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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

Renewable energies can reduce emissions from fossil fuel-based power production by a significant amount, reducing climate change. Among the several options being investigated, hydrogen is now recognized as one of the primary enabling technologies for future large-scale and long-term green storage of renewable energy. However, using clean and renewable energy sources like water and sunlight is the best option. According to recent studies, photoelectrochemical (PEC) water splitting is a potential technology for creating hydrogen using free solar energy since hydrogen and oxygen gases may be easily identified in PEC. This study uses bibliometric and systematic literature review methodologies to examine the scientific understanding of PEC water splitting and hydrogen generation, evaluating 936 articles issued in the Web of Science database from 1970 to 2022. The authors looked at how PEC water splitting research has developed compared to prior research, what criteria make up practical approaches, and what subjects have emerged as new trends in reacting to changing situations. The key findings from the article analysis, future research potential, and practical implications for the field are discussed.

Years of study have shown that creating a commercial photoelectrode to solve particular bottlenecks, such as low charge separation and injection efficiency, short carrier diffusion length and lifespan, and poor stability, requires the employment of a variety of components. Developing photovoltaic-electrolysis, photocatalytic, and photoelectrochemical approaches to accelerate hydrogen production from solar energy has been highly competitive. Photoelectrochemical water splitting utilizing nanoporous materials is one of the promising approaches to produce hydrogen more efficiently, cost-effectively, and on a long-term basis. Nanoporous materials have been highly used in photoelectrochemical water-splitting systems and are crucial in numerous applications. Those materials have a porous structure and excellent conductivity, enabling the deposition of transition metal atoms and electrochemically active chemicals on a large active surface area. However, there remains a dearth of review articles exploring the application of nanoporous materials in photoelectrochemical reactions. Therefore, this review provides bibliometric statistics and various perspectives on a range of nanoporous materials, including indium, nickel, gold, copper, lead, silver, aluminum, silicon, tin, iron, zinc, titanium, bismuth vanadate, cadmium sulfide, and zeolites. Additionally, this review offers a comprehensive assessment of worldwide studies on utilizing nanoporous materials in photoelectrochemical cells. We show how morphological modifications to materials may improve charge transfer and, as a consequence, overall power conversion efficiency.ke The superior catalytic performance of nanostructures with varying levels of complexity has been discovered in photoelectrochemical reactions. Finally, signif

The development of efficient catalysts with a large number of active sites, tunable bandgap, and large surface area has been very challenging. In addition, a significant bottleneck in the application of catalysts for water treatment is their dissolution under extreme conditions, such as highly acidic or highly alkaline conditions that lead to poor application of the reported materials in real-world applications. In this study, the lanthanum (La)-doped molybdenum disulfide (MoS2) nanosheets are reported for efficient breakdown of toxic pollutants from wastewater under a wide pH range from strongly alkaline to strongly acidic solutions. The La-MoS2 nanosheets (NSs) are prepared by a facile hydrothermal approach using a two-step methodology. A redshift is observed upon La doping, indicating that the bandgap is lowered after La doping in MoS2. The changes in bandgap and electronic structure are further investigated using the density functional theory (DFT), which reveal that doping of La introduces new states within the bandgap region, allowing for further induced energy transitions. The La-MoS2, having a doping concentration of 2%, exhibits the highest catalytic activity against methylene blue (MB) in neutral, acidic, and alkaline solutions, as well as substantial inhibitory activity for bacterial strains such as Escherichia coli (E. coli). In summary, the modified catalyst provides a pathway to design highly efficient catalysts for all pH range water treatment as well as good activity against microbes.

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.

Huge plastic consumption and depletion of fossil fuels are at the top of the world's envi-ronmental and energy challenges. The scientific community has tackled these issues through differ-ent approaches. Catalytic pyrolysis of plastic wastes to valuable products has been proved as a sustainable route which fits with the circular economy aspects. The design of catalytic materials is the central factor for performing the catalytic conversion of plastic wastes. This review aims to conduct a Bibliometric analysis of the pyrolysis of plastic wastes and non-precious-based catalysts by mapping research studies over the last fifty years. The analysis was developed via VOSviewer and RStudio tools. It showed the historical progress regarding plastic waste pyrolysis to produce valu-able products and chemicals worldwide. The research shows that the top five countries with the highest citations and publications in this field were Spain, China, England, the USA and India. The Journal of Analytical and Applied Pyrolysis had the most comprehensive coverage of plastic waste. The relationship between the catalyst and the mechanism of plastic waste can influence the production yield and selectivity. The research gap and underrepresented research topics were iden-tified, and previous research studies on developing non-precious-based catalysts that were most rel-evant to the current topic were reviewed and discussed. The challenges and perspectives on catalyst preparation and development for material complexity were critically discussed. Challenges of pre-vious studies and directions for future research were provided. This report might guide the reader to take a general look at plastic waste valorization by pyrolysis and easily understand the main chal-lenges. (c) 2023 The Author(s). Publis

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.

