Search Results (31)

From the lanthanide group, part of the rare earth elements (REEs), lanthanum is one of the most important elements given its application potential. Although it does not have severe toxicity to the environment, its increased usage in advanced technologies and medical fields and scarce natural reserves point to the necessity also of recovering lanthanum from diluted solutions. Among the multiple methods for separation and purification, adsorption has been recognized as one of the most promising because of its simplicity, high efficiency, and large-scale availability. In this study, a xerogel based on silicon and iron oxides doped with zinc oxide and polymer (SiO₂@Fe₂O₃@ZnO) (SFZ), obtained by the sol–gel method, was considered as an adsorbent material. Micrography indicates the existence of particles with irregular geometric shapes and sizes between 16 μm and 45 μm. Atomic force microscopy (AFM) reveals the presence of dimples on the top of the material. The specific surface area of the material, calculated by the Brunauer–Emmet–Teller (BET) method, indicates a value of 53 m²/g, with C constant at a value of 48. In addition, the Point of Zero Charge (pH_pZc) of the material was determined to be 6.7. To establish the specific parameters of the La(III) adsorption process, static studies were performed. Based on experimental data, kinetic, thermodynamic, and equilibrium studies, the mechanism of the adsorption process was established. The maximum adsorption capacity was 6.7 mg/g, at a solid/liquid ratio = 0.1 g:25 mL, 4 < pH < 6, 298 K, after a contact time of 90 min. From a thermodynamic point of view, the adsorption process is spontaneous, endothermic, and occurs at the adsorbent–adsorbate interface. The Sips model is the most suitable for describing the observed adsorption process, indicating a complex interaction between La(III) ions and the adsorbent material. The material can be reused as an adsorbent material, having a regeneration capacity of more than 90% after the first cycle of regeneration. The material was reused 3 times with considerable efficiency. Full article

This study introduces a novel approach to biodiesel production by repurposing starfish, an abundant marine waste, as a sustainable catalyst material. Starfish, primarily composed of Ca-Mg carbonate, were calcined to produce calcium oxide (CaO) and magnesium oxide (MgO), which were subsequently doped with varying zinc loadings through hydrothermal treatment. This innovative use of marine waste not only addresses environmental concerns but also provides a cost-effective catalyst source. Among the tested compositions, the catalyst doped with 10 wt% Zn achieved the highest biodiesel yield of 96.6%, outperforming both lower and higher Zn loadings. Zinc incorporation significantly improved the catalyst’s surface area, pore volume, and active site density, as confirmed by X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and Brunauer–Emmett–Teller (BET) surface analysis. These enhancements facilitated a biodiesel yield of 96.6% within 10 h, a substantial increase compared to the undoped catalyst (86.5%) under identical conditions. Reusability tests further confirmed the catalyst’s high activity over three consecutive cycles, with yields of 96.6%, 94.2%, and 86.5%, respectively, while SEM-EDS analysis demonstrated effective Zn retention after repeated use. This study demonstrates a pioneering strategy for transforming marine waste into a high-performance catalyst, paving the way for sustainable biodiesel production. Full article

This study synthesized graphene oxide (GO)/zinc oxide (ZnO)/silver (Ag) composite materials and investigated their photocatalytic degradation performance for ciprofloxacin (CIP) under visible light irradiation. GO/ZnO/Ag composites with different ratios were prepared via an impregnation and chemical reduction method and characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FT-IR), and X-ray photoelectron spectroscopy (XPS). The results demonstrated that under optimal conditions (20 mg/L CIP concentration, 15 mg catalyst dosage, GO/ZnO-3%/Ag-doping ratio, and pH 5), the GO/ZnO/Ag composite exhibited the highest photocatalytic activity, achieving a maximum degradation rate of 82.13%. This catalyst effectively degraded ciprofloxacin under light irradiation, showing promising potential for water purification applications. Full article

