The aim of the work was to prepare a polymer matrix composite doped by silver nanoparticles and analyze the influence of silver nanoparticles (AgNPs) on polymers’ optical and toxic properties. Two different colloids of AgNPs were prepared by chemical reduction. The first colloid, a blue one, contains stable triangular nanoparticles (the mean size of the nanoparticles was ~75 nm). UV–vis spectrophotometry showed that the second colloid, a yellow colloid, was very unstable. Originally formed spherical particles (~11 nm in diameter) after 25 days changed into a mix of differently shaped nanoparticles (irregular, triangular, rod-like, spherical, decahedrons, etc.), and the dichroic effect was observed. Pre-prepared AgNPs were added into the PVA (poly(vinyl alcohol)) polymer matrix and PVA–AgNPs composites (poly(vinyl alcohol) doped by Ag nanoparticles) were prepared. PVA–AgNPs thin layers (by a spin-coating technique) and fibers (by electrospinning and dip-coating techniques) were prepared. TEM and SEM techniques were used to analyze the prepared composites. It was found that the addition of AgNPs caused a change in the optical and antibiofilm properties of the non-toxic and colorless polymer. The PVA–AgNPs composites not only showed a change in color but a dichroic effect was also observed on the thin layer, and a good antibiofilm effect was also observed.

A chemical method was successfully used to synthesize silver nanoparticles (AgNPs) with various shapes. The shape of the nanoparticles affects the color of the colloid (spherical—yellow solution, triangular—blue, a mixture of spherical and triangular—green). The NaBH₄, which acts as the main reducing agent and H₂O₂ have a significant impact on the shape of AgNPs. It has also been shown that the ratio between precursor, reducing, and the stabilizing agent is crucial for the formation of the required nanoparticles. The light sensitivity of AgNPs and the presence of H₂O₂ lead to a significant change in AgNPs’ shape and size with time and to the formation of the dichroic effect. UV–vis spectrophotometry, TEM, SEM/FIB, and EDX methods were used to analyze the shape, size, and composition of the nanoparticles. Polymer matrix composite with AgNPs was prepared by the “ex-situ” method.

The Fe₃O₄@SiO₂@ZnO composite was synthesized via the simultaneous deposition of SiO₂ and ZnO onto pre-prepared Fe₃O₄ nanoparticles. Physicochemical methods (TEM, EDXS, XRD, SEM, FTIR, PL, zeta potential measurements, and low-temperature nitrogen adsorption/desorption) revealed that the simultaneous deposition onto magnetite surfaces, up to 18 nm in size, results in the formation of an amorphous shell composed of a mixture of zinc and silicon oxides. This composite underwent modification to form Fe₃O₄@SiO₂@ZnO*, achieved by activation with H₂O₂. The modified composite retained its structural integrity, but its surface groups underwent significant changes, exhibiting pronounced catalytic activity in the photodegradation of methyl orange under UV irradiation. It was capable of degrading 96% of this azo dye in 240 min, compared to the initial Fe₃O₄@SiO₂@ZnO composite, which could remove only 11% under identical conditions. Fe₃O₄@SiO₂@ZnO* demonstrated robust stability after three cycles of use in dye photodegradation. Furthermore, Fe₃O₄@SiO₂@ZnO* exhibited decreased PL intensity, indicating an enhanced efficiency in electron-hole pair separation and a reduced recombination rate in the modified composite. The activation process diminishes the electron-hole (e⁻)/(h⁺) recombination and generates the potent oxidizing species, hydroxyl radicals (OH˙), on the photocatalyst surface, thereby playing a crucial role in the enhanced photodegradation efficiency of methyl orange with Fe₃O₄@SiO₂@ZnO*.

The synthesis of silver nanoparticles (AgNPs) using sustainable and non-toxic methods has become an important research focus due to the limitations of conventional chemical approaches, which often involve hazardous reagents and produce unstable products. In particular, the effects of reaction conditions on the quality and stability of AgNPs obtained via green synthesis remain insufficiently understood. This study addresses this gap by examining the influence of pH and temperature on the synthesis of AgNPs using Rosmarinus officinalis extract as both reducing and stabilizing agents. UV-vis spectroscopy and TEM analysis revealed that optimal conditions for producing uniform, stable, and spherical AgNPs were achieved at pH 8, with a narrow size distribution (~17.5 nm). At extreme pH values (≤3 or ≥13), nanoparticle formation was hindered by aggregation or precipitation, while elevated temperatures mainly accelerated reaction without altering particle morphology. HRTEM and SAED confirmed the crystalline face-centered cubic structure, and colloids synthesized at pH 8 showed excellent stability over 30 days. Overall, the results demonstrate that precise pH control is critical for obtaining high-quality AgNPs via a simple, scalable, and environmentally friendly approach. Their stability and homogeneous size highlight potential applications in biomedicine, food packaging, and sensing, where reproducibility and long-term functionality are essential.