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This paper reports the optical properties of zinc oxide nanofilm fabricated by using organic natural products from Salvia officinalis leaves (SOL) extract and discusses the effect of the nanocrystal (NC) structure (nanoyarn and nanomat-like structure) on nanofilm optical properties. The surface-active layer of the nanofilm of ZnO nanoparticles (ZnO NPs) was passivated with natural organic SOL leaves hydrothermally, then accumulated on zinc oxide nanorods (ZnO NRs). The nanofilms were fabricated (with and without PEO) on glass substrate (at 85 °C for 16 h) via chemical solution deposition (CSD). The samples were characterized by UV-vis, PL, FESEM, XRD, and TEM measurements. TEM micrographs confirmed the nucleation of ZnO NPs around 4 nm and the size distribution at 1.2 nm of ZnO QDs as an influence of the quantum confinement effect (QCE). The nanofilms fabricated with SOL surfactant (which works as a capping agent for ZnO NPs) represent distinct optoelectronic properties when compared to bulk ZnO. FESEM images of the nanofilms revealed nanoyarn and nanomat-like structures resembling morphologies. The XRD patterns of the samples exhibited the existence of ZnO nanocrystallites (ZnO NCs) with (100), (002), and (101) growth planes. The nanofilms fabricated represented a distinct optical property through absorption and broad emission, as the optical energy band gap reduced as the nanofilms annealed (at 120℃). Based on the obtained results, it was established that phytochemicals extracted from organic natural SOL leaves have a distinct influence on zoic oxide nanofilm fabrication, which may be useful for visible light spectrum trapping. The nanofilms can be used in photovoltaic solar cell applications.

A series of Co-doped and Cr-doped Ba1-xCoxFe12-yCryO19 nanoparticles (NPs) were synthesized via the microemulsion route. The effects of Co and Cr substitution on the structural, dielectric, optical, and photocatalytic properties of the NPs were investigated. The Ba1-xCoxFe12-yCryO19 NPs were characterized using Fourier-transform infrared spectroscopy, X-ray diffraction analysis, scanning electron microscopy, Raman scattering, and dielectric measurements. The Ba1-xCoxFe12-yCryO19 NPs were obtained in a single phase with an average crystallite size of 18 nm. The dielectric constant of the NPs decreased, while the dielectric loss and tangent loss increased with increasing dopant (Co and Cr) contents. The photocatalytic activities (PCAs) of the Ba1-xCoxFe12-yCryO19 and BaFe12O19 NPs were appraised by carrying out the degradation of CV (crystal violet) dye under solar light irradiation. The doping improved the PCA of BaFe12O19, and up to 64.23% of the CV dye could be degraded within 60 min under visible light irradiation. The Ba1-xCoxFe12-yCryO19 NPs showed great potential for application as an economic photocatalyst as they required solar light irradiation for the degradation of CV.

Obtaining H2 energy from H2O using the most abundant solar radiation is an outstanding approach to zero pollution. This work focuses on studying the effect of Co doping and calcination on the structure, morphology, and optical properties of spin-coated SnO2 films as well as their photoelectrochemical (PEC) efficiency. The structures and morphologies of the films were investigated by XRD, AFM, and Raman spectra. The results confirmed the preparation of SnO2 of the rutile phase, with crystallite sizes in the range of 18.4–29.2 nm. AFM showed the granular structure and smooth surfaces having limited roughness. UV-Vis spectroscopy showed that the absorption spectra depend on the calcination temperature and the Co content, and the films have optical bandgap (Eg) in the range of 3.67–3.93 eV. The prepared samples were applied for the PEC hydrogen generation after optimizing the sample doping ratio, using electrolyte (HCl, Na2SO4, NaOH), electrode reusability, applied temperature, and monochromatic illumination. Additionally, the electrode stability, thermodynamic parameters, conversion efficiency, number of hydrogen moles, and PEC impedance were evaluated and discussed, while the SnO2 films were used as working electrodes and platinum sheet as an auxiliary or counter electrode (2-electrode system) and both were dipped in the electrolyte. The highest photocurrent (21.25 mA/cm2), number of hydrogen moles (20.4 mmol/h.cm2), incident photon-to-current change efficiency (6.892%@307 nm and +1 V), and the absorbed photon-to-current conversion efficiency (4.61% at ~500 nm and +1 V) were recorded for the 2.5% Co-doped SnO2 photoanode that annealed at 673 K.

