Search Results (21)

Se-doped CdTe thin films were grown employing a simple two-electrode electrochemical deposition method using glass/tin-doped indium oxide (glass/ITO). Cadmium acetate dihydrate [Cd (CH₃CO₂)₂. 2H₂O], selenium dioxide (SeO₂), and tellurium dioxide (TeO₂) were used as precursors. Instruments including X-ray diffraction for structural investigation, UV-Vis spectrophotometry for optical properties, and scanning probe microscopy for morphological properties were employed to investigate the physico-chemical characteristics of the resulting Se-doped CdTe thin-film. The films are polycrystalline with a cubic phase, according to X-ray diffraction (XRD) data. More ions are deposited on the substrate, which makes the material more crystalline and intensifies the characteristic peaks that are seen. It is observed from the acquired optical characterization that the film’s bandgap is greatly influenced by the deposition time. The bandgap dropped from 1.92 to 1.62 as the deposition period increased from 25 to 45 min, making the film more transparent and absorbing less light at shorter deposition durations. Images from scanning electron microscopy (SEM) show that the surface morphology is homogenous with closely packed grains and that the grain forms become less noticeable as the deposition time increases. This work is novel in that it investigates the influence of the deposition time on the structural, optical, and morphological properties of Se-doped CdTe thin films deposited using a cost-effective, simplified two-electrode electrochemical method—a fabrication route that remains largely unexplored for this material system. Full article

A continuous flow with reagent injection method on a novel inlaid microfluidic platform for nitrite determination has been successfully developed. The significance of the high-frequency monitoring of nutrient fluctuations in marine environments is crucial for understanding our impacts on the ecosystem. Many in-situ systems face limitations in high-frequency data collection and have restricted deployment times due to high reagent consumption. The proposed microfluidic device employs automatic colorimetric absorbance spectrophotometry, using the Griess assay for nitrite determination, with minimal reagent usage. The sensor incorporates 10 solenoid valves, four syringes, two LEDs, four photodiodes, and an inlaid microfluidic technique to facilitate optical measurements of fluid volumes. In this flow system, Taylor–Aris dispersion was simulated for different injection volumes at a constant flow rate, and the results have been experimentally confirmed using red food dye injection into a carrier stream. A series of tests were conducted to determine a suitable injection frequency for the reagent. Following the initial system characterization, seven different standard concentrations ranging from 0.125 to 10 µM nitrite were run through the microfluidic device to acquire a calibration curve. Three different calibrations were performed to optimize plug length, with reagent injection volumes of 4, 20, and 50 µL. A straightforward signal processing method was implemented to mitigate the Schlieren effect caused by differences in refractive indexes between the reagent and standards. The results demonstrate that a sampling frequency of at least 10 samples per hour is achievable using this system. The obtained attenuation coefficients exhibited good agreement with the literature, while the reagent consumption was significantly reduced. The limit of detection for a 20 µL injection volume was determined to be 94 nM from the sample intake, and the limit of quantification was 312 nM. Going forward, the demonstrated system will be packaged in a submersible enclosure to facilitate in-situ colorimetric measurements in marine environments. Full article

Steel slag waste produced by the steel industry accumulates in open areas or is disposed of in landfills, causing harm to the environment and human health. Valorizing steel slag through comprehensive data analysis is imperative and could add value to the product with respect to energy conversion and storage applications. This study investigated the morphological, structural, and optical characteristics of a thermally annealed steel slag composite generated from iron and steel factories. Scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), Raman spectroscopy, and UV–visible spectrophotometry were subsequently used to evaluate the impact of thermal treatment on the morphology, structure, elemental composition, and optical properties. It was found that the pre-treated slag composites contained a variety of irregular grain sizes and microscale fragments, primarily composed of C (18.55%), O (50.85%), and Fe (29.41%), with lower amounts of Mg (0.31%), Si (0.44%), and Ca (0.44%), indicating the natural formation of a disordered iron composite. Thermal treatment at different temperatures (300 °C, 600 °C, and 900 °C) increased the grain density and clustering, resulting in denser two-dimensional microstructures at 900 °C. Additionally, XRD and Raman analyses of both untreated and thermally treated slag composites revealed the presence of a disordered iron oxide composite, including (Fe₃O₄), hematite (α-Fe₂O₃), and maghemite (γ-Fe₂O₃) phases. A significant increase in optical absorbance was also observed after annealing at 600 °C, highlighting the successful optimization of the elemental composition of the slag composite. A band gap energy of approximately 2.2 eV was obtained from this optimization at 600 °C. The optical conductivity of the composite reached 2.1 × 10⁶ S⁻¹ at 600 °C, which indicates an enhancement in charge transfer among the optimized chemical elements in the waste composite. These findings suggest an optimization method for novel composites derived from steel slag waste, indicating its potential as a low-cost material for energy storage systems (batteries, supercapacitors, and fuel cells) and optoelectronic devices. Full article

