Increase In Surface Area Research Articles

Light Drought Stress Positively Influenced Root Morphological and Endogenous Hormones in Pinus massoniana Seedlings Inoculated with Suillus luteus

Aims An ectomycorrhizal fungus (ECMF) may enhance plant drought resistance. However, there is limited information regarding the effects of ECMFs on drought resistance in Pinus massoniana Lamb., a native species representing an afforestation pioneer tree in subtropical regions of China. Methods In this study, a pot experiment was conducted to determine the effects of ECMF Suillus luteus inoculation on the root morphology and endogenous hormones of P. massoniana, including roots, leaves, and stems, under various water treatment conditions. Four water levels (regular, light, moderate, and severe drought) and three inoculations (inoculated Suillus luteus, numbered S12 and S13, and non-ECMF-inoculated) were compared using a factorial design. Results Under drought stress, P. massoniana seedlings inoculated with S12 and S13 had significantly increased root morphology development (p < 0.05). Light drought positively influenced root development, resulting in a more than twofold increase in root length and root surface area compared to non-inoculated seedlings. Concentrations of gibberellic acid (GA), zeatin riboside (ZR), and indole-3-acetic acid (IAA) in roots, stems, and leaves of inoculated S12 and S13 plants were elevated, whereas abscisic acid (ABA) concentrations were significantly lower, compared to non-inoculated seedlings. The ABA concentrations in the roots of S12 and S13 inoculated seedlings under light drought stress were 1.5 times lower than those in non-inoculated controls. Moreover, root development was positively correlated with plant total GA, IAA, and ZR but negatively correlated with ABA. ConclusionsS. luteus can promote the root growth and development of P. massoniana seedlings, notably by regulating the balance in the concentration of endogenous hormones, thus improving the drought resistance of P. massoniana seedlings.

Tailoring Cell Attachment onto Melt Electrowritten Scaffolds via a Phase Separated Hydrogel Coating with Peptide Functionalization

AbstractHighly porous scaffolds with a high surface area can be designed and fabricated via melt electrowriting (MEW). Here, the study introduces morphological features onto the MEW microfibers via a hydrogel coating of phase‐separated poly(2‐hydroxyethyl methacrylate) (pHEMA). This coating is achieved by capturing phase‐separated droplets of pHEMA onto poly(ε‐caprolactone) (PCL) microfibers via dip‐coating, resulting in a hydrogel coating with webbed structures across pores of the MEW scaffold. Excess pHEMA droplets are removed and phase separation is quenched by washing in water, and then functionalized by dipping the pHEMA coated scaffold into a buffered peptide solution. It is demonstrated that a cysteine‐terminated peptide sequence (Cys‐Gly‐Arg‐Gly‐Asp‐Ser‐Gly (CG‐RGD‐SG)) promotes fibroblast adhesion on the hydrogel‐coated MEW scaffolds compared to unmodified pHEMA and compared to scrambled peptide sequence. Due to the protein‐resistant nature of pHEMA, the hydrogel‐coated scaffolds show less cell attachment than non‐coated PCL scaffolds, while RGD‐functionalized pHEMA scaffolds achieve 2.8‐fold increase in cell attachment (p = 0.02) when compared to non‐functionalized pHEMA. The study therefore presents a platform that combines PCL scaffolds of microscale fibers with a phase‐separated pHEMA hydrogel coating that maintains the high porosity of MEW scaffolds yet increases surface area and, importantly, introduces the capability for tailoring cell attachment via peptide functionalization.

Effect of Plasma Treatment on Self-Cleaning Features of Acrylic Paint/TiO2-Coated Surfaces for Environmental Pollutant Removal

This study investigates the characterization and performance of self-cleaning TiO2 surfaces synthesized through a one-step preparation process, followed by enhancement via plasma treatment. The process involved coating aluminum foil with an acrylic paint mixture containing nanoparticles of different mass compositions and subsequent plasma treatment using a continuous plasma arc. Scanning electron microscopy revealed the morphology of the treated surfaces, showing an increase in surface area of plasma-treated materials. Energy-dispersive X-ray spectroscopy revealed changes in oxygen and titanium in acrylic paint/TiO2 surfaces as the TiO2 content increased, indicating successful TiO2 incorporation. Raman spectroscopy showed that the bulk structure of self-cleaning acrylic paints is mainly preserved after plasma treatment. Alternating current impedance spectroscopy assessed that plasma treatment reduced agglomeration and increased active sites, especially for the acrylic paint/TiO2 surfaces with 0.5 mg/cm3 TiO2. The contact angle measurements indicated that plasma treatment enhanced the superhydrophobic characteristics and potential self-cleaning abilities of produced acrylic paint/TiO2 surfaces. The efficacy of these plasma-treated surfaces in self-cleaning was evaluated by testing their performance against puddle sediment and automotive oil samples. The study demonstrated that plasma treatment positively impacted the self-cleaning ability of the acrylic paint/TiO2 surfaces, particularly those with 0.5 mg/cm3 TiO2. This enhancement was attributed to the formation of functional groups, improved water repellency, and possible increases in surface area, which collectively contribute to the sustainable self-cleaning properties of the treated surfaces.