In this study, various concentrations of strontium (Sr) into a fixed amount of starch (St) and Fe2O3 nanostructures (NSs) were synthesized with the co-precipitation approach to evaluate the antibacterial and photocatalytic properties of the concerned NSs. The study aimed to synthesize nanorods of Fe2O3 with co-precipitation to enhance the bactericidal behavior with dopant-dependent Fe2O3. Advanced techniques were utilized to investigate the structural characteristics, morphological properties, optical absorption and emission, and elemental composition properties of synthesized samples. Measurements via X-ray diffraction confirmed the rhombohedral structure for Fe2O3. Fourier-transform infrared analysis explored the vibrational and rotational modes of the O-H functional group and the C-C and Fe-O functional groups. The energy band gap of the synthesized samples was observed in the range of 2.78-3.15 eV, which indicates that the blue shift in the absorption spectra of Fe2O3 and Sr/St-Fe2O3 was identified with UV-vis spectroscopy. The emission spectra were obtained through photoluminescence spectroscopy, and the elements in the materials were determined using energy-dispersive X-ray spectroscopy analysis. High-resolution transmission electron microscopy micrographs showed NSs that exhibit nanorods (NRs), and upon doping, agglomeration of NRs and nanoparticles was observed. Efficient degradations of methylene blue increased the photocatalytic activity in the implantation of Sr/St on Fe2O3 NRs. The antibacterial potential for Escherichia coli and Staphylococcus aureus was measured against ciprofloxacin. E. coli bacteria exhibit inhibition zones of 3.55 and 4.60 mm at low and high doses, respectively. S. aureus shows the measurement of inhibition zones for low and high doses

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.

The pollution of synthetic dyes in wastewater exerts many negative impacts on the environment and human health. There is an increasing demand for the degradation of dyes, with an emphasis on photocatalysis. Here, we investigated the bio-mediated synthesis of ZnO using Chrysanthemum spp. flower extract and its utilization for the removal of methylene blue dye under sunlight irradiation. The bandgap energy of green ZnO nanoparticles was determined to be 3.0. The Taguchi L9 (34) orthogonal array design was applied to optimize the photocatalytic degradation of methylene blue dye by green ZnO particles. Four parameters, including the initial concentration (10–50 mg/L), ZnO dosage (0.33–1.0 mg), contact time (30–120 min), and pH (4–10) of the solution, were surveyed based on the Taguchi design. We found that the test result (99.0%) at 10 mg/L was almost equivalent to the predicted value (99.5%) of degradation efficiency. The reaction mechanisms shed light on the major role of reactive oxygen species (•O2−, •OH). More importantly, the green ZnO particles could be reused for at least five cycles and demonstrated high stability.

Microplastic pollution has adversely affected the aquatic ecosystem, living creatures, and human health. Several studies in Malaysia have provided baseline information on the existence of microplastics in surface water, ingestion by marine life and sediment. Also, humans are exposed to microplastic due to consumption of contaminated abiotic and biotic products, such as processed seafood. Nonetheless, knowledge is still scarce among Malaysian on the potential remediation and pollution management of microplastics, which poses a significant challenge to preserve a good environmental status. Green technologies also other alternative to mitigate the contamination of microplastics for sustainable future. Hence, this review aims to provide an overview of microplastic's occurrence, fate, and implications in Malaysia's aquatic environment. Detection of microplastics from the water surface, ingestion by aquatics, and sediment samples are highlighted. Available different treatment processes toward microplastic remediation are also discussed. Additionally, the potential challenges, current perspective for plastic management in Malaysia, as well as green strategies for reducing microplastic contamination are also put forward. The goal of this work is to improve the understanding of the seriousness of microplastic contamination in aquatic environments, thus encouraging key concerns that need to be investigated further.

