Synthesis Of Ag Nanoparticles Research Articles

Synthesis and characterization of zinc oxide nanoparticles from aqueous extract of elephant grass (Pennisetum purpureum)

Objective: To synthesise and characterise Pennisetum purpureum zinc oxide nanoparticles from aqueous extracts of elephant grass (Pennisetum purpureum). Methodology: Zinc oxide nanoparticles were synthesised with aqueous extract of elephant grass (Pennisetum purpureum) and zinc acetate dihydrate. It was characterized by using various dispersion methods such as UV-visible spectrophotometry, Transmission Electron Microscopy (TEM), Fourier Transform Infrared (FTIR) Spectroscopy and X-ray diffraction (XRD) to determine the morphology, crystallographic structure, chemical composition, physical properties and crystalline size of the nanoparticles. Results: The results showed that Zinc oxide nanoparticles were synthesized and characterized using various dispersion methods. UV–Vis spectra showed typical absorption peaks around 370nm (Pennisetum purpureum). FTIR revealed the presence of biomolecules and functional groups (C-O, O-H, CH, C≡C, C=C, N-O) that performs various functions like stabilizers, capping and coating agents in nanoparticle synthesis. XRD revealed the crystallographic structure, chemical composition, physical properties and crystalline size of the nanoparticles. The average crystalline size of zinc oxide nanoparticles was calculated using Debye–Scherer equation and the average size was 23.37nm. Conclusion: In this study, simple and green method for the synthesis of zinc oxide nanoparticles using aqueous extract of elephant grass (Pennisetum purpureum) and characterization using various dispersion methods was described. The formation of zinc oxide nanoparticle was confirmed by UV-Visible spectroscopy. The FTIR spectrum showed that the phytochemicals found in the plant extract was incorporated into the zinc oxide nanoparticle as capping and stabilizing agents. XRD results revealed the average size of 23.37nm (Pennisetum purpureum ZnO) and Transmission Electron microscopy (TEM) confirmed the morphology to be spherical.

Cyrene as solvent for metal nanoparticle synthesis

Enormous advances have been made in the synthesis of metal nanoparticles (NPs) affording a high degree of control over their size, shape, and composition. In recent years, a growing effort has been dedicated to incorporating principles of green chemistry in different aspects of NPs, ranging from reagents/solvents to their fate in the environment. In this report, we focus on the use of Cyrene (dihydrolevoglucosenone) as an alternative green solvent for the synthesis of metal NPs. We begin with the synthesis of Ag NPs, given their prominence in the literature. Through control reactions, we show that Cyrene has a dual role of solvent and reducing agent. Additionally, the conversion yield for the Ag NPs synthesis was studied with respect to temperature and the Ag precursor. We then expand on the synthetic methodology to access Pd, Pt, and Bi NPs. The functionality of the synthesized NPs is assessed by employing them as electrocatalysts for furfural reduction and the hydrogen evolution reaction. We envision the use of Cyrene as a green solvent can be extended toward the synthesis of NPs of other metals and classes of materials.Graphical

Green Synthesized Ag Nanoparticles as Promising Antibacterial and Antitumor Agents: In Vitro Studies

Green Synthesized Ag Nanoparticles as Promising Antibacterial and Antitumor Agents: In Vitro Studies

Bare copper bonding with facilely synthesized Ag nanoparticles decorated Cu microparticles paste

Bare copper bonding with facilely synthesized Ag nanoparticles decorated Cu microparticles paste

Green synthesis of silver nanoparticles using Pandanus tectorius aerial root extract: Characterization, antibacterial, cytotoxic, and photocatalytic properties, and ecotoxicological assessment

