UV-visible Reflectance Spectroscopy Research Articles

XPS valence band observable light-responsive system for photocatalytic acid Red114 dye decomposition using a ZnO–Cu2O heterojunction

ZnO–Cu2O composites were made as photocatalysts in a range of different amounts using an easy, cheap, and environment-friendly coprecipitation method due to their superior visible light activity to remove pollutants from the surrounding atmosphere. X-ray diffraction and Fourier transform infrared spectroscopy (FT-IR) have demonstrated that ZnO–Cu2O catalysts are made of highly pure hexagonal ZnO and cubic Cu2O. X-ray photoelectron spectroscopy has confirmed that there is a substantial interaction between the two phases of the resultant catalyst. The optical characterizations of the synthesized ZnO–Cu2O composite were done via UV–vis reflectance spectroscopy. Due to the doping on ZnO, the absorption range of the ZnO–Cu2O catalyst is shifted from the ultraviolet to the visible region due to diffuse reflection. The degradation efficiency is affected by the Ratio of ZnO: Cu2O and ZnO–Cu2O composite with a proportion of 90:10 exhibited the most prominent photocatalytic activity on Acid Red 114, with a pseudo-first-order rate constant of 0.05032 min−1 that was 6 and 11 times greater than those of ZnO and Cu2O, respectively. The maximum degradation efficiency is 97 %. The enhanced photocatalytic activity of the composite is caused by the synergistic interaction of ZnO and Cu2O, which improves visible light absorption by lowering band gap energy and decreasing the rate at which the electron-hole pairs recombine. The scavenging experiment confirmed that hydroxyl radical was the dominant species for the photodegradation of Acid Red 114. Notably, the recycling test demonstrated the ZnO–Cu2O photocatalyst was highly stable and recyclable. These results suggest that the ZnO–Cu2O mix might be able to clean up environmental pollutants when it meets visible light.

Not all apparently gynandromorphic butterflies are gynandrous: The case of Polyommatus icarus and its relatives (Lepidoptera: Lycaenidae)

Beside the more than two thousand normal specimens of Polyommatus icarus (Rottemburg, 1775) yielded by rearing experiments, there was one perfectly bilateral dichromatic individual first considered to be gynandrous. On the basis of analysing genitalia traits, wing surface covering scale micromorphology, and the spectral characteristics of the blue colour generated by the cover scales, the gender of the specimen has been identified as female. This exemplar was investigated in comparison with gynandrous specimens from the collections of the Hungarian Natural History Museum exhibiting various degrees of intermixing of blue and brown coloration. Focus stacking microscopy for detailed scale morphology and UV–visible reflectance spectroscopy was used for the characterization of the optical properties. Inspecting literature references and the Lycaenidae collection of the museum, further examples have been found for female bilateral dichromatism in the closely related polyommatine lycaenid species Lysandra bellargus (Rottemburg, 1775) and Lysandra coridon (Poda, 1761) what suggests that polyommatine female dichromaticity may be displayed by the manner of bilaterality and mosaicism, phenomena hitherto solely connected to gynandromorphy.

Preparation of high color fastness structural colored cotton fabric via SiO2@PDA photonic crystal

Structural color is an important way to achieve the ecological coloring of textiles. SiO2 microspheres with sizes in the range of 200–337 nm were synthesized by the Stober method and then covered with highly light-absorbing melanin PDA to form SiO2@PDA photonic crystals. The SiO2@PDA photonic crystals were assembled onto the surface of white cotton fabrics by gravity deposition to achieve structural color. The addition of polyvinylpyrrolidone (PVP) enhances interfacial bonding by forming multiple hydrogen bonds between its lactam group and the phenolic hydroxyl group of PDA, resulting in a structured color cotton fabric with high color fastness. Scanning electron microscopy (SEM) was used to study the structure and morphology of SiO2@PDA microspheres. The chemical compositions of PDA and PVP were surveyed by Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD). The surface structural color of cotton fabrics was investigated by UV–Vis reflectance spectroscopy.

