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This study focuses on the solution combustion approach to examine the nanostructures of undoped and doped ZnO with different concentrations of Al (0.1 % and 0.2 %). Various physical techniques were utilized to characterize the synthesized nanoparticles. X-ray diffraction (XRD) revealed the crystalline materials, while scanning electron microscopy (SEM) with energy-dispersive X-ray (EDX) findings confirmed the products with particle size and the insertion of Al into the ZnO lattice. Fourier-transform infrared spectra (FTIR) confirmed the presence of different functional groups in the obtained material. The results indicate that Al-doped ZnO (Al-ZnO) nanoparticles show promising properties for optoelectronics and photoluminescence. Photoluminescence analysis indicated that an increase in Al3+ (0.2 %) concentration resulted in a decrease in peak intensity and an increase in the full width at half maximum. The band gap was calculated using the Taucs plot. The study also highlights the effectiveness of Zn1-xAlxO nanostructures in degrading organic pollutants, particularly in adsorbing Malachite Green (MG) dye. Among the samples, the 0.2 % Al-doped ZnO exhibited superior dye degradation efficiency due to its enhanced adsorption capacity and smaller particle size, as evidenced by multilayer adsorption capacity and chemisorption during the degradation process. This study provides valuable insights into the potential applications of Al-doped ZnO nanoparticles in various environmental and technological fields, emphasizing their significance in the degradation of organic pollutants.

RESUMEN

Energy-efficient sol-gel synthesis was achieved through the microwave assisted self-combustion route to produce hexagonal Tungsten oxide semiconductor (WO3). The photocatalytic activity was enhanced by doping Cobalt (Co) into the crystalline structure of the nanoparticle, which were subsequently sintered at 400 °C for an hour. The structural and morphological properties of the Co-doped WO3 were revealed using X-ray diffraction (XRD) characterization. The nanoparticles exhibited an amorphous structure before annealing, due to the short heating time during combustion synthesis. Sintering the nanoparticle transformed the nanoparticle from a monoclinic phase to orthorhombic phase structure. Additional analysis techniques, including scanning electron microscopy (SEM), transmission electron microscopy (TEM) and energy dispersive X-ray spectrum analysis (EDS). To assess the photocatalytic performance of these particles, Acid Blue 74 (AB 74) was employed in photodegradation experiments under UV light irradiation within a semi-continuous reactor. The photodegradation of dye molecules was evaluated utilizing a UV-Vis spectrophotometer, and the mineralization efficiency of the dye was determined through total organic carbon analysis (TOC). The results indicated that the dimension of the synthesized nano catalyst fell within the range of 70-120 nm, and it exhibited the ability to completely degrade a solution with an initial dye concentration of 20 ppm within 60 min. Various parameters affecting the photocatalytic reaction, including the photocatalyst dosage, initial dye concentration, pH and temperature of the dye solution were also investigated. The experiments were designed using Response surface methodology (RSM), through which a mathematical model for the dye removal process was developed.

RESUMEN

This paper presents a research investigation into the synthesis of vanadate oxides M3 (VO4 )2 (M: Mg or Zn) using the solution combustion method and investigates their structural, photoluminescence, and photocatalytic properties after introducing cerium (Ce) as a dopant. The resulting synthesized samples all display an orthorhombic crystalline structure with crystallite sizes ranging from 71 to 110 nm. Morphological diversity among the samples is revealed through field-emission scanning electron microscopy (FESEM) imagery. Diffuse reflectance spectroscopy discloses that the introduction of Ce3+ as a dopant leads to an increase in the band gap energy. Notably, when excited at a wavelength of 340 nm, the photoluminescence emission intensity reaches its peak across all samples. This intensity undergoes enhancement due to Ce3+ doping, causing a slight shift toward shorter wavelengths attributable to the augmented band gap resulting from the dopant. Markedly, among the investigated materials, Ce3+ -activated Mg3 (VO4 )2 stands out with the most pronounced emission intensity, positioning it as a highly promising luminescent material. Additionally, the incorporation of Ce3+ has a positive effect on the photocatalytic performance of Mg3 (VO4 )2 , resulting in notable improvement.

