Optimization of a New ZnO Nanorods Hydrothermal Synthesis Method for Solid State Dye Sensitized Solar Cells Applications

We report on the growth control of zinc oxide nanorods to point out the effect of the ZnO nanorods quality on the power conversion efficiency (PCE) of transparent conductive oxide (TCO)/ZnO nanorods/dye/spiro-OMe-TAD/metal electrode photovoltaic devices. A promising PCE of 0.61% was measured for the best nanorods growth conditions. A careful control of all the growth parameters during the seeds layer deposition and the hydrothermal synthesis was necessary to reach such a high PCE for this kind of device. A regular nanorod layer with a flat upper surface was obtained for ethylenediamine to zinc acetate dihydrate molar ratio equal to 1.74 and a pH of 8.2. The growth was performed at 65 degrees C for 2 h to avoid zinc oxide brushes deposition on the surface, arising from zinc hydroxyacetate decomposition during the hydrothermal treatment. The effect of ZnO nanorods length (ranging from 1 to 3 mu m) on solar cell efficiency was tested. Although the UV-vis absorption increases when the nanorods length increases, the best photovoltaic parameters were measured for the shortest nanorods length studied (1 mu m)

Effect of ball-milling and Fe-/Al-doping on the structural aspect and visible light photocatalytic activity of TiO2 towards Escherichia coli bacteria abatement

Escherichia coil abatement was studied in liquid phase under visible light in the presence of two commercial titania photocatalysts, and of Fe- and Al-doped titania samples prepared by high energy ball-milling. The two commercial titania photocatalysts, Aeroxide P25 (Evonik industries) exhibiting both rutile and anatase structures and MPT625 (Ishihara Sangyo Kaisha), a Fe-, Al-, P- and S-doped titania exhibiting only the rutile phase, are active suggesting that neither the structure nor the doping is the driving parameter. Although the MPT625 UV-visible spectrum is shifted towards the visible domain with respect to the P25 one, the effect on bacteria is not increased. On the other hand, the ball milled iron-doped P25 samples exhibit low activities in bacteria abatement under visible light due to charge recombinations unfavorable to catalysis as shown by photoluminescence measurements. While doping elements are in interstitial positions within the rutile structure in MPT625 sample, they are located at the surface in ball milled samples and in isolated octahedral units according to Fe-57 Mossbauer spectrometry. The location of doping elements at the surface is suggested to be responsible for the sample cytotoxicity observed in the dark. (C) 2014 Elsevier B.V. All rights reserved