Electrochemical nanostructuring of (111) oriented GaAs crystals: from porous structures to nanowires.

A comparative study of the anodization processes occurring at the GaAs(111)A and GaAs(111)B surfaces exposed to electrochemical etching in neutral NaCl and acidic HNO3 aqueous electrolytes is performed in galvanostatic and potentiostatic anodization modes. Anodization in NaCl electrolytes was found to result in the formation of porous structures with porosity controlled either by current under the galvanostatic anodization, or by the potential under the potentiostatic anodization. Possibilities to produce multilayer porous structures are demonstrated. At the same time, one-step anodization in a HNO3 electrolyte is shown to lead to the formation of GaAs triangular shape nanowires with high aspect ratio (400 nm in diameter and 100 µm in length). The new data are compared to those previously obtained through anodizing GaAs(100) wafers in alkaline KOH electrolyte. An IR photodetector based on the GaAs nanowires is demonstrated.

Band tail state related photoluminescence and photoresponse of ZnMgO solid solution nanostructured films.

A series of Zn1- x Mg x O thin films with the composition range x = 0.00-0.40 has been prepared by sol-gel spin coating on Si substrates with a post-deposition thermal treatment in the temperature range of 400-650 °C. The morphology of the films was investigated by scanning electron microscopy and atomic force microscopy while their light emission properties were studied by photoluminescence spectroscopy under excitation at 325 nm. It was found that annealing at 500 °C leads to the production of macroscopically homogeneous wurtzite phase films, while thermal treatment at higher or lower temperature results in the degradation of the morphology, or in the formation of ZnO particles embedded into the ZnMgO matrix, respectively. Local compositional fluctuations leading to the formation of deep band tails in the gap were deduced from photoluminescence spectra. A model for the band tail distribution in the bandgap is proposed as a function of the alloy composition. Thin films were also prepared by aerosol spray pyrolysis deposition using the same sol-gel precursors for the purpose of comparison. The prepared films were tested for photodetector applications.

Strong light scattering and broadband (UV to IR) photoabsorption in stretchable 3D hybrid architectures based on Aerographite decorated by ZnO nanocrystallites.

In present work, the nano- and microscale tetrapods from zinc oxide were integrated on the surface of Aerographite material (as backbone) in carbon-metal oxide hybrid hierarchical network via a simple and single step magnetron sputtering process. The fabricated hybrid networks are characterized for morphology, microstructural and optical properties. The cathodoluminescence investigations revealed interesting luminescence features related to carbon impurities and inherent host defects in zinc oxide. Because of the wide bandgap of zinc oxide and its intrinsic defects, the hybrid network absorbs light in the UV and visible regions, however, this broadband photoabsorption behavior extends to the infrared (IR) region due to the dependence of the optical properties of ZnO architectures upon size and shape of constituent nanostructures and their doping by carbon impurities. Such a phenomenon of broadband photoabsorption ranging from UV to IR for zinc oxide based hybrid materials is novel. Additionally, the fabricated network exhibits strong visible light scattering behavior. The developed Aerographite/nanocrystalline ZnO hybrid network materials, equipped with broadband photoabsorption and strong light scattering, are very promising candidates for optoelectronic technologies.

Light-Induced Motion of Microengines Based on Microarrays of TiO2 Nanotubes.

An electrochemical approach for manufacturing light-driven nanostructured titanium dioxide (TiO2 ) microengines with controlled spatial architecture for improved performance is reported. The microengines based on microscale arrays of TiO2 nanotubes with variable (50-120 nm) inner diameter show a quasi-ordered arrangement of nanotubes, being the smallest tubular entities for catalytic microengines reported to date. The nanotubes exhibit well defined crystalline phases depending upon the postfabrication annealing conditions that determine the microengines' efficiency. When exposed to UV-light, the microarrays of TiO2 nanotubes exhibiting conical internal shapes show directed motion in confined space, both in the presence and absence of hydrogen peroxide. In the former case, two different motion patterns related to diffusiophoresis and localized nanobubble generation inside of the tubes due to the photocatalytic decomposition of H2 O2 are disclosed. Controlled pick-up, transport, and release of individual and agglomerated particles are demonstrated using the UV light irradiation of microengines. The obtained results show that light-driven microengines based on microarrays of TiO2 nanotubes represent a promising platform for controlled micro/nanoscale sample transportation in fluids as well as for environmental applications, in particular, for the enhanced photocatalytic degradation of organic pollutants due to the improved intermixing taking place during the motion of TiO2 microengines.