Pyreno-chalcone dendrimers as an additive in the redox couple of dye-sensitized solar cells

Novel pyreno-chalcone dendrimers 1, 2, and 3 were synthesized and their ability to act as an additive in the redox couple (I⁻/I₃ ⁻) of dye-sensitized nanocrystalline TiO₂ solar cell has been tested. The redox couple doped with pyreno-chalcone dendrimer 3 gave a short circuit photocurrent density (J _sc) of 7.40 mA/cm², open circuit voltage (V _oc) of 820 mV, and a fill factor of 0.51, corresponding to an overall conversion efficiency (η) of 7.89% under 40 mW/cm² irradiation.     

Anisotropic interface induced formation of Sb nanowires on GaSb(111)A substrates

The growth of Sb nanowires on GaSb(111)A substrates is studied by in?situ azimuthal scan reflection high-energy electron diffraction (ARHEED). Bulk and layer contributions can be distinguished in the ARHEED transmission pattern through the Sb nanowires. The three-dimensional structure of the growing Sb nanowires is identified by post-growth atomic force microscopy (AFM) and x-ray diffraction (XRD). The lattice match of the Sb crystal along the [Formula: see text] and the GaSb crystal along [Formula: see text] directions lead to a preferential orientation of the Sb nanowires. The Sb adsorption and desorption kinetics is studied by thermal desorption spectroscopy.     

Surface adsorption and anticorrosive behavior of benzimidazolium inhibitor in acid medium for carbon steel corrosion

Corrosion inhibition property of a newly synthesized 3-(4-chlorobenzoylmethyl) benzimidazolium bromide inhibitor against carbon steel corrosion in 1 N hydrochloric acid solution was studied and analyzed utilizing various electrochemical methods. Electrochemical impedance study inferred that the inhibition efficiency increased with increasing inhibitor concentration and give 93.5% at 250 ppm. Potentiodynamic polarization study emphasized that inhibitor acted as a mixed type inhibitor and the adsorption of inhibitor on the metal surface followed Langmuir adsorption isotherm. The noise results were in good correlation with other electrochemical results obtained. The increase of inhibition efficiency with concentrations of inhibitor is attributed to the blocking of the active area by the inhibitor adsorption on the metal surface. The thermodynamic parameter values were calculated and discussed to explain the adsorption mechanism of inhibitor in an acidic medium. The protective surface morphology governed by the inhibited medium was investigated using the scanning electron microscopic technique. The surface roughness of the sample in the absence and presence of inhibitor was obtained using atomic force microscopic study. The effect and reactivity of the inhibitor are further clarified with quantum chemical analysis. Finally, the corrosion protection mechanism is proposed on the ground of experimental and theoretical studies.

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Proton conducting composite membranes for fuel cell application

Composites were fabricated by blending SPSEBS (Sulfonated Poly Styrene Ethylene Butylene Poly Styrene) with Boron phosphate (BPO₄) for proton conducting applications in fuel cells. The effects of boron phosphate and its relative loading were analyzed in terms of IEC and proton conductivity. Water and methanol uptake of these membranes were also studied.The membranes were characterized by IR spectroscopy. Thermal stability was studied by TGA and DSC analyses. Surface morphology was done by Scanning Electron Microscopy (SEM). The XRD studies indicated the existence of a certain level of crystallinity in the SPSEBS, and the composite membranes. Mechanical strength of the membranes was measured by Universal Testing Machine (UTM). This paper presents the result of recent investigations to develop an optimised in-house membrane electrode assembly (MEA) preparation technique combining catalyst ink spraying and assembly hot pressing. Easy steps were chosen in this preparation technique aiming at simplification and cost reduction.     

Effect of Vernonia cinerea Less flower extract in adjuvant-induced arthritis

Denatured lysozyme was refolded by a dilution method. The refolding yield depended greatly on the lysozyme concentration in the refolding mixture. When the concentration of denatured lysozyme was 0.02 g/L, the refolding yield was as high as 60%. However, when the concentration of denatured lysozyme was 0.2 g/L, the refolding yield was as low as 10% due to the formation of aggregates. To prevent the formation of aggregates and to increase the refolding yield at a low cost, inexpensive additives were screened. The addition of acetone, acetoamide, or urea derivatives was very effective for improving the refolding yield. To clarify why the addition of acetoamide in the refolding mixture improved the refolding yield at the high lysozyme concentration, the time courses of the concentration and the average diameter of the aggregates in the refolding mixture were monitored by the dynamic light scattering method. The experimental results showed that acetoamide played a role in preventing the formation and growth of aggregates and secondary aggregation between the lysozyme aggregates.     

Formation and Stability of Equiatomic and Nonequiatomic Nanocrystalline CuNiCoZnAlTi High-Entropy Alloys by Mechanical Alloying

Nanocrystalline equiatomic high-entropy alloys (HEAs) have been synthesized by mechanical alloying in the Cu-Ni-Co-Zn-Al-Ti system from the binary CuNi alloy to the hexanary CuNiCoZnAlTi alloy. An attempt also has been made to find the influence of nonequiatomic compositions on the HEA formation by varying the Cu content up to 50 at. pct (Cu _x NiCoZnAlTi; x = 0, 8.33, 33.33, 49.98 at. pct). The phase formation and stability of mechanically alloyed powder at an elevated temperature (1073 K [800 °C] for 1 hour) were studied. The nanocrystalline equiatomic Cu-Ni-Co-Zn-Al-Ti alloys have a face-centered cubic (fcc) structure up to quinary compositions and have a body-centered cubic (bcc) structure in a hexanary alloy. In nonequiatomic alloys, bcc is the dominating phase in the alloys containing 0 and 8.33 at. pct of Cu, and the fcc phase was observed in alloys with 33.33 and 49.98 at. pct of Cu. The Vicker’s bulk hardness and compressive strength of the equiatomic nanocrystalline hexanary CuNiCoZnAlTi HEA after hot isostatic pressing is 8.79 GPa, and the compressive strength is 2.76 GPa. The hardness of these HEAs is higher than most commercial hard facing alloys (e.g., Stellite, which is 4.94 GPa).