Two series of the bismuth tantalate pyrochlore samples, codoped with Mg,Mn and Zn,Mn, were synthesized via solid-phase reaction. It was established that the Bi₂Mg(Zn)_xMn_1−xTa₂O_9.5−Δ (x = 0.3; 0.5; 0.7) samples contain the main phase of cubic pyrochlore (sp. gr. Fd-3m) and an admixture of triclinic BiTaO₄ (sp. gr. P-1). In both sets, the amount of BiTaO₄ is proportional to the amount of manganese doping, however, zinc-containing samples have a higher level of impurities than magnesium-containing ones. The unit cell parameter of the Zn,Mn codoped bismuth tantalate phase increases with an increasing content of zinc ions in the samples from 10.4895(5) (x = 0.3) to 10.5325(5) Å (x = 0.7). The unit cell parameter of Mg,Mn codoped bismuth tantalate pyrochlores increases uniformly with an increasing index x(Mg) from 10.4970(8) at x = 0.3 to 10.5248(8) Å at x = 0.7, according to the Vegard rule. The NEXAFS and XPS data showed that the ions were found to have oxidation states of Bi(+3), Ta(+5), Zn(+2) and Mg(+2). In the Ta 4f XPS spectrum of both series of samples, a low energy shift of the absorption band characteristic of tantalum ions with an effective charge of (+5-δ) was observed. The XPS spectra of Bi4f7/2 and Bi4f5/2 also show a shift of bands towards lower energies which is attributed to the presence of some low-charge ions of transition elements in the bismuth position. The NEXAFS spectroscopy data showed that manganese ions in both series of samples have predominantly 2+ and 3+ oxidation states. XPS data indicate that in zinc-containing preparations the proportion of oxidized manganese ions is higher than in magnesium-containing ones. Full article

Zinc oxide (ZnO) nanoparticles were synthesized hydrothermally using zinc acetate dihydrate and sodium thiosulfate pentahydrate precursors. The synthesized powders were sintered in air at 600 °C for different durations with a Cl-doping concentration of 25 mg/g. The optimal sintering time was found to be 5 h, resulting in the successful formation of the ZnO phase with small particle sizes of around 90 nm, nominal atomic fractions of Zn and O (~50%, ~50%), and increased luminescence intensity. The ideal concentration of Cl was discovered to be 25 mg/g of ZnO, which resulted in the highest luminescence intensity. The ZnO luminescence characteristics were observed in emission bands peaking at approximately 503 nm attributed to the transition from oxygen vacancies. A considerable improvement in the emission intensity was observed with increased Cl doping concentration, up to eight orders of magnitude, compared to pristine ZnO nanoparticles. However, the luminescence intensity decreased in samples with higher concentrations of Cl doping due to concentration quenching. These preliminary outcomes suggest that Cl-doped ZnO nanoparticles could be used for radiation detector development for radon monitoring and other related applications. Full article

Free-form factor optoelectronics is becoming more important for various applications. Specifically, flexible and transparent optoelectronics offers the potential to be adopted in wearable devices in displays, solar cells, or biomedical applications. However, current transparent electrodes are limited in conductivity and flexibility. This study aims to address these challenges and explore potential solutions. For the next-generation transparent conductive electrode, Al-doped zinc oxide (AZO) and silver (AZO/Ag/AZO) deposited by in-line magnetron sputtering without thermal treatment was investigated, and this transparent electrode was used as a transparent organic light-emitting diode (OLED) anode to maximize the transparency characteristics. The experiment and simulation involved adjusting the thickness of Ag and AZO and OLED structure to enhance the transmittance and device performance. The AZO/Ag/AZO with Ag of 12 nm and AZO of 32 nm thickness achieved the results of the highest figure of merit (FOM) (Φ₅₅₀ = 4.65 mΩ⁻¹) and lowest roughness. The full structure of transparent OLED (TrOLED) with AZO/Ag/AZO anode and Mg:Ag cathode reached 64.84% transmittance at 550 nm, and 300 cd/m² at about 4 V. The results demonstrate the feasibility of adopting flexible substrates, such as PET, without the need for thermal treatment. This research provides valuable insights into the development of transparent and flexible electronic devices. Full article

