Field Emission Scanning Electron Microscopy Research Articles

Studies on the retarded recrystallization of tungsten in CIMPLE-PSI exposed under very-high target temperature and long He+-fluence

Abstract Experiments are carried out in CIMPLE-PSI, to understand the recrystallization behavior of tungsten (W) exposed under very-high target temperature and ITER relevant long He+-fluence. The effect of helium bubbles on possible retardation of the recrystallization process is also studied. W samples are simultaneously exposed under He plasma and annealed by the plasma heat-load, in contrast to previously reported experiments in literature, which were carried out sequentially. Exposed samples are characterized by field emission scanning electron microscopy (FESEM), Vickers surface micro-hardness, nano-hardness and electron backscattered diffraction (EBSD). It is observed that the sample exposed to plasma under the highest temperature (1866 K) suffered acute retarded grain growth. This also contained small, unrecovered grains on the exposed surface. FESEM imaging of the cross-sections confirm relatively smaller helium bubbles still form even at the very high temperature conditions, which can impede the grain growth locally, whenever they are forming right on the grain boundaries. This results in an inhomogeneous mixture of surface grains with sizes from few micrometer to few tens of micrometer. EBSD estimates that the plasma exposed surface was only 34% recrystallized. The second sample exposed at a lower temperature (1699 K) but for three times higher fluence (ion fluence: 1.19×1027 m-2) was almost fully recrystallized, which shows retardation diminishes very fast with the duration of the exposure. Hardness measurements were undertaken to understand the variation with plasma exposure/annealing temperature and the extent of recrystallization, with three different probing length scales, spanning from few hundreds of nanometer to several micrometers. Both helium plasma exposed W samples are observed to undergo retarded softening up to a depth of few hundred nanometers from the surface, compared to when the metal may be recrystallized by simple heating, without any plasma exposure.

The impact of carbon quantum dots derived from spent coffee grounds on the droplet combustion of diesel/n-butanol blend

As global concerns surrounding climate change mount and fossil fuel reserves diminish, the application of additives in internal combustion engines is increasingly prevalent. Butanol and carbonaceous nanomaterials, such as carbon quantum dots (CQD), are being employed as additives to increase engine efficiency and mitigate the emission of pollutants. Nevertheless, understanding the impact of these additives on combustion behavior at the droplet scale through combustion assessments before their use in engines is crucial. In this study, our main objective was to assess the impact of incorporating CQD dispersed in n-butanol as additives to conventional diesel fuel on the combustion characteristics at the droplet scale. CQD were obtained from spent coffee grounds (SCGs) using n-butanol as a solvent. The product obtained was mixed with Colombian commercial diesel (10 % vol. palm oil biodiesel), and its combustion was evaluated using the droplet combustion method. Before the CQD synthesis, SCGs were characterized by thermogravimetric analysis (TGA) and field emission scanning electron microscopy (FESEM). CQD were characterized via Fourier transform infrared (FTIR) spectroscopy, Transmission Electron Microscopy (TEM), UV–vis, and fluorescence spectroscopy. Results indicated that adding n-butanol and CQD to commercial diesel leads to a 5.4 % and 16.5 % increase in droplet ignition delay, respectively. These additives also cause droplet contraction and expansion cycles, resulting in unstable combustion. However, CQD reduces the frequency of microexplosions caused by boiling n-butanol inside the droplet, which mitigates instabilities during droplet combustion. Including CQD can enhance fuel evaporation by increasing the density of nucleation sites for bubble formation and preventing micro-explosions, thereby leading to stable combustion. These attributes can significantly influence the performance of blends in Compression Ignition (CI) Engines.

The impact of proton ion irradiation on Se70Te20In10 thin films: Linear and non-linear optical properties for photonic applications

The examination of the linear and non-linear optical features was conducted on amorphous ternary Se70Te20 In10 thin films, which were exposed to proton irradiation energy of 3 MeV at varying fluences of 5×1013, 5×1014, 5×1015 and 5×1016 ions/cm2. The bulk sample was produced using the melt quenching method, and subsequently, thin films were obtained through electron beam evaporation. Calculations of linear and non-linear optical parameters were carried out based on transmittance and reflectance data acquired from UV–Vis–NIR spectroscopy spanning 300–2500 nm. Field emission scanning electron microscopy (FESEM) and X-ray diffraction (XRD) confirmed an amorphous phase in the films. The optical parameters showed strong dependency on the proton radiation fluence. In addition, the existence of minima or maxima for a number of parameters at a fluence of 5×1014 ions/cm2 showed that this was the optimum fluence. The linear and non-linear properties showed that the sample have potential applications in photonic devices.

