The adsorption of crystal violet (CV) onto date palm fibers (DPFs) was examined in aqueous solution at 25°C. The experimental maximum adsorption capacity value was0.66×10−6. Langmuir, Freundlich, Elovich and Temkin models were applied to describe the equilibrium isotherms. The influence of pH and temperature on dye removal was evaluated. The percentage removal of CV dye by adsorption onto DPF at different pH and temperatures showed that these factors play a role in the adsorption process. Thermodynamic analysis was performed, and the Gibbs free energyΔGο, enthalpy changeΔHο, and entropyΔSοwere calculated. The negative values ofΔGοindicate spontaneous adsorption. The negative value ofΔHοindicates that the interaction between CV and DPF is exothermic, and the positive value ofΔSοindicates good affinity between DPF and CV. The kinetic data were fitted to a pseudo-second-order model.

A series of virgin and lithia-doped Ni ferrites was synthesized using egg-white-mediated combustion. Characterization of the investigated ferrites was performed using several techniques, specifically, X-ray Powder Diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), and High-resolution transmission electron microscopy (HRTEM). XRD-based structural parameters were determined. A closer look at these characteristics reveals that lithia doping enhanced the nickel ferrite lattice constant (a), unit cell volume (V), stress (ε), microstrain (σ), and dislocation density (δ). It also enhanced the separation between magnetic ions (LA and LB), ionic radii (rA, rB), and bond lengths (A-O and B-O) between tetrahedral (A) and octahedral (B) locations. Furthermore, it enhanced the X-ray density (Dx) and crystallite size (d) of random spinel nickel ferrite displaying opposing patterns of behavior. FTIR-based functional groups of random spinel nickel ferrite were determined. HRTEM-based morphological properties of the synthesized ferrite were investigated. These characteristics of NiFe2O4 particles, such as their size, shape, and crystallinity, demonstrate that these manufactured particles are present at the nanoscale and that lithia doping caused shape modification of the particles. Additionally, the prepared ferrite’s surface area and total pore volume marginally increased after being treated with lithia, depending on the visibility of the grain boundaries. Last, but not least, as the dopant content was increased through a variety of methods, the magnetization of virgin nickel ferrite fell with a corresponding increase in coercivity. Uniaxial anisotropy, rather than cubic anisotropy, and antisite and cation excess defects developed in virgin and lithia-doped nickel ferrites because the squareness ratio (Mr/Ms) was less than 0.5. Small squareness values strongly recommend using the assessed ferrites in high-frequency applications.

The spread of organic pollutants in water spoils the environment, and among the best-known sorbents for removing organic compounds are carbonaceous materials. Sunflower seed waste (SFSW) was employed as a green and low-cost precursor to prepare carbon nanoparticles (CNPs) via pyrolysis, followed by a ball-milling process. The CNPs were treated with a nitric–sulfuric acid mixture (1:1) at 100 °C. The scanning electron microscopy (SEM) showed a particle size range of 38 to 45 nm, and the Brunauer–Emmett–Teller (BET) surface area was 162.9 m2 g−1. The elemental analysis was performed using energy-dispersive X-ray spectroscopy, and the functional groups on the CNPs were examined with Fourier transform infrared spectroscopy. Additionally, an X-ray diffractometer was employed to test the phase crystallinity of the prepared CNPs. The fabricated CNPs were used to adsorb ciprofloxacin (CFXN) and malachite green (MLG) from water. The experimentally obtained adsorption capacities for CFXN and MLG were 103.6 and 182.4 mg g−1, respectively. The kinetic investigation implied that the adsorption of both pollutants fitted the pseudo-first-order model, and the intraparticle diffusion step controlled the process. The equilibrium findings for CFXN and MLG sorption on the CNPs followed the Langmuir and the Fredulich isotherm models, respectively. It was concluded that both pollutants spontaneously adsorbed on the CNPs, with physisorption being the likely mechanism. Additionally, the FTIR analysis of the adsorbed CFXN showed the disappearance of some functional groups, suggesting a chemisorption contribution. The CNPs showed an excellent performance in removing CFXN and MLG from groundwater and seawater samples and possessed consistent efficiency during the recycle–reuse study. The application of CNPs to treat synthetically contaminated natural water samples indicated the complete remediation of polluted water using the ball-mill-fabricated CNPs.

In this study, the adsorption of malachite green (MG) onto date palm fibers (DPF) was examined in aqueous solutions. The Langmuir and Freundlich adsorption isotherm models were employed to describe the equilibrium adsorption data. The Freundlich isotherm model was found to fit the adsorption data The removal percentage of MG dye from aqueous solutions via adsorption onto DPF adsorbent varied with pH and temperature, showing that these factors play a key role in the adsorption process. The removal percentage was found to increase with decrease in the solution temperature and in alkaline media. The adsorption kinetic data were fitted with a pseudo-secondorder model.

The sensors are effectively used in the determination of Hq and Cat in a real water sample.

Perovskite solar cells (PSCs) are considered highly efficient and hold great potential for next‐generation photovoltaic devices due to their excellent properties. However, there are some challenges that hinder their mass production, such as toxicity in lead‐based PSCs, nonstability, and high manufacturing costs. This study aims to address these challenges by proposing a device modeling approach to optimize the design of highly efficient lead‐free cesium titanium bromide (Cs2TiBr6) perovskite solar cells. Cs2TiBr6‐based perovskite solar cells have low performance due to the lack of suitable electron and hole transport layers. Therefore, this study utilizes numerical simulations in SCAPS‐1D to investigate the effect of different parameters, including the doping density of optimized hole and electron transport layers, the thickness of the absorber layer, the NA/ND of the absorption layer, and the defect concentration. The study models six different device structures with different hole transport layerss. However, an optimized novel structure device Se/CuSbS2/Cs2TiBr6/IZGO/FTO/Glass has been proposed, with a theoretical power conversion efficiency of 29.19%. This device has a VOC of 1.33 V, JSC of 24.28 mA cm−2, and FF of 90.46%. Overall, this study demonstrates the potential of Cs2TiBr6 as a promising material for perovskite solar cells, providing a nontoxic, green renewable energy solution for the future.

The innovative lead‐free formamidinium tin‐based perovskite solar cell structure is considered nontoxic and potentially more stable than lead‐based, although its performance is not yet excellent. This research aims to enhance the power conversion efficiency of perovskite solar cells and reduce the recombination losses. According to device modeling, the FASnI3 perovskite solar cell demonstrates a packing conversion efficiency of 14.3% (open circuit voltage (Voc) = 0.899 V, fill factor (FF) = 58.9%, and current density (Jsc) = 26.06 mA cm−2) by employing Bi hole transporting layers, a copper oxide, and crystalline silicon layers. Some features that affect the device include the thickness of each layer, the doping density of copper oxide and a silicon layer, and the back contact metalwork function. It is proposed that Bi‐HTL reduce the carriers to enter hole transport layer (HTL) as the doping change so that decreasing charge carriers recombination and enhancing the device efficiency in tin‐based perovskite solar cell with the structure of ITO/TiO2/FASnI3/CuO/Si/C. Furthermore, the impacts of various charge transport layers on energy band alignment, recombination, electric field, and IV properties are thoroughly explored.

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