Study of the Enhancement of the Efficiency of the Monocrystalline Silicon Solar Cell by Optimizing Effective Parameters Using PC1D Simulation

Silicon - In this paper, simulation of a monocrystalline silicon solar cell was done using PC1D software. The impact of different solar cell parameters, with their effects on power and efficiency,...     

Radiation crosslinked polyvinyl alcohol/polyvinyl pyrrolidone/acrylic acid hydrogels: swelling,crosslinking and dye adsorption study

Iranian Polymer Journal - Hydrogels were produced from mixtures of polyvinyl alcohol (PVA), polyvinyl pyrrolidone (PVP), and acrylic acid (AAc) using γ-radiation at doses of 3, 7, and...     

Effects of hydrothermal process parameters on the physical,magnetic and thermal properties of Zn0.3Fe2.7O4 nanoparticles for magnetic hyperthermia applications

Effects of hydrothermal temperature and time on physical, magnetic and thermal properties of Zn-substituted magnetite nanoparticles (Zn_0.3Fe_2.7O₄) were assessed. The magnetic nanoparticles were synthesized via citric acid-assisted hydrothermal reduction route at temperatures of 150, 175 and 200 °C for duration of 10, 15 and 20 h. The nanoparticles were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM), vibrating sample magnetometer (VSM) and specific loss power (SLP) measurements. The results showed that temperature and time of the hydrothermal process both had significant effects on nanoparticles composition and properties. It was observed that at 150 °C, heat generation was insufficient to produce activation energy required for nucleation of Zn_0.3Fe_2.7O₄ spinel nanoparticles, even after a long time. At 175 °C, although temperature was low, but the suitable condition for nucleation of nanoparticles was made and spinel nanoparticles with the size of about 13 nm were formed after 15 h. Nonetheless, since crystallinity and SLP of the nanoparticles was low, they showed weak performance for magnetic hyperthermia. At 200 °C, the required activation energy was provided for nanoparticles nucleation; however, the spinel was oxidized to hematite, resulting in a decrease in thermal and magnetic properties. In overall, the nanoparticles synthesized at 200 °C for 15 h possessed the best characteristics of reasonable purity, saturation magnetization of about 35.9 emu/g and SLP of 18.7 W/g.     

Effect of seed layer on the growth of rutile TiO2 nanorod arrays and their performance in dye-sensitized solar cells

In order to improve the performance of TiO₂ photoanode-based dye sensitized solar cells (DSSCs), rutile TiO₂ nanorod arrays (NRAs) were grown on SnO₂:F (FTO) conductive glass coated with TiO₂ seed layer by a hydrothermal method. The TiO₂ seed layer was obtained by spin-coating titanium tetraisopropoxide (TTIP) isopropanol solution with concentration in the range of 0~0.075 M. Then the effect of the thin TiO₂ seed layer on the crystal structure and surface morphology of TiO₂ NRAs and the photoelectric conversion properties of the corresponding DSSCs were investigated. It is found that TiO₂ NRAs are vertically oriented, about 1.7 μm long and the average diameter is about 35 nm for the samples derived from TTIP in the range of 0.005~0.05 M, which are more uniform and better separated from each other than those without TiO₂ seed layer (average diameter 35~85 nm). The photoelectric conversion efficiency of DSSCs based on TiO₂ NRAs with TiO₂ seed layer is larger than that without TiO₂ seed layer. Typically, the energy efficiency of DSSCs obtained from the seed solution of 0.025 M TTIP is 1.47%, about 1.8 times greater than that without TiO₂ seed layer. The performance improvement is attributed to the thinner, denser and better oriented NRAs grown on seeded-FTO substrate absorbing more dye and suppressing charge recombination at the FTO substrate/electrolyte interface.     