Investigating the catalytic and antibacterial behavior of cesium-doped MoO3 nanostructures against methylene blue dye and MDR E. coli with DFT analysis

Water pollution, exacerbated by inadequate water management practices, has compromised the effectiveness of traditional water treatment technologies. The integration of metal oxide-based nanomaterials in treatment systems has the potential to revolutionize the field of wastewater treatment, providing a sustainable and efficient solution to the growing global water crisis. This study focused on the fabrication of hexagonal cesium (Cs) doped MoO3 nanostructures (NSs) for their potential use as catalytic and antibacterial agents. Various structural, optical, and morphological analysis was conducted to examine these NSs. The UV–Vis spectroscopy results showed that as Cs concentration increased, the band gap energies of MoO3 decreased from 3.5 eV to 3.0 eV. The field emission scanning electron microscopy (FESEM) investigation revealed the plate-like structural morphology of MoO3 formed by overlapping one layer onto another. Cs doping effectively inhibited the recombination of photo-generated charge carriers, resulting in a significant reduction in PL peak intensity for Cs-doped MoO3 compared to MoO3. The prepared NS-reduced methylene blue dye in the absence of light under different pH conditions, reaching 86.8% with 2% Cs-doped MoO3. Density functional theory (DFT), utilizing the Heyd-Scuseria-Ernzerhof hybrid (HSE06) method, was employed to model and compute the interactions between methylene blue (MB) and Cs-doped MoO3 during MB adsorption. Bactericidal experiments on multidrug-resistant Escherichia coli showed that the NSs had remarkable antibacterial action, generating an inhibition zone of 9.15 mm at higher doses using 6% Cs-doped MoO3. Consequently, these findings offer potential significance for research in developing and implementing wastewater disinfection systems.

Synthesis mechanism of TiO2 nanoparticles via high frequency electrical arc discharge

Abstract The rapid advancement of nanofabrication techniques has significantly increased the utilization of nanoparticles in recent years. This study investigates the synthesis of titanium dioxide (TiO₂) nanoparticles, highlighting their unique properties and diverse applications across scientific and industrial fields. These nanoparticles are valued for their biocompatibility and advantageous optical, electrical, and physical properties. Various synthesis methods—chemical, physical, and biological—are reviewed, with a particular focus on the electric arc discharge method. This method is distinguished by its efficiency and environmental friendliness, enabling the production of highly pure nanoparticles. Utilizing continuous and alternating sparks between two electrodes, the technique generates spherical nanoparticles with adjustable sizes, controlled by the energy of each spark. An RC circuit-based device was designed for this electrical discharge process. Dynamic light scattering (DLS) measurements revealed an average particle size of 164.51 nm with a standard deviation of 44.08 nm. Field emission scanning electron microscopy (FESEM) images showed both solid and hollow spherical TiO2 nanoparticles. Energy dispersive spectroscopy (EDS) confirmed that the TiO2 particles contained only titanium and oxygen, with no other elements detected. X-ray diffraction (XRD) analysis verified the crystal structure, predominantly identifying the anatase phase of the synthesized nanoparticles. This research enhances the understanding of TiO2 nanoparticle synthesis and characterization, providing a foundation for future innovations in their extensive applications.

Synthesis and characterization of Er2O3-doped Y2O3 nanoparticle incorporated optical fiber for use as optical amplifier