Anchoring Perovskite-Like Bi4Ti3O12 and Plasmonic Bi on Defect-Rich Yellow TiO2-x for Enhanced Catalytic Activity toward Degradation of Pollutants upon Visible Light.

The efficiency of heterogeneous photocatalytic processes is currently limited due to the fast recombination of photocarriers, poor light absorption, and inefficient surface catalytic characteristics. In this study, defect-rich yellow TiO2-x nanoparticles (abbreviated as D-TiO2) with high surface area and significant absorption in the visible range were integrated with perovskite-like Bi4Ti3O12 to synthesize binary D-TiO2/Bi4Ti3O12 nanocomposites. To overcome the problem of insufficient activity, we integrated the optimized D-TiO2/Bi4Ti3O12 nanocomposite with plasmonic Bi nanoparticles. Significantly, the optimized D-TiO2/Bi4Ti3O12/Bi-2 nanocomposite efficiently removed tetracycline (TC) in 50 min through production of •OH, h+, and •O2- species, whose removal rate promoted 10.6, 3.18, 5.01, and 1.84 compared with the white TiO2 (abbreviated as W-TiO2), D-TiO2, Bi4Ti3O12, and D-TiO2/Bi4Ti3O12 (20%) photocatalysts, respectively. The outstanding performance of the D-TiO2/Bi4Ti3O12/Bi photocatalyst was attributed to its quantum dot size, low resistance for charge migration, increased surface area, oxygen vacancies in D-TiO2, and developed n-n heterojunction among D-TiO2 and Bi4Ti3O12, which accelerated charge transfer and promoted the generation of active species. Furthermore, the stability tests showed that the TC degradation efficiency still reached 96% after four recycles, indicating the remarkable stability of the photocatalyst. Eventually, the biocompatible nature of the treated solution over the optimized photocatalyst was also revealed from an investigation of the growth of lentil seeds.

An Observational Study on Implication of Postoperative Visceral Edema, Assessed by CT Scan, on Complications Following Bowel Resection and Anastomosis, in a Tertiary Care Hospital in Maharashtra, India

Introduction: Surgeries involving bowel resection and anastomosis are quite common. Fluid overload, leading to tissue edema and impaired tissue perfusion, may contribute to anastomotic leak, which is one of the most dreaded complication. Methods: In our current study, CT scan, done on postoperative day-4, was used to assess visceral edema, and its effect on development of complications post bowel anastomosis and increase in value of cross section of body trunk area ≥20% was taken as an independent risk factor of severe complication. Results: Twenty three patients were enrolled in the study, 7 of them developed complications. The most common complication observed was wound infection (Clavein Dindo grade II). Only 2 patients (28.57%) had an increase in CT area >20%. Among patients who developed complications, 33.3% had an increase in CT area and 28.6% did not. Various other factors – preoperative albumin level, timing of surgery, duration of surgery – also lead to development of complications. Statistically, no significant association could be derived between the increase in CT area and development of complications. Conclusion: As per the findings of the current study, higher fluid balance was not reflected by an increase in body surface area on CT Scan. Hence, use of CT scan as a tool to assess visceral edema needs further evaluation.

Molecular signatures of cortical expansion in the human foetal brain

The third trimester of human gestation is characterised by rapid increases in brain volume and cortical surface area. Recent studies have revealed a remarkable molecular diversity across the prenatal cortex but little is known about how this diversity translates into the differential rates of cortical expansion observed during gestation. We present a digital resource, μBrain, to facilitate knowledge translation between molecular and anatomical descriptions of the prenatal brain. Using μBrain, we evaluate the molecular signatures of preferentially-expanded cortical regions, quantified in utero using magnetic resonance imaging. Our findings demonstrate a spatial coupling between areal differences in the timing of neurogenesis and rates of neocortical expansion during gestation. We identify genes, upregulated from mid-gestation, that are highly expressed in rapidly expanding neocortex and implicated in genetic disorders with cognitive sequelae. The μBrain atlas provides a tool to comprehensively map early brain development across domains, model systems and resolution scales.

