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Designing efficient catalysts that possess large number of active sites, high catalytic activity and selectivity while also exhibiting strong antimicrobial activity is a challenging task because of poor control over material fabrication. Therefore, developing new and innovative approaches for the synthesis of catalytic materials is crucial for addressing these challenges. Here, we report the controlled fabrication of GQDs/Y-doped MgO nanoparticles achieved by co doping of yttrium (Y) and graphene quantum dots (GQDs) in magnesium oxide (MgO) based nanostructures (NSs) using the co-precipitation method. The co-doping of GQDs and Y was controlled by manipulating the ratio of precursors where introduction of GQD resulted in higher surface area and enhanced conductivity while the doping of Y enhanced the number of active sites in the final product. The GQDs/Y-doped MgO exhibited an average particle size of similar to 50 nm and a bandgap of 3.6 eV. Owing to these excellent characteristics, the GQDs/Y-doped MgO was utilized as a catalyst for treatment of the organic pollutants from water as well as antibacterial activity. The modified GQDs/Y-doped MgO nanostructure exhibited excellent activity of over 99.9 % for dye removal and versatility in a broad range of pH which clearly indicated the application in a range of different environments. Furthermore, the GQDs/Y-doped MgO exhibited excellent antibacterial activity against Escherichia Coli (E. Coli) bacteria. To gain further insights into the origins of this excellent activity response, the molecular docking simulations (MDS) is utilized against DNA gyrase and FabI (two enzymes critical to nucleic acid and fatty acid biosynthesis, respectively), to uncover the mechanism behind the observed antibacterial effects. In summary, the

The removal of cationic dyes from water has received a great attention of researchers considering their influence on environment and ecosystem. In current work, starch-grafted-poly acrylic acid (St-g-PAA) doped BaO nanostrucutures have been synthesized by co-precipitation approach. The aim of this research was to reduce the harmful methylene blue dye and evaluate the antibacterial activity of St-g-PAA doped BaO. XRD spectra exhibited the tetragonal structure of BaO and no variations occurred upon doping. The optical properties of St-g-PAA doped BaO have been evaluated by UV–Vis spectrophotometer. The existence of a dopant in the product was verified using EDS spectroscopy. TEM revealed the formation of cubic-shaped NPs of BaO and upon the addition of St-g-PAA, a few nanorod-like structures. The higher concentration of St-g-PAA doped BaO exhibit a remarkable reduction of methylene blue in a basic environment. Furthermore, St-g-PAA doped BaO revealed higher antimicrobial efficacy against Staphylococcus aureus in comparison to Escherichia coli. In silico studies were conducted against enoyl-[acylcarrier-protein] reductase (FabI) and beta-lactamase enzyme to evaluate the potential of both St-g-PAA and St-g-PAA doped BaO nanocomposites as their inhibitors and to rationalize their possible mode of action.

Vanadium oxide (V2O5) and carbonspheres(Cs)-doped NiO2 nanostructures (NSs) were prepared usingthe co-precipitation approach. Several spectroscopic and microscopictechniques, including X-ray diffraction (XRD), UV-vis, FTIR,TEM, and HR-TEM investigations, were used to describe the as-synthesizedNSs. The XRD pattern exhibited the hexagonal structure, and the crystallitesize of pristine and doped NSs was calculated as 29.3, 32.8, 25.79,and 45.19 nm, respectively. The control sample (NiO2) showedmaximum absorption at 330 nm, and upon doping, a redshift was observed,leading to decreased band gap energy from 3.75 to 3.59 eV. TEM ofNiO(2) shows agglomerated nonuniform nanorods exhibited withvarious nanoparticles without a specific orientation; a higher agglomerationwas observed upon doping. The (4 wt %) V2O5/Cs-dopedNiO(2) NSs served as superior catalysts with a 94.21% MBreduction in acidic media. The significant antibacterial efficacywas estimated against Escherichia coli by measuring the zone of inhibition (3.75 mm). Besidestheir bactericidal analysis, V2O5/Cs-doped NiO2 was shown to have a binding score of 6.37 for dihydrofolatereductase and a binding score of 4.31 for dihydropteroate synthasein an in silico docking study of E. coli.