To obtain good economic and environmental benefits, LaMgNi3.6M0.4 (M = Al, Mn, Ni, Co, Cu) alloys are investigated for the hydrogen storage. The absorption data of hydrogen in the tested alloys are measured experimentally at 373 K. The hydrogen absorption isotherms are analyzed using three models derived from statistical physics formalism. The adequate model permits to discover significant details about the absorption phenomenon via determining the density of the interstitial sites (Dm), the number of hydrogen atoms per site (n) and the energetic parameter ΔE. The results indicate that multi-atomic (n > 1) and multi-linking (n

In the current investigation, we report a theoretical study to acquire the highest feasible efficiency of cadmium telluride (CdTe) thin-films. It is well recognized that CdTe crystallizes in cubic zinc-blende structure and its direct band gap of 1.5 eV turned it out as a potential candidate for photovoltaic (PV) applications. Our calculations are founded on Shockley-Queisser (SQ) limit to simulate the open-circuit voltage, current density, and filling factor versus the variation of photon energy up to 4.0 eV. These key parameters of SQ change with the variation of energy between 0.3 to 3.5 eV. This is owing to the strong optical absorption (> 104 cm−1) and direct band gap of 1.5 eV, which make CdTe thin-film suitable for single junction solar cell and ideal for PV applications. It is observed that the optical absorption enhances as the thickness of the absorbed layer increases. This will effectively provide a theoretical support to the industry of global solar energy that is anticipated to be sustainable in the future.

In our simulations, we considered two typical magnetic materials, while the first one includes the 3d-transition metal, such as cobalt which is responsible of the presence of magnetism in pyrochlore structure Rb3CoCl5. The second magnetic material was chosen to have 4f-rare earth metal, namely dysprosium that can induce magnetism in garnet material Dy3Al5O12. A general agreement was found between our results and the previous works. In our calculations, we employed the classical Ising model for the above mentioned realistic materials. We specifically studied the magnetic properties over a range of temperature including the critical temperature and above it. To understand the magnetic phase transition, the effect of magnetic field was involved in the classical Ising model.

We study the emission spectrum and quantum-state fidelity for an atomic system interacting with radiation fields of quantum systems described by power-law potentials. We consider a set of manifold fields that are characterizable by their level-energy differences. They include triangular, infinite, and harmonic potentials as special cases. We present the time evolution of the spectrum and fidelity for this class of potentials with respect to model parameters of the physical system. The results indicate that the spectrum and fidelity during the dynamics are highly sensitive to the value of the photon-transition number and exponent parameter.

In this paper, we investigate the emission spectrum of a two-level atomic system interacting with an optical radiation field based on photon-added coherent states of a pseudo-harmonic oscillator (PACSPHO). Also, the purity of the optical field initially prepared in the PACS-PHO is studied through the evolution of the field entropy. We examine the influence of the intensity-dependent field and the photon-transition number on the dynamic behavior of the emission spectrum and field purity. We explore the link between the field purity and the emission spectrum during the time evolution. Finally, we show how the emission spectrum is affected and changed according to the main physical parameters. We find that there is some kind of correlation between the emission spectrum and the field purity, which will be useful in different applications of quantum physics and spectroscopy.

A p-n nanocomposite based on TiO

New homologues series of liquid crystalline materials namely, (E)-3-methoxy-4-[(p-tolylimino)methyl]phenyl 4-alkloxybenzoates (I-n), were designed and evaluated for their mesomorphic and optical behavior. The prepared series constitutes three members that differ from each other by the terminally attached alkoxy chain group, these vary between 6 and 12 carbons. A laterally OCH3 group is incorporated into the central benzene ring in meta position with respect to the ester moiety. Mesomorphic characterizations of the prepared derivatives are conducted using differential scanning-calorimetry (DSC), polarized optical-microscopy (POM). Molecular structures were elucidated by elemental analyses and NMR spectroscopy. DSC and POM investigations revealed that all the synthesized derivatives are purely nematogenic exhibiting only nematic (N) mesophase, except for the longest chain derivative (I-12) that is dimorphic possesses smectic A and N phases. Moreover, all members of the group have a wide mesomorphic range with high thermal nematic stability. A comparative study was established between the present derivative (I-6) and their previously prepared isomer. The results indicated that the location exchange of the polar compact group (CH3) influences the N mesophase stability and range. The electrical measurements revealed that all synthesized series I-n show Ohmic behaviors with effective electric resistances in the GΩ range. Under white light illumination, the effective electric conductivity for the compound I-8 is five times that obtained in dark conditions. This derivative also showed two direct optical band gaps in the UV and visible light range. In addition, I-6 has band energy gaps of values 1.07 and 2.79 eV, which are suitable for solar energy applications.