In this paper, we investigate the decomposition of a toxic organic compound, Rhodamine B, by the photocatalytic activities of undoped and nitrogen-doped ZrO₂ thin films, deposited using the HiPIMS technique. The investigation was performed in the presence and in the absence of H₂O₂, for two types of experimental arrangements: the irradiation of the films, followed by dipping them in the Rhodamine B solutions, and the irradiation of the films dipped in the solution. The two situations were named “direct irradiation” and “indirect irradiation”, respectively. Methods like XRD, AFM, XPS, DRS, water/film surface contact angle, and spectrophotometry were used to obtain information on the films’ structure, surface morphology, elemental composition of the films surface, optical band gap, hydrophilicity, and photocatalytic activity, respectively. All these properties were described and correlated. By N-doping ZrO₂, the films become absorbent in the visible domain, so that the solar light could be efficiently used; the films’ hydrophilic properties improve, which is an important fact in self-cleaning applications; and the films’ photocatalytic activity for the decomposition of Rhodamine B becomes better. The addition of hydrogen peroxide acted as an inhibitor for all systems and not as an accelerator of the photocatalytic reactions as expected. Full article

In this study, a novel approach for characterizing the optical properties of inhomogeneous thin films is presented, with a particular focus on samples exhibiting absorption in some part of the measured spectral range. Conventional methods of measuring the samples only from the film side can be limited by incomplete information at the lower boundary of the film, leading to potentially unreliable results. To address this issue, depositing the thin films onto non-absorbing substrates to enable measurements from both sides of the sample is proposed. To demonstrate the efficacy of this approach, a combination of variable-angle spectroscopic ellipsometry and spectrophotometry at near-normal incidence was employed to optically characterize three inhomogeneous polymer-like thin films. The spectral dependencies of the optical constants were modeled using the Kramers–Kronig consistent model. It was found that it is necessary to consider thin, weakly absorbing transition layers between the films and the substrates. The obtained results show excellent agreement between the fits and the measured data, providing validation of the structural and dispersion models, as well as the overall characterization procedure. The proposed approach offers a method for optically characterizing a diverse range of inhomogeneous thin films, providing more reliable results when compared to traditional one-sided measurements. Full article

The separation of red blood cells (RBCs) from blood plasma and the analysis of individual RBCs are of great importance, as they provide valuable information regarding the health of their donor. Recent developments in microfluidics and microfabrication have contributed to the fabrication of microsystems with complex features to promote the separation and analysis of RBCs. In this work, the separation capacity of a multi-step crossflow microfluidic device was evaluated by using a blood analogue fluid made by Brij L4 micelles and human RBCs separated from whole blood, suspended in a solution with hematocrits (Ht) of 0.5 and 1%. All the samples collected at the outlets of the device were experimentally analyzed and compared. The absorbance spectrum was also measured for the prepared blood samples. The results indicate that the tested blood analogue fluid has exhibited a flow behavior similar to that of blood. In addition, the optical absorbance spectrophotometry revealed that it was possible to evaluate the separation efficiency of the microfluidic device, concluding that the concentration of cells was lower at the most lateral outside outlets of the microchannel due to the cumulative effect of the multiple cross-flow filters. Full article