Nanotechnology, a rapidly developing field of research, has several applications in various disciplines of applied science. The eco-friendly synthesis method presented here provides a sustainable alternative to traditional methods that frequently rely on harmful chemicals. Following the synthesis, the antibacterial and anti-cancer properties of the nanoparticles produced through this environmentally-friendly. In the present study, the reducing agents for the fabrication of silver nanoparticles (Ag-NPs) were aqueous extracts of the aerial root of Pandanus tectorius. The green synthesized Ag nanoparticles were characterized by UV–vis, FTIR, XRD, and SEM, as well as EDX analysis. Artemia nauplii larvae were used to test the nanoparticles’ eco-toxicity, cytotoxicity against HeLa cells, and antibacterial activity using the well diffusion assay. The synthesized Ag-NPs exhibited maximum absorbance in the visible band at 415 nm. In the XRD spectrum of crystalline Ag-NPs, four prominent peaks with 2θ values of 38.12°, 54.14°, 64.18°, and 77.48° are observed. These peaks correspond to the crystallographic planes 111, 200, 220, and 311, respectively. The synthesized nanoparticles SEM-TEM image revealed a spherical shape. EDX spectral peak was found at 3.0 keV. Maximum growth inhibitory activity was noticed against P. aeruginosa (14 mm) through determining the zones of inhibition on disc diffusion method. The studied bacterial strains have demonstrated effective inhibition by these Ag-NPs. In vitro cytotoxicity assessment of Ag-NPs exhibited an IC50 value of 47.58 μg/mL against HeLa cancer cells. Methylene blue (MB) dye degradation under solar radiation was investigated for its photocatalytic properties. The findings demonstrated that after 120 min in the light, MB deteriorated by 82.6 %. Overall, the results of this investigation suggest that Ag-NPs biosynthesized by P. tectorius may have photocatalytic, antibacterial and anticancer properties.

Continuous On‐Chip Synthesis of Ag Nanoparticles Assisted by Resonant Microwave Heating Using a Post‐Wall Waveguide

Microfluidics made of dimethylpolysiloxane were developed for chemical synthesis using microwave heating at 24.125 GHz, and microwave efficiency was enhanced by the microwave resonance effect. In addition, the device was fabricated using a mold created using a 3D printer to reduce production costs. The microchip structure comprised a post‐wall waveguide and a microchannel that passed through the waveguide. This post‐wall waveguide also comprises metal columns (post‐wall) instead of a conductor side wall, and easily introduces microchannels through the gaps between the metal columns. The waveguide length was adjusted to achieve a resonance frequency of 24 GHz using an electromagnetic wave simulation, assuming that the microchannel was filled with pure water. Microwaves with an input power of 4 W caused a maximum temperature increase of 93 °C; this result is ~10 °C higher than that of a microchip with non‐resonant structure. In this study, Ag nanoparticles were synthesized using a chemical reaction induced by microwave irradiation of a chip flow system. Owing to irradiating the mixing reagent with microwaves of an input power of 4 W while controlling the flow rate at 0.7 μl/min, the formation of Ag nanoparticles with an average particle size of ~19.2 ± 2.4 nm was demonstrated by absorbance measurements and dynamic light scattering. It is expected that microwave microfluidics enhanced by the resonance effect will substantialize nanoparticle synthesis and high‐efficiency automated chemical synthesis combined with multichemical unit operations. © 2024 Institute of Electrical Engineers of Japan and Wiley Periodicals LLC.

Utilizing Biomolecule-Rich Citrus Fruit Waste as a Medium for the Eco-Friendly Preparation of Silver Nanoparticles with Antimicrobial Properties