Porous anodic alumina membranes coated with Pt nanoparticles (PAAM/Pt) have been employed as pH sensor electrodes for H+ ion detection. The PAAM was designed using a two-step anodization process. Pt nanoparticles were then sputtered onto the membrane at different deposition times. The membrane’s morphological, chemical, and optical characteristics were carefully assessed following the fabrication stage using a variety of analytical techniques. The potential of the PAAM/Pt sensor electrode was investigated by measuring the potential using a simple potentiometric method. The effects of depositing Pt nanoparticles for 3–7 min on sensor electrode sensitivity were examined. The optimal potentiometric Nernstian response slope for the PAAM/Pt sensor electrode with 5 min Pt sputter coating is 56.31 mV/decade in the pH range of 3.0 to 10 at 293 K. Additionally, the PAAM/Pt sensor electrode’s stability and selectivity in various ions solutions were examined. The sensor electrode had a lifetime of more than six weeks and was kept in a normal air environment.

Indium Tin Oxide (ITO) films were deposited on glass substrate using radiofrequency (RF) magnetron sputtering technique. To improve the physical characteristics of the ITO film, AlN and HfO2 buffer layers were deposited on glass prior to the film deposition. The ITO/glass, ITO/AlN/glass and ITO/HfO2/glass films were annealed using CO2 laser and electrical oven heating methods. The crystallinity of the ITO film was improved due to the incorporation of AlN and HfO2 buffer layers and also by the post-deposition annealing process. The optical transmittance of the ITO was also increased due to the presence of the buffer layers. Similarly, the annealed ITO films grown on buffer layers exhibited lower values of the sheet resistance as compared to the film deposited without buffer layers. The laser annealing technique was more found to be more effective in reducing the ITO sheet resistance.

This article is mainly a complementary study of a novel part of π-conjugated copolymers based on the poly (N-vinylcarbazole) (PVK) and poly (9,9-dioctylfluorene-co-bithiophene) (F8T2) unit based on the Density Functional Theory (DFT) and Time-Dependent Density Functional Theory (TD-DFT). This study is carried out to explore the structural and optoelectronic characteristics of a new organic material named PVK-F8T2. First, the structural, optical (absorption, photoluminescence, optical transition), electronic (molecular orbital (MO), energy-level diagram) and vibratory parameters of infrared (IR) were computed and compared with experimental studies. In addition, we calculated the level energy of the excited states and their corresponding transitions. Obviously, electronic parameters such as highest occupied and lowest unoccupied molecular orbital (HOMO and LUMO), ionization potential (IP), electronic affinity (EA) and the energy band gap (Eg) were computed in order to elucidate the intramolecular charge transport and to establish the energetic diagrams of the PVK-F8T2 copolymer for different states. The results obtained looked with precision at future optoelectronic applications. From these results, we have shown that the PVK-F8T2 has significant optoelectronic properties and seems usable as an active layer in organic light-emitting diodes (OLEDs).

New mesomorphic series, 4-hexadecyloxy phenyl-imino-4′-(3-methoxyphenyl)-4″-alkoxybenzoates (An), were prepared and investigated with different thermal and mesomorphic techniques. The synthesized homologous series constitutes four members that differ from each other in the terminal length of flexible chain (n) attached to phenyl ester moiety, which varies between n = 6, 8, 10, and 12 carbons. A lateral CH3O group is attached to the central benzene ring in the meta position with respect to the ester moiety. Molecular structures of all newly prepared homologues were elucidated via FT-IR, 1H and 13C NMR spectroscopy. Mesomorphic and thermal properties were examined by differential scanning calorimetry (DSC), thermogravimetric analysis (TGA) and the mesophases identified by polarized optical microscopy (POM). DSC and POM examinations revealed that all members of the present series (An) exhibit a purely enantiotropic nematic (N) phase. Comparative evaluations and binary phase diagrams were established between the present homologues and their corresponding shorter one (Bn). The examination revealed that, the length of the flexible alkoxy chain incorporated into the phenylimino moiety is highly effective on the temperature range and stability of the mesophase observed. With respect to the binary mixtures An/Bn, the exhibited N phase showed to cover the whole composition range with eutectic behavior.

