SnO₂ nanoparticle production using thermal treatment with tin(II) chloride dihydrate and polyvinylpyrrolidone capping agent precursor materials for calcination was investigated. Samples were analyzed using X-ray diffraction (XRD), Scanning Electron Microscopy (SEM), energy dispersive X-ray (EDX), transmission electron microscopy (TEM), Fourier Transform Infrared Spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), diffuse UV-vis reflectance spectra, photoluminescence (PL) spectra and the electron spin resonance (ESR). XRD analysis found tetragonal crystalline structures in the SnO₂ nanoparticles generated through calcination. EDX and FT-IR spectroscopy phase analysis verified the derivation of the Sn and O in the SnO₂ nanoparticle samples from the precursor materials. An average nanoparticle size of 4–15.5 nm was achieved by increasing calcination temperature from 500 °C to 800 °C, as confirmed through TEM. The valence state and surface composition of the resulting nanoparticle were analyzed using XPS. Diffuse UV-vis reflectance spectra were used to evaluate the optical energy gap using the Kubelka-Munk equation. Greater calcination temperature resulted in the energy band gap falling from 3.90 eV to 3.64 eV. PL spectra indicated a positive relationship between particle size and photoluminescence. Magnetic features were investigated through ESR, which revealed the presence of unpaired electrons. The magnetic field resonance decreases along with an increase of the g-factor value as the calcination temperature increased from 500 °C to 800 °C. Finally, Escherichia coli ATCC 25922 Gram (–ve) and Bacillus subtilis UPMC 1175 Gram (+ve) were used for in vitro evaluation of the tin oxide nanoparticle’s antibacterial activity. This work indicated that the zone of inhibition of 22 mm has good antibacterial activity toward the Gram-positive B. subtilis UPMC 1175.

In this study, a series of Li₂O-Al₂O₃-B₂O₃ glasses doped with various concentrations of Dy₂O₃ (where x = 0.0, 0.2, 0.4, 0.6, 0.8, and 1.0 mol%) were prepared by using a conventional melt-quenching technique. The structural, physical and optical properties of the glasses were examined by utilising a variety of techniques instance, X-ray diffraction (XRD), UV–Vis-NIR spectrometer, Fourier transform infrared (FTIR) and photoluminescence (PL). The XRD spectra demonstrate the amorphous phase of all glasses. Furthermore, the UV-vis-NIR spectrometers have registered optical absorption spectra a numbers of peaks which exist at 1703, 1271, 1095, 902, 841, 802, 669, 458, 393 and 352 nm congruous to the transitions from the ground of state (⁶H_15/2) to different excited states, ⁶H_11/2, ⁶F_11/2 + ⁶H_9/2, ⁶F_9/2 + ⁶H_7/2, ⁶F_7/2, ⁶F_5/2, ⁶F_3/2, ⁴F_9/2, ⁴I_15/2, ⁴F_7/2 and ⁶P_7/2, respectively. The spectra of emission exhibit two strong emanation bands at 481 nm and 575 nm in the visible region, which correspond to the transitions ⁴F_9/2 → ⁶H_15/2 and ⁴F_9/2 → ⁶H_13/2. All prepared glass samples doped with Dy₂O₃ show an increase in the emission intensity with an increase in the concentration of Dy³⁺. Based on the obtained results, the aforementioned glass samples may have possible applications, such as optical sensor and laser applications.

In the present study, binary oxide (cadmium oxide [CdO])_x (zinc oxide [ZnO])_1–x nanoparticles (NPs) at different concentrations of precursor in calcination temperature were prepared using thermal treatment technique. Cadmium and zinc nitrates (source of cadmium and zinc) with polyvinylpyrrolidone (capping agent) have been used to prepare (CdO)_x (ZnO)_1–x NPs samples. The sample was characterized by X-ray diffraction (XRD), scanning electron microscopy, energy-dispersive X-ray (EDX), transmission electron microscopy (TEM), and Fourier transform infrared (FTIR) spectroscopy. XRD patterns analysis revealed that NPs were formed after calcination, which showed a cubic and hexagonal crystalline structure of (CdO)_x (ZnO)_1–x NPs. The phase analysis using EDX spectroscopy and FTIR spectroscopy confirmed the presence of Cd and Zn as the original compounds of prepared (CdO)_x (ZnO)_1–x NP samples. The average particle size of the samples increased from 14 to 33 nm as the concentration of precursor increased from x=0.20 to x=0.80, as observed by TEM results. The surface composition and valance state of the prepared product NPs were determined by X-ray photoelectron spectroscopy (XPS) analyses. Diffuse UV–visible reflectance spectra were used to determine the optical band gap through the Kubelka–Munk equation; the energy band gap was found to decrease for CdO from 2.92 to 2.82 eV and for ZnO from 3.22 to 3.11 eV with increasing x value. Additionally, photoluminescence (PL) spectra revealed that the intensity in PL increased with an increase in particle size. In addition, the antibacterial activity of binary oxide NP was carried out in vitro against Escherichia coli ATCC 25922 Gram (-ve), Salmonella choleraesuis ATCC 10708, and Bacillus subtilis UPMC 1175 Gram (+ve). This study indicated that the zone of inhibition of 21 mm has good antibacterial activity toward the Gram-positive B. subtilis UPMC 1175.