Erbium oxide (Er2O3)-doped optical fibers (EDF) are well-known for their applications in optical amplification at 1550 nm. In this study, we present the synthesis of Er2O3-doped yttrium oxide (Y2O3) nanoparticles (NPs) using a homogeneous coprecipitation technique and their integration into optical fibers for enhanced optical amplification. A series of NP samples with varying Y/Er molar ratios were synthesized to identify the optimal composition for incorporation into optical fibers. X-ray diffraction (XRD) analysis revealed that the nanoparticles crystallize in a cubic geometry (space group Ia3) with crystallite sizes ranging from 20 to 41 nm. These sizes increased approximately to 90 nm as the calcination temperature was raised from 1000°C to 1400°C. Field emission scanning electron microscopy (FESEM) corroborated the XRD results, while high-resolution transmission electron microscopy (HRTEM) confirmed the crystalline structure and an average particle size of approximately 100 nm. Photoluminescence studies showed that emission and excitation intensities were functions of the Y/Er molar concentration ratio and calcination temperature, with the lifetime extending up to 6.86 ms for a sample with a 0.25:0.01 Y2O3:Er2O3 ratio calcined at 1400°C. To assess the performance of the synthesized NPs, an optical preform was prepared using the Vapor Phase Delivery (VPD) method combined with the Solution Doping (SD) technique. The preform was then drawn into fiber, and its amplification performance was evaluated. The resulting fiber demonstrated efficient amplification with a gain of 14.9 dB with respect to 0 dBm input signal at 1550 nm under 150 mW pump power from 9 m active fiber, indicating its potential as a gain medium for constructing erbium-doped fiber amplifiers (EDFAs).

Natural Kapok fiber-derived two-dimensional carbonized sheets as sustainable electrode material

Natural biomass-derived carbon nanostructures have attracted research interest because of their unique surface and electrochemical properties. The present study embodied the carbonized micro-nano sheets derived from the low-cost natural source Kapok silk fiber. The material was obtained via a facile thermal pyrolysis process. Diffraction analysis showed a broad graphene structure-like peak, indicating the formation of graphene-like carbon nanosheets. Field emission scanning electron microscope (FESEM) and transmission electron microscopic (TEM) images confirmed the presence of fragmented carbon sheets, some of which were folded to form a tube-like structure. Raman study showed the presence of D and G band with the Id/Ig ratio of 0.96 which indicated the formation of few-layered carbon nanosheets. Furthermore, the electrochemical performance was evaluated for lithium-ion battery as well as supercapacitor. A specific capacity of 465 mAh.g-1 at 0.1 C rate for Li-ion battery and a specific capacitance of 473.61 F.g-1 for supercapacitor have been obtained with the capacitance retention of 95 %. This study provides insights into a strategy for the sustainable production and utilization of natural fiber-based carbon in energy storage systems.

A reactive melamine-DOPO based flame retardant for superior thermal stability and flame retardancy in rigid polyurethane foam

The flame-retardant effect of 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide (DOPO) and its derivatives in reducing the flammability of polymeric materials are well known. In this study, flame-retardant rigid polyurethane foams (FR-RPUF) were synthesized using a melamine-DOPO-based flame-retardant (MDFR). Additionally, MDFR was also used for preparation of a flame-retardant elastomeric polyurethane (FR-PUE). The chemical structure and thermal properties of the FR-RPUF and FR-PUE samples were studied with Fourier transform infrared (FTIR), field emission-scanning electron microscopy (FE-SEM), and thermogravimetric analysis (TGA). TGA results revealed that the incorporation of MDFR into the PU matrix significantly increased the char residue. The char residue of FR-RPUF with 0.5 wt% MDFR increased from 4.75% to 44.36%, as compared to the pure RPUF. Results from the microscale combustion calorimeter (MCC) test illustrated that the peak of heat release rate (pHRR), total heat release (THR), and heat release capacity (HRC) of the FR-RPUF and FR-PUE samples were reduced, as compared to the pure PU samples. The pHRR value of FR-RPUF with 3 wt% of MDFR decreased 12%, as compared to the pure RPUF, while the pHRR was obtained 34% lower than of the pure PUE. Furthermore, FR-RPUFs successfully passed the UL94 testing, achieving a V-0 grade.

The role of BaTiO3 nanoparticles as photocatalysts in the synthesis and characterization of novel fruit dyes is investigated.

