Sub‐nano‐sized Ag‐clusters represent an intermediate class between isolated atoms and nanoparticles, and they can possess new, unexpected properties differing from bulk and nano‐sized particles. A simple, fast, one‐step, cost‐effective protocol was revealed to prepare stable sub‐nano‐sized Ag‐clusters with green synthesis. The synthesis conditions included the low silver concentration (0.02 wt.%), excess of PVP (1.5 wt.%) as a stabilizer, pH 4, and use of water P. ruderale extract as a reducing agent. UV–visible and photoluminescence spectroscopies were used for the identification and characterization of sub‐nano‐sized Ag clusters, and FT‐IR, SEM, STEM, and dynamic light scattering were used for the characterization of the complete particles, which included three components: the extract, the stabilizer, and Ag clusters. The sub‐nano‐size (<1 nm) of the synthesized Ag clusters was revealed by the photoluminescence emission band and by absorption peaks at wavelengths less than 400 nm in the UV–visible spectra. The synthesized sub‐nano‐sized Ag clusters were reproducible and stable for up to 30 days, which represents a significant achievement since such clusters usually tend to fast aggregation. SEM and STEM revealed the presence of complete particles (Ag clusters, the extract, and the stabilizer) with cubic and spherical morphologies with sizes of 60 nm (nanoparticles) and 200–300 nm (microparticles), respectively. Dynamic light scattering confirmed the bimodal distribution of these particles and revealed their negative charge (−10 mV). The sub‐nano‐sized Ag clusters showed antiproliferative activity against the MCF‐7 breast cancer lying in the interval typical for the activity of different formulations of silver nanoparticles studied earlier.
The present paper presents a straightforward method for producing thin film layers of sulfide quantum dots (PbS-QDs) on a glass substrate using chemical solution deposition (CSD) assisted by dipcoating technique. The deposited PbS-QDs films were subjected to a comprehensive analysis using atomic force microscopy (AFM), energy dispersive X-ray (EDX) scanning electron microscopy (SEM), X-ray diffraction (XRD), UV–vis–IR absorption, and photoluminescence spectroscopic (PL) techniques to investigate the effects of varying concentrations of diethanol amine (DEA) on their morphology, crystal structure, elemental composition, light absorption, and emission characteristics. The spherical shape of the PbS-QDs was confirmed by AFM and SEM images with average sizes around 100 and 50 nm, respectively. The energy dispersive X-ray (EDX) analysis provides evidence the existence of Pb and S elements within the PbS matrix. X-ray diffraction (XRD) results validate that the deposited films exhibit high crystallinity, with a preferential orientation along the (111) plane and a face-centered cubic lattice structure of PbS. The crystallite size of PbS is measured to be 46.6 nm. Based on the optical absorption measurements, we have determined the size range of PbS nanocrystals to be between 4.3 and 11.5 nm. The optical studies reveal the presence of two optical absorption edges within the visible and infrared spectrum, two direct band gap energy, two cut-off wavelengths, two confinement energy, two Urbach energy tail, and dual emission peaks of PbS-QDs at room temperature. The analysis reveals the presence of two distinct band gap energies, one in the visible range (1.3–2.28 eV) and the other in the infrared range (0.65–0.88 eV), which can be attributed to the formation of two distinct sizes of quantum dots situated in two different layers. The first layer, deposited directly on the glass substrate, comprises quantum dots with an average size of approximately 5.2 nm, while the second layer contains quantum dots with an average size of about 9.5 nm. This ability to tune the band gap of PbS in the visible range up to the IR band (0.65–2.28 eV) is a critical feature that holds the potential for the development of innovative optoelectronic devices.