A straightforward manufacture strategy is proposed to obtain an efficient and robust palladium-alumina (Pd0/Al2O3) cermet monolithic catalyst, specifically designed to perform safe microwave assisted organic synthesis (MAOS). In this approach, a cermet catalyst with high surface area, controlled composition and adapted shape and dimensions to a microwave reactor vessel is generated via 3D printing technology and sintering. The resulting catalyst has been explored in heterogeneous Suzuki, Sonogashira, Stille and Heck cross-coupling reactions, in MAOS. The Pd0 catalyst is permanently active, stable, without leaching and can be recycled and reused at least 200 reaction cycles. The generation of hot spots, sparking or hazardous discharges is controlled by the effective immobilization of the palladium in the monolithic structure during the reaction. The palladium content is forming part of both the internal and external structure, providing greater mechanical resistance and catalytic activity with respect to the basic ceramic material (alumina).

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.

Environmental pollution, climate change, and fossil fuel extinction have aroused serious global interest in the search for alternative energy sources. The dry reforming of methane (DRM) could be a good technique to harness syngas, a starting material for the FT energy process from greenhouse gases. Noble metal DRM catalysts are effective for the syngas generation but costly. Therefore, they inevitably, must be replaced by their Ni-based contemporaries for economic reasons. However, coking remains a strong challenge that impedes the industrialization of the FT process. This article explains the secondary reactions that lead to the production of detrimental graphitic coke deposition on the surface of active nickel catalyst. The influence of nickel particle size, impact of extra surface oxygen species, interaction of Ni catalysts with metal oxide supports/promoters, and larger fraction of exposed nickel active sites were addressed in this review. Size of active metal determines the conversion, surface area, metal dispersion, surface reactions, interior diffusion effects, activity, and yield. The influence of oxygen vacancy and coke deposition on highly reported metal oxide supports/promoters (Al2O3, MgO and La2O3) was postulated after studying CIFs (crystallographic information files) obtained from the Crystallography open database (COD) on VESTA software. Thus, overcoming excessive coking by La2O3 promotion is strongly advised in light of the orientation of the crystal lattice characteristics and the metal-support interaction can be used to enhance activity and stability in hydrogen reforming systems.

The catalytic conversion of CO(2)via the Reverse Water Gas Shift (RWGS) reaction for CO production is a promising environment-friendly approach. The greenhouse gas emissions from burning fossil fuels can be used to produce valuable fuels or chemicals through CO2 hydrogenation. Therefore, this project was to study the CO2 conversion via RWGS over various Cu/ZnO catalysts supported by regenerated spent bleaching earth (RSBE) prepared by wet impregnation technique with different Cu : Zn ratios (0.5, 1.0, 1.5, 2.0, 3.0). The causes of environmental pollution from the disposal of spent bleaching earth (SBE) from an edible oil refinery can be eliminated by using it as catalyst support after the regeneration process. The synthesized catalysts were characterized by thermogravimetric analysis (TGA), X-ray diffraction (XRD), temperature-programmed reduction of hydrogen (TPR-H-2), pyridine-adsorbed Fourier transform infrared (FTIR-pyridine), temperature programmed desorption of carbon dioxide (TPD-CO2), N-2 physisorption, and Fourier transform infrared (FTIR) analysis. The RWGS reaction was carried out in a slurry reactor at 200 degrees C, with a pressure of 3 MPa, a residence time of 4 h, and catalyst loading of 1.0 g with an H-2/CO2 ratio of 3. According to experimental data, the Cu/Zn ratio significantly impacts the catalytic structure and performance. The catalytic activity increased until the Cu : Zn ratio reached the maximum value of 1.5, while a further increase in Cu/Zn ratio inhibited the catalytic performance. The CZR3 catalyst (Cu/Zn ratio of 1.5) with a higher catalytic reducibility, high copper dispersion with small crystalline size, lower total pore volume as well as higher basicity showed superior catalytic performance in terms of CO2 conversion (40.67%) and CO yiel

In-situ pyrolysis-catalytic steam reforming reaction of polystyrene waste (PSW) liquefied in phenol can generate hydrogen from phenol and valuable liquid fuel from the PSW and thus has been studied recently. However, due to the complexity of phenol compounds and plastic waste, this reaction suffers from high energy consumption and coking. Herein, Ti, 4Ti3Cu and 3Ti3Cu nano-catalysts were facilitatively prepared using hydrothermal and impregnation methods and the physical and chemical properties of the fresh and used samples were deeply characterized. The experimental results show that almost complete phenol conversion with 97.90% H2 yield was achieved at 800 oC using 3Ti3Cu nano-catalyst. The catalytic pyrolysis products were ethylamine, tert-butyl hydroperoxide (TBHP) and benzene (1,1-dimethylethoxy) (BDE). The correspondence of the preparation, morphology and catalytic activity in this research elucidates the synthesis of anti-coking and stable nano-catalysts for in-situ pyrolysis-catalytic steam reforming reaction.

