An electrochemical approach for manufacturing light-driven nanostructured titanium dioxide (TiO ) microengines with controlled spatial architecture for improved performance is reported. The microengines based on microscale arrays of TiO 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 TiO 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 H O 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 TiO 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 TiO microengines.

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.

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In this paper, we show that long-duration-photoconductivity decay (LDPCD) and persistent photoconductivity (PPC) in porous InP structures fabricated by anodic etching of bulk substrates can be controlled through the modification of the sample morphology. Particularly, the PPC inherent at low temperatures to porous InP layers with the thickness of skeleton walls comparable with pore diameters is quenched in structures consisting of ultrathin walls produced at high anodization voltages. The relaxation of photoconductivity in bulk InP substrates, porous layers, and utrathin membranes is investigated as a function of temperature and excitation power density. The obtained results suggest that PPC in porous InP layers is due to porosity induced potential barriers which hinder the recombination of photoexcited carriers, while the photoconductivity relaxation processes in ultrathin membranes are governed by surface states.

Titania nanotube arrays have been prepared by anodic oxidation of titanium foils in an electrolyte solution containing a mixture of hydrofluoric acid, ethylene glycol, and phosphoric acid. The initially amor phous nanotubes were found to crystalize in an anatase phase upon thermal treatment at 500°C. Anatase crys talline phase showed a significant improvement in the photocatalytic properties of the prepared samples, which was evaluated by studying their efficiency towards Rhodamine B dye degradation. Additionally, the effect of doping titania nanotubes with noble metals (e.g. Ag, Pt, and Au), or covering their surface with noble metal nanoparticles, was studied regarding their capabilities towards the photocatalytic degradation of Rhodamine B dye. A positive effect when samples were doped with Ag was revealed.

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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.