This review addresses the importance of Zn for obtaining multifunctional materials with interesting properties by following certain preparation strategies: choosing the appropriate synthesis route, doping and co-doping of ZnO films to achieve conductive oxide materials with p- or n-type conductivity, and finally adding polymers in the oxide systems for piezoelectricity enhancement. We mainly followed the results of studies of the last ten years through chemical routes, especially by sol-gel and hydrothermal synthesis. Zinc is an essential element that has a special importance for developing multifunctional materials with various applications. ZnO can be used for the deposition of thin films or for obtaining mixed layers by combining ZnO with other oxides (ZnO-SnO₂, ZnO-CuO). Also, composite films can be achieved by mixing ZnO with polymers. It can be doped with metals (Li, Na, Mg, Al) or non-metals (B, N, P). Zn is easily incorporated in a matrix and therefore it can be used as a dopant for other oxidic materials, such as: ITO, CuO, BiFeO_3, and NiO. ZnO can be very useful as a seed layer, for good adherence of the main layer to the substrate, generating nucleation sites for nanowires growth. Thanks to its interesting properties, ZnO is a material with multiple applications in various fields: sensing technology, piezoelectric devices, transparent conductive oxides, solar cells, and photoluminescence applications. Its versatility is the main message of this review. Full article

In this study, a valuable adsorbent was functionalized using commercial ZnO and a mango seed extract (MS-Ext) as a green approach for synthesis. Fourier-transform infrared spectroscopy, transmission electron microscopy, scanning electron microscopy, and energy-dispersive X-ray analysis spectraconfirmed the presence of bioactive phenolic compounds and ${\mathrm{Cu}}^{2+}$ ions on the surface of ZnO. Functionalized Cu-doped ZnO/MS-Ext exhibits high efficacy in acidic, neutral, and alkaline medium, as indicated by 98.3% and 93.7% removal of methylene blue (MB) and crystal violet (CV) dyes, respectively. Cu-doped ZnO/MS-Ext has a zeta potential significantly lower than pristine zinc oxide (p-ZnO), which results in enhanced adsorption of cationic MB and CV dyes. In binary systems, both MB and CV were significantly removed in acidic and alkaline media, with 92% and 87% being removed for CV in acidic and alkaline media, respectively. In contrast, the removal efficiency of methyl orange dye (MO) was 16.4%, 6.6% and 11.2% for p-ZnO, ZnO/Ext and Cu-doped ZnO/Ext, respectively. In general, the adsorption kinetics of MB on Cu-doped ZnO/MS-Ext follow this order: linear pseudo-second-order (PSO) > nonlinear pseudo-second-order (PSO) > nonlinear Elovich model > linear Elovich model. The Langmuir isotherm represents the adsorption process and indicates that MB, CV, and MO are chemisorbed onto the surface of the adsorbent at localized active centers of the MS-extract functional groups. In a binary system consisting of MB and CV, the maximum adsorption capacity (q_m) was 72.49 mg/g and 46.61 mg/g, respectively. The adsorption mechanism is governed by electrostatic attraction and repulsion, coordination bonds, and π–π interactions between cationic and anionic dyes upon Cu-doped ZnO/Ext surfaces. Full article

A new type of perovskite solar cell based on mixed tin and germanium has the potential to achieve good power conversion efficiency and extreme air stability. However, improving its efficiency is crucial for practical application in solar cells. This paper presents a quantitative analysis of lead-free FA_0.75MA_0.25Sn_0.95Ge_0.05I₃ using a solar cell capacitance simulator to optimize its structure. Various electron transport layer materials were thoroughly investigated to enhance efficiency. The study considered the impact of energy level alignment between the absorber and electron transport layer interface, thickness and doping concentration of the electron transport layer, thickness and defect density of the absorber, and the rear metal work function. The optimized structures included poly (3,4-ethylenedioxythiophene)polystyrene sulfonate (PEDOT:PSS) as the hole transport layer and either zinc oxide (ZnO) or zinc magnesium oxide (Zn_0.7Mg_0.3O) as the electron transport layer. The power conversion efficiency obtained was 29%, which was over three times higher than the initial structure. Performing numerical simulations on FA_0.75MA_0.25Sn_0.95Ge_0.05I₃ can significantly enhance the likelihood of its commercialization. The optimized values resulting from the conducted parametric study are as follows: a short-circuit current density of 30.13 mA·cm⁻²), an open-circuit voltage of 1.08 V, a fill factor of 86.56%, and a power conversion efficiency of 28.31% for the intended solar cell. Full article