RESUMEN

A study on the influence of magnesium ferrite nanoparticles on the optical and dielectric attributes of Polyaniline has been conducted. Magnesium nano Ferrite powder is synthesized by the self-propagating solution combustion method. Polyaniline-Magnesium nano ferrite composites are synthesized by chemical oxidative polymerization of aniline with the addition of Magnesium nanoparticles. The samples are characterized with XRD and UV-Vis spectrometer, in the wavelength range of 200-800 nm and studied for optical properties. Dielectric properties are studied in the frequency range of 50 Hz to 5 MHz. X-ray diffraction reveals single phase formation of Magnesium ferrite, whereas Polyaniline shows an amorphous nature. In the XRD of the composites, we see the crystalline peaks of ferrite becoming more intense with the addition of ferrite and whereas the peak of Polyaniline diminishes. The crystallite size is quantified with the Debye-Scherrer formula, and it increases as the content of ferrite in the composites increases. The micro-strain decreases in the composites as the percentage of ferrite enhances in the composites. In the UV-Vis absorption spectra of composites, the peaks of Polyaniline shift to higher wavelength and there is also an absorption band in the spectra of composites corresponding to that of Magnesium ferrite particles. Both direct and indirect band gaps are calculated with the Tauc plot, and both the optical band gap decrease as the percentage of ferrite increases in the composite. The dielectric loss and dielectric constant both decrease with frequency in all the samples, and the dielectric response are in good agreement with Maxwell-Wagner model. Ferrite-polymer composites with both conducting and magnetic properties are considered useful for electromagnetic shielding and microwave absorption.

RESUMEN

The noble metal nanoparticles have attracted attention due to their excellent catalytic performance for CO oxidation at low temperatures. M-CeO2(M = Pd, Ag, Au) catalysts with different atomic ratios of M/Ce were deposited via solution combustion method. Among them, 3 at% Pd-CeO2, 5 at% Ag-CeO2and 1 at% Au-CeO2catalysts have better catalytic performances. Especially, 5 at% Ag-CeO2catalyst shows better low-temperature CO oxidation performance. The catalytic activity for CO oxidation follows the follows the following sequence: 5 at% Ag-CeO2(T50 = 69 °C) > 3 at% Pd-CeO2(T50 = 99 °C) >1 at% Au-CeO2(T50 = 115 °C). Meanwhile, the catalysts are characterized by means of powder x-ray diffraction, scanning electron microscope, transmission electron microscopy, Raman spectroscopy, x-ray photoelectron spectroscopy, Brunauer-Emmett-Teller and H2-TPR. The characterization results show that the 5 at% Ag-CeO2catalyst has excellent catalytic activity due to the good dispersion of Ag nanoparticles, the specific surface area of the material, and the reduction catalyst between different valence ions. Moreover, the surface of the catalyst enhances the mutual synergy, effectively promotes the generation of oxygen vacancies, and increases the active oxygen content of the catalyst surface. Finally, the catalytic mechanism of M-CeO2catalysts is summarized.

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In the current investigation, a series of NaCa1-x PO4 :xDy3+ (x = 0.1, 0.3, 0.5, 0.7, 1.0, 1.5 and 2 mol%) phosphors were synthesized using a solution combustion method and citric acid as fuel. The investigated results from the X-ray diffraction (XRD) pattern showed phase purity of the synthesized material and orthorhombic crystal structure with space group Pna21. Photoluminescence properties of the synthesized phosphors were investigated. The synthesized Dy3+ -activated phosphor displayed blue (482 nm) and yellow (576 nm) emission under near-ultraviolet or blue excitations. These emission bands were ascribed due to the 4 F9/2 →6 H15/2 and 4 F9/2 →6 H13/2 transitions of Dy3+ ions. Commission International de l'Eclairage chromaticity coordinates showed emission in the near-white region for the proposed phosphors under different excitations. In addition, the current-voltage (I-V) characteristics of the NaCa1-x PO4 :xDy3+ (x = 1.5 mol%) phosphor-coated silicon solar cell and an uncoated solar cell were investigated under a solar simulator. The I-V characteristics of the proposed phosphor-coated silicon solar cell showed enhancement in solar cell efficiency by ~7.92%. The entire studies and their outcomes showed that synthesized phosphors have potential as white light emitting diodes and for solar applications.