Er3+/Yb3+ co-doped bioactive glasses with up-conversion luminescence prepared by containerless processing

Er³⁺/Yb³⁺ co-doped bioactive glasses were prepared via containerless processing in an aerodynamic levitation furnace. The as-prepared glasses were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM) equipped with energy dispersive X-Ray spectroscopy (EDX). The up-conversion luminescence of as-prepared glasses was measured using an Omni- 3007 spectrometer. Furthermore, the in vitro bioactivity was evaluated by soaking the materials in simulated body fluid, and the biocompatibility was evaluated in MC3T3-E1 cell culture.The results show that containerless processing is a unique method to prepare homogeneous rare earth doped bioactive glasses. The obtained Er³⁺/Yb³⁺ co-doped glasses show green and red up-conversion luminescence at the excitation of 980 nm laser. The XRD analysis confirmed that calcium silicate powders, as starting materials, were completely transformed from the original multi-crystalline phase (CS-P) into the amorphous-glassy phase (CS-G, EYS, LCS) via containerless processing. The SEM observation combined with EDX and FTIR analyses showed that the as-prepared glasses were bioactive. The cell proliferation assay also revealed that the as-prepared glasses were biocompatible and nontoxic to MC3T3-E1 cells. This study suggests that the luminescent bioactive glasses prepared by containerless processing could be used for studying biodegradation of bone implantation materials.     

Impacts of CO2 emission constraints on technology selection and energy resources for power generation in Bangladesh

This paper examines the impacts of CO₂ emission reduction target and carbon tax on future technologies selection and energy use in Bangladesh power sector during 2005–2035. The analyses are based on a long-term energy system model of Bangladesh using the MARKAL framework. The analysis shows that Bangladesh will not be able to meet the future energy demand without importing energy. However, alternative policies on CO₂ emission constraints reduce the burden of imported fuel, improve energy security and reduce environmental impacts. The results show that the introduction of the CO₂ emission reduction targets and carbon taxes directly affect the shift of technologies from high carbon content fossil-based to low carbon content fossil-based and clean renewable energy-based technologies compared to the base scenario. With the cumulative CO₂ emission reduction target of 10–20% and carbon tax of 2500 Taka/ton, the cumulative net energy imports during 2005–2035 would be reduced in the range of 39–65% and 37%, respectively, compared to the base scenario emission level. The total primary energy requirement would be reduced in the range of 4.5–22.3% in the CO₂ emission reduction targets and carbon tax 2500 Taka/ton scenarios and the primary energy supply system would be diversified compared to the base scenario.     

Proton conductivity in stoichiometric and sub-stoichiometric yittrium doped SrCeO3 ceramic electrolytes

The crystal structure and electrical properties of stoichiometric perovskite proton conductors SrCe_1−xY_xO_3−δ (where x = 0.025, 0.05, 0.075, 0.1, 0.15, and 0.2 and δ = x/2) and substoichiometric Sr_0.995Ce_0.95Y_0.05O_3−δ have been investigated. The conductivities of the samples were measured as a function of the partial pressure of oxygen at 600 and 800 °C, and at two water vapor pressures (P_H2O=0.01 and 0.001 atm). A P_O2 range of 1 atm (pure O₂) to approximately 1 × 10⁻²⁵ atm (N₂/H₂ mix) allowed for the separation of n-(electron), p-(hole), and i-(ionic) type conductivities.In the case of stoichiometric perovskite proton conductors, the unit cell volume (UCV) and calculated density decrease with increasing yttrium content. The ionic and p-type components of the conductivity show threshold effect with Y-doping, which may be related to the double substitution of Y on both A- and B-sites. A maximum ionic conductivity of 5 mS/cm is found at 10% Y, whereas p-type conductivity increases with increasing yttrium concentration. A conductivity component appearing at low oxygen partial pressures decreases with yttrium doping. The substoichiometric material showed a drop in unit cell volume of approximately 0.34 Å³ compared to its stoichiometric partner. The conductivity components of substoichiometric material are higher than the conductivities of corresponding stoichiometric material, being approximately 7 mS/cm for both P_H2O levels.     

Synthesis of β-MoO3 by vacuum drying and its structural and electrochemical characterisation

The β-MoO₃ was obtained successfully free of α-MoO₃ through soft chemistry methods. The formation of β-MoO₃ with high purity was determined by the formation of the precursor MoO₃·2H₂O when a solution of Na₂MoO₄·2H₂O was passed through a cation-exchange resin. A structural, spectroscopic and thermal study of the polymorph synthesised was made by XRD, electron dispersion spectroscopy (EDS), FTIR and TGA/DTA techniques, respectively, in order to make a study about the possibilities of β-MoO₃ as active material in a lithium battery. Electrochemical experiments showed a high ability of the β-MoO₃ to form lithium molybdenum bronzes via a lithium insertion reaction.