This work demonstratesthe degradation of toxic RhB (rhodamineB) dye from polluted water in various pH environments. It assessesthe antibacterial action of CDs (carbon dots)/CS (chitosan)-dopedLa(2)O(3) (lanthanum oxide) NRs (nanorods). CS andCDs have been introduced as dopants to modify the characteristicsof La2O3 to achieve efficient outcomes. Theinfluence of doping on the structural, morphological, optical, andelemental properties of synthesized La2O3 NRswas investigated through a number of analytical techniques. The structuralanalysis of XRD revealed a hexagonal phase. The rod-like structureof pure La2O3 and reduction in the size of NRsupon doping were exhibited by TEM micrographs. From UV-visspectroscopy, increased absorption upon doping and introduction ofredshift that led to reduced bandgap energy were observed. The FTIRspectra indicate the presence of functional groups of pure and integratedsamples. The catalytic activity of specimens in basic medium towarddye showed excellent results (94.57%). The inhibition zone of diameter4.15 mm was evaluated by 6 mL of CDs/CS-doped La2O3 NRs against Escherichia coli once the surface area increased by dopants. In silico experimentswere performed for enoyl-[acyl-carrier-protein] reductase (FabI) andDNA gyrase enzymes to assess the potency of CS-doped La2O3 and CDs/CS-doped La2O3 as theirinhibitors and to justify their possible mechanism of action.

Carbon materials and their diverse allotropes have played important roles in our daily lives and the advancement of material science. After 0D “Carbon 60” and 1D “carbon-nanotube,” 2D-graphene nanomaterials have attracted significant attention since 2004 because of their unique and exciting properties. Over the last decade, 3D-graphene nanomaterials have been developed to efficiently use 2D-graphene nanosheets in applications like energy storage, environmental remediation, and electrochemical catalysis. We describe 3D graphene materials, classify them, briefly discuss their history, and cover this review's basic synthesis chemical procedures. Special attention is given to their bibliometric analysis, advancement, synthesis, technical applications of energy storage devices, environmental applications, and supercapacitor-based applications. The CiteSpace (6.1. R3) software is used for the bibliometric analysis findings from 2012 to 2023 for keywords, countries, journals, co-occurrence, and co-author networks. Data were taken from 1142 papers, 71 review articles, and 1071 article proceedings over 12 years, from 2012 to 2023. The date of retrieval, November 10, 2022, was the latest.

Undoped V2O5 is characterized by a small surface area and rapid electron-hole recombination, thus rendering it ineffective as a catalytic and antimicrobial agent. In this study, co-precipitation was employed to synthesize vanadium oxide (V2O5) and carbon spheres (CS) followed by doping with specific concentrations (3 and 6 wt%) of graphene oxide (GO) to produce GO/CS-doped V2O5 nanorods (NRs). The enhancement in catalytic and antibacterial activity provided by GO/CS-doped V2O5 was utilized to treat wastewater more efficiently. XRD analysis validated the orthorhombic and tetragonal structure of the synthesized samples. The polycrystalline nature of V2O5 was shown by vibrant circular rings in selected area electron diffraction (SAED) micrographs. TEM analysis endorsed formation of NRs, whereas UV–vis, luminescence (PL) and fourier transform infrared spectroscopy (FTIR), probed the absorption and emission along with stretching and bending vibrations in V-O-V bond. The chemically synthesized NRs exhibited excellent catalytic activity (93.71%) against rhodamine B (RhB) dye in the vicinity of NaBH4. In addition, NRs were used to evaluate in-vitro antimicrobial efficiency of 3.75 mmfor Escherichia coli (E. coli) using inhibition zone measurement. Docking investigations of GO/CS-V2O5 NRs for FabH and FabI of E. coli suggested suppression of above-mentioned enzymes as a possible mechanism. These findings demonstrate that (3 and 6 wt%) GO/CS-V2O5 possessed ample potency for industrial dye degradation and antimicrobial activity.