High performance Co3O4/Sn-ZnO nanocomposite photocatalyst for removal of methylene blue dye

Methylene blue is a toxic, carcinogenic, and non-biodegradable synthetic dye discharged from factories and industries that causes severe harm to human health and environmental pollution. Therefore, in this work, Co3O4/Sn-ZnO nanocomposite was synthesized using a simple sol–gel method for efficient photocatalytic removal of methylene blue dye in an aqueous basic medium. The structural, optical, photoluminescence, morphological, and compositional properties were studied. The XRD result revealed that the crystal size increases as the full width at half maxima (FWHM) decreases when Co3O4 are coupled with Sn-ZnO. From UV-visible diffusive reflectance and photoluminescence spectroscopies, a narrowing of the band gap and a reduction of the charge carrier’s recombination rate were observed, respectively. The photocatalytic efficiency and degradation rate constant of 95.1% and 0.03251 min−1 were recorded for methylene blue dye upon the use of optimized catalyst dosage of 60 mg Co3O4/Sn-ZnO nanocomposite catalyst under an irradiation time of 100 min at room temperature for optimized pH value of 9 in an aqueous basic medium.

Immobilization of Bi2WO6 on Polymer Membranes for Photocatalytic Removal of Micropollutants from Water - A Stable and Visible Light Active Alternative.

In this work, bismuth tungstate Bi2WO6 is immobilized on polymer membranes to photocatalytically remove micropollutants from water as an alternative to titanium dioxide TiO2. A synthesis method for Bi2WO6 preparation and its immobilization on a polymer membrane is developed. Bi2WO6 is characterized using X-ray diffraction and UV-vis reflectance spectroscopy, while the membrane undergoes analysis through scanning electron microscopy, X-ray photoelectron spectroscopy, and degradation experiments. The density of states calculations for TiO2 and Bi2WO6, along with PVDF reactions with potential reactive species, are investigated by density functional theory. The generation of hydroxyl radicals OH• is investigated via the reaction of coumarin to umbelliferone via fluorescence probe detection and electron paramagnetic resonance. Increasing reactant concentration enhances Bi2WO6 crystallinity. Under UV light at pH 7 and 11, the Bi2WO6 membrane completely degrades propranolol in 3 and 1 h, respectively, remaining stable and reusable for over 10 cycles (30 h). Active under visible light with a bandgap of 2.91eV, the Bi2WO6 membrane demonstrates superior stability compared to a TiO2 membrane during a 7-day exposure to UV light as Bi2WO6 does not generate OH• radicals. The Bi2WO6 membrane is an alternative for water pollutant degradation due to its visible light activity and long-term stability.

Synthetization and Characterization of Zinc Oxide Nanoparticles by X- Ray Diffractometry (XRD), Fourier Transforms, Infra-Red Spectroscopy (FT-IR), Scanning Electron Microscopy (SEM) and Antibacterial Activity Test

Purpose: Nanomaterials with their derivable potentials offer wide obtain ability and have recently aroused much attention for biomedical applications. Nowadays, nanomaterials-based colorimetric sensing is a quickly emerging field of sensing applications. Nanomaterials are considered as the main component of colorimetric determination of hydrogen peroxide to replace the natural enzyme-based sensors because of some associated intrinsic drawbacks. Considering the advantageous properties of ionic liquid (IL) for various applications, significant attention has been made to the use of ionic liquid stabilized metal NPs which may serve as a regulator to enhance the catalytic performance of the metal nanoparticles in the different IL reaction medium. 
 Methodology: The peroxidase-like activity of IL coated metal NPs (IL-MNPs) have been considered for the catalytic oxidation reaction of chromogenic substrate 3,3,5,5- tetramethylbenzidine (TMB) in the presence of H2O2 at an estimated wavelength of 652 nm.
 Results: The synthesized metal nanoparticles (Ag) were produced using a chemical reduction method. Various characterization techniques like FTIR, UV-Visible spread Reflectance Spectroscopy [UV-VIS DRS], were employed, which verified the structure, nano-size and successful combination of metal dopant ion into the samples. The molecular structure of ionic liquid with varying cations was produced and confirmed by 1H-NMR spectroscopy. The ionic liquid was coated on metal nanoparticles to enhance their conductivity. 
 Unique Contribution to Theory, Practice and Policy: Optimized reaction conditions like pH, temperature and catalyst dosage affect catalytic activity and color sensing properties. The coating of [Min] Ac on Ag achieved low detection limits and colorimetric detection of [Pyr] based Ag.

