Entrapment of organic fluorophores in calcium phosphate nanoparticles with slow release

Two organic fluorophores, fluorescein (F) and rhodamine B (Rd), were entrapped in calcium phosphate nanoparticles. The as-obtained nanoparticles can be used for biological release applications. For this aim, calcium phosphate nanoparticles were synthesized using the precipitation method. Structural analysis of these nanoparticles was performed using XRD, FTIR, and Raman spectroscopy, confirming that the synthesized nanoparticles were hydroxyapatite. TEM and SEM analyses demonstrated that these nanoparticles had a size of 20 nm and a well-defined morphology. F and Rd (about 0.5 wt.%) were entrapped in these nanoparticles and their release, as a function of time, was studied via UV-Vis spectroscopy. The obtained results showed that the release of both fluorophores was progressive over time. The trapping efficiencies of the fluorophores were 67.15% and 90.76% for F and Rd, respectively.     

Beyond Perovskite Solar Cells: Tellurium Iodide as a Promising Light‐Absorbing Material for Solution‐Processed Photovoltaic Application

Searching new light‐absorbing materials to replace toxic lead halide in solar cells is very important and highly desirable. In this research, we firstly demonstrated that tellurium iodide (TeI₄) could be used as a light‐absorbing material in solar cells due to its suitable optical band gap and the active lone‐pair electron orbital in Te⁴⁺. The best power conversion efficiency (PCE=3.56%) was achieved with a concentration of 0.9 M TeI₄ in DMF:DMSO (4 : 1, v,v) without any heat treatment or antisolvent dripping. Our study indicates the promising potential of TeI₄ for photovoltaic and optoelectronic applications.     

Characterization and catalytic performance of basaltic dust as an efficient catalyst in the liquid‐phase esterification of acetic acid with n‐butanol

Three natural basaltic samples were collected and used as efficient catalysts for the liquid‐phase synthesis of n‐butyl acetate. The samples were characterized by X‐ray fluorescence analysis (XRF), X‐ray diffraction (XRD), thermogravimetry (TG), differential thermal analysis (DTA), Fourier transform infrared (FT‐IR), scanning electron microscopy (SEM), and N₂ sorption. The acidity of the samples was determined using isopropanol dehydration, and the strength of the acid sites was measured using chemisorption of basic probes. The catalytic activity of the samples towards the esterification of acetic acid with n‐butanol was extensively examined. The influence of different parameters, such as the reaction refluxing time, molar ratio, catalyst loading, reusability, and calcination temperature, on the esterification reaction was studied in detail. The results revealed that all samples had high catalytic activity with a selectivity of 100% to n‐butyl acetate formation. In addition, the sample obtained from the top hill of Volcano had the highest activity with a 80% yield of n‐butyl acetate. Moreover, the significant catalytic performances were well correlated with the acidity of the samples and to the reaction rate constants.     

Oscillation criteria for higher order nonlinear dynamic equations

In this paper, we will consider the higher‐order functional dynamic equations of the form on an above‐unbounded time scale , where and , . The function is a rd‐continuous function such that . The results extend and improve some known results in the literature on higher order nonlinear dynamic equations.     

Numerical simulation of a coupling effect on electronic states in quantum dots

Lasers operating at 1.3 μm have attracted considerable attention owing to their potential to provide efficient light sources for next-generation high-speed communication systems. InAs/GaAs quantum dots (QDs) were pointed out as a reliable low-cost way to attain this goal. However, due to the lattice mismatch, the accumulation of strain by stacking the QDs can cause dislocations that significantly degrade the performance of the lasers. In order to reduce this strain, a promising method is the use of InAs QDs embedded in InGaAs layers. The capping of the QD layer with InGaAs is able to tune the emission toward longer and controllable wave-lengths between 1.1 and 1.5 μm. In this work, using the effective-mass envelope-function theory, we investigated theoretically the optical properties of coupled InAs/GaAs strained QDs based structures emitting around 1.33 μm. The calculation was performed by the resolution of the 3D Schrödinger equation. The energy levels of confined carriers and the optical transition energy have been investigated. The oscillator strengths of this transition have been studied with and without taking into account the strain effect in the calculations. The information derived from the present study shows that the InGaAs capping layer may have profound consequences as regards the performance of an InAs/GaAs QD based laser. Based on the present results, we hope that the present work make a contribution to experimental studies of InAs/GaAs QD based structures, namely the optoelectronic applications concerning infrared and mid-infrared spectral regions as well as the solar cells.     

Solvability of a Mixed Nonlocal Problem for a Nonlinear Singular Viscoelastic Equation

The present paper deals with a nonlinear viscoelastic equation having a dissipation term. With the equation some classical and non classical boundary conditions are combined. Based on some a priori bounds, iteration processes and density arguments, we simultaneously solve the nonlinear and the associated linear problems.     

Structural and Catalytic Activity of V2O5-Supported on AlPO4 Catalysts

Summary. A series of AlPO₄-V₂O₅ (APV) systems with various vanadia amounts 1–30mol% were prepared by the impregnation method and calcinated at 400 and 600°C for 4h. The catalysts were characterized by TG/DTG, DSC, IR spectroscopy, XRD, N₂ adsorption, and electrical conductivity measurements. The surface acidity and basicity of the catalysts were studied by the dehydration-dehydrogenation of isopropyl alcohol and the adsorption of pyridine. The catalytic gas phase esterification of acetic acid with ethyl alcohol was carried out at 210°C in a flow system at 1atm using air as a carrier gas. The results showed that the catalysts calcinated at 400°C were active and selective towards the formation of ethyl acetate whereas the calcination of samples at 600°C led to a drastic reduction in both activity and selectivity. Good correlations were obtained between catalytic activities towards ester formation and acidity of the prepared catalysts.