Pesticide residues are harmful to the environment and human and animal health even at low levels because of long-term bioaccumulation. In this study, photolysis was applied to treat three representative water samples: aqueous atrazine and dimethoate solutions as target pesticides, as well as wastewater and agriculture wastewater containing pesticide residue. It was performed using ultraviolet (UV) irradiation at two wavelengths (254 and 306 nm) with exposure times ranging from 2 to 12 h in the presence and absence of a photocatalyst to identify the optimal degradation conditions. Extraction and analyzation process were performed by the Quick Easy Cheap Effective Rugged Safe (QuEChERS) methods and gas chromatography–tandem mass spectrometry with triple quadrupole detector (GC–MSMS/TQD), respectively. Photodegradation increased with an increase in exposure time and the TiO2 catalyst was beneficial for degradation. Both selected irradiation wavelengths were effective, although the wavelength of λ = 306 nm was the most efficient.

We propose a new kind of Schr&ouml, dinger cat state introduced as a superposition of spin coherent states in the framework of noncommutative spaces. We analyze the nonclassical features for these noncommutative deformed states in terms of the main physical parameters. The physical importance of deformed states is that they provide a convenient description of a large set of laser systems. As an application, we develop the Jaynes&ndash, Cummings model by considering the interaction among atoms and cat state fields associated to deformed spin algebras. In this context, we show the dynamical behavior of the nonlocal correlation and nonclassical properties in these quantum systems.

This work presents a study on the characteristics of the radiation attenuating behavior of oxy-fluoro borotellurite glasses with general formula TeO2–B2O3–LiF–BaO–Bi2O3. The mass attenuation coefficient (MAC) decreases pointedly as the energy goes up from 15 keV–0.15 MeV. The MAC for the tested samples lies within the range 40.032–50.170 cm2/g at 15 keV. We examined the effective atomic number (Zeff), and the results revealed that initially Zeff reaches the maximum values up to around 0.1 MeV and then Zeff decreases and reaches the minimum values between around 1 and 4 MeV. The Zeff lies within the range of 56.11–57.85 (at 15 keV). The Zeff of the tested samples increases with the increasing content of TeO2. The half value layer (HVL) was evaluated, and the effect of TeO2 and the energy on this parameter was discussed. The minimum HVL was reported at 15 keV and varied between 0.00463–0.00226 cm.

One of the most serious environmental concerns worldwide is the consequences of industrial wastes and agricultural usage leading to pesticide residues in water. At present, a wide range of pesticides are used directly to control pests and diseases. However, environmental damage is expected even at their low concentration because they are sustained a long time in nature, which has a negative impact on human health. In this study, photolysis and photocatalysis of the pesticides dieldrin and deltamethrin were tested at two UV wavelengths (254 and 306 nm) and in different test media (distilled water, wastewater, and agricultural wastewater) to examine their ability to eliminate pesticides. TiO2 (0.001 g/10 mL) was used as a catalyst for each treatment. The purpose was to determine the influence of UV wavelength, exposure time, and catalyst addition on the pesticide decomposition processes in different water types. Water was loaded with the tested pesticides (2000 µg) for 12 h under UV irradiation, and the pesticide concentrations were measured at 2 h intervals after UV irradiation. The results showed a clear effect of UV light on the pesticides photodegradations that was both a wavelength- and time-dependent effect. Photolysis was more effective at λ = 306 nm than at λ = 254 nm. Furthermore, TiO2 addition (0.001 g/10 mL) increased the degradation at both tested wavelengths and hence could be considered a potential catalyst for both pesticide degradations. Deltamethrin was more sensitive to UV light than dieldrin under all conditions.

A quaternary glass system was fabricated via the melting quenching method. The mentioned glass system consists of five samples described by the chemical composition 50B2O3 + 30BaF2 + (20-x)Li2O + xAg2O, 0.0