Assembling ZnMnFe2O4@Ag-AgVO3 nanostructure heterojunctions for photocatalytically degrading RhB and Pseudomonas aeruginosa bacteria under visible irradiation

Improving the separation of photocarriers is a vital approach to create highly effective heterojunction photocatalysts for the photodegradation of environmental pollutants. In this work, coprecipitation and hydrothermal methods were employed to develop a new heterojunction of Zn0.5Mn0.5Fe2O4@Ag-AgVO3 magnetic nanocomposite as photocatalysts for the photodegradation of Rhodamine B (RhB) and bacterial inactivation of Pseudomonas aeruginosa (P. aeruginosa) when exposed to illumination of visible light. FESEM, EDX, UV–vis reflectance spectroscopy (DRS), N2 adsorption/desorption, TEM, PL, Brunauer-Emmett-Teller (BET) surface area, Vibrating Sample Magnetometer (VSM), and XRD techniques were used to investigate the structural and optical properties of synthesized materials. The Zn0.5Mn0.5Fe2O4@Ag-AgVO3 photocatalyst demonstrated noticeably higher photocatalytic activity for RhB degradation when compared to the pure constituents AgVO3, Ag-AgVO3, and Zn0.5Mn0.5Fe2O4 samples. The results revealed that when RhB was used at a concentration of 20 ppm, the Zn0.5Mn0.5Fe2O4@Ag-AgVO3 possessed a high degradation rate (93.43 % within 180 min), and this was sufficient to get the highest total organic carbons (TOC) removal (90 %). Besides, Zn0.5Mn0.5Fe2O4@Ag-AgVO3 possesses complete inactivation efficiency (log(CFU) decreased from 6.5 to 0.00001) toward P. aeruginosa in 120 min of visible illumination. The photodegradation mechanism was explained by the surface plasmonic resonance Z-type heterostructure, and tested by trapping experiments. It can beinferredthat the Zn0.5Mn0.5Fe2O4@Ag-AgVO3 photocatalyst was very stable and efficient in removing different organic pollutants and pathogenic bacteria from wastewater.

Efficient sunlight-assisted degradation of organic dyes using V2O3/g-C3N4 nanocomposite catalyst

This study reports the synthesis of vanadium oxide (V2O3) and graphitic carbon nitride (g-C3N4) nanocomposite for simple sunlight-assisted degradation of Methylene Blue(MB) and Rhodamine B (RhB) dyes. Herein, the V2O3 and g-C3N4 are synthesized via hydrothermal and thermal decomposition techniques, respectively. X-ray diffraction (XRD) analysis confirms the formation of the rhombohedral and hexagonal structures of V2O3 and g-C3N4 in the nanocomposite, respectively, while scanning electron microscopy (SEM) reveals the sheet-like morphology of g-C3N4 and V2O3 nanoparticles. The optical band gap of the nanocomposite is estimated as 1.89 eV using a Tauc's plot generated from UV–Vis reflectance spectroscopy. The as-synthesized nanocomposite exhibits an excellent dye degradation efficacy displaying a 100 % degradation of RhB and 90 % degradation of MB dyes within 1 h of exposure to daylight. This performance is attributed to the synergistic effect of the V2O3/g-C3N4 nanocomposite wherein the composite benefits from the large surface area and high visible light adsorption of g-C3N4, combined with the active catalytic sites of the rhombohedral V2O3 structure, resulting in its high efficiency for photocatalytic dye degradation. Scavenger studies confirm the hydroxyl (.OH) radicals and oxygen (O2−.) radicals as the primary reactive species in the degradation process MB. Furthermore, the catalyst exhibited remarkable stability over three cycles of photocatalysis thus confirming its utility for real-time environmental remediation applications.

Mixed Nanosphere Assemblies at a Liquid-Liquid Interface.