Layered high-entropy sulfides: boosting electrocatalytic performance for hydrogen evolution reaction by cocktail effects

Abstract This study explores high-entropy sulfides (HESs) as potential electrocatalysts for the hydrogen evolution reaction (HER). Novel Pa-3 and Pnma structured HESs containing Fe, Mn, Ni, Co and Mo, were synthesized via a facile mechanochemical method. Structural and chemical properties were extensively characterized using x-ray diffraction, transmission electron microscopy, energy-dispersive x-ray spectroscopy, and x-ray photoelectron spectroscopy. The electrocatalytic performance of four as-prepared HESs in alkaline electrolyte for HER reveals the remarkable outperformance compared to medium-entropy and conventional sulfides. Particularly, (Fe0.2Mn0.2Ni0.2Co0.2Mo0.2)S2 demonstrated outstanding activities, with minimal overpotentials (187 mV at 10 mA cm–2) and outstanding durability under harsh alkaline conditions (a mere polarization increase ΔE = 17 mV after 14 h via chronopotentiometry). The remarkable catalytic activities can be attributed to synergistic effects resulting from the cocktail effects within the high-entropy disulfide. The introduction of Mo contributes to the formation of a layered structure, which leads to an increased surface area and thus to a superior HER performance compared to other HES and conventional sulfides. This work demonstrates the promising potential of HES and underscores that further development for catalytic applications paves the way for innovative routes to new and more efficient active materials for HER catalysis.

A highly-efficient peroxymonosulfate activator using a sewage sludge derived biochar supported cobalt oxide: Mechanism and characteristics

The application of biochar derived from sewage sludge (BS) in Fenton-like reactions for contaminant removal has attracted considerable attention. Herein, a BS-supported Co3O4 (BS-Co3O4) catalyst was synthesized using a simple two-step hydrothermal-calcination process to achieve highly efficient activation of peroxymonosulfate (PMS). The introduction of biochar effectively inhibited the aggregation of Co3O4 and reduced cobalt leaching. Compared to Co3O4, the mesoporous BS-Co3O4 exhibited an 8-fold increase in specific surface area (SSA) to 111.92 m2∙g−1, and a 46 %-66.4 % reduction in crystal plane size. The interaction between biochar and cobalt oxide resulted in several notable enhancements in the BS-Co3O4 composite. Specifically, there was an increase in sp2 carbon content, a 42.69 % rise in capacitance, and a 79.99 % reduction in charge transfer resistance. These improvements contributed to enhanced PMS activation performance. The BS-Co3O4 also contained a higher content of Co(II), sp2 carbon, and oxygen vacancies (OV). Co(II) played a crucial role in the redox reaction, accelerating the formation of SO4•− and 1O2 during the PMS activation process. Additionally, OV acted as electron capture centers, further promoting the generation of 1O2. Evidence from reactive species investigations and electron paramagnetic resonance (EPR) tests indicated that SO4•− and 1O2 were the main reactive radicals for eliminating tetracycline (TC). Based on the identification of TC intermediates, two potential degradation pathways were proposed, and a reduction in intermediate toxicity was observed. Experiments involving interference and repetition demonstrated that the BS-Co3O4 catalyst was stable and reusable. This work provides a solution with low metal leaching, high recycling performance, and safety for antibiotic wastewater treatment.

Enzymatic bimetallic Cu-Ni micromotor sensor for xanthine detection

Enzymatic bimetallic Cu-Ni micromotors modified screen-printed electrodes were designed for the determination of xanthine. The bimetallic Cu-Ni micromotors were prepared by electrochemical template deposition. Morphological and structural characterization revealed that the smaller size and active mobility of the particles contribute to a larger specific surface area. The increase in surface area enhances electro-catalytic activities and sensitivity. These improved properties enable the newly created xanthine oxidase-modified Cu-Ni micromotors to function effectively as a high-performance sensor. Designed specifically for detecting xanthine, this sensor boasts high sensitivity, a broad measurement range, low detection limits, and excellent reproducibility and stability. The enzymatic bimetallic micromotor-based sensor was also successfully employed to measure xanthine levels. The limits of detection were determined to be 15.7 nM and 21.53 μM for xanthine concentration ranges of 0.1 μM–1 μM and 10 μM–300 μM, respectively, based on electrochemical signals under a magnetic field. Besides, the detection limit was calculated as 9.02 μM for xanthine concentrations ranging from 0.3 μM to 20 μM, based on the speed of the micromotors under a magnetic field (S/N = 3). The impressive results highlight the significant potential of bimetallic Cu-Ni micromotors as sensors, suggesting their promising applications in monitoring food freshness and enhancing security technology.