This study investigates the co-precipitation synthesis of (2 and 4 wt%) Ag and polyacrylic acid-doped SrO nanocomposites for bactericidal activities and catalytic Rhodamine B (RhB) decolorization. The objective of the investigation was to minimize the rate of electron-hole recombination of SrO to enhance charge transfer. The influence of Ag and PAA on the crystal structure, morphology, absorbance wavelength, and exciton recombination rate of SrO was studied using a systematic characterization. The binary dopants were added into SrO to reduce the crystallite size, which produces the new active sites (reduces the recombination rate) and may generate reactive oxygen species (ROS). In a neutral medium with sodium borohydride (NaBH4), the synthesized nanocomposites demonstrated reasonable results for catalytic reduction of RhB dye (74.3 %). The bactericidal efficiency (96.6 %) of prepared samples was measured for Escherichia coli (E. coli) at various concentrations. Molecular docking studies were performed to rationale the antibacterial activity of PAA-SrO and Ag/PAA-SrO nanocomposites against DHFRE. coli, DHPSE. coli, and FabIE.coli suggested their role as inhibitors.

In this research work, pristine and various concentrations (2.4 wt%) of graphene oxide (GO)/carbon sphere (CS)–doped Al2O3 nanostructures (NSs) were synthesized with the chemical sol–gel method. Aluminum oxide (Al2O3) exhibits quick recombination of electrons and holes with a low specific surface to limit catalytic and antibacterial activities. Al2O3 doped with CS is good in wastewater treatment and reduces the size of NSs. The incorporation of graphene oxide (GO) into Al2O3 at different concentrations (2 and 4 wt%) enhances both the structural and chemical stabilities of the resulting material while concurrently decreasing the number of charge carriers and reducing the band gap energy. This modified Al2O3-GO composite exhibits promising potential for utilization in dye degradation and antibacterial activity. A series of characterizations were performed to investigate the structural, morphological, and optical properties. The NSs exhibited excellent catalytic activity (CA) against rhodamine B (RhB) dye in acidic, basic, and neutral media. The antimicrobial activity was tested against Escherichia coli. Pairs of electrons and holes are the primary building blocks for the production of reactive oxygen species (ROS), which causes bacteria to die. The significant inhibition zones against E. coli were calculated to be approximately 5.65 mm when compared to ciprofloxacin. Moreover, in silico investigations have revealed the possible inhibitory impact of produced nanomaterials (GO/CS-doped Al2O3) on DNA gyrase and FabI enzymes of fatty acid biosynthesis.

This research lays the groundwork for preparing graphene oxide (GO)-doped CaO nanocomposites for efficient antibacterial potential and dye degradation. The study aimed to reduce the recombination rate of the electron hole (e−/h+) of CaO and improve charge transfer. This issue can be minimized by doping high-surface area GO into CaO quantum dots (QDs). Herein, the one-pot co-precipitation technique has prepared various concentrations (1, 3, and 5 wt%) of GO-doped CaO. Characterization techniques were used to investigate optical, elemental analysis, microstructural, functional, and morphological properties. The addition of GO into QDs showed excellent catalytic activity (CA) to control sample CaO against methylene blue (MB) in basic and acidic media compared to the neutral media. The synergistic effect of morphological alternation attributed to an increase in the mechanism of CA upon doping. Various concentrations of GO to QDs promised remarkable bactericidal potency against Escherichia coli.

As the population grows, the scientific community remains focused on researching new materials, methods, and devices to ensure the availability of safe drinking water. The main aim of this research was to decrease the recombination rate of the charge carriers of La2O3 and enhance the catalytic and antimicrobial activity by employing Y/Cs- doped La2O3, respectively. In the current study, different concentrations of yttrium (Y) and a fixed amount of carbon spheres (Cs) doped into lanthanum oxide (La2O3) nanostructures (NSs) were synthesized by the coprecipitation technique. Cs are used as a cocatalyst as they have a high surface area and small size attributed to increased active sites and decreased recombination rate. Moreover, Y was further incorporated as it activates the generation of reactive oxygen species in the inhibition zone, enhancing the antibacterial activity and reducing the emission intensity. Advanced techniques were utilized to determine the structural properties, optical emission and absorption, elemental composition, and d-spacing of the synthesized samples. The reported ternary catalyst works efficiently, improving the catalytic activity and bactericidal potential. Moreover, in silico molecular docking studies, Cs-doped La2O3 and Y/Cs-doped La2O3 nanostructures toward DNA gyrase Escherichia coli showed good efficacy for antibacterial activity.

