Determination of the Junction Recombination Velocity Initiating the Short Circuit Situation Sfsc of a Bifacial Silicon Solar Cell Irradiated Under Magnetic Field in Dynamic Frequency Regime

The object of this work, a study of the junction recombination velocity limiting the short circuit (Sfsc) of a silicon solar cell under magnetic field in the dynamic frequency regime is presented. From the continuity equation, the density of minority Charge carrier’s in the base and the photocurrent are determined. The study of this photocurrent, according to the junction recombination velocity, allows us to determine the junction recombination velocity limiting the short circuit. The photocurrent density is studied as a function of the junction recombination velocity for different modulation frequencies. From the variation profile of the photocurrent density as a function of the junction recombination velocity, a technique for determining junction recombination velocity initiating the short-circuit situation is presented.

     

Face-Specific Data Augmentation for Unconstrained Face Recognition

International Journal of Computer Vision - We identify two issues as key to developing effective face recognition systems: maximizing the appearance variations of training images and minimizing...     

Implementing flipped learning approach based on ‘first principles of instruction’ in mathematics courses

This study investigates the effect of E-learning (EL), blended learning (BL) and flipped learning (FL) approaches on the mathematics achievement, self-regulation and mathematics self-efficacy. Participants consist of 163 first-year students attending an associate degree program (a 2-year program) of a state university. The EL, BL and FL settings in the research were designed based on Merrill's ‘First Principles of Instruction Design Theory’. In the research in which a quasi-experimental pre-test–post-test research design was used, the data were obtained by means of mathematics achievement test, self-regulation and self-efficacy questionnaires. The experimental results showed that the mathematics achievement post-test scores of FL students were significantly higher than those of the students of EL and BL. No significant difference was found between BL and EL settings. In addition, FL students showed significantly higher self-regulation and mathematics self-efficacy than the other groups' students. According to these results, it can be said that the usage of FL approach in mathematics courses has a positive effect on the learning process of students. It is expected that the findings will be helpful in the future design and implementation of mathematics courses at vocational colleges.     

Thermo-economic analysis of chlor-alkali electrolysis for hydrogen production in the electrochlorination plant: Real case

This study deals with the implementations of electrochemical technology for the on-site production of sodium hypochlorite (NaOCl) and hydrogen from seawater for utilization in the steam power plant. The effects of electrical current and seawater temperature on the performance of electrochlorination system are investigated. The obtained results show that current efficiency increases with increasing electrical current. The current efficiency of the system is calculated as 94% at a maximum electric current with a value of 4000 A and maximum temperature with a value of 30 °C. Electricity consumption increases for the unit generation of available chlorine in the case of both enhancements of electrical current and seawater. Hydrogen generation is directly proportional to the variation of the electrical current. Also, improvement in seawater temperature provides more efficient hydrogen generation. Moreover, energy and exergy efficiencies of the whole system are positively affected by an increase of current. However, energy and exergy efficiencies are determined to be 50.4% and 3.04%, respectively, under the best operational conditions. Besides, the cheapest product cost of the hydrogen gas is calculated as $4.04/kg under the greatest electrical current and seawater temperatures.     

Highly active and stable CeO2 supported nickel-complex catalyst in hydrogen generation

Cerium oxide supported 5-Amino-2,4-dichlorophenol-3,5-ditertbutylsalisylaldimine-Nickel complex for the first time was used to produce H₂ from hydrolysis of sodium borohydride. Cerium oxide supported Nickel complex catalyzed hydrolysis system was studied depend on temperature, concentration of sodium hydroxide, amount of Cerium oxide supported Ni complex catalyst, concentration of Ni complex and concentration of sodium borohydride. Cerium oxide supported Ni(II) complex display highly effective catalytic activity in sodium borohydride hydrolysis reaction. The obtained Cerium oxide supported Ni(II) complex catalyst was characterized by using Fourier Transform Infrared Spectroscopy, Scanning Electron Microscope, Transmission Electron Microscope, Brunauer-Emmett-Teller Surface Area Analysis, X-Ray Diffraction Analysis techniques. The catalyst stability was tested, even the fifth recycle the catalytic activity was maintained at 100%. Additionally the proposed Cerium oxide supported-Ni (II) complex catalyzed sodium borohydride hydrolysis mechanism was determined carefully. The experimental results showed that Cerium oxide supported Ni (II) complex catalyst accelerate sodium borohydride hydrolysis with 43,392 and 19,630 mL H₂ g_cat^?1 min^?1 hydrogen production rates at 50 °C and 30 °C respectively and 20,587 kJ mol^?1 activation energy.     

