.0 V, which value is lower than 1.3 V of the oxidized needle coke-cell with 1.2 M TEABF4/acetonitrile solution. After first charge/discharge, the cell using TEMABF4 electrolyte exhibited smaller electrode resistance of 0.05 omega, and larger specific volume capacitance of 25.5 F/ml at the two-electrode system in the potential range 0-2.5 V than those of the cell using TEABF4 electrolyte. Compared to the TEABF4 electrolyte, better electrochemical performance of the TEMABF4 electrolyte in the oxidized needle coke may be caused by the smaller cation (TEMA+) size and better ion mobility in the nanopores between inter-layers.