Solar cells consisting of phenazine dyes in polymer matrix

We have constructed p−n heterojunction solar sandwich cells with phenazine dyes in a thin film of polyvinyl alcohol placed between a conducting glass coated with indium oxide and a platinum foil. The current-voltage relations of the cells have been measured in the dark and light under both forward and reverse biases.     

In vitro antioxidant activity of different cultivars of banana flower (Musa paradicicus L.) extracts available in India

Abstract: Six different cultivars of banana flowers (Musa paradicicus) (Kathali, Bichi, Shingapuri, Kacha, Champa, and Kalabou) were analyzed for the content of polyphenol expressed as gallic acid equivalent and flavonoid expressed as quercetein equivalent, and the in vitro total antioxidative activities of the flower extracts were compared with standard and expressed as trolox equivalent. The reducing power, 1,1‐diphenyl‐2‐picrylhydrazyl (DPPH) and 2,2‐azinobis(3‐ethylbenzothiazoline‐6‐sulfonic acid) radical cation (ABTS?⁺) scavenging activities, inhibition of lipid peroxidation in a linoleic acid emulsion system, and liposome peroxidation system were measured and compared with respective standard antioxidants. Iron‐mediated Fenton reaction was carried out to evaluate the protective effect of the extract of banana flower (Kacha cultivar) against H₂O₂‐induced DNA damage. The Kacha variety contains the maximum amount of polyphenol (11.94 ± 0.03 mg of gallic acid equivalent/g of dry weight) and flavonoid (0.174 ± 0.001 g of quercetin equivalent/g of polyphenol). It also has the highest total antioxidant capacity, DPPH radical scavenging activity, and ABTS?⁺ radical scavenging activity with a least EC₅₀ value of 0.051 mg/mL. Hepatic cell damage in iron‐mediated Fenton reaction caused by free radicals is reduced by the banana flower extract. On the basis of the results obtained, the banana flowers are found to be a potential source of natural antioxidants. This is the first report on the antioxidant properties of the extracts from banana flowers. The study suggests that the flowers of M. paradicicus that are found in India and consumed as vegetable can provide valuable functional ingredients that help in the prevention of oxidative stress.     

Highly dispersed platinum nanoparticles on graphitic carbon nitride: A highly active and durable electrocatalyst for oxidation of methanol,formic acid and formaldehyde

Finding efficient electrocatalyst for oxidation of small organic molecules such as methanol (CH₃OH), formic acid (HCOOH), formaldehyde (HCHO) etc. is essential for the development of their respective direct fuel cells. We report here highly dispersed platinum nanoparticles (PtNPs) on carbon nitride (CN_x) were successfully synthesized by the ultrasound mediated sodium borohydride reduction of H₂PtCl₆ in presence of CN_x nanosheets. This platinum–carbon nitride (Pt/CN_x) composite exhibited superior electrocatalytic activity towards oxidation of CH₃OH, HCOOH and HCHO in acid media. The mass activity, onset potential, tolerance to carbon monoxide (CO) poisoning and long term durability for the catalytic oxidation of CH₃OH, HCOOH, HCHO on Pt/CN_x catalyst in acid media is much higher than that of commercial Pt/C catalyst. The mass activity of Pt/CN_x catalyst at ～0.64 V (forward scan) is 310 mA/mg_Pt which is 2.7 time higher than that of commercial Pt/C for methanol oxidation. The electrooxidation of HCOOH on Pt/CN_x occurs via dual mechanism with greatly enhanced oxidation through dehydrogenation pathway in comparison with commercial Pt/C. The mass activity on Pt/CN_x at 0.3 V (vs. NHE) is 25 times higher than that of Pt/C for oxidation of HCOOH. The superior catalytic activity and durability of this Pt/CN_x catalyst can be attributed to high dispersion of PtNPs and strong catalyst support interaction.     

Kinetics of temperature-dependent photoinduced redox reactions in a photoelectrochemical cell

The effect of temperature on the electrode kinetics of photovoltage generation in photoelectrochemical (PEC) cells consisting of a phenazine dye-EDTA system, separated from an aqueous solution of an electron acceptor like iodine by a salt bridge has been studied. The phenazine dyes used are phenosafranin, safranin-O, and safranin-T. The maximum photovoltages (V_oc) generated and the sunlight engineering efficiency (SEE) have been found to increase with increasing temperature, but there is a fixed critical temperature for each dye above which the V_oc decreases: 29°C for phenosafranin, 35°C for safranin-T, and 40°C for safranin-O. The photovoltage growth and decay follow the functional forms related to the relaxation times. The rate constants for the forward and backward reactions have been calculated from these relaxation times at different temperatures. The rate of the photoinduced chemical reaction increases with an increase in temperature from 20°C–50°C for all the dyes, with concomitant decrease for the backward reaction. The free energies of electron transfer across the electrode/electrolyte interface have been calculated. The activation energies calculated from the rate constants at different temperatures for phenosafranin-EDTA, safranin-T-EDTA, and safranin-O-EDTA reactions are 5.14, 5.60, and 5.63 kJ mol⁻¹ respectively.     

A study of thin‐flame quasisteady sphericosymmetric combustion of multicomponent fuel droplets. Part I: modelling for droplet surface regression and non‐unity gas‐phase Lewis number

A model for sphericosymmetric thin‐flame combustion of multicomponent fuel droplets has been developed in the first part of this two‐part work. The model incorporates effects of droplet surface regression and gas‐phase Lewis number. It is observed that both these effects affect the results substantially. The study also reveals the transient nature of the combustion process. Copyright © 1999 John Wiley and Sons, Ltd.     

Neural perceptron & strict lossless secret sharing oriented cryptographic science: fostering patients’ security in the “new normal” COVID-19 E-Health

Multimedia Tools and Applications - Patients’ data security is an open challenge on any telemedicine system. The challenge has been extended enough in this unprecedented corona virus led...     

Physicochemical and Adhesion Characteristics of High-Density Polyethylene when Treated in a Low-Pressure Plasma under Different Electrodes

The present investigation studys the effects of different electrodes such as copper, nickel, and stainless steel under low-pressure plasma on physicochemical and adhesion characteristics of high-density polyethylene (HDPE). To estimate the extent of surface modification, the surface energies of the polymer surfaces exposed to low-pressure plasmas have been determined by measuring contact angles using two standard test liquids of known surface energies. It is observed that the surface energy and its polar component increase with increasing exposure time, attain a maximum, and then decrease. The increase in surface energy and its polar component is relatively more important when the polymer is exposed under a stainless-steel electrode followed by a nickel and then a copper electrode. The dispersion component of surface energy remains almost unaffected. The surfaces have also been studied by optical microscopy and electron spectroscopy for chemical analysis (ESCA). It is observed that when the HDPE is exposed under these electrodes, single crystals of shish kebab structure form, and the extent of formation of crystals is higher under a stainless-steel electrode followed by nickel and then copper electrodes. Exposure of the polymer under low-pressure plasma has essentially incorporated oxygen functionalities on the polymer surface as detected by ESCA. Furthermore the ESCA studies strongly emphasize that higher incorporation of oxygen functionalities are obtained when the polymer is exposed to low-pressure plasma under a stainless-steel electrode followed by nickel and then copper electrodes. These oxygen functionalities have been transformed into various polar functional groups, which have been attributed to increases in the polar component of surface energy as well as the total surface energy of the polymer. Therefore, the maximum increase in surface energy results in stronger adhesion of the polymer when the polymer is exposed under a stainless-steel electrode rather than nickel and copper electrodes.