Facile synthesis of CQD/g-C3N4 as a highly effective metal-free photocatalyst for the degradation of carmoisine and indigo carmine dye

The development of extensive dye pollution in the water ecosystem seriously endangers the health of the living organism. For effectively eradicating dyecontaminants from water bodies, photocatalysis is consideredan effective, energy-consumption, inexpensive disinfection technique. As an alternative to conventional metal-based catalysts, heterogeneous metal-free photocatalysts are more sustainable and kinder to the environment. Here, we reported the simplehydrothermalchemical production of Carbon Quantum dots (CQD)-doped graphitic carbon nitride(GCN). Analytical instruments such as XRD, SEM, FE-SEM, HR-TEM, EDX, FT-IR, thesurface area of BET analysis, photoluminescence, and UV–vis spectroscopy, zeta potentialwere used to characterize the as-prepared CQD doped GCN (CDCN). The degradation studies reveal that the CDCN catalyst displays the highest rate of degradation performance than pure GCN. Within 60 min, it shows 96 % degradation toward indigo Carmine (IC) and 93 % decomposition towards carmoisine dye (CM). Significant e−/h+ separation, an increased surface area, and a high redox potential capacity to induce charge bears may all contribute to the CDCN catalyst’s enhanced photocatalytic degradation efficiency. The efficiency of the photocatalytic process was optimized by studying and altering many variables. These include Dye concentration, catalyst concentration, and variation of the pH solution were some of these. The nanocomposite exhibited excellent stability after three successive runs of the photocatalytic procedure. According to the kinetics analysis results indicate that the photocatalytic decomposition of Indigo Carmine (IC) and carmoisine (CM) dye follows pseudo-first-order kinetics. For better photodegradation performance, a potential photocatalytic method employing several pairs of electron-hole acceptor scavengershas been put forth. Based on the positionsof the band gap and the result of the characterization, a feasible mechanismpathway for charge carriers was also presented.

Effect of flame temperature on structure and CO oxidation properties of Pt/CeO2 catalyst by flame-assisted spray pyrolysis

Flame synthesis offers the potential for the synthesis of structure-controlled catalysts. In this study, Pt/CeO2 nanoparticles were synthesized via flame-assisted spray pyrolysis (FASP) and used as CO oxidation catalysts. The catalysts were synthesized using a burner diffusion flame at three different flame temperatures (maximum flame temperatures, Tf = 1556, 1785, and 2026 K), and their particle structure and CO oxidation activity were evaluated. The synthesized Pt/CeO2 catalysts had a bimodal structure containing 100 nm-scale CeO2 loaded with 10 nm-scale Pt and fine CeO2 less than 10 nm loaded with highly dispersed Pt (less than 1 nm). As the flame temperature increases from 1556 to 2026 K, the formation of fine CeO2 particles dominates, resulting in an increase in BET specific surface area from 7.97 to 112 m2/g and Pt dispersion from 4.67 to 20.6%. Insight into the particle formation routes that determine the catalyst structure is provided by numerical simulation of droplet evaporation in a burner flame. CO oxidation experiments showed that the temperature at which CO conversion reached 100% (T100) decreased from 513 to 378 K with increasing flame temperature in FASP. In addition, the thermal stability test showed that the Pt dispersion after thermal degradation was higher for Pt/CeO2 catalyst made by FASP at Tf = 2026 K than that prepared by the impregnation method, and the T100 for CO oxidation was lower by 20 K.