An ample amount of fruit waste is generated as agro-industrial waste, leading to significant nutritional, economic, and environmental challenges. Fruit peels are rich in many valuable bioactive compounds with the potential for developing nanoparticles. This study examined fresh juices of two citrus fruit peel wastes (Citrus sinensis: C. sinesis and Citrus limon: C. limon) for antioxidants and total protein. Then, we investigated their ability to produce silver nanoparticles, which were further analyzed for anti-microbial activity against thirteen pathogenic microbes. Both Citrus peel juices were rich in secondary metabolites. The formation of Ag nanoparticles was initially confirmed by UV-vis spectroscopy, with peaks at 400 nm for C. sinensis peel Ag nanoparticles and 430 nm for C. limon peel Ag nanoparticles. Further characterization was conducted using zeta sizer, zeta potential, Transmission Electron Microscopy (TEM), Scanning Electron Microscope (SEM), Energy-dispersive X-ray spectroscopy (EDX) and Fourier transform infrared (FTIR) spectroscopy. The antimicrobial activity was tested using the well diffusion method against 11 bacterial strains (five Gram-positive and six Gram-negative) and two fungal strains of Candida. TEM and SEM results revealed a spherical shape, with an average diameter of about 13 nm for C. sinensis and 21 nm for C. limon Ag. EDX confirmed the presence of silver in both nanoparticles. The FTIR spectrum of the extract indicated the presence of biomolecules, which facilitated the reduction and capping of the synthesized Ag nanoparticles. The prepared nanoparticles showed remarkable antimicrobial activity, but the nanoparticles from C. sinensis exhibited stronger antibacterial properties because of their smaller size. Citrus peel waste is a suitable medium for the eco-friendly production of silver nanoparticles.

A facile detachable catalyst support: Green synthesis of Ag nanoparticles, immobilizing into waste corn husk fibers, evaluation of photocatalytic performance and bioactivity analysis

The escalating demand for metallic nanoparticles (Nps) is propelled by their expanding utility in environmental and biomedical disciplines. To enhance the efficiency of wastewater treatment, nanotechnology, renowned for its environmentally friendly properties, has been strategically employed. Nano-metals, distinguished for their photocatalytic and antimicrobial capabilities, were harnessed in this investigation. A biochemical synthesis method involving the green synthesis of environmentally friendly and non-toxic AgNps, utilizing Myrtus communis leaf extract, was implemented. The subsequent immobilization of these synthesized nanoparticles into corn husk fibers facilitated the photocatalytic degradation of Crystal Violet dye, yielding an impressive 96 % removal efficiency. The optimization of methodologies using Central Composite Design was validated through ANOVA. Surface properties were comprehensively assessed through SEM-EDS and FT-IR analyses, while crystal structure elucidation was achieved via XRD analysis. The synthesized AgNps showcased notable antioxidant activity, registering 90.61 % efficacy even at a modest concentration of 100 mg/L. Microdilution assays underscored the consequential antibacterial and antifungal activities against diverse microorganisms. Notably, AgNps exhibited substantial antibiofilm efficacy, reaching peak rates of 89.63 % and 81.75 % against S. aureus and P. aeruginosa at 20 mg/L, respectively. Furthermore, E. coli cell viability was markedly impeded, displaying a 95.87 % reduction compared to the control at a concentration of 20 mg/L. In summation, AgNps manifest noteworthy antimicrobial, antioxidant, cell viability, and antidiabetic potential. Their integration into photocatalytic processes offers a nuanced strategy for environmental remediation, coupling heightened pollutant degradation with inherent antibacterial attributes, thereby advancing the evolution of effective and sustainable water treatment technologies.

Green Synthesis of Silver Nanoparticles Using Plant Extract Blends and Its Impact on Antibacterial and Biological Activity