In the present work, the photocatalytic activity against the natural dye extracted from the novel fruits has been studied by the BaTiO3 nanoparticles (NPs) under a ultra-violet (UV) light source. The large concentrations of an essential phenolic agent present in this phytochemical extract superimposed with cloths fibers make strong stain and degrade into another form of toxic, which is excluded from the many textiles industries as the colorful waste waters without recycling and removal of that dye pigments have been investigated using both photodegradation and photoluminescence techniques. The entitled nanoparticles (NPs) were prepared using the soft chemical root-modified solvothermal synthesis combo method and exposure to heat treatment such that the annealing process has been done for different temperatures ranging from 100°C to 250°C. As for as concern the characterization, as a start, structural and morphology studies have been reported here that highly crystalline oriented peaks data using powder x-ray diffraction techniques (PXRD) as well as the surface morphology including the size, shape, and mass distribution using the field emission scanning electron microscopy (FESEM) techniques, which purely belong to rutile tetragonal structure of the crystal system and circular and noncircular flakes like rough surface morphology materials respectively. The lattice dissociation constant 'ε' value of the BaTiO3 NPs has determined to be ~2.71 × 10-3 using the Williamson-Hall (W-H plot) analysis of crystallographic data. In the UV visible spectroscopy findings, since the extreme quantum confinement of BaTiO3 nanoflakes/nanodisc, the optical energy bandgap has been estimated to be a range of 1.98 to 2.67 eV (~2.48 eV) found from the Tauc plot analysis, which contributes to the significantly owing to the enhanced photocatalytic efficiency with excellent performance along exciton formation, superoxide ions, and hydroxyl free radicals generations under UV-vis light irradiation resulting in efficient degradation of typical novel fruit organic dye. Photoluminescence spectra observed at room temperature and low temperature have been observed for the BaTiO3 nanoflakes, which exhibit the blue emission due to the crystalline defects such as the appearance of Ba vacancies leads to the conceivable beginning of p-type conductivity and the origination of free exciton emission reveals the direct bandgap transition nature of nanoflakes. RESEARCH HIGHLIGHTS: According to our findings, 89.71% of the natural syzygium cumin is degraded by photocatalysis reaction. As a plausible mechanism for the destruction of natural dyes under solar light, photocatalytic destruction has been proposed. The reaction between these reactive free radical species leads to high efficiency photodegradation with a short decay time. In addition to water treatment and environmental cleaning applications, the excellent performance of this photocatalyst makes it a promising candidate for other applications. Hence, the synthesized BaTiO3 nanoflakes showcase a highly significant advancement towards the development of a textiles dye recycling method.

Hydrothermal synthesis of rGO and MnCoS composite for enhanced supercapacitor application

Nanostructured materials incorporating transition metal sulfides have demonstrated considerable potential across various applications, particularly in the realms of energy production and storage. Sulfide-based material preparation is a challenging and costly procedure that requires a high temperature and reducing atmosphere. This work reports that manganese cobalt sulfide (MCS) and reduced graphene oxide composite manganese cobalt sulfide (rMCS) were successfully prepared through a hydrothermal method. Various characterization techniques were employed to analyze the prepared materials, including X-ray diffraction, field emission scanning electron microscopy, transmission electron microscopy, Brunauer-Emmett-Teller analysis, and X-ray photoelectron spectroscopy. In a three-electrode system, MCS and rMCS electrodes exhibit an excellent specific capacitance of 1695 and 1925 F g−1 at 1 A g−1 current density respectively. MCS delivers the capacitance retention of 99% and rMCS exhibits the capacitance retention of 100% capacitance retention over 5000 consecutive cycles. The constructed asymmetric supercapacitor electrode (rMCS//rGO) exhibits the energy and power density of 64 Wh kg−1 at 799 W kg−1, respectively with outstanding cyclic stability of 97.4% even after 10,000 cycles. The exceptional electrochemical properties of MCS with rGO composite electrode indicate that they would make an outstanding electrode material for cutting-edge energy storage devices.

Influence of exfoliation method of graphene on physical properties of graphene/High Density Polyethylene nanocomposites: Semiconductor‐like electrical conductivity, glass transition, and melting temperature