Adsorption Properties of Alkali-activated Stone Wool

Alkali-activated materials are actively studied as adsorbents for toxic metals, nutrients, and dyes from wastewater. They are produced using an environmentally friendly process from low-cost aluminosilicate precursors, and thus have significant potential for fostering the development of clean technology. One of the potential precursors is stone and glass wool, for which alkali activation has been successfully demonstrated in construction products. In this study, alkali-activated stone wool was assessed for adsorption for the first time. Stone wool manufactured without organic resin (SW) and another stone wool with organic resin being removed by heat treatment (SW-O) were alkali activated using NaOH, Na2CO3, NaAlO2, or Na silicate solution, and characterized by X-ray diffraction, scanning electron microscopy, Fourier-transform infrared spectroscopy, thermogravimetry–mass spectrometry, and potentiometric titrations to understand the surface properties affecting adsorption. Comparative adsorption experiments were conducted using methylene blue (MB), cobalt (Co(II)), arsenite (As(III)), and NH4+ at 100 mg × L −1 concentration, 1 g/L adsorbent dose, 24 h contact time, and pH of 7. The raw stone wools demonstrated almost no adsorption, whereas the alkali-activated stone wools adsorbed up to 78, 42, 3, and 18 mg × g−1 of MB, Co(II), As(III), and NH4+, respectively. The samples prepared with the SW Na silicate demonstrated higher adsorption capacities for MB and Co(II). For As(III), an adsorption capacity was similar regardless of the mixture. The highest adsorption capacity for NH4+ was achieved with SW-O NaOH. The increased adsorption capacities were related to the increase in the specific surface area, more negative zeta potential, formation of tobermorite-like structures, and an increase in the quantity of surface OH groups. The varying adsorption levels of specified contaminants are possibly governed by their speciation at pH 7, aqueous radii, and the adsorption mechanism. This study demonstrated that stone wool-based adsorbents have practically relevant potential for wastewater treatment.

Deciphering the role of nonylphenol adsorption in soil by microplastics with different polarities and ageing processes.

In the soil environment, microplastics (MPs) commonly coexist with organic pollutants such as nonylphenol (NP), affecting the migration of NP through adsorption/desorption. However, few studies have focused on the interaction between NP and MPs in soil, especially for MPs of different types and ageing characteristics. In this study, non-polar polypropylene (PP) and polar polyamide (PA) MPs were aged either photochemically (144 h) or within soil (60 days), then used to determine the effect of 5 % MPs on the adsorption behaviour of NP (0.1-4.0 mg/L) in soil. Results showed that both ageing processes significantly promoted the conversion of -CH3 groups to C-O and CO on the surface of PPMPs, while PAMPs exhibited amide groups changes and a reduction in average particle size due to ageing. Additionally, both ageing processes promoted the adsorption of NP by soil containing PPMPs, due to an increase in oxygen-containing functional groups and specific surface area. In contrast, the NP adsorption capacity of soil containing PAMPs decreased by 15.4 % following photochemical ageing due to hydrolysis of amide groups, but increased by 21.15 % after soil ageing due to reorganization of amide groups, respectively. The soil-PAMPs systems exhibited a stronger affinity for NP compared to the soil-PPMPs systems, which was primarily attributed to the dominant role of hydrogen bonding. NP was found to be distributed mainly on soil particles in the soil-PPMPs systems, while it tended to be adsorbed by MPs in the soil-PAMPs systems, especially in the soil aged MPs system. This study provides a comprehensive analysis of the complex effects of MPs on coexisting pollutants in soil environments, highlighting the effect of MP characteristics on the adsorption of organic pollutants, which is essential for understanding the transport behaviour of organic pollutants.

Enhanced electrochemical activity of boron doped cobalt oxide nanoparticles towards supercapacitor application

Doping via metal/nonmetal/metalloid dopants in to the crystal structural surface of cobalt oxide nanoparticles are promising for creating electroactive supercapacitors with excellent electrochemical performance. Herein, we fabricate boron doped cobalt oxide nanoparticles (B@Co3O4) via a facile co-precipitation route for supercapacitor applications. The incorporation of boron into cobalt oxide nanoparticles (3M B@Co3O4) brings a ∼4.2-fold increase in a specific surface area (548.126 m2g-1), decrease in band gap energy and reduced in crystalline size. Consequently, the B doped Co3O4 NPs displays a maximum specific capacitance of 998.12 F/g, which is ∼1.50-fold increased as compared to 668.79 F/g of the pristine Co3O4 NPs at current density 1.5mA/cm2 and scan rate 2mV/s in 1M KOH electrolyte solution. Moreover, 3M B@Co3O4 NPs demonstrates excellent power density 711.14W/kg and high energy density 195.96Wh/kg Wh/kg. Hence, we believe that boron doped cobalt oxide nanoparticles are a promising electroactive material for the supercapacitive applications.