The in-plane packing of gold (Au), polystyrene (PS), and silica (SiO2) spherical nanoparticle (NP) mixtures at a water-oil interface is investigated in situ by UV-vis reflection spectroscopy. All NPs are functionalized with carboxylic acid such that they strongly interact with amine-functionalized ligands dissolved in an immiscible oil phase at the fluid interface. This interaction markedly increases the binding energy of these nanoparticle surfactants (NPSs). The separation distance between the Au NPSs and Au surface coverage are measured by the maximum plasmonic wavelength (λmax) and integrated intensities as the assemblies saturate for different concentrations of non-plasmonic (PS/SiO2) NPs. As the PS/SiO2 content increases, the time to reach intimate Au NP contact also increases, resulting from their hindered mobility. λmax changes within the first few minutes of adsorption due to weak attractive inter-NP forces. Additionally, a sharper peak in the reflection spectrum at NP saturation reveals tighter Au NP packing for assemblies with intermediate non-plasmonic NP content. Grazing incidence small angle X-ray scattering (GISAXS) and scanning electron microscopy (SEM) measurements confirm a decrease in Au NP domain size for mixtures with larger non-plasmonic NP content. The results demonstrate a simple means to probe interfacial phase separation behavior using in situ spectroscopy as interfacial structures densify into jammed, phase-separated NP films.

Structural transition and magnetization reversal in rare earth doped R0.5Sr0.5Fe0.5Cr0.5O3 (R[dbnd]La, Nd and Sm) perovskite oxides containing mixed valent cations at B site: Magnetic, optical and transport properties

In the current paper, the effect of lanthanide metal cation substitution on structural, magnetic, optical and transport properties of R0.5Sr0.5Fe0.5Cr0.5O3 (RLa, Nd and Sm) perovskite oxides have been investigated. Structural investigations reveal that there is a phase transition from cubic to orthorhombic symmetry with the doping of heavier rare earth ion. The findings of XPS studies point to the existence of mixed valence states of Cr and Fe ions. The change in magnetization in response to an external magnetic field reveals that the phases have a mostly antiferromagnetic character with some trace amounts of ferromagnetic components. In temperature dependent magnetization studies, magnetic reversal has been observed in Nd doped sample, while La and Sm doped samples only show positive magnetization. The band gap energies of the synthesized materials determined from the UV–vis reflectance spectroscopy lie in the range of 1.60–1.78 eV indicating the semi-conducting nature of the samples. The temperature-dependent resistivity measurements show semi-conducting behaviour of the samples with decreasing temperature which finally become insulating at low temperature. It has been shown that the VRH model provides the best fit for the resistivity data when compared to the other transport mechanism models that were used to describe the electrical conduction process of synthesized phases.

High-Selectivity Hydrogen Gas Sensors based on Mesoporous PbOx -ZnO Nanocomposites.

Hydrogen heralded as a promising renewable and environmentally friendly energy carrier, carries inherent risks owing to its highly flammable nature. A mere 4 % concentration of hydrogen in the air can trigger an explosion. To counteract this peril, a composite material comprising PbOX -ZnO (2 : 1) was synthesized, characterized, and subsequently employed to fabricate a hydrogen sensing device. Various analytical tools were used to characterize as-deposited materials, including X-ray diffraction, Scanning electron microscopy /Energy Dispersive X-ray Spectroscopy, Transmission electron microscopy UV-Vis Reflectance Spectroscopy and Fourier-transform infrared spectroscopy. The device exhibited favorable properties, such as good selectivity, stability, and a low detection limit for hydrogen. At ambient room temperature, the device demonstrated a sensing signal reaching 468.7, with a response time (T90) of 155 seconds and a recovery time (Tr90) of 69 seconds when exposed to a hydrogen concentration of 5 ppm. This performance underscores the device's rapid and effective response to hydrogen exposure. Moreover, the PbOX-ZnO (2 : 1) composite-based device exhibited a detection limit of 2.4 ppm, functioning accurately within a linear range spanning from 5 ppm to 50 ppm. This capability confirms its precision in accurately detecting hydrogen concentrations within this designated range.

Compositional Influence of Synthesized Magnetic Nanoparticles on Epoxy Composites: Dielectric, Magnetic, and Optical Characteristics