Surfaces of commercial molybdenum (Mo) plates have been textured by fs-laser treatments with the aim to form low-cost and efficient solar absorbers and substrates for thermionic cathodes in Concentrated Solar Power conversion devices. Morphological (SEM and AFM), optical (spectrophotometry), and structural (Raman spectroscopy) properties of the samples treated at different laser fluences (from 1.8 to 14 J/cm²) have been characterized after the laser treatments and also following long thermal annealing for simulating the operating conditions of thermionic converters. A significant improvement of the solar absorptance and selectivity, with a maximum value of about four times higher than the pristine sample at a temperature of 800 K, has been detected for sample surfaces treated at intermediate fluences. The effects observed have been related to the light trapping capability of the laser-induced nanotexturing, whereas a low selectivity, together with a high absorptance, could be revealed when the highest laser fluence was employed due to a significant presence of oxide species. The ageing process confirms the performance improvement shown when treated samples are used as solar absorbers, even though, due to chemical modification occurring at the surface, a decrease of the solar absorptance takes place. Interestingly, the sample showing the highest quantity of oxides preserves more efficiently the laser texturing. The observation of this behaviour allows to extend the applicability of the laser treatments since, by further nanostructuring of the Mo oxides, it could be beneficial also for sensing applications. Full article

Background: The photocatalytic degradation of toxic organic compounds has received great attention for the past several years. Dyes, such as methyl orange (MO), are one of the major pollutants which create environmental hazards in the hydrosphere, living organisms and human beings. During photocatalytic degradation, NPs are activated in the presence of UV–Vis radiation which in turn creates a redox environment in the system and behaves as a sensitizer for light-induced redox mechanisms. Tin oxide (SnO₂) is one of the prominent, but less investigated, nanomaterials compared to titanium oxide (TiO₂) and Zinc oxide (ZnO) nanoparticles (NPs). Methods: Herein, Buxus wallichiana (B. wallichiana) leaf extract was utilized as a reducing and capping agent for the biosynthesis of SnO₂ NPs. The effects of the calcination temperature on their photocatalytic, structure and surface properties were then examined. The degree of crystallinity and the crystallite size were determined through X-ray diffraction (XRD) analysis. The pore size and surface area were calculated by Burnett–Emmitt–Teller (BET) and Barrett–Joyner–Halenda (BJH) methods based on nitrogen desorption data. Morphological changes were assessed by scanning electron microscopy (SEM). The optical behavior was analyzed through UV–Vis diffuse reflectance spectroscopy (DRS) data and the band gap subsequently calculated. The photocatalytic efficiency of SnO₂ NPs was evaluated by double beam UV–Vis spectrophotometry under the influence of initial MO concentration, catalyst dose and pH of MO solution. The surface functional moieties were identified using Fourier transform infrared (FTIR) spectroscopy. All the calcined SnO₂ NPs were used as photocatalysts for the mineralization of MO in aqueous media. Results: The degree of crystallinity and the crystallite size increased with the calcination temperature. The transmittance edge obtained for all the calcined SnO₂ NPs shows a maximum absorbance in the visible range (λ-max = 464 nm). Moving toward higher wavelengths, a sudden intense red shift (from 464 nm to 500 nm), attributed to the incorporation of a hydroxyl radical at the ortho-position in the benzene ring associated with the dimethylamine group of MO, was observed in the absorbance of the samples calcined up to 300 °C. The percentage degradation of MO was found to decrease with increasing calcination temperatures. The optimal photocatalytic activity toward MO (15 ppm) in a solution of pH = 6 was obtained with 15 mg SnO₂ NPs calcined at 100 °C. Conclusions: UV–Vis absorption spectroscopy demonstrates that the absorption spectra of MO are strongly modified by the calcination temperature. This work opens new avenues for the use of SnO₂ NPs as photocatalysts against the degradation of industrial effluents enriched with different dyes. Full article

