New phase-pure nanohybrids of dichlorprop[2(2,4-dichlorophenoxy)propionate]-intercalated Zn/Al-LDH were successfully prepared using either co-precipitation or ion exchange methods. The basal spacing expansion from 8.9 Å in the layered double hydroxide (LDH) to 18.7 and 21.7 Å of the nanohybrids was observed. This together with FTIR, DTG/TGA and compositional studies show that dichlorprop was successfully intercalated into the Zn/Al-layered double hydroxides interlayer. Release study of dichlorprop showed that it is dependent on the concentration of the incoming ionic species and governed by the pseudo-second order kinetic. This study suggests that the layered double hydroxide might be used as a matrix for controlled release formulation for a herbicide, dichlorprop and the release of the herbicide can be tuned using parameters such as method of synthesis and the concentration of the incoming ionic species to be ion exchange with. This is towards new generation of agrochemicals which are safer as well as user- and environmentally-friendly.
An artificial neural network (ANN) was applied for the determination of V(V) based on immobilized fatty hydroxamic acid (FHA) in poly(methyl methacrylate) (PMMA). Spectra obtained from the V(V)-FHA complex at single wavelengths was used as the input data for the ANN. The V(V)-FHA complex shows a limited linear dynamic range of V(V) concentration of 10 - 100 mg/ L. After training with ANN, the linear dynamic range was extended with low calibration error. A three layer feed forward neural network using backpropagation (BP) algorithm was employed in this study. The input layer consisted of single neurons, 30 neurons in hidden a layer and one output neuron was found appropriate for the multivariate calibration used. The network were trained up to 10000 epochs with 0.003 % learning rate. This reagent also provided a good analytical pedormance with reproducibility characters of the method yielding relative standard deviation (RSD) of 9.29% and 7.09% for V(V) at concentrations of 50 mg/ L and 200 mg/ L, respectively. The limit of detection of the method was 8.4 mg/ L.
Quantum dots-sensitized solar cell (QDSSC) is one of the third generation solar cell that is
the most promising low cost, easy to manufacture and highly efficient solar cell. Compared to Dyesensitized
solar cell (DSSC), quantum dots (QDs) of QDSSC has a narrow bandgap and possess
excellent properties such as tunable band gaps, strong light absorption and high multiple electron
generation. Titanium dioxide or titania (TiO2) is an oxides semiconductor material that is frequently
used as a photoanode in this photovoltaic system due to high stability under visible light illumination.
TiO2 is also known as a good photocatalyst and an excellent choice in environmental purification. The
efficiencies of electron injection and light harvesting in QDSSC are affected by the nature, size
morphology, and quantity of this nanomaterial. In this review, the concept and principles of the
QDSSCs are reviewed. The preparation and fabrication method ofTiO2 electrode in QDSSC are also
discussed. It is worthwhile to know the architecture of TiO2 in order to enhance the efficiency of
QDSSC.
Titania nanotube is gaining tremendous interest for its unique features including high
surface area, ion-exchange ability, photocatalytic potential and prominent electrical properties. Many
attempts were made to manipulate the unique properties of titania nanotubes for supercapacitor
application. In this review a comprehensive list of literatures on fabrication of titania nanotubes via
anodisation method in fluoride-based electrolytes and its application as supercapacitor are discussed.
This review shows that the nanotube morphology can be optimized by varying the anodisation
parameter such as electrolyte concentration, pH, voltage, and bath temperature. The review also
includes studies on the application of titania nanotubes as supercapacitor on improving the specific
capacitance value by doping with metal oxides and conducting polymers.
ZnO/γ-Fe2O3 catalysts were fabricated via a simple precipitation route using zinc acetate and iron acetate as the precursors and ammonia as the precipitant. The resulted nanocatalysts were subjected to heat treatment at 450°C for 2 h. The characteristics of the nanocomposite were investigated by various characterization techniques. The synthesized nanocomposite has an average particle size of 13 nm and a surface area of 17 m2/g. The photocatalytic activity of ZnO/γ- Fe2O3 nanocomposite was evaluated by photodegrading 2,4-dichlorophenoxyacetic acid (2,4-D) under UV irradiation. The results showed that ZnO/γ-Fe2O3 nanocomposite exhibited enhanced photoactivity compared to pure ZnO with almost 20% increment within 4 h of reaction time. The result indicated the applicability of ZnO/γ-Fe2O3 nanocomposite to be used as photocatalyst in removing organic pollutants in wastewater.