Epoxy nano-magnetic composites exhibit remarkable and promising properties by synergistically combining the properties of epoxy resin and magnetic nanofillers. The current study deals with the synthesis of Fe3O4, NiFe2O4, and CoFe2O4 nanoparticles and their respective nanoparticles-doped epoxy composites, as well as the structural, optical, and dielectric characterization of the resultant nano-composites. To investigate the surface morphology of the synthesized nanoparticles, field emission electron microscopy (FESEM) analysis was employed. By measuring electron diffraction spectroscopy (EDS), the presence of various chemicals was verified. X-ray diffraction (XRD) was used to determine the structural details of the synthesized nanoparticles and nanoparticles-doped epoxy composites. The structural chemistry and surface functionality of the nano-epoxy composites were investigated using Fourier transform infrared spectroscopy (FTIR). The magnetic properties of the synthesized nanoparticles and nanoparticles loaded epoxy composites were also studied using a vibrating sample magnetometer (VSM). UV–visible reflection spectroscopy was also carried out to find the optical properties of the synthesized nanoparticles, neat (undoped) epoxy, and nanoparticles-doped epoxy composites. Dielectric spectroscopy measurements of nanoparticles-doped epoxy composites were performed using an Agilent E4980A precision LCR (Inductance Capacitance Resistance) meter with an Agilent 16451B-test fixture LCR and vector network analyzer (VNA) in the frequency span of 10 kHz to 2 MHz and 200 MHz to 20 GHz, respectively. The influence of the synthesized nanoparticles on the neat (undoped) epoxy composites and the results in view of future applications are fully discussed.

Morphological and semiconductive properties of the anodic oxide layers made on Fe3Al alloy by anodizing in tartaric-sulfuric acid mixture

It has recently been found that the anodizing of FeAl alloys allows the formation of iron-aluminum oxide layers with interesting semiconducting properties. However, the lack of systematic research on different anodizing regimes is hampering their full exploitation in numerous photoelectrochemical-related applications. This study address, for the first time, the systematic effect of the electrolyte composition on the formation of self-ordered oxide films by anodizing on cast Fe3Al alloy. The Fe3Al alloy was anodized in 3 electrolytes with different water-ethylene glycol (EG) ratios (pure water, 25 vol.%-EG, and 50 vol.%-EG solutions) at a constant tartaric-sulfuric acids concentration, different voltages (10–20 V) and treatment times (2–60 min). After anodizing, all anodic oxide layers were annealed at 900 °C to form semiconductive iron-aluminum crystalline phases. Conventional techniques were used to systematically ascertain the morphological (SEM/EDS, XRD, eddy-current measurements) and semiconductive (UV–VIS reflectance spectroscopy) properties of these oxide layers. The results confirmed the formation of homogeneous and self-ordered anodic oxide layers at 10 and 15 V, regardless of the electrolyte composition. Namely, anodic films formed in electrolytes containing EG showed lower pore sizes, growth rates, and film thicknesses than those anodic films formed in the aqueous-based electrolyte. The annealing post-treatment results in different Fe-Al oxides (FexOy, FeAl2O4, etc.) with superior band gap values than those for non-annealed films.

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TiO2 nanotubes (NT) offer several advantages over other geometries for photoelectrochemical (PEC) applications. However, their performance in PEC water-splitting application has remained unsatisfactory due to its wide bandgap. To address this limitation, one approach is the incorporation of other materials as co-catalysts. Hence, in this study, a composite of TiO2 NT and cobalt sulfide (CoxSy) was successfully synthesized, and its potential as a photoelectrode for water molecules splitting was evaluated. The TiO2 NT was synthesized using electrochemical anodization of Ti foil, followed by annealing at 500 °C. Subsequently, CoxSy was added to the TiO2 NT using hydrothermal method, and the composite was further annealed at 400 °C. Characterization technique, such as FESEM and XRD were employed to identify the morphological and phase structures, while UV-Vis reflectance spectroscopy was used for optical analysis. The efficiency of CoxSy deposited on to TiO2 NT were evaluated by measuring the photocurrent generation. Remarkably, the sample of 60_CoxSy/TiO2 NT exhibited photocurrent as high as 0.375 mA/cm2 which is over sixfold higher than the bare TiO2 NT. The results reported in this study were higher than those reported previously.