Cationic dyes present in industrial effluents significantly reduce the effectiveness of remediation operations. Considering the terrible impact of these pollutants on environment and biodiversity, investigating strategies to remove potentially harmful compounds from water is becoming an increasingly intriguing issue. In this work, we employed a simple hydrothermal technique to synthesize Fe-doped CdO (2, 4, and 6 wt %) nanostructures and assessed their efficacy in degrading methylene blue (MB) dye and inhibiting the growth of Staphylococcus aureus and Escherichia coli, respectively. Structural, morphological, and optical characterization of produced nanomaterials was also performed using X-ray diffraction, TEM, and UV absorption spectra. The photocatalytic decomposition of MB was significantly enhanced (58.8%) by using Fe (6 wt %)-doped CdO catalysts for 80 min under irradiation. In addition, 2.05-5.05 mm inhibitory zones were seen against Gram-positive bacteria (S. aureus), whereas the range for Gram-negative bacteria (E. coli) was 1.65-2.75 mm. These nanostructures were shown to be very effective inhibitors of beta-lactamase, d-alanine-d-alanine ligase B, and fatty acid synthase inhibitor by in silico molecular docking investigations.

Various concentrations of samarium-grafted-carbon nitride (Sm-g-C3N4) doped-bismuth oxobromide (BiOBr) quantum dots (QDs) are prepared by the co-precipitation method. Elemental evaluation, morphological, optical, and functional group assessment are studied employing characterization techniques. Based on the XRD pattern analysis, it is determined that BiOBr exhibits a tetragonal crystal structure. The electronic spectroscopy revealed an absorption peak for BiOBr at 315 nm and the bandgap energy (Eg) decreasing from 3.9 to 3.8 eV with the insertion of Sm-g-C3N4. The presence of vibrational modes related to BiOBr at 550 cm−1 is confirmed through FTIR spectra. TEM revealed that pure BiOBr possessed non-uniform QDS, and agglomeration increased with the addition of Sm-g-C3N4. The catalytic performance of Sm-g-C3N4 into BiOBr (6 mL) in a neutral medium toward rhodamine B exhibited excellent results (99.66%). The bactericidal activity is evaluated against multi-drug resistance (MDR) Escherichia coli once the surface area is increased by dopant and the measured inhibition zone is assessed to be 3.65 mm. Molecular docking results supported the in vitro bactericidal potential of Sm-g-C3N4 and Sm-g-C3N4 doped-BiOBr as DNA gyraseE. coli inhibitors. This study shows that the novel Sm-g-C3N4 doped-BiOBr is a better catalyst that increases specific semiconductor's catalytic activity (CA).

In this research, a fixed concentration (3 wt%) of Ag/PAA and PAA/Ag doped graphene quantum dots (GQDs) were synthesized using the co-precipitation technique. A variety of characterization techniques were employed to synthesize samples to investigate their optical, morphological, structural, and compositional analyses, antimicrobial efficacy, and dye degradation potential with molecular docking analysis. GQDs have high solubility, narrow band gaps, and are suitable for electron acceptors and donors but show less adsorption and catalytic behavior. Incorporating polyacrylic acid (PAA) into GQDs increases the catalytic and antibacterial activities due to the carboxylic group (-COOH). Furthermore, introducing silver (Ag) increased the degradation of dye and microbes as it had a high surface-to-volume ratio. In addition, molecular docking studies were used to decipher the mechanism underlying the bactericidal action of silver and polyacrylic acid-doped graphene quantum dots and revealed inhibition of & beta;-lactamase and DNA gyrase.In this research, a fixed concentration (3 wt%) of Ag/PAA and PAA/Ag doped graphene quantum dots (GQDs) were synthesized using the co-precipitation technique.