Condensed tannins from black wattle as a promising nutritional additive for Nile tilapia: growth, immune and antioxidant responses, and gut morphology

The present study aimed to investigate the potential of condensed tannins (CT), derived from black wattle (Acacia mearnsii) tree bark, as a nutritional additive for Nile tilapia (Oreochromis niloticus) juveniles. CT are known for their antioxidant and immune-modulating properties, and their inclusion in aquafeeds may enhance fish health and performance. In this study, six diets were formulated: one control diet (Con) with no additives, and five experimental diets supplemented with CT extract at concentrations of 150, 250, 500, 750, and 1000mg/kg (CT150, CT250, CT500, CT750, CT1000, respectively). The selection of these doses was based on previous studies indicating that lower concentrations (below 1000mg/kg of diet) of tannins may offer benefits, while higher concentrations could exhibit antinutritional effects. After a 90-day feeding trial, fish fed the CT150 diet exhibited significantly higher growth compared to the control group. Additionally, fish in the CT150 group showed higher plasma lysozyme activity, while myeloperoxidase activity and hemolytic activity of the complement system were significantly higher in all tannin-fed groups compared to the control. Notably, CT150-fed fish demonstrated liver antioxidant responses comparable to or better than the control group, with no significant increase in lipid peroxidation, suggesting antioxidant protection. Histological analysis revealed a significant increase in intestinal villi density in the CT150 and CT500 groups compared to the control. While all groups showed an increase in absorption surface area (ASA), this increase was statistically significant only in the CT250, CT500, and CT750 groups when compared to the control. Furthermore, the CT150 diet led to the highest survival rate (80%) following a bacterial challenge. These findings suggest that dietary supplementation with 150mg/kg of CT from black wattle bark provides the most beneficial effects on growth, immune response, and survival in Nile tilapia juveniles.

Effect of γ-irradiation combined with enzymatic modification on the physicochemical properties of defatted rice bran dietary fiber

This study comprehensively examines how combining γ-irradiation and enzymatic modification influences the microstructure and physicochemical properties of dietary fiber (DF) obtained from defatted rice bran. The resulting yields of soluble dietary fiber (SDF) and insoluble dietary fiber (IDF) were measured at 13.38 ± 0.40 g/100 g and 52.19 ± 0.97 g/100 g, respectively. The modifications led to a diminish in particle size, an increase in specific surface area, and an improvement in water-holding capacity, oil-holding capacity, swelling capacity, glucose adsorption capacity, and cholesterol adsorption capacity. Furthermore, the modified DF exhibited enhanced anti-digestive properties and probiotic activity. Cluster and principal component analysis results revealed that the modified SDF exhibited superior functional properties. Correlation analysis indicated a noticeable relationship between the monosaccharide composition of DF and its functional characteristics. These findings suggest that γ-irradiation combined with enzymatic modification represents a viable approach for enhancing the quality of rice bran DF.

Modulating Drug Retention and Release via Surface Anchors Using Hyperthermia and Photothermal Effects of Fe3O4-SiO2 Core-shell Mesoporous Nanoparticles

Core-shell nanocarriers (Fe3O4-MSN-TESPA-PEG/DOX) with a core-shell structure were created as possible materials for controlled drug retention and release. With a notable increase in pore volume and surface area, the 3-(Trimethylsilyl)propionic acid (TESPA) anchors on the pore walls of SiO2 nanoparticles (MSN). The doxorubicin (DOX) is controlled and stored by a network of polyethylene glycol (PEG) layers that cover the MSN pore by TESPA anchor as a result of interactions between the layers and the high density of functional groups at the pore mouth. Rather than the Brownian motion contribution, magnetic hysteresis losses account for the magnetic hyperthermia contribution to the heating efficiency of the investigated core-shell configuration. Fe3O4 NPs' magnetism and capacity for photothermal conversion make its core an appealing choice for photothermal treatment. By appropriately adjusting the following variables, the combination of magnetic field and NIR irradiation can control localized heating: i. NIR irradiation density; ii. magnetic field intensity; iii. time of use; and iv. concentration of Fe3O4-MSN-TESPA-PEG/DOX core-shell solution. This combination is ideal for bioapplications and clinical trials. The two-step NIR irradiation procedure or magnetic field intensity control allows for the rapid delivery of roughly seven times the maximum amount of stored doxorubicin in only five minutes. Fe3O4-MSN-TESPA-PEG nanocarriers with their core-shell structure have great potential as therapeutic agents with controllable drug delivery and targetability.