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.

An exponential rise in global pollution and industrialization has led to significant economic and environmental problems due to the insufficient application of green technology for the chemical industry and energy production. Nowadays, the scientific and environmental/industrial communities push to apply new sustainable ways and/or materials for energy/environmental applications through the so-called circular (bio)economy. One of today's hottest topics is primarily valorizing available lignocellulosic biomass wastes into valuable materials for energy or environmentally related applications. This review aims to discuss, from both the chemistry and mechanistic points of view, the recent finding reported on the valorization of biomass wastes into valuable carbon materials. The sorption mechanisms using carbon materials prepared from biomass wastes by emphasizing the relationship between the synthesis route or/and surface modification and the retention performance were discussed towards the removal of organic and heavy metal pollutants from water or air (NOx, CO2, VOCs, SO2, and Hg0). Photocatalytic nanoparticle-coated biomass-based carbon materials have proved to be successful composites for water remediation. The review discusses and simplifies the most raised interfacial, photonic, and physical mechanisms that might take place on the surface of these composites under light irradiation. Finally, the review examines the economic benefits and circular bioeconomy and the challenges of transferring this technology to more comprehensive applications.© 2023. The Author(s).

In this study, MoO3 nanostructures were prepared, doped with various concentrations of graphene oxide (2 and 4% GO) and a fixed amount of polyvinylpyrrolidone (PVP) using the co-precipitation method. The motive of this study was to examine the catalytic and antimicrobial efficacy with evidential molecular docking analyses of GO/PVP-doped MoO3. GO and PVP were utilized as doping agents to reduce the exciton recombination rate of MoO3 by providing more active sites that increase the antibacterial activity of MoO3. The prepared binary dopant (GO and PVP)-dependent MoO3 was used as an effective antibacterial agent against Escherichia coli (E. coli). Notably, 4% GO/PVP-doped MoO3 showed good bactericidal potential against E. coli at higher concentrations in comparison to ciprofloxacin. Furthermore, in silico docking revealed the possible inhibitory impact of the synthesized nanocomposites on folate and fatty acid synthesis enzymes, dihydrofolate reductase and enoyl-[acyl carrier protein] reductase, respectively.

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.

Breast cancer is considered the second-leading cancer after lung cancer and is the most prevalent cancer among women globally. Currently, cancer immunotherapy via vaccine has gained great attention due to specific and targeted immune cell activity that creates a potent immune response, thus providing long-lasting protection against the disease. Despite peptides being very susceptible to enzymatic degradation and poor immunogenicity, they can be easily customized with selected epitopes to induce a specific immune response and particulate with carriers to improve their delivery and thus overcome their weaknesses. With advances in nanotechnology, the peptide-based vaccine could incorporate other components, thereby modulating the immune system response against breast cancer. Considering that peptide-based vaccines seem to show remarkably promising outcomes against cancer, this review focuses on and provides a specific view of peptide-based vaccines used against breast cancer. Here, we discuss the benefits associated with a peptide-based vaccine, which can be a mainstay in the prevention and recurrence of breast cancer. Additionally, we also report the results of recent trials as well as plausible prospects for nanotechnology against breast cancer.

Contaminants removal is usually becoming an exciting subject of research from water considering their environmental and ecological effects. This work provides pathways to remove organic pollutants from water via nanomaterials and is used as an antibiotic against bacteria like Escherichia coli (E. coli). In this study, molybdenum trioxide (MoO3) and yttrium (Y) doped (2 and 4%) MoO3 nanorods were synthesized by co-precipitation method. Advanced characterization techniques have been introduced to study textural structures, morphological developments, and optical characteristics of produced products. X-ray diffraction studied multiple crystalline structures of prepared samples as hexagonal, orthorhombic, and monoclinic of pure MoO3 with decrease in crystallinity and crystallite size upon Y doping. UV-visible spectroscopy unveiled a redshift (bathochromic effect) in absorption pattern attributed to band gap energy (Eg) decreases. Photoluminescence spectra examined the recombination rate of electrons (e-) and holes (h+) as charge carriers. A sufficient catalytic activity (CA) was observed against methylene blue (MB) dye in an acidic medium (99.74%) and efficient bactericidal action was studied against (E. coli) with zone of inhibition (5.20 mm) for 4% Y-doped MoO3. In addition, in silico docking demonstrated potential inhibitory effect of produced nanomaterials on FabH and FabI enzymes of fatty acid biosynthesis.Copyright © 2023 The Authors. Published by Elsevier Ltd.. All rights reserved.

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).