A wide range of hard contaminants in wastewater is generated from different industries as byproducts of the organic compound. In this review, various metal oxide-based nanomaterials are employed for the photocatalytic removal of malachite green (MG) dye from wastewater. Some cost-effective and appropriate testing conditions are used for degrading these hard dyes to get higher removal efficiency. The effects of specific parameters are considered such as how the catalyst is made, how much dye is in the solution at first, how much nanocatalyst is needed to break down the dye, the initial pH of the dye solution, the type of light source used, the year of publications, and how long the dye has to be exposed to light to be removed. This study suggests that Scopus-based core collected data employ bibliometric methods to provide an objective analysis of global MG dye from 2011 to 2022 (12 years). The Scopus database collects all the information (articles, authors, keywords, and publications). For bibliometric analysis, 658 publications are retrieved corresponding to MG dye photodegradation, and the number of publications increases annually. A bibliometric study reveals a state-of-art review of metal oxide-based nanomaterials' effects on photocatalytic degradation of MG dyes (12 years).

The emergence of multi-drug resistance (MDR) in aquatic pathogens and the presence of cationic dyes are the leading causes of water contamination on a global scale. In this context, nanotechnology holds immense promise for utilizing various nanomaterials with catalytic and antibacterial properties. This study aimed to evaluate the catalytic and bactericidal potential of undoped and Sr-doped Cr2O3 nanostructures (NSs) synthesized through the co-precipitation method. In addition, the morphological, optical, and structural properties of the resultant NSs were also examined. The optical bandgap energy of Cr2O3 has been substantially reduced by Sr doping, as confirmed through extracted values from absorption spectra recorded by UV-Vis studies. The field-emission scanning electron microscopy (FE-SEM) and transmission electron microscopy (TEM) micrographs illustrate that the composition of Cr2O3 primarily consisted of agglomerated, irregularly shaped NSs with a morphology resembling nanoflakes. Moreover, the presence of Sr in the lattice of Cr2O3 increased the roughness of the resulting NSs. The catalytic activity of synthesized NSs was analyzed by their reduction ability of Rhodamine B (RhB) dye in the dark under different pH conditions. Their antibacterial activity was evaluated against MDR Escherichia coli (E. coli). Sr doping increased antibacterial efficiency against MDR E. coli, as indicated by inhibition zone measurements of 10.15 and 11.75 mm at low and high doses, respectively. Furthermore, a molecular docking analysis was conducted to determine the binding interaction pattern between NSs and active sites in the target cell protein. The findings corroborated antimicrobial test results indicating that Sr-Cr2O3 is the most effective inhibitor of FabH and DHFR enzymes.

In the present study, different concentrations (1 and 3%) of Bi were incorporated into a fixed amount of molybdenum disulfide (MoS2) and SnO2 quantum dots (QDs) by co-precipitation technique. This research aimed to increase the efficacy of dye degradation and bactericidal behavior of SnO2. The high recombination rate of SnO2 can be decreased upon doping with two-dimensional materials (MoS2 nanosheets) and Bi metal. These binary dopants-based SnO2 showed a significant role in methylene blue (MB) dye degradation in various pH media and antimicrobial potential as more active sites are provided by nanostructured MoS2 and Bi3+ is responsible for producing a variety of different oxygen vacancies within SnO2. The prepared QDs were described via morphology, optical characteristics, elemental composition, functional group, phase formation, crystallinity, and d-spacing. In contrast, antimicrobial activity was checked at high and low dosages against Escherichia coli (E. coli) and the inhibition zone was calculated utilizing a Vernier caliper. Furthermore, prepared samples have expressed substantial antimicrobial effects against E. coli. To further explore the interactions between the MB and Bi/MoS2-SnO2 composite, we modeled and calculated the MB adsorption using density functional theory and the Heyd-Scuseria-Ernzerhof hybrid (HSE06) approach. There is a relatively strong interaction between the MB molecule and Bi/MoS2-SnO2 composite.