AbstractDespite the wide range of applications of polyethylene (PE), many efforts are being made to improve its properties with carbon allotropes such as graphene. The addition of graphene can improve the electrical, thermal, and mechanical properties of this polymer. Through the present study, the effects of exfoliated graphene nanoplatelets (XGNPs) and few‐layer graphene (FLG) on the electrical conductivity and thermal properties of high‐density polyethylene (HDPE) were investigated. XGNPs were synthesized by ultrasonication of graphite nanoplatelets, and FLG was synthesized by shear exfoliation of flake graphite. Finally, HDPE powder particles were coated with dispersed XGNPs and FLG. Then XGNPs/HDPE nanocomposites and FLG/HDPE nanocomposites were fabricated by compression molding. The morphology, structural, electrical, and thermal properties of the graphite, graphene, PE, and nanocomposites were observed and comparatively studied by transmission electron microscopy, field emission scanning electron microscope, x‐ray diffraction (XRD), Raman spectroscopy, and conductivity measurements. The graphene's D, G, and 2D bands were revealed by Raman spectroscopy of nanocomposites and verified the existence of the graphene in the polymer matrix. XRD revealed that the graphene did not affect the original crystalline structure of the HDPE matrix, and the Fourier‐transform infrared spectroscopy revealed that the nanocomposite was obtained without the formation of any functional groups. The electrical properties of the nanocomposites were comparatively studied. After adding XGNPs (7 wt%), volumetric electrical conductivity in a sample reached from 10−16 to 10−3 S/m. The highest volumetric conductivity, 1.1 × 10−2 S/m, that is, semiconductor‐like conductivity, was achieved after adding 7 wt% of FLG. The glass transition temperatures (Tg), melting temperatures (Tm), and thermal stability were investigated by differential scanning calorimetry and TGA, respectively, and it was concluded that Tg and Tm increase by adding the graphene. This study shows that shear exfoliation of graphene is the best and the most facile method to prepare mass‐scale graphene for the production of graphene/polyolefin nanocomposites.Highlights Two types of graphene were produced by using sonication and shear‐exfoliation. HDPE powders were coated with two types of graphene and then hot pressed. The method of (G) preparation is crucialparameter on electrical conductivity. In the sample containing 7 wt% (XGNPs), the highest conductivity is 10−3 S/m. In the sample containing 7 wt% (FLG), the highest conductivity is 10−2 S/m.

On the Electrochemical Properties of Poly(Vinylidene Fluoride)/Polythiophene Blends Doped with Lithium‐Based Salt

AbstractIn this study, polymer blends of polythiophene (PTH) and poly(vinylidene fluoride) (PVDF) are investigated by focusing on their structural and electrochemical characteristics. These blends displayed immiscibility confirmed through field emission scanning electron microscopy (FE‐SEM) and interaction assessments. PTH's role as a plasticizer is evident, diminishing crystallinity. A rise in PTH level led to a lower glass transition temperature and a higher melting point, suggesting reduced intermolecular forces and increased polymer chain flexibility. Conversely, a dispersed phase presence elevated the melting point, restricting chain movement and crystallization. The thermal properties of blends are enhanced by increased PTH content. Applying the Vogel–Tammann–Fulcher model to ionic conductivity measurements, it observed a direct relationship between temperature and free volume, impacting conductivity and ion transport numbers. Certain materials exhibit increased activation energies, indicating substantial thermodynamic barriers to local motion. Higher PTH content within the PVDF matrix notably increased the lithium ion transfer number from 0.22 to 0.71, a change tied to the C–S–C structure of polythiophene. However, elevated PTH levels also led to diminished negative charge transfer and ionic conductivity in the PTH‐PVDF blend compared to pure PVDF, likely due to an ionic conduction hindrance.

Manufacturing Radially Aligned PCL Nanofibers Reinforced With Sulfated Levan and Evaluation of its Biological Activity for Healing Tympanic Membrane Perforations.

The main objective of this study is to construct radially aligned PCL nanofibers reinforced with levan polymer and investigate their in vitro biological activities thoroughly. First Halomonas levan (HL) polysaccharide is hydrolyzed (hHL) and subjected to sulfation to attain Sulfated hydrolyzed Halomonas levan (ShHL)-based material indicating heparin mimetic properties. Then, optimization studies are carried out to produce coaxially generated radially aligned Poly(caprolactone) (PCL) -ShHL nanofibers via electrospinning. The obtained nanofibers are characterized with Fourier Transform Infrared Spectroscopy (FTIR)and Field Emission Scanning Electron Microscopy with Energy Dispersive X-Ray (FESEM-EDX) analysis, and mechanical, contact angle measurement, biodegradability, and swelling tests as well. Afterward, cytotoxicity of artificial tympanic membranes is analyzed by MTT (3-(4,5-Dimethylthiazol-2-yl) -2,5 Diphenyltetrazolium Bromide) test, and their impacts on cell proliferation, cellular adhesion, wound healing processes are explored. Furthermore, an additional FESEM imaging is performed to manifest the interactions between fibroblasts and nanofibers. According to analytical measurements it is detected that PCL-ShHL nanofibers i) are smaller in fiber diameter, ii) are more biodegradable, iii) are more hydrophilic, and iv) demonstrated superior mechanical properties compared to PCL nanofibers. Moreover, it is also deciphered that PCL-ShHL nanofibers strongly elevated cellular adhesion, proliferation, and in vitro wound healing features compared to PCL nanofibers. According to obtained results it is assumed that newly synthetized levan and PCL mediated nanofibers are very encouraging for healing tympanic membrane perforations.