The purpose of this investigation is to study the physical, structural and optical characteristics of a newly fabricated SrO2 doped lithium bismuth borate glass system. The current glass system was fabricated according to the chemical formula 50B2O3 + 25Bi2O3 + (25-x) Li2O + xSrO2, utilizing the solid state- conventional method. It was noticed that The glass density increased from 4.821 to 5.952 g cm−3 whilst the molar volume was decreasing in the range from 32.93 to 30.44 cm3 mol−1 with increase the SrO2 insertion from 0 (BBLSr0 glasses) to 25 (BBLSr25) respectively. The structure of the fabricated glasses was inspected utilizing X-ray diffraction method which clarified that the insertion of SrO2 didn’t affect the amorphous nature of the tested samples. Furthermore, the UV–vis absorption spectrum was utilized to study the UV absorption characteristics for the fabricated glasses. The UV–vis absorption spectrum showed that the absorption and transition bands increase with insertion of the SrO2 contents. Based on the UV/Vis data, several important optical features were calculated like the energy gap (Eg), Urbach energy (Eu), oscillator energy (Eo) and energy of distribution (Ed). Increasing the SrO2 substitution ratio led to increase the optical properties where the refractive index was found to increase from 3.056 to 5.710.

In the present work, the optical, electronic and thermoelectric (TE) characteristics of NaTaO3 are investigated with implementation of pressure ranging 0 to 140 GPa.The calculations were done in the framework of density functional theory (DFT) within Perdew-Burke-Ernzerhof generalized gradient approximation (PBE-GGA) scheme implemented within WIEN2K package. The semiconducting Eg behavior of NaTaO3compound has been revealed at all applied pressures. Results indicated that the value of Eg increments from 2.29 eV (0 GPa) to 2.82 eV (140 GPa), however, the characteristics of Eg transformed to direct from indirect with the increment in pressure. The optical characteristics are also explored in the form of dielectric constants, reflectivity (R (ω)) and absorption coefficient (α (ω)). Moreover, the TE characteristics are also investigated. TE and optical features disclosed that NaTaO3 is a good candidate for optical and TE devices.

A very interesting challenge concerns the elaboration of nanowires from organic polymers with the aim to design novel nanoelectronic devices. The new VK-Stilbene copolymer based on organic nanowires was developed and characterized in this context. The VK-Stilbene nanowires were made with a template method by filling nanopores of AOO membranes. The prepared nanowires wereinvestigated by morphological spectroscopy and micro-Raman Rinshaw analysis. The modifications of photoemissive properties from microscopy film to nanowires were described by steady-state optical techniques combinedwith time-resolved photoluminescence spectroscopy. A blue shift of the luminescence are observed in the case of nanowires proceed from structural order and shortening of effective conjugation lengths. Therefore, VK-Stilbene nanowires exhibit a remarkably quasi-exponential long-lived and blue-shifted ascribed to a confinement-effect of intra-chain singlet excitons. Additionally, these nano-objects show an increase in the quantum yield with respect to bulk samples. The acquired optical data confirm that VK-Stilbene nanomaterials may be suitable for nanotechnologies.

In this research, the radiation safety features and the optical properties of novel prepared glass samples with nominal compositions 45P2O5 + 25B2O3 + 20Bi2O3 + (10-x)Li2O+xCdO where x = 0, 2.5, 5, 7.5, and 10 have been studied. The XRD was utilized to exclude the crystal structure nature of the glass samples. The density of the samples increases while the molar volume decreases with the rise of the CdO incrementation ratio. The UV-Vis NIR spectroscopy was utilized to measure the absorbance rate of the fabricated glass sample. Based on the measured absorbance, some important parameters were evaluated, such as the energy gap, Urbach energy, refractive index. The Monte-Carlo simulation code was utilized to evaluate the radiation attenuation properties of the current glass samples in the energy range 0.015 till 15 MeV.

The nanostructured materials from Ag and Au@Ag core/shell bimetallic were synthesized by pulsed infrared laser ablation process in different liquid media technique in just one-pot step. By varying the surrounding media by metallic precursor solution and the laser energy, the monometallic nanoparticles were changed to bimetallic nanocomposites in a form of core/shell structure with tuning their shell thickness. The prepared nanostructured materials were examined by different spectroscopic techniques to inform their physicochemical properties. The characterization techniques proved that the crystallinity of prepared samples. Besides, the bimetallic nanocomposite structure has a core/shell form with Au in the core and Ag in shell. Also, as the laser intensity raises, the Ag-shell’s thickness grows, and the core/shell diameter increases, which was affected in their linear and nonlinear optical properties. Their linear properties were investigated depended on Mie theory. Besides, the nonlinear optical parameters were determined by Z-scan technique, which demonstrated that the nonlinear optical properties of a shell can be tuned depending on their thickness. The prepared core/shell nanocomposites with different particle sizes confirmed the capability for possible application in optoelectronic applications as good optical limiting materials.

An amendment to this paper has been published and can be accessed via a link at the top of the paper.