Bi3Zn2Ta3O14, ‘P’, was crystallised in a cubic unit cell with lattice parameter of a=10.5437 (9) Å. The material had permittivity, ε’, of around 58 and dielectric loss, tan δ, of 2.3 × 10-3 at 30oC, 1 MHz; temperature coefficient of capacitance (TCC) of -156 ppm/oC in the range of 30oC to 300oC at 1 MHz. Chemical doping was carried out at either A (Bi1.5Zn0.5-xMx)(Zn0.5Ta1.5)O7, or B site (Bi1.5Zn0.5)(Zn0.5-xMxTa1.5)O7 in search of better performance materials. Various divalent cations such as Cd2+, Ca2+, Mg2+, Ni2+, Pb2+, and Cu2+ were used as dopants. Solid solutions formed were: Bi3Zn2-xCdxTa3O14 (0≤x≤0.5), Bi3Zn2-xMgxTa3O14(0≤x≤0.2), Bi3Zn2-xNixTa3O14 (0≤x≤0.4), Bi3Zn2-xPbxTa3O14 (0≤x≤0.3), Bi3Zn2-xCaxTa3O14 (0≤x≤0.3) and Bi3Zn2-xCuxTa3O14 (0≤x≤0.1). Electrical properties of the materials were investigated using impedance spectroscopy. Conductivities of the solid solutions were higher than that of the parent material Bi3Zn2Ta3O14. These doped materials exhibited similar behaviour as Bi3Zn2Ta3O14, showing a high degree of dispersion of permittivity at low frequencies (<1 kHz) and at temperatures above 500oC. Between 100 kHz and 1000 kHz, non-frequency dependence was observed in the range of 100 – 300oC. An increase in dielectric loss below 10 kHz was observed. Dielectric loss decreased with frequencies when temperature was above 500oC. Dielectric loss of all divalent cation doped materials was higher than that of the parent material; maximum permittivity value of 68 was recorded at x = 0.3 in Bi3Zn2-xCaxTa3O14. TCC obtained in this study had negative values; no obvious correlation between TCC and composition of the doped materials can be deduced.
In the recent years, electronic packaging provides significant research and development challenges
across multiple disciplines such as performance, materials, reliability, thermals and interconnections.
New technologies and techniques frequently adopted can be implemented in soldering alloys of
semiconductor sectors in terms of optimisation. Wetting contact angle or wettability of solder alloys
is one of the important factors which has got the attention of scholars. Hence in this study, due to the
remarkable similarity over classical solder alloys (Pb-Sn), Bi-Ag solder was investigated. Data were
collected through the effects of aging time variation and different weight percentages of Ag in solder
alloys. The contact angle of the alloys with Cu plate was measured by optical microscopy. Artificial
neural networks (ANNs) were applied on the measured datasets to develop a numerical model for further
simulation. Results of the experiments and simulations showed that the coefficient of determination (R2
)
is around 0.97, which signifies that the ANN set up is appropriate for the evaluation.
This studies are directed towards measuring the electrical conductivity of the (CuSe)1-xSex metal chalcogenide semi-conductor composites, with different stoichiometric compositions of Se (x = 0, 0.2, 0.4, 0.5, 0.6, 0.8,1.0) in bulk form. The electrical conductivity measurement was carried out at room temperature, using the parallel plate technique. The (CuSe)1-xSex composites were prepared using solid state reaction, by varying the ratio of CuSe:Se, in the reaction mixture. The electrical conductivity of (CuSe)1-xSex was determined to be in the range of 1.17 x 10-8 to 1.02 x 10-1 S/cm. The finding indicated that the electrical conductivity value tended to decrease as the concentration of Se increased. The effect of the concentration of Se, on electrical conductivity of (CuSe)1-xSex composites, is discussed in this paper.
Tin selenide (SnSe) and copper indium diselenide (CuInSe2) compounds were synthesized by high temperature reaction method using combination of sealed ampoule (at relatively low pressure ~10-1 Pa without inert gas) and heating at specific temperature profile in rocking furnace. Powder X-Ray diffraction analysis showed that the products involved only single phases of SnSe and of CuInSe2 only. Using the reaction products as source materials, the SnSe and CuInSe2 thin films were vacuum-deposited on glass substrates at room temperature. Structural, elemental, surface morphological and optical properties of the as-deposited films were studied by X-Ray diffraction (XRD), energy dispersive X-Ray (EDX) analysis, field emission scanning electron microscopy (FESEM) and UV-Vis-NIR spectroscopy. Single phase of SnSe and CuInSe2 films were obtained by thermal evaporation technique from synthesized SnSe and CuInSe2 compound without further treatment.