Fabrication of a molecularly imprinted poly(methyl methacrylate) decorated graphite electrode for detection of aloe emodin in Aloe vera

In this work, the authors represent a comprehensive approach for the development and validation of a novel graphite-supported molecularly imprinted poly(methyl methacrylate) electrode for the selective and sensitive detection of aloe emodin (AE) in aloe-based cosmetic products. The electrocatalytic activity of the electrode was evaluated using cyclic voltammetry and differential pulse voltammetry techniques in phosphate buffer saline. Surface morphology, structural characteristics, and imprinting endorsement were investigated using field emission scanning electron microscopy, Fourier-transform infrared spectroscopy, and UV-Vis spectroscopy. Under the optimal conditions, the electrode showed an oxidative differential pulse voltammetry peak at -0.2931±0.011 V (vs. Ag/AgCl, saturated KCl). The current was increased linearly with increasing concentrations of AE from 0.0005 to 350 µM, with a low detection limit of 0.0003 µM. The voltammetric analysis has been validated by reverse-phase high-performance liquid chromatography (RP-HPLC) methods. A partial least square regression model was developed to correlate the results obtained from the proposed system with the reference values obtained by RP-HPLC. The model showed a high prediction accuracy of 95.95 % for the detection of AE in cosmetic samples. The developed electrode provides a low-cost, rapid, easy, and convenient method for the detection of AE in cosmetic products, offering potential benefits for quality control and safety assessment in the cosmetic industry.

To investigate the effect of discharge energy and addition of nano-powder on processing of micro slots using EDM assisted µ-milling operation

ABSTRACT Micro-electric Discharge-Milling (µ-ED-M) is a non-contact process that uses an electrical spark to remove the material from a submerged workpiece with an electrode in a dielectric. The present paper focuses on optimizing process energizing (Capacitor, Voltage) and process stabilizing (Tool Travel Speed, Nano-Powder) parameters for controlling the size and surface characteristics of micro-crater. The present work focuses on the effect of nano-powder concerning dimensional aspects and surface characteristics at high and low capacitance levels. A µ-slot has been generated on the copper material by a tungsten carbide electrode. The experimentation is performed with two capacitor levels and three voltage and tool travel speed levels using full factorial design technique using with and without mixing of nano-powder in dielectric. The desirability functional multi-objective optimization approach is used to analyze the MRR, TWR, Width, and Depth. Field emission scanning electron microscopy (FESEM), non-contact optical profilometer, and x-ray diffraction (XRD) techniques are used to analyze the surface morphology of machined surfaces. The ANOVA is used to optimize the results; at low discharge energy, tool travel speed contributes 41% and promotes a higher thickness of recast layer 12.7 µm, whereas high discharge energy and nano-powder concentration contribute approx.—36% with 8.56 µm of recast layer.

Corrosion resistance and biocompatibility of carbon ion implanted AZ31B magnesium alloy

The poor corrosion resistance of magnesium limits its clinical applications. Accordingly, in the present study, carbon ions were incorporated into a AZ31b magnesium alloy surface via carbon plasma immersion ion-implantation to improve its corrosion resistance and biocompatibility. The surface morphology and properties of the modified alloy were evaluated by field-emission scanning electron microscopy, water contact angle measurement, Raman scattering, X-ray photoelectron spectroscopy, and energy dispersive X-ray spectroscopy. Furthermore, compositional depth profiles were obtained by glow discharge optical emission spectroscopy, revealing a Gaussian-like distribution of carbon concentration. Electrochemical and hydrogen-evolution analysis demonstrated the successfully improved corrosion resistance of the AZ31b Mg alloy, while its biocompatibility was demonstrated by MTT and cell-adherence assays.