Polypropylene (PP), a promising engineering thermoplastic, possesses the advantages of light weight, chemical resistance, and flexible processability, yet preserving insulative properties. For the rising demand for cost-effective electronic devices and system hardware protections, these applications require the proper conductive properties of PP, which can be easily modified. This study investigates the thermal and electrical properties of isotactic polypropylene/copper nanowires (i-PP/CuNWs). The CuNWs were harvested by chemical reduction of CuCl₂ using a reducing agent of glucose, capping agent of hexadecylamine (HDA), and surfactant of PEG-7 glyceryl cocoate. Their morphology, light absorbance, and solution homogeneity were investigated by SEM, UV-visible spectrophotometry, and optical microscopy. The averaged diameters and the length of the CuNWs were 66.4 ± 16.1 nm and 32.4 ± 11.8 µm, respectively. The estimated aspect ratio (L/D, length-to-diameter) was 488 ± 215 which can be recognized as 1-D nanomaterials. Conductive i-PP/CuNWs composites were prepared by solution blending using p-xylene, then melt blending. The thermal analysis and morphology of CuNWs were characterized by DSC, polarized optical microscopy (POM), and SEM, respectively. The melting temperature decreased, but the crystallization temperature increasing of i-PP/CuNWs composites were observed when increasing the content of CuNWs by the melt blending process. The WAXD data reveal the coexistence of Cu₂O and Cu in melt-blended i-PP/CuNWs composites. The fit of the electrical volume resistivity (ρ) with the modified power law equation: ρ = ρ_o (V − Vc)^−t based on the percolation theory was used to find the percolation concentration. A low percolation threshold value of 0.237 vol% and high critical exponent t of 2.96 for i-PP/CuNWs composites were obtained. The volume resistivity for i-PP/CuNWs composite was 1.57 × 10⁷ Ω-cm at 1 vol% of CuNWs as a potential candidate for future conductive materials. Full article

This study aims to produce green zinc oxide nanoparticles (ZnO-NPs) derived from red seaweed (Pterocladia Capillacea) and evaluate their potential to absorb Ismate violet 2R (IV2R) ions from an aqueous solution. UV-vis spectrophotometry, Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), X-ray diffraction (XRD), and a Brunauer–Emmett–Teller surface area analysis (BET) were used to analyze the structural, morphological, and optical features of the synthesized nanoparticles. The change in color of the chemical solution revealed the formation of zinc oxide nanoparticles. The FTIR examination confirmed the synthesis of both Zn and ZnO nanoparticle powder, with a BET surface area of 113.751 m² g⁻¹ and an average pore size of 2.527 nm for the synthesized adsorbent. Furthermore, the maximum removal effectiveness of IV2R was 99% when 0.08 g ZnO-NPs was applied at a pH of 6, a temperature of 55 °C, and a contact time of 120 min. The dye adsorption capacity of the ZnO-NPs was 72.24 mg g⁻¹. The adsorption process was also controlled by the Freundlich adsorption model and pseudo-second-order reaction kinetics. The adsorption of IV2R ions onto the ZnO-NPs could be represented as a nonideal and reversible sorption process of a nonuniform surface, according to Freundlich adsorption isotherms. In addition, the constant values of the model parameters were determined using various nonlinear regression error functions. Moreover, thermodynamic parameters such as entropy change, enthalpy change, and free energy change were investigated; the adsorption process was spontaneous and endothermic. The high capacity of the ZnO-NPs synthesized by red seaweed promotes them as promising substances for applications in water treatment for the removal of IV2R dye from aqueous systems. Full article

Cupric oxide is a semiconductor with applications in sensors, solar cells, and solar thermal absorbers. To improve its properties, the oxide was doped with a metallic element. No studies were previously performed on Cr-doping using the ion implantation technique. The research goal of these studies is to investigate how Cr ion implantation impacts the properties of the oxide thin films. CuO thin films were deposited using magnetron sputtering, and then chromium ions with different energies and doses were implanted. Structural, optical, and vibrational properties of the samples were studied using X-ray diffraction, X-ray reflectivity, infra-red spectroscopy, Raman spectroscopy, and spectrophotometry. The surface morphology and topography were studied with ellipsometry, atomic force microscopy, and scanning electron microscopy. A simulation of the range of ions in the materials was performed. Ion implantation had an impact on the properties of thin films that could be used to tailor the optical properties of the cupric oxide and possibly also its electrical properties. A study considering the influence of ion implantation on electrical properties is proposed as further research on ion-implanted CuO thin films. Full article

Enhancing the weatherability of bamboo-based products is essential for increasing their application lifespan. In this study, a composite protective coating containing organic and inorganic UV absorbers and a hindered amine light stabilizer (HALS) was investigated for outdoor bamboo scrimber (OBS). The optical properties of weathered coated and uncoated samples were investigated by colorimetry and UV-Vis spectrophotometry. Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), and thermal gravimetric analysis (TGA) were used to determine the physicochemical properties of the coating. The addition of HALS improved the photostability of the coating and preserved the properties of OBS. Compared to resin-coated samples, alicyclic amines in HALS inhibit photooxidation reactions between bamboo lignin and the coating adhesive. This inhibition is critical for maintaining the UV-shielding performance of the coating. We have developed a photostable protective coating for bamboo-based products whose widespread use can significantly help conserve critical forest resources. Full article

