Articles you may be interested inThe Cr-substitution concentration dependence of the structural, electric and magnetic behaviors for Aurivillius Bi5Ti3FeO15 multiferroic ceramics J. Appl. Phys. 114, 234101 (2013); 10.1063/1.4849055Conversion of CH4/CO2 to syngas over Ni-Co/Al2O3-ZrO2 nanocatalyst synthesized via plasma assisted coimpregnation method: Surface properties and catalytic performance Synthesis of TiO 2 nanoparticles by hydrolysis and peptization of titanium isopropoxide solution AIP Conf.The structural, optical and dielectric properties of as-grown Cr 2 O 3 nanostructures are demonstrated in this paper. Powder X-ray diffractometry analysis confirmed the rhombohedral structure of the material with lattice parameter, a = b = 4.953 Å; c = 13.578 Å, and average crystallize size (62.40 ± 21.3) nm. FE-SEM image illustrated the mixture of different shapes (disk, particle and rod) of as-grown nanostructures whereas; EDS spectrum confirmed the elemental purity of the material. FTIR spectroscopy, revealed the characteristic peaks of Cr-O bond stretching vibrations. Energy band gap (3.2 eV) of the nanostructures has been determined using the results of UV-VIS-NIR spectrophotometer. The dielectric properties of the material were checked in the wide frequency region (100Hz-30 MHz). In the low frequency region, the matrix of the dielectric behaves like source as well as sink of electrical energy within the relaxation time. Low value of dielectric loss exhibits that the materials posses good optical quality with lesser defects. The ac conductivity of the material in the high frequency region was found according to frequency power law. The physical-mechanism and the theoretical-interpretation of dielectric-properties of Cr 2 O 3 nanostructures attest the potential candidature of the material as an efficient dielectric medium. C 2014 Author(s). All article content, except where otherwise noted, is licensed under a Creative Commons Attribution 3.0 Unported License.
Anatase titania films with a thickness of up to 20 μm and deposited over a fluorine-doped tin-oxide substrate are impregnated with ruthenium dyes N-719 and N-749 using Dip and supercritical-fluid methods for the purpose of fabricating dye-sensitized solar cell devices. The dyes are dissolved in different solvent mixtures, including supercritical carbon dioxide, as well as combinations of more traditional solvents including mixtures of acetonitrile, and t-butanol. Analytical studies included thin-film analyzing and scanning electron microscopy to measure titania film thickness and porosity, UV-Vis spectroscopy to quantify dye concentration, and current-voltage device characterizations to assess energy conversion efficiency, as well as open-circuit voltage decay measurements and quantum efficiency to examine electron collection efficiency. A significant result is that using the dye N-749 in a solvent that includes supercritical carbon dioxide leads to energy conversion efficiencies that are higher for devices with a thick 20 μm semiconductor film than for the case of devices with thinner films, including the 10 μm film thickness that is traditionally considered an upper threshold. The supercritical-fluid method for the N-719 dye also enabled shorter impregnation duration than more conventional classical Dip Methods.
The formation of methylammonium lead iodide (CH3NH3PbI3) perovskite into mesoporous titania (TiO2) scaffold via a sequential deposition method is known to offer high quality films for good photovoltaic device performance. The local kinetics at the lower interface between the mesoporous TiO2 film and the collecting electrode govern perovskite growth and formation. Here, we have used a NanoPlasmonic Sensing (NPS) approach with gold (Au) nanosensors to monitor the formation of CH3NH3PbI3 perovskite at the lower interface of up to 650 nm mesoporous TiO2 films. This technique provides time-resolved spectral shifts of the localized surface plasmon resonance at different operating temperatures and methylammonium iodide (CH3NH3I3) concentrations by recording changes in the local vicinity of the Au nanosensors at the mesoporous TiO2 film interface. Analytical studies included ellipsometry, scanning electron microscopy, X-ray diffraction, and photoluminescence spectroscopy. The results show that both the intensity of the NPS response and NPS rate constants are correlated with the operating concentrations and temperatures of CH3NH3I3 as well as CH3NH3PbI3 perovskite growth in mesoporous TiO2.
A new nondestructive quantitative method is developed to measure the adsorption of dyes in solid titania films for dye-sensitized solar cells. UV-vis spectroscopy study showed that the absorbance of dye in the solid film can be directly related to the absorbance measured by the typical destructive method used to quantify concentration. Concentrations of N-719 and N-749 dyes on solid titania films were successfully extracted using molar extinction coefficients of dye on solid titania films with value of 6916 and 6454 L•cm −1 •mol −1 respectively determined using the spectral peaks at 512 and 586 nm.
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