The structural and optical characterizations of nanocomposite films of polymethyl methacrylate (PMMA) and SiO₂/TiO₂ composites prepared via the spin-coating technique were investigated using different SiO₂:TiO₂ ratios. The SiO₂/TiO₂ nanocomposites were synthesized using the sonochemical process with Si:Ti precursor ratios of 1:0.1, 1:0.5, 1:1, 1:2, 1:4, and 0:1. All characterizations of ultrafine SiO₂/TiO₂ particles were loaded at 1 wt.% in a PMMA matrix for the fabrication of transparent SiO₂/TiO₂/PMMA composite films. The phase structure and morphology of SiO₂/TiO₂/PMMA composite films were monitored using X-ray diffraction, optical microscopy, and field-emission scanning electron microscopy. A surface roughness analysis of SiO₂/TiO₂/PMMA nanocomposite films was conducted using atomic force microscopy. For optical characterization, transmission properties with different incident angles of SiO₂/TiO₂/PMMA composite films were analyzed with UV-vis spectrophotometry. The water contact angles of SiO₂/TiO₂/PMMA composite films were analyzed to identify hydrophilic properties on film surfaces. Photocatalytic reactions in SiO₂TiO₂ composite films under UV irradiation were evaluated using rhodamine B dye degradation. The optimal condition of SiO₂/TiO₂/PMMA nanocomposite films was obtained at a 1:1 SiO₂:TiO₂ ratio in self-cleaning applications, resulting from good particle dispersion and the presence of the TiO₂ phase in the composite.

In this work, Er-doped BiVO₄/BiFeO₃ composites are prepared using the sonochemical process with a difference of rare earth loading compositions. The crystallinity and chemical and morphological structure of as-synthesized samples were investigated via X-ray diffraction, Raman scattering, and electron microscopy, respectively. The diffuse reflectance technique was used to extract the optical property and calculate the optical band gap of the composite sample. The piezo-photocatalytic performance was evaluated according to the decomposition of a Rhodamine B organic compound. The decomposition of the organic compound was achieved under ultrasonic bath irradiation combined with light exposure. The Er-doped BiVO₄/BiFeO₃ composite heterojunction material exhibited significant enhancement of the piezo-photocatalytic activity under both ultrasonic and light irradiation due to the improvement in charge generation and separation. The result indicates that Er dopant strongly affects the phase transformation, change in morphology, and alternation in optical band gap of the BiVO₄ matrix. The incorporation of BiFeO₃ in the composite form with BiVO₄ doped with 1%Er can improve the photocatalytic performance of BiVO₄ via piezo-induced charge separation and charge recombination retardment.

The article reports the successful fabrication of Eu³⁺-doped WO₃ thin films via the radio-frequency magnetron sputtering (RFMS) technique. To our knowledge, this is the first study showing the tunable visible emission (blue to bluish red) from a WO₃:Eu³⁺ thin film system using RFMS. X-ray diffractograms revealed that the crystalline nature of these thin films increased upto 3 wt% of the Eu³⁺ concentration. The diffraction peaks in the crystalline films are matched well with the monoclinic crystalline phase of WO₃, but for all the films’, micro-Raman spectra detected bands related to WO₃ monoclinic phase. Vibrational and surface studies reveal the amorphous/semi-crystalline behavior of the 10 wt% Eu³⁺-doped sample. Valence state determination shows the trivalent state of Eu ions in doped films. In the 400–900 nm regions, the fabricated thin films show an average optical transparency of ~51–85%. Moreover, the band gap energy gradually reduces from 2.95 to 2.49 eV, with an enhancement of the Eu³⁺-doping content. The doped films, except the one at a higher doping concentration (10 wt%), show unique emissions of Eu³⁺ ions, besides the band edge emission of WO₃. With an enhancement of the Eu³⁺ content, the concentration quenching process of the Eu³⁺ ions’ emission intensities is visible. The variation in CIE chromaticity coordinates suggest that the overall emission color can be altered from blue to bluish red by changing the Eu³⁺ ion concentration.

In this study, we investigated the impact of polyvinyl alcohol (PVA) incorporation on the optical properties and oxygen detection performance of a titanium dioxide/methylene blue (TiO₂/MB) nanocomposite colorimetric indicator for packaging applications. The nanocomposite was synthesized via mechanical milling of TiO₂ nanoparticles with MB and citric acid. PVA, at varying concentrations (0, 3, 9, and 14 wt%), was introduced during the wet milling process to produce a homogeneous composite film. Spin coating was employed to fabricate TiO₂/MB nanocomposite films for oxygen detection evaluation. The influence of PVA loading on the films’ chemical functionalities and surface morphologies was assessed using Fourier-transform infrared spectroscopy (FTIR) and field-emission scanning electron microscopy (FE-SEM). The indicator’s activation process, involving a color change between bleached and colored states, and its recovery time were monitored via optical imaging and UV-VIS-NIR spectrophotometry. The results revealed that a PVA content of 9 wt% yielded well-defined films with enhanced stability of the TiO₂/MB nanocomposite’s oxygen detection performance.

ZnO nanopowders were synthesized via a solvent-mediated green route using Mitragyna speciosa Korth. leaf extract as reducing and stabilizing agents. Deionized water and methanol were employed to tailor the phytochemical composition of the extracts. The influence of extract concentration (5–20 mL) and solvent polarity on structural, morphological, and functional properties was systematically investigated. Structural analyses confirmed the formation of Zn-O bonds and a phase-pure hexagonal wurtzite ZnO without secondary phases. Surface morphology revealed solvent-dependent morphological evolution toward spherical shapes and reduced aggregation in the methanol-derived system. For antibacterial activity, green ZnO nanopowders demonstrated enhanced biocidal effects against Gram-negative Escherichia coli and Gram-positive Staphylococcus aureus, comparable to that of commercial ZnO nanoparticles. Enhanced piezo-photocatalytic degradation of rhodamine B was achieved under combined light and ultrasonic irradiation, with superior performance observed for methanol-derived ZnO. This enhancement is attributed to the synergistic interplay of solvent-induced defect states, reduced particle size, and piezoelectric field-driven charge separation. Scavenger analysis confirmed that superoxide radicals (${·\mathrm{O}}_2^{-}$) dominate the degradation pathway by green-synthesized ZnO nanopowders prepared from different solvent extracts. Thus, a correlation between solvent-mediated phytochemical environments and piezo-photocatalytic activity provides new insights for the design of sustainable, high-performance ZnO-based catalysts.