Synthesis and spectroelectrochemistry of dithieno(3,2‐b:2′,3′‐d)pyrrole derivatives

New π‐conjugated polymers containing dithieno(3,2‐b:2′,3′‐d)pyrrole (DTP) were successfully synthesized via electropolymerization. The effect of structural differences on the electrochemical and optoelectronic properties of the 4‐[4H‐dithieno(3,2‐b:2′,3′‐d)pyrrol‐4‐yl]aniline (DTP–aryl–NH₂), 10‐[4H‐dithiyeno(3,2‐b:2′,3′‐d)pirol‐4‐il]dekan‐1‐amine (DTP–alkyl–NH₂), and 1,10‐bis[4H‐dithieno(3,2‐b:2′,3′‐d)pyrrol‐4‐yl] decane (DTP–alkyl–DTP) were investigated. The corresponding polymers were characterized by cyclic voltammetry, NMR (¹H‐NMR and ¹³C‐NMR), and ultraviolet–visible spectroscopy. Changes in the electronic nature of the functional groups led to variations in the electrochemical properties of the π‐conjugated systems. The electroactive polymer films revealed redox couples and exhibited electrochromic behavior. The replacement of the DTP–alkyl–DTP unit with DTP–aryl–NH₂ and DTP–alkyl–NH₂ resulted in a lower oxidation potential. Both the poly(10‐(4H‐Dithiyeno[3,2‐b:2′,3′‐d]pirol‐4‐il)dekan‐1‐amin) (poly(DTP–alkyl–NH₂)) and poly(1,10‐bis(4H‐dithieno[3,2‐b:2′,3′‐d]pyrrol‐4‐yl) decane) (poly(DTP–alkyl–DTP)) films showed multicolor electrochromism and also fast switching times (<1 s) in the visible and near infrared regions. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40701.     

Propham mineralization in aqueous medium by anodic oxidation using boron-doped diamond anode: influence of experimental parameters on degradation kinetics and mineralization efficiency

This study aims the removal of a carbamate herbicide, propham, from aqueous solution by direct electrochemical advanced oxidation process using a boron-doped diamond (BDD) anode. This electrode produces large quantities of hydroxyl radicals from oxidation of water, which leads to the oxidative degradation of propham up to its total mineralization. Effect of operational parameters such as current, temperature, pH and supporting electrolyte on the degradation and mineralization rate was studied. The applied current and temperature exert a prominent effect on the total organic carbon (TOC) removal rate of the solutions. The mineralization of propham can be performed at any pH value between 3 and 11 without any loss in oxidation efficiency. The propham decay and its overall mineralization reaction follows a pseudo-first-order kinetics. The apparent rate constant value of propham oxidation was determined as 4.8×10⁻⁴ s⁻¹ at 100 mA and 35 °C in the presence of 50 mM Na₂SO₄ in acidic media (pH: 3). A general mineralization sequence was proposed considering the identified oxidation intermediates.     

A two-dimensional material for high capacity supercapacitors: S-doped graphene

In this work, sulfur-doped graphene-coated electrodes are prepared by cyclic voltammetry in different potential ranges and different cycles (from 10 to 50) for selective modification of electrodes by different functional groups. The prepared electrodes are characterized by spectroscopic, microscopic and electrochemical methods. In scanning electron microscopic analysis, formation of graphene layers and their porous structure have been determined. Electrochemical impedance spectroscopic and cyclic voltammetric analyses are also used in electrochemical characterization of the electrodes. Then, the prepared sulfur-doped graphene-coated electrodes by using cyclic voltammetry in one-step and low cost are used as electrode materials of supercapacitor for the first time in the literature. Since the mesoporous structure of the electrodes prepared in lower potential ranges increases, specific capacitance of the electrodes increases from 74 to 1833 mF cm⁻² with 10 mA cm⁻² current density. This result shows that specific capacitances of prepared electrodes are higher than those of the electrodes prepared with metal-doped in the literature.