Metal-conducting polyaniline (PANI)-based nanocomposite materials have attracted attention in various applications due to their synergism of electrical, mechanical, and optical properties of the initial components. Herein, metal-PANI nanocomposites, including silver nanoparticle-polyaniline (AgNP-PANI), zinc oxide nanoparticle-polyaniline (ZnONP-PANI), and silver-zinc oxide nanoparticle-polyaniline (Ag–ZnONP-PANI), were prepared using the two processes. Nanocomposite-based electrode platforms were prepared by depositing AgNPs, ZnONPs, or Ag–ZnONPs on a PANI modified glass carbon electrode (GCE) in the presence of 1-ethyl-3-(3-dimethyl aminopropyl) carbodiimide/N-Hydroxysuccinimide (EDC/NHS, 1:2) as coupling agents. The incorporation of AgNPs, ZnONPs, and Ag–ZnONPs onto PANI was confirmed by UV-Vis spectrophotometry, which showed five absorbance bands at 216 nm, 412 nm, 464 nm, 550 nm, and 831 nm (i.e., transition of π-π*, π-polaron band transition, polaron-π* electronic transition, and AgNPs). The FTIR characteristic signatures of the nanocomposite materials exhibited stretching arising from C–H aromatic, C–O, and C–N stretching mode for benzenoid rings, and =C–H plane bending vibration formed during protonation. The CV voltammograms of the nanocomposite materials showed a quasi-reversible behavior with increased redox current response. Notably, AgNP–PANI–GCE electrode showed the highest conductivity, which was attributed the high conductivity of silver. The increase in peak currents exhibited by the composites shows that AgNPs and ZnONPs improve the electrical properties of PANI, and they could be potential candidates for electrochemical applications. Full article

Modification has been made to TiO₂ thin film to improve the wettability and the absorption of light. The sol-gel spin coating method was successfully used to synthesize GO/TiO₂ thin films using a titanium (IV) isopropoxide (TTIP) as a precursor. Different amounts of polyethylene glycol (PEG) (20 to 100 mg) were added into the parent sol solution to improve the optical properties and wettability of the GO/TiO₂ thin film. The effect of different amounts of PEG was characterized using X-ray diffraction (XRD) for the phase composition, scanning electron microscopy (SEM) for microstructure observation, atomic force microscopy (AFM) for the surface topography, ultraviolet–visible spectrophotometry (UV-VIS) for the optical properties and wettability of the thin films by measuring the water contact angle. The XRD analysis showed the amorphous phase. The SEM and AFM images revealed that the particles were less agglomerated and surface roughness increases from 1.21 × 10² to 2.63 × 10² nm when the amount of PEG increased. The wettability analysis results show that the water contact angle of the thin film decreased to 27.52° with the increase of PEG to 80 mg which indicated that the thin film has hydrophilic properties. The optical properties also improved significantly, where the light absorbance wavelength became wider and the band gap was reduced from 3.31 to 2.82 eV with the presence of PEG. Full article

The term disentangled refers to polymers with fewer entanglements in the amorphous regions, a metastable condition that can significantly affect the material’s properties and processing behavior. The lower entanglement density in ultra-high molecular weight polyethylene (dis-UHMWPE) facilitates the solid-state processability into uniaxially-oriented specimens reaching very high draw ratios and crystallinities. In this study, Au/dis-UHMWPE nanocomposites were formulated and processed at variable draw ratios. Polarized light microscopy suggests gold nanoparticles are oriented in arrays following the drawing of polymer chains. The structural features, upon orientation, are studied by means of Raman spectroscopy, wide- and small-angle X-ray scattering, and near-infrared spectrophotometry. Crystallinity is found to increase by 15%, as calculated by wide-angle X-ray scattering. The change in optical absorbance in the visible spectrum indicates that, with orientation, the average size of gold aggregates increases, supported quantitatively by small-angle X-ray scattering. Since the gold nanoparticles are expected to be found within amorphous chain segments, the aforementioned findings are attributed to the increase of crystallinity and thus the decrease of available (amorphous) space. Full article