Effect of water intercalation into tungsten trioxide structure (WO3·xH2O) (x = 0,1,2): Correlation between structure and photocatalytic performances

Tungsten oxide (WO3) is a potential photoanode material for water oxidation, however, its employment is still restricted by its limited light absorption (Eg ∼ 2.75 eV). A particular interest was devoted to tuning its electronic structure and optical bandgap in order to enhance its photocatalytic performance in hydrogen production as well as in advanced oxidation process. One of the promising alternatives for the enhancement of these photocatalytic performances, is the introduction of guest molecules into the tungsten oxide structure. In this paper, the photocatalytic performances of tungsten trioxide were highly improved by the intercalation of water into its structure. The intercalated compounds of chemical formula WO3·xH2O were prepared and characterized by TGA-DSC, PXRD, FT-IR, Raman spectroscopy, SEM-EDS and XPS. The structures of intercalated materials were refined using Rietveld method and the electronic proprieties including bandgap energy, CB and VB edges were estimated using UV–visible reflectance spectroscopy. The obtained results show that the intercalation of water molecules into tungsten oxide structure reduces the gap energy of the WO3 (2.4 eV) to 2.16 eV for WO3∙H2O and to 2.31 eV for WO3∙2H2O. The photocatalytic efficiency of the obtained materials was studied through oxygen evolution reaction tests in the presence of an electron acceptor (Ag+) and the oxidative photodegradation of the orange G dye pollutant. We found that intercalated samples exhibit the highest efficiencies compared with anhydrous samples. These findings are correlated with the increase in the average W-O-W tilt angle in WO3∙2H2O and WO3∙H2O compared to that of WO3. This improvement in the tilt angle induces the shrinkage of the energy bandgap and increases the photocatalytic performance. Furthermore, the stability of the investigated materials was studied as a function of pH, the results reveal that the intercalation of water molecules is beneficial for the chemical stability of the hydrated tungsten oxides. These findings shed light on new alternatives for band-gap engineering and improvement of materials stability through intercalation with water molecules.

La3+ substituted Ni0.5 Co0.5 Fe2 O4 nanoferrites: Magnetically separable catalysts for sunlight-driven photo-oxidative degradation of Methylene Blue

LaxNi0.5Co0.5Fe2−xO4 nanoparticles (x = 0.0, 0.03, 0.06, 0.09, 0.12) were investigated in the current work as Methylene Blue degradation catalysts. Using the citrate-aided sol-gel auto-combustion approach, the nanoferrites with homogenous size distribution were produced. Powder X-ray diffraction was used to analyse the structure of the material. The optical characteristics of ferrite nanoparticles were investigated using diffused UV–visible reflectance spectroscopy. It was noted that when the concentration of La3+ increased, the band gap of produced ferrites shrank. Morphological and compositional studies were performed by FE-SEM and EDX spectra. Surface area was depicted using BET analysis. Raman Spectroscopy was used to estimate the parameters of vibration. Testing has been done on synthesized nanoferrites to see whether they can remove Methylene Blue's concentration in water. In addition, it was examined how La3+ incorporation in Ni0.5Co0.5Fe2O4 nanocomposites resulted in aspects of doping ratio, reaction time and amount of catalyst. The most effective material, La0.06Ni0.5Co0.5Fe1.94O4, achieved a 98.69 per cent efficiency in 140 min. Due to three positive characteristics, including high recycling (up to five cycles), stability, and simplicity of separation using an external magnet, toxic dyes in actual wastewaters can be photodegraded in sunlight using La3+ substituted Ni0.5Co0.5Fe2O4 nanoferrites as an efficient and competitive catalyst.

Polyoxometalate Archetype-Boosted Stability and Charge Storage of 2D Graphene Nanosheets

In this study, the potential of impregnation of phosphotungstic acid (PTA), a polyoxometalate in enhancing specific capacitance (C sp) and diminishing the well-known restacking phenomenon of graphene nanosheets was explored. Graphene nanosheets were prepared chemically from graphite powder through the formation of graphene oxide (GO) and then the subsequent reduction of GO to the reduced GO (rGO). Impregnation of PTA in rGO-PTA (rGP) composites was carried out by simply dispersing rGO and PTA derived from tungstic acid. Scanning electron microscopy, X-ray diffraction analysis, UV–vis reflectance spectroscopy, and Fourier-transform infrared spectroscopy were used to analyze the elemental composition, microstates, and morphology of the composites. The charge-storing capacity and stability of the prepared rGP composites casted on a graphite electrode were examined with cyclic voltammetric, chronopotentiometric, and electrochemical impedance techniques. The effect of ions on the charging capacity of the electrodes was verified using electrolytes with different ion sizes. About 100% enhancement of C sp of rGO with 87% capacitance retention for 2000 charging-discharging cycles was achieved by impregnating rGP composites with only 1% PTA.