Nanotechnology has emerged as a promising field in pharmaceutical research, involving producing unique nanoscale materials with sizes up to 100 nm via physiochemical and biological approaches. Nowadays more emphasis has been given to eco-friendly techniques for developing nanomaterials to enhance their biological applications and minimize health and environmental risks. With the help of green nanotechnology, a wide range of green metal, metal oxide, and bimetallic nanoparticles with distinct chemical compositions, sizes, and morphologies have been manufactured which are safe, economical, and environment friendly. Due to their biocompatibility and vast potential in biomedical (antibacterial, anticancer, antiviral, analgesic, anticoagulant, biofilm inhibitory activity) and in other fields such as (nanofertilizers, fermentative, food, and bioethanol production, construction field), green metal nanoparticles have garnered significant interest worldwide. The metal precursors combined with natural extracts such as plants, algae, fungi, and bacteria to get potent novel metal, metal oxide, and bimetallic nanoparticles such as Ag, Au, Co, Cu, Fe, Zr, Zn, Ni, Pt, Mg, Ti, Pd, Cd, Bi2O3, CeO2, Co3O4, CoFe2O4, CuO, Fe2O3, MgO, NiO, TiO2, ZnO, ZrO2, Ag-Au, Ag-Cr, Ag-Cu, Ag-Zn, Ag-CeO2, Ag-CuO, Ag-SeO2, Ag-TiO2, Ag-ZnO, Cu-Ag, Cu-Mg, Cu-Ni, Pd-Pt, Pt-Ag, ZnO-CuO, ZnO-SeO, ZnO-Se, Se-Zr, and Co-Bi2O3. These plant-mediated green nanoparticles possess excellent antibacterial and anticancer activity when tested against several microorganisms and cancer cell lines. Plants contain essential phytoconstituents (polyphenols, flavonoids, terpenoids, glycosides, alkaloids, etc.) compared to other natural sources (bacteria, fungi, and algae) in higher concentration that play a vital role in the development of green metal, metal oxide, and bimetallic nanoparticles because these plant-phytoconstituents act as a reducing, stabilizing, and capping agent and helps in the development of green nanoparticles. After concluding all these findings, this review has been designed for the first time in such a way that it imparts satisfactory knowledge about the antibacterial and anticancer activity of plant-mediated green metal, metal oxide, and bimetallic nanoparticles together, along with antibacterial and anticancer mechanisms. Additionally, it provides information about characterization techniques (UV–vis, FT-IR, DLS, XRD, SEM, TEM, BET, AFM) employed for plant-mediated nanoparticles, biomedical applications, and their role in other industries. Hence, this review provides information about the antibacterial and anticancer activity of various types of plant-mediated green metal, metal oxide, and bimetallic nanoparticles and their versatile application in diverse fields which is not covered in other pieces of literature.
The preparation of metallic nanoparticles using green synthetic approaches and its application toward the efficient degradation of environmentally hazardous dyes constitutes an attractive alternative to currently employed methods. In the current report, the green synthesis of silver nanoparticles (AgNPs) was successfully achieved using Actinidia deliciosa (kiwifruit) peel aqueous extract as a bioreducing agent under optimized synthesis conditions. The experimental parameters were optimized in terms of reactant ratio, reaction temperature, and reaction time. The biogenic nanoparticles exhibited SPR absorption band at λmax 480 nm. Transmission electron microscopy (TEM) and scanning electron microscopy (SEM) images revealed quasispherical monodisperse nanoparticles which were 36 nm in diameter. The hydrodynamic diameter of the nanoparticles was 106 nm as determined by dynamic light scattering, and the highly negative ζ-potential (−34 mV) supported its superior colloidal stability. Energy dispersive X-ray confirmed that silver is a major constituent of the nanoparticles. X-ray diffraction (XRD) diffractograms confirmed the crystallinity of the nanoparticles and its face-centered cubic (fcc) lattice structure. The functional groups in the plant’s phytochemicals facilitating the reduction of Ag+ ions and stabilization of the formed AgNPs were identified by fourier transform infrared (FTIR) spectroscopy. In specific, the bands in the FTIR spectra at 3,412, 1,618, 1,419, and 1,237 cm−1 suggested the presence of phenolic compounds. Phytochemical analysis by colorimetric assays revealed that the kiwifruit peel extract was rich in phenolic compounds. When evaluated in the catalytic degradation of organic dyes, the biosynthesized AgNPs induced instant and complete discoloration of the methylene blue dye when 1.6 mg of nanoparticles was used. At a lower dose of AgNPs (0.4 mg), 80% degradation of the dye occurred after 3 hr of treatment. The degradation reaction followed second-order kinetics with a rate constant of 0.01083 mM−1s−1. The current study highlights the immense potential of the prepared nanoparticles as efficient catalysts for the degradation of hazardous organic dyes such as methylene blue and presents an intriguing argument for investigating the catalytic efficiency of the biogenic AgNPs for the degradation of other structurally different dye pollutants.
This research aims to improve antimicrobial materials based on functional silica nanoparticles. Three different methods were used in the study to create silica nanoparticles with other properties. The nanoparticles’ morphological structures are porous, hollow, and filled with spherical forms. The surface of these nanoparticles was grafted with poly(1-vinyl-1,2,4-triazole) (PVTri). The morphological properties of nanocomposites were used for analysis. In contrast, thermal gravimetric analysis was used to characterize the thermal properties of nanocomposites (thermogravimetric analysis). The silica nanoparticles were evaluated for their in vitro antimicrobial activity against Escherichia coli , Staphylococcus aureus , and Saccharomyces cerevisiae using minimum inhibitory concentration measurement. Silica nanoparticles have different antifungal and antibacterial properties related to their structure. The cytotoxic effects of the silica nanoparticles on HaCaT cells were performed with an MTS assay. In this study, we observed that high doses of HSS and e-SiO 2 decreased cell growth, while HSS and e-SiO 2 composite with PVTri increased cell proliferation.