There is a strong interest in using green resources for synthesizing nanoparticles (NPs) of industrial and biomedical utility in a way to maintain desired material properties throughout use while not inducing any harmful effects. The use of various plant extracts as reducing, capping, or stabilizing agents is widely attempted in green nanotechnology. However, very little has been explored about incorporating plant extract blends into green NP synthesis routes. Here, we used the combination of tea and olive leaf extracts for the synthesis of silver NPs and evaluated the advantages it provided over both chemical and single-plant-mediated synthesis routes. Four different reducing agents (tannic acid, black tea leaves extract, olive leaves extract and their blend) were used to synthesize silver NPs (Ag NP) from silver nitrate (AgNO[Formula: see text]. The synthesized Ag NP was characterized by scanning electron microscopy (SEM), dynamic light scattering (DLS), and ultraviolet-visible (US-Vis) spectroscopy. The antimicrobial properties of Ag NP were assessed against Escherichia coli (E. Coli) and Staphylococcus aureus (S. Aureus) using the colony-forming unit (CFU) assay and the minimum inhibitory concentration (MIC) assay. The cytotoxic potential of Ag NP on human colorectal adenocarcinoma (Caco-2) cells was assessed by the WST-1 assay. Results showed that Ag NP synthesized using plant extract mixtures had a primary particle size of 40[Formula: see text]nm and were very effective antibacterial agents, with the MIC values ranging from [Formula: see text]g/mL to 10[Formula: see text][Formula: see text]g/mL. While the particle size obtained in chemical synthesis was slightly lower, the resultant Ag NP did not serve as an effective antibacterial agents at low doses. Further understanding of how best to integrate extracts of different plants into green NP synthesis routes will enable wider and safer biomedical applications.

Facile synthesis of Ag/AgCl/PAF-54 heterojunction photocatalysts for TC degradation

Photocatalysis plays an increasingly important role in the field of water treatment. Among the catalysts, Ag nanoparticles (NPs), a type of noble metal NP, show extraordinary potential for photocatalysis. Nevertheless, the aggregation caused by high surface energy limits their applications. The simple synthesis of Ag NPs with uniform size remains a challenge. In this work, a nitrogen-rich porous organic polymer (POP) with reduction ability, porous aromatic framework (PAF)-54, was chosen as the carrier for the in-situ synthesis of Ag NPs. By virtue of the reducing framework of PAF-54 and the formation of the AgCl/PAF-54 heterojunction, the in-situ reduction of Ag(I) was realized, and thus Ag NPs with the particle size of 20-25 nm were uniformly distributed on PAF-54, which exhibit a strong localized surface plasmon resonance (LSPR) effect. Furthermore, the Ag/AgCl/PAF-54 heterojunction effectively suppresses the recombination of photogenerated electrons and holes, leading to the enhanced photocatalytic ability of the composite material. Even with a small catalyst dosage, rapid tetracycline (TC) degradation can be achieved, and the degradation rate of TC reached 94.8% in 30 min. This study offers a facilitated approach for fabricating Ag-based POP composites with superior photocatalytic properties.

Acoustofluidic one-step production of plasmonic Ag nanoparticles for portable paper-based ultrasensitive SERS detection of bactericides

SERS measurements for monitoring bactericides in dairy products are highly desired for food safety problems. However, the complicated preparation process of SERS substrates greatly impedes the promotion of SERS. Here, we propose acoustofluidic one-step synthesis of Ag nanoparticles on paper substrates for SERS detection. Our method is economical, fast, simple, and eco-friendly. We adopted laser cutting to cut out appropriate paper shapes, and aldehydes were simultaneously produced at the cutting edge in the pyrolysis of cellulose by laser which were leveraged as the reducing reagent. In the synthesis, only 5 μL of Ag precursor was added to complete the reaction, and no reducing agent was used. Our recently developed acoustofluidic device was employed to intensely mix Ag+ ions and aldehydes and spread the reduced Ag nanoparticles over the substrate. The SERS substrate was fabricated in 1 step and 3 min. The standard R6G solution measurement demonstrated the excellent signal and prominent uniformity of the fabricated SERS substrates. SERS detection of the safe concentration of three bactericides, including tetracycline hydrochloride, thiabendazole, and malachite green, from food samples can be achieved using fabricated substrates. We take the least cost, time, reagents, and steps to fabricate the SERS substrate with satisfying performance. Our work has an extraodinary meaning for the green preparation and large-scale application of SERS.