Phytomediated-Assisted Preparation of Cerium Oxide Nanoparticles Using Plant Extracts and Assessment of Their Structural and Optical Properties.

Cerium oxide nanoparticles were obtained using aqueous extracts of Chelidonium majus and Viscum album. X-ray diffractometry analysis confirmed the crystalline structure of the synthesized cerium oxide nanoparticles calcined at 600 °C. Scanning electron microscopy, UV-Vis reflectance and Raman spectroscopy, XPS, and fluorescence studies were utilized to interpret the morphological and optical properties of these nanoparticles. The STEM images revealed the spherical shape of the nanoparticles and that they were predominantly uniform in size. The optical band gap of our cerium nanoparticles was determined to be 3.3 and 3.0 eV from reflectance measurements using the Tauc plots. The nanoparticle sizes evaluated from the Raman band at 464 cm-1 due to the F2g mode of the cubic fluorite structure of cerium oxide are close to those determined from the XRD and STEM data. The fluorescence results showed emission bands at 425, 446, 467, and 480 nm. The electronic absorption spectra have exhibited an absorption band around 325 nm. The antioxidant potential of the cerium oxide nanoparticles was estimated by DPPH scavenging assay.

Phyto-assisted synthesis of zinc oxide nanoparticles for developing antibiofilm surface coatings on central venous catheters.

Medical devices such as Central Venous Catheters (CVCs), are routinely used in intensive and critical care settings. In the present scenario, incidences of Catheter-Related Blood Stream Infections (CRBSIs) pose a serious challenge. Despite considerable advancements in the antimicrobial therapy and material design of CVCs, clinicians continue to struggle with infection-related complications. These complications are often due colonization of bacteria on the surface of the medical devices, termed as biofilms, leading to infections. Biofilm formation is recognized as a critical virulence trait rendering infections chronic and difficult to treat even with 1,000x, the minimum inhibitory concentration (MIC) of antibiotics. Therefore, non-antibiotic-based solutions that prevent bacterial adhesion on medical devices are warranted. In our study, we report a novel and simple method to synthesize zinc oxide (ZnO) nanoparticles using ethanolic plant extracts of Eupatorium odoratum. We investigated its physio-chemical characteristics using Field Emission- Scanning Electron Microscopy and Energy dispersive X-Ray analysis, X-Ray Diffraction (XRD), Photoluminescence Spectroscopy, UV-Visible and Diffuse Reflectance spectroscopy, and Dynamic Light Scattering characterization methods. Hexagonal phase with wurtzite structure was confirmed using XRD with particle size of ∼50nm. ZnO nanoparticles showed a band gap 3.25eV. Photoluminescence spectra showed prominent peak corresponding to defects formed in the synthesized ZnO nanoparticles. Clinically relevant bacterial strains, viz., Proteus aeruginosa PAO1, Escherichia coli MTCC 119 and Staphylococcus aureus MTCC 7443 were treated with different concentrations of ZnO NPs. A concentration dependent increase in killing efficacy was observed with 99.99% killing at 500μg/mL. Further, we coated the commercial CVCs using green synthesized ZnO NPs and evaluated it is in vitro antibiofilm efficacy using previously optimized in situ continuous flow model. The hydrophilic functionalized interface of CVC prevents biofilm formation by P. aeruginosa, E. coli and S. aureus. Based on our findings, we propose ZnO nanoparticles as a promising non-antibiotic-based preventive solutions to reduce the risk of central venous catheter-associated infections.

Interaction between acetylsalicylic acid and a cationic amphiphile model: An experimental approach using surface techniques

Mechanical and morphological effects of monolayers of octadecylamine upon aspirin adsorption are monitored by Langmuir isotherms measurements and Brewster angle microscopy. Aspirin induced a notable expansion of the corresponding isotherms and a concentration-dependence of the mechanical stability of the films as a consequence of the subtle balance between the solubility of the amine and the monolayer stabilization induced by the ion-pairs, as corroborated by Brewster Angle Microscopy images. The incorporation of the aspirin into the interface was confirmed by UV–vis reflection spectroscopy. Some comments on the feasibility of using aliphatic amines for drug delivery of anionic species are presented.