On the determination of the glass forming ability of AlxZr1−x alloys using molecular dynamics, Monte Carlo simulations, and classical thermodynamics J. Appl. Phys. 112, 073508 (2012) Enhanced photoanode properties of epitaxial Ti doped α-Fe2O3 (0001) thin films Appl. Phys. Lett. 101, 133908 (2012) Structure and optical band gap of ZnO1−xSx thin films synthesized by chemical spray pyrolysis for application in solar cells J. Appl. Phys. 112, 063708 (2012) Roto-flexoelectric coupling impact on the phase diagrams and pyroelectricity of thin SrTiO3 films J. Appl. Phys. 112, 064111 (2012) Plasmonic effects of ultra-thin Mo films on hydrogenated amorphous Si photovoltaic cells
Two-dimensional silicon nanodome arrays are prepared on large areas up to 50 cm² exhibiting photonic band structure effects in the near-infrared and visible wavelength region by downscaling a recently developed fabrication method based on nanoimprint-patterned glass, high-rate electron-beam evaporation of silicon, self-organized solid phase crystallization and wet-chemical etching. The silicon nanodomes, arranged in square lattice geometry with 300 nm lattice constant, are optically characterized by angular resolved reflection measurements, allowing the partial determination of the photonic band structure. This experimentally determined band structure agrees well with the outcome of three-dimensional optical finite-element simulations. A 16% photonic bandgap is predicted for an optimized geometry of the silicon nanodome arrays. By variation of the duration of the selective etching step, the geometry as well as the optical properties of the periodic silicon nanodome arrays can be controlled systematically.
A systematic study was carried out on the equilibrium phases after slow solidification of the Zr41Ti14Cu12.5Ni10Be22.5 alloy. The crystalline microstructure of the slowly cooled melt of the alloy shows “polygons” and “plates” embedded in a fine-grained two-component matrix. To analyze the crystal structure of the different components, microdiffraction technique combining convergent beam electron diffraction and conventional selected-area electron diffraction were used. The stoichiometry of these phases was confirmed by field ion microscopy with atom probe and energy-dispersive x-ray analysis in a transmission electron microscope. The polygons were determined to be cubic (a = 1.185 nm) with space group Fm3m (cF116). The plates were found to be tetragonal (a = 0.37 nm, c = 1.137 nm) with space group I4/mmm (tI6). Its composition is (Cu + Ni)(Zr + Ti)2. One phase of the fine-grained two-component matrix was rich in Ti and poor in Be; the other one was rich in Be and poor in Ti. The Ti-rich phase was determined to be hexagonal (a = 0.536 nm, c = 0.888 nm) with space group P63/mmc.
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