Asunto(s)

Disprosio , Luminiscencia , Difracción de Rayos X

RESUMEN

Zirconia (ZrO2) nanoparticles were synthesized by solution combustion using urea as an organic fuel. Brunauer-Emmett-Teller (BET), X-ray diffraction (XRD), thermal gravimetric analysis (TGA), transmission electron microscopy (TEM), UV-vis and Fourier transform infrared (FTIR) measurements were performed in order to characterize the catalyst. The calculated crystallite size of ZrO2, calculated with the help of the Scherrer equation, was around 30.3 nm. The synthesized ZrO2 was scrutinized regarding its role as catalyst in the oxidation of carbon monoxide (CO). It showed 100% CO conversion at 240 °C, which is the highest conversion rate reported for ZrO2 in literature to date. It is found that through solution combustion, Pt2+ ions replace Zr4+ ions in the ZrO2 lattice and because of this, oxygen vacancies are formed due to charge imbalance and lattice distortion in ZrO2. 1% Pt was doped into ZrO2 and yielded excellent CO oxidation. The working temperature was lowered by 150 °C in comparison to pure ZrO2. Further, it is highly stable for the CO reaction (time-on-stream ≈ 40 h). This is because of a synergic effect between Pt and Zr components, which results in an increase of the oxygen mobility and oxygen vacancies and improves the activity and stability of the catalyst. The effects of gas hourly space velocity (GHSV) and initial CO concentration on the CO oxidation over Pt(1%)-ZrO2 were studied.

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Surface Enhanced Raman Spectroscopic technique has been employed to investigate the orientation of 2-bromo-3-methylamino-1,4-naphthoquinone (BMANQ) on silver nanoparticles. Silver nanoparticles have been prepared by solution combustion method with citric acid as fuel. Silver nanoparticles were characterized by X-ray Diffraction (XRD), High Resolution Transmission Electron Microscopy (HRTEM) and Scanning Electron Microscopy (SEM). XRD and morphological results confirmed the nanocrystalline nature of the prepared silver nanoparticles. The observed intense CO stretching, CBr stretching and NH2 vibration suggests that the BMANQ molecule may be adsorbed in a 'stand-on' orientation to the silver surface. The calculated highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) energy show that charge transfer occurs within the molecule.

RESUMEN

Silver nanoparticles have been synthesized by a simple and inexpensive solution combustion method with urea as fuel. The structural and morphology of the silver nanoparticles were investigated through X-ray powder diffraction (XRD), Field Emission Scanning Electron Microscopy (FESEM) and Energy Dispersion Spectra (EDS) techniques. Structural and morphological results confirmed the nanocrystalline nature of the silver nanoparticles. Density Functional Theory (DFT) calculations were also performed to study the ground and excited state behavior of 2-bromo-1,4-naphthoquinone (2-BrNQ) and 2-BrNQ on silver nanoparticles. Surface-Enhanced Raman Scattering (SERS) spectra of 2-BrNQ adsorbed on silver nanoparticles were investigated. The CO, CH in-plane bending and CBr stretching modes were enhanced in SERS spectrum with respect to normal Raman spectrum. The spectral analysis reveals that the 2-BrNQ adsorbed 'stand-on' orientation on the silver surface. Density Functional Theory (DFT) calculations are also performed to study the vibrational features of 2-BrNQ molecule and 2-BrNQ molecule on silver surface.

Asunto(s)

Naftoquinonas/química , Espectrometría Raman/métodos , Adsorción , Nanopartículas del Metal/química , Nanopartículas del Metal/ultraestructura , Modelos Moleculares , Difracción de Polvo , Teoría Cuántica , Plata/química , Propiedades de Superficie , Difracción de Rayos X