Efficient RhB degradation and antimicrobial activity with molecular docking study of polymers doped ZnSe nanostructure

A facile coprecipitation approach was adopted to synthesize zinc selenide (ZnSe) doped with a fixed amount (3 wt%) of cetyltrimethylammonium bromide (CTAB) and different concentrations (2 and 4 wt%) of eudragit to form ternary nanostructure (NSs). Eud and CTAB inhibit the dimension and reduce the rate of recombination of NSs to intensify catalytic performance against rhodamine B (RhB) and bactericidal action against MDR Staphylococcus aureus (S. aureus). Doped ZnSe increase active sites, porosity, and surface area to enhance the degradation of RhB dye and antimicrobial efficacy to kill pathogenic S. aureus. Assessment of 4 wt% Eud/CTAB exhibited effective performance for degradation of RhB and bactericidal potential highlights an impressive 94.3 % degradation efficiency and 8.85 ± 0.05 mm of the inhibition zone against MDR S. aureus. Computational molecular docking studies suggest that NSs, such as Eud/CTAB-doped ZnSe, have the ability to inhibit the DNA gyrase enzyme in MDR S. aureus.

Boosted Hydrogen evolution reaction based on synergistic effect of graphene, MoS2 and RuO2 ternary electrocatalyst

Hydrogen holds the promise of replacing fossil fuels and offers a sustainable pathway for energy generation. However, the large-scale production of hydrogen via the environment friendly electrocatalytic process relies heavily on the performance of electrocatalysts. In this study, we investigate the electrocatalytic performance of graphene nanosheets (GNS), molybdenum disulfide (MoS2), ruthenium dioxide (RuO2), and their composites for hydrogen evolution reaction (HER), a novel combination that has not been explored in previous literature. We synthesize the materials using Liquid Phase Exfoliation at 500 and 1000 RPMs for GNS and MoS2 and via hydrothermal methods for RuO2 nanosheets and nanoparticles, aiming to exploit synergistic effects for enhanced activity and stability. The synthesized GNS-1000/MoS2-1000/RuO2-NSs composite demonstrates promising HER results, showcasing a low overpotential of 63 mV and a reduced Tafel slope of 59 mV/dec. This improvement indicates enhanced electron transfer, improved active site dispersion, and increased surface area due to the synergistic effects, which also aids in long-term electrochemical stability. Our study underlines the potential of GNS/MoS2/RuO2 composites, particularly the GNS-1000/MoS2-1000/RuO2-NSs, in transforming hydrogen production methods and promoting efficient, sustainable energy solutions. The implications of our findings extend the boundaries of materials engineering, edging us closer to a sustainable energy future.

Reduced Graphene Oxide/Silica Based Electrode Material: Synthesis and Characterization

<span lang="EN-US">Developing a Reduced Graphene Oxide (rGO) synthesis method based on rice husk as a composite electrode material with silica has garnered particular attention for designing high-quality electrode materials. This research successfully synthesized rGO-Si material from rice husk-derived activated carbon through a one-step thermal reduction process at 200 °C. This method offers a simple, efficient, cost-effective, and environmentally friendly synthesis approach. The resulting samples' morphology, surface composition, crystal structure, surface area, and pore diameter size were characterized using FE-SEM, EDX, XRD, and SAA-BET. EDX characterization results confirmed the predominance of carbon content in the samples. At the same time, the natural emergence of Si without external addition due to thermal reduction at 200 °C was an intriguing initial finding. The spherical crystal structure of silica between the wrinkled rGO layers was confirmed through FE-SEM and XRD analysis. The synergistic effect between Si and rGO significantly increased the sample's surface area, with a value of 34.17 m<sup>2</sup>/g for the rGO sample before thermal reduction, which increased to 121.24 m<sup>2</sup>/g after the thermal reduction process at 200 °C. This process also positively impacted the reduction in pore size of rGO-Si, with a value decreasing from 9.33 nm before thermal reduction to 4.89 nm after the thermal reduction process. The results of this study demonstrate that rGO-Si synthesized from rice husk-derived activated carbon holds great potential as a high-performance electrode material, combining the advantages of thermal reduction, natural Si content, and increased surface area for diverse applications.</span>