Environmentally benign preparation of Ag nanoparticles & Ag-rGO nanocomposite and evaluation of their photocatalytic, sensing, antioxidant and antimicrobial activities

Environmental pollution and fossil fuel depletion are becoming major issues on a worldwide scale, posing serious threats to both the environment and human health. Finding effective and affordable pollution cleanup technologies as well as the alternate source of energy is very important. The present study is concerned with the synthesis of Ag nanoparticles and Ag-rGO composite employing environment affable and cost-effective green combustion method. The fuel used for the preparation of NPs was the Malus domastica juice. The synthesized materials were subjected for the characterization techniques like XRD, TEM, SEM, Raman and UV-Visible spectral studies. The synthesized nanocomposite was analyzed for photocatalytic dye degradation, electrochemical nitrate sensing, antibacterial as well as antioxidant activities. Ag-rGO degraded methylene blue dye completely by 70 min. Further, the material was subjected for recyclability test and it was efficient and stable upto 5th cycle. Effect of various parameters such as catalytic load, dye concentration and pH on efficiency of dye degradation was analyzed. Nitrite sensing studies revealed that the LOD was found to be 19.8 µg. Further, Ag-rGO exhibited antibacterial activity on Pseudomonas aeroginosa bacterial strain to a greater extent compared to all the other bacterial strains tested. The Ag-rGO nanocomposite was found to be the potent antioxidant with IC50 value of 1489 µg/mL. Therefore, this work exemplifies the easy and eco-friendly green synthetic route for the large-scale industrial production of versatile Ag-rGO nanocomposite.

Green synthesis of silver nanoparticles decorated on graphene oxide for crystal violet dye removal

In this study, we demonstrate a facile and environmentally benign method for the synthesis of Ag nanoparticles using a green reducing agent and their subsequent deposition onto GO sheets. The synthesized GO@Ag nanocomposite was characterized using various analytical techniques such as FTIR, XRD, FESEM, EDX and BET. The results confirmed the successful formation of cubic Ag nanoparticles with diameter 30–40 nm on the GO surface. The theoretical surface area of GO@Ag was found to be 89 m2/g. The adsorption efficiency of GO@Ag nanocomposite toward CV dye was evaluated through batch adsorption experiments. The above experimental results revealed that CV adsorption on to the GO@Ag surface was pH dependent and maximum adsorption capacity was found to be 48.78 mg/g at pH = 8. The adsorption process followed pseudo-second-order kinetics and Langmuir isotherm models, indicating monolayer adsorption with chemisorption as the rate-limiting step. Furthermore, the recyclability and stability of the nanocomposite were assessed through multiple adsorption-desorption cycles, demonstrating its potential for practical applications in wastewater treatment for the removal of cationic dyes. The mechanism of CV adsorption on to the GO@Ag surface mainly involves electrostatic attraction and π-π interaction.

Green synthesized AgNPs as a probe for colorimetric detection of Hg (II) ions in aqueous medium and fluorescent imaging in liver cell lines and its antibacterial activity

The present research aimed at green synthesis of Ag nanoparticles (AgNPs) based colorimetric sensor using persimmon leaf extract (PLE) for selective detection of mercuric ion (Hg2+). Optimization of reaction conditions viz. pH, concentration of PLE, time was done and further AgNPs were characterized using UV, IR, FE-SEM, EDX, XRD and TEM analysis. The developed AgNPs were evaluated for the selective colorimetric detection of Hg2+ in aqueous medium and fluorescence imaging of Hg2+ ions in liver cell lines. Later, the antibacterial activity of AgNPs was performed against S. aureus and E. coli. The findings of the study revealed that PLE mediated AgNPs exhibited notable limit of detection up to 0.1 ppb, high efficiency, and stability. The antibacterial study indicated that developed AgNPs has impressive bacterial inhibiting properties against the tested bacterial strains. In conclusion, developed biogenic AgNPs has high selectivity and notable sensitivity towards Hg2+ ions and may be used as key tool water remediation.Graphical abstract