Hardystonite-based (HT) bioceramic foams were easily obtained via thermal treatment of silicone resins and reactive oxide fillers in air. By using a commercial silicone, incorporating strontium oxide and magnesium oxide precursors (as well as CaO and ZnO), and treating it at 1100 °C, a complex solid solution (Ca_1.4Sr_0.6Zn_0.85Mg_0.15Si₂O₇) that has superior biocompatibility and bioactivity properties compared to pure hardystonite (Ca₂ZnSi₂O₇) can be obtained. Proteolytic-resistant adhesive peptide mapped on vitronectin (D2HVP), was selectively grafted to Sr/Mg-doped HT foams using two different strategies. Unfortunately, the first method (via protected peptide) was unsuitable for acid-sensitive materials such as Sr/Mg-doped HT, resulting in the release of cytotoxic levels of Zinc over time, with consequent negative cellular response. To overcome this unexpected result, a novel functionalization strategy requiring aqueous solution and mild conditions was designed. Sr/Mg-doped HT functionalized with this second strategy (via aldehyde peptide) showed a dramatic increase in human osteoblast proliferation at 6 days compared to only silanized or non-functionalized samples. Furthermore, we demonstrated that the functionalization treatment does not induce any cytotoxicity. Functionalized foams enhanced mRNA-specific transcript levels coding IBSP, VTN, RUNX2, and SPP1 at 2 days post-seeding. In conclusion, the second functionalization strategy proved to be appropriate for this specific biomaterial and was effective at enhancing the material’s bioactivity. Full article

Magnesium hydrides (MgH₂) have drawn a lot of interest as a promising hydrogen storage material option due to their good reversibility and high hydrogen storage capacity (7.60 wt.%). However, the high hydrogen desorption temperature (more than 400 °C) and slow sorption kinetics of MgH₂ are the main obstacles to its practical use. In this research, nickel zinc oxide (Ni_0.6Zn_0.4O) was synthesized via the solid-state method and doped into MgH₂ to overcome the drawbacks of MgH₂. The onset desorption temperature of the MgH₂–10 wt.% Ni_0.6Zn_0.4O sample was reduced to 285 °C, 133 °C, and 56 °C lower than that of pure MgH₂ and milled MgH₂, respectively. Furthermore, at 250 °C, the MgH₂–10 wt.% Ni_0.6Zn_0.4O sample could absorb 6.50 wt.% of H₂ and desorbed 2.20 wt.% of H₂ at 300 °C within 1 h. With the addition of 10 wt.% of Ni_0.6Zn_0.4O, the activation energy of MgH₂ dropped from 133 kJ/mol to 97 kJ/mol. The morphology of the samples also demonstrated that the particle size is smaller compared with undoped samples. It is believed that in situ forms of NiO, ZnO, and MgO had good catalytic effects on MgH₂, significantly reducing the activation energy and onset desorption temperature while improving the sorption kinetics of MgH₂. Full article

Renewable energy can be harnessed from wastewater, whether from municipalities or industries, but this potential is often ignored. The world generates over 900 km³ of wastewater annually, which is typically treated through energy-consuming processes, despite its potential for energy production. Environmental pollution is a most important and serious issue for all and their adulterations to the aquatic system are very toxic in very low concentrations. Photocatalysis is a prominent approach to eliminating risky elements from the environment. The present study developed Zinc oxide (ZnO), Copper-doped Zinc oxide (CuZnO), and Cobalt-doped Zinc oxide (CoZnO) nanostructures (NSs) by facile hydrothermal route. The crystalline and structural stability of the synthesized nanostructures were evident from XRD and FESEM analysis. Metal, and oxygen bond and their interaction on the surfaces and their valency were explored from XPS spectra. Optical orientations and electron movements were revealed from UV-Visible analysis. After 100 min exposure time with 1 g of catalyst concentration 60%, 70%, and 89% of dye degraded, for dye concentration (5 mg/L to 50 mg/L), the huge variation observed (70% to 22%), (80% to 16%), (94% to 10%). The highest photodegradation rate (55%, 75%, 90%) was observed on pH~12 using ZnO, CoZnO, and CuZnO respectively. Photodegradation of methylene blue confirmed the largest surface area, rate of recombination, photo-excited charge carriers, photo-sensitivity range, and radical generations of ZnO, CuZnO, and CoZnO. The present study, therefore, suggested that CuZnO would be preferred to produce nanomaterials for industrial wastewater treatment like methylene. Full article