Plasmon-driven substitution of 4–mercaptophenylboronic acid to 4-nitrothiophenol monitored by surface-enhanced Raman spectroscopy

Plasmon-driven reactions on plasmonic nanoparticles (NPs) occur under significantly different conditions from those of classical organic synthesis and provide a promising pathway for enhancing the efficiency of various chemical processes. However, these reactions can also have undesirable effects, such as 4-mercaptophenylboronic acid (MPBA) deboronation. MPBA chemisorbs well to Ag NPs through its thiol group and can subsequently bind to diols, enabling the detection of various biological structures by surface-enhanced Raman scattering (SERS), but not upon its deboronation. To avoid this reaction, we investigated the experimental conditions of MPBA deboronation on Ag NPs by SERS. Our results showed that the level of deboronation strongly depends on both the morphology of the system and the excitation laser wavelength and power. In addition, we detected not only the expected products, namely thiophenol and biphenyl-4,4-dithiol, but also 4-nitrothiophenol (NTP). The crucial reagent for NTP formation was an oxidation product of hydroxylamine hydrochloride, the reduction agent used in Ag NP synthesis. Ultimately, this reaction was replicated by adding NaNO2 to the system, and its progress was monitored as a function of the laser power, thereby identifying a new reaction of plasmon-driven −B(OH)2 substitution for –NO2.

A Catalytic Reduction of 4-Nitrophenol Utilizing Bimetallic CuO-Co3O4 Nanoparticles Synthesized via Wrightia tinctoria Extract: A Green Approach

In this investigation, copper oxide (CuO), cobalt oxide (Co3O4) and bimetallic copper oxide-cobalt oxide (CuO-Co3O4) nanoparticles were synthesized using an aqueous extract of Wrightia tinctoria leaves and characterized through UV-Vis, FT-IR, XRD, TEM and zeta potential analyses. The FT-IR analysis identified that specific phytoconstituents are responsible for the reduction and capping agents in nanoparticle synthesis. TEM analysis determined size and shape and zeta potential analysis assessed stability. The CuO and Co3O4 NPs, synthesized through an eco-friendly approach, were employed for 4-nitrophenol reduction with sodium borohydride. The reaction rate, was computed at 1 × 10-4 s-1, which indicated the pseudo-first-order kinetics. The synthesis of 4-aminophenol was also successfully acheived demonstrated that the excellent catalytic activity of CuO, Co3O4 and CuO-Co3O4 nanoparticles as catalysts.

Green Synthesis and Antimicrobial Study on Jujube Seed Extract Functionalized Ag Nanoparticles

AbstractGreen synthesis of Ag nanoparticles (AgNPs) by using the plant extract is a very important strategy to gain efficient antimicrobial agents with strong antimicrobial activity and low toxicity. In this study, jujube seed extract (JSE) is utilized to green synthesis of AgNPs by both hydrothermal process and solution‐based approaches. UV–vis absorption spectroscopy and infrared spectroscopy (FTIR) spectra confirm that jujube seed extract functionalized Ag nanoparticles are formed by both approaches and jujube seed extract covered on the surface of Ag nanoparticles. Transmission electron microscopy (TEM) images indicate that the JSE‐AgNPs are spherical with the average diameter of 17.7 and 14.2 nm for the hydrothermal process and solution‐based approaches, respectively. X‐ray diffraction (XRD) results indicate that the JSE‐AgNPs prepared by both approaches have face‐centered cubic crystal structure. The antimicrobial activity test reveals that minimum inhibitory concentrations (MIC) of JSE‐AgNPs by the solution‐based method are 62.5, 125, and 62.5 µg mL−1 against Escherichia coli, Staphylococcus aureus, and Candida albicans, respectively. These results imply that the JSE‐AgNPs have potential to be developed as efficient antimicrobial agents.

Low temperature one-step synthesis of Ag nanoparticles on BaTiO3 for synergistic piezo-photocatalytic properties

It is a major constraint that complex synthesis methods limit the application of catalysts. Herein, Ag/BaTiO3 catalyst is synthesized via a facile method, which demonstrates the outstanding catalytic properties. Investigations reveal that Ag-loading BaTiO3 could increase carrier concentration, reduce the electronic impedance and enhance carrier’s separation efficiency under ultrasonic vibration, leading to superior piezocatalytic performance. Therefore, Ag/BaTiO3 catalyst presents the high degradation efficiency of 95.4 % in 50 min for RhB dye solution at light illumination and ultrasonic vibration. Moreover, when Ag content is 0.33 %, the degradation ratio of the sample still remains 81.9 % after 5th cycles, which indicates Ag/BaTiO3 catalyst has good stability. This work provides a novel and easy implement strategy for designing high performance catalysts, and could be extended to other catalytic material.

Selective Flocculation and H2O2-Free Oxidative Etching-Based Synthesis of Highly Monodisperse Ag Nanospheres for Uniform Quantum Dot Photoluminescence-Enhancing Plasmonic Cavity Applications.

Ag nanoparticles have garnered significant attention for their excellent plasmonic properties and potential use as plasmonic cavities, primarily because of their intrinsically low ohmic losses and optical properties in the visible range. These are particularly crucial in systems involving quantum dots that absorb light at low wavelengths, where the need for a high threshold energy of interband transitions necessitates the incorporation of Ag nanostructures. However, the synthesis of Ag nanoparticles still encounters challenges in achieving structural uniformity and monodispersity, along with chemical stability, consequentially inducing inconsistent and poorly reliable optical responses. Here, we present a two-step approach for synthesizing highly uniform spherical Ag nanoparticles involving depletion-induced flocculation and Cu(II)-mediated oxidative etching. We found that the selective flocculation of multitwinned Ag nanocrystals significantly enhances the uniformity of the resulting Ag nanostructures, leaving behind only single-crystalline and single-twinned nanostructures. Subsequent oxidative etching, in which cupric ions are directly involved in the reaction, was designed based on Pourbaix diagrams to proceed following thermodynamically favorable states and circumvent the generation of reactive chemical species such as H2O2. This leads to perfectly spherical shapes of final Ag nanoparticles with a synthetic yield of 99.5% and additionally reduces the overall reaction time. Furthermore, we explore the potential applications of these monodisperse Ag nanospheres as uniform plasmonic cavities. The fabricated Ag nanosphere films uniformly enhanced the photoluminescence of InP/ZnSe/ZnS quantum dots, showcasing their capabilities in exhibiting consistent plasmonic responses across a large area.

Recent Advancements and Unexplored Biomedical Applications of Green Synthesized Ag and Au Nanoparticles: A Review.

Green synthesis of silver (Ag) and gold (Au) nanoparticles (NPs) has acquired huge popularity owing to their potential applications in various fields. A large number of research articles exist in the literature describing the green synthesis of Ag and Au NPs for biomedical applications. However, these findings are scattered, making it time-consuming for researchers to locate promising advancements in Ag and Au NPs synthesis and their unexplored biomedical applications. Unlike other review articles, this systematic study not only highlights recent advancements in the green synthesis of Ag and Au NPs but also explores their potential unexplored biomedical applications. The article discusses the various synthesis approaches for the green synthesis of Ag and Au NPs highlighting the emerging developments and novel strategies. Then, the article reviews the important biomedical applications of green synthesized Ag and Au NPs by critically evaluating the expected advantages. To expose future research direction in the field, the article describes the unexplored biomedical applications of the NPs. Finally, the articles discuss the challenges and limitations in the green synthesis of Ag and Au NPs and their biomedical applications. This article will serve as a valuable reference for researchers, working on green synthesis of Ag and Au NPs for biomedical applications.