Kesterite Cu₂ZnSnS₄ (CZTS) thin films using various 1,8-diiodooctane (DIO) polymer additive concentrations were fabricated by the electrochemical deposition method. The optical, electrical, morphological, and structural properties of the CZTS thin films synthesized using different concentrations of 5 mg/mL, 10 mg/mL, 15 mg/mL, and 20 mg/mL were investigated using different techniques. Cyclic voltammetry exhibited three cathodic peaks at −0.15 V, −0.54 V, and −0.73 V, corresponding to the reduction of Cu²⁺, Sn²⁺, Sn²⁺, and Zn²⁺ metal ions, respectively. The analysis of the X-ray diffraction (XRD) pattern indicated the formation of the pure kesterite crystal structure, and the Raman spectra showed pure CZTS with the A1 mode of vibration. Field emission scanning electron microscopy (FE-SEM) indicated that the films are well grown, with compact, crack-free, and uniform deposition and a grain size of approximately 4 µm. For sample DIO-20 mg/mL, the elemental composition of the CZTS thin film was modified to Cu:Zn:Sn: and S = 24.2:13.3:12.3:50.2, which indicates a zinc-rich and copper-poor composition. The X-ray photoelectron spectroscopy (XPS) results confirmed the existence of Cu, Sn, Zn, and S elements and revealed the element oxidation states. The electrochemical deposition synthesis increased the absorption of the CZTS film to more than 10⁴ cm⁻¹ with a band gap between 1.62 eV and 1.51 eV. Finally, the photovoltaic properties of glass/CZTS/CdS/n-ZnO/aluminum-doped zinc oxide (AZO)/Ag solar cells were investigated. The best-performing photovoltaic device, with a DIO concentration of 20 mg/mL, had a short-circuit current density of 16.44 mA/cm², an open-circuit voltage of 0.465 V, and a fill factor of 64.3%, providing a conversion efficiency of 4.82%. Full article

In this work, acetone gas sensors were fabricated using pre-annealing metal oxide zinc oxide (pa-ZnO)-doped perovskite cesium lead bromide (CsPbBr₃). The ZnO nanopowder, before it was doped into CsPbBr₃ solution, was first put into a furnace to anneal at different temperatures, and formed the pa-ZnO. The properties of pa-ZnO were different from ZnO. The optimized doping conditions were 2 mg of pa-ZnO nanopowder and pre-annealing at 300 °C. Under these conditions, the highest sensitivity (gas signal current-to-air background current ratio) of the ZnO-doped CsPbBr₃ perovskite acetone sensor was 1726. In addition, for the limit test, 100 ppm was the limit of detection of the ZnO-doped CsPbBr₃ perovskite acetone sensor and the sensitivity was 101. Full article

In the current study, nanocomposites were prepared by combining $k$-carrageenan, polyvinyl alcohol (PVA), and doped nanoparticles (Magnesium oxide) MgO, (Magnesium Zinc oxide) MgZnO 1%, MgZnO 3%, and MgZnO 5%. The nanoparticles were synthesized by a sol–gel method and mixed with a mixture of $k$-carrageenan/PVA (Ca/PVA) in various ratios. The structure of the composites was analyzed using thermogravimetric analysis (TGA), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR). The Ca/PVA mixture was then mixed with nanoparticles and loaded with active ingredient, catechin. Scanning electron microscope (SEM) and texture analysis were performed to analyze the nanocomposites. Entrapment efficiency (EE%) and drug release studies confirmed that $k$-carrageenan/PVA/MgZnO 5% had the highest EE% at 81.58% and a drug release of 75.21% $\pm$ 0.94. The EE% of $k$-carrageenan/PVA/MgO was 55.21% and its drug release was 45%. This indicates that ZnO plays an effective role in the structure and performance of Ca/PVA composites. The SEM images of MgO composites show smoother surfaces compared to MgZnO composites. This may be one of the reasons for the increased EE% and drug release of MgZnO composites. The addition of ZnO to the composite structure can lead to the appearance of pores on the surface of the composite, increasing entrapment and drug release. Full article