Green synthesis of boehmite-reinforced cashew gum/polypyrrole biopolymer blend for advanced biomaterials

Electrically conducting biopolymer blend nanocomposites based on different contents of boehmite (BHM) reinforced cashew gum (CG) /polypyrrole (PPy) blend is synthesized by an in situ polymerization technique using water as a green solvent. The resulting bio-blend nanocomposites underwent comprehensive analysis concerning their structural, morphology, thermal, and electrical properties, such as dielectric constant, dielectric loss, electric modulus, and AC conductivity. The Fourier transform infrared spectroscopy (FTIR) spectra revealed the presence of metal oxide stretching in the blended nanocomposite at 512 cm−1. Field emission scanning electron microscopy (FE-SEM) confirmed the attachment and uniform dispersion of BHM within the CG/PPy blend at 7 wt% loading, and beyond this loading, the nanoparticles get agglomerated in the biopolymer blend. The glass transition temperature and thermal stability of all the blended nanocomposites are higher than that of the pure CG/PPy blend and these thermal properties increase with the loading of nanoparticles. Conductivity experiments demonstrated that as the nanofiller content increases up to 7 wt%, there is a concurrent rise observed in AC conductivity, dielectric loss, and dielectric constant. There is a substantial difference of 1.21 Scm−1 between the maximum and minimum AC electrical conductivity, at 102 Hz. However, a decrease in electrical properties is observed at the highest loadings of BHM due to the agglomeration of nanoparticles in the polymer blend matrix. The lowest activation energy value (0.049 × 10−4 eV) is also exhibited by 7 wt% BHM nanocomposites. Furthermore, the electrical properties of both CG/PPy and CG/PPy/BHM nanocomposites exhibited a temperature-dependent behavior, progressively increasing until reaching maximum values. This study suggests that such bio-based polymer dielectrics could be promising materials for various applications, offering enhanced thermal and electrical properties through careful control of nanofiller content and dispersion.

Temperature-modulated acetone monitoring using Al2O3-coated evanescent wave fiber optic sensors

This paper presents an experimental study of a fiber-optic-based acetone sensor and its temperature effects for use as a breath analyzer to detect acetone in exhaled breath. The study employs fiber optic evanescent wave-based acetone sensing, utilizing sputter coated Aluminium Oxide (Al2O3)-coated probes fabricated via clad modification technique. The optical fibers were coated with Al2O3 to achieve thicknesses of 247.03 nm, 334.05 nm, and 468.75 nm. The sensor probes were characterized using, Field Emission Scanning Electron Microscopy (FESEM), Energy Dispersive Spectroscopy (EDS), X-ray Diffraction (XRD), Ultraviolet-Visible (UV-Vis) Spectroscopy, and Spectroscopic Ellipsometry for uniformity, elemental, optical constants, and thickness of the Al2O3. The spectral responses of the probes were analyzed for acetone concentrations ranging from 0 to 100 ppm, with temperature modulation from room temperature to 100 °C. The probe with a ∼334 nm thick Al2O3 coating exhibited the highest response, reaching 6.2 % at 100 °C in 100 ppm acetone. Linear regression revealed that the ∼334 nm coated probe had the highest sensitivity at 5.98 counts/ppm. The sensor showed response and recovery times of approximately 12 and 17 seconds, respectively. This study underscores the stability and repeatability of temperature-modulated Al2O3-coated fiber optic sensors for selective acetone detection in various non-invasive applications.

Effects of Pt doping on surface properties and quenching of band edge emission in ZnO

Pt doped ZnO thin films were synthesized on soda-lime glass substrates using a cost-effective sol-gel method, followed by spin coating and thermal annealing at various temperatures. Several characterization techniques such as UV–Vis absorption spectroscopy, photoluminescence (PL), field emission scanning electron microscopy (FESEM), time-of-flight secondary ion mass spectroscopy (ToF-SIMS), Raman spectroscopy, and X-ray photoelectron spectroscopy (XPS) are exploited to investigate the Pt doping effects on surface and optical properties of ZnO thin films. UV–Vis analysis demonstrated a slight decrease in the optical band gap from 3.3 eV to 3.2 eV with increased annealing, indicating enhanced suitability for optoelectronic applications. FESEM imaging revealed distinct worm-like structures and small Pt metal nanoparticles in unannealed samples, while thermal treatment supported the formation of spherical Pt nanoparticles and improved conductive pathways in the films. The Wagner diagram, coupled with Auger line transitions from XPS, quantified the oxidation states and chemical environments of Zn and Pt, respectively. Notably, the observed changes in the binding energy of the Zn-2p junction and the kinetic energy of the Zn-LMM Auger junction were significantly influenced by the Pt doping and the electronic properties of the substrate. The Wagner diagram provided a comprehensive visual representation of the parameters, facilitating a deeper understanding of electronic interactions and structural dynamics at the atomic level. XPS results confirmed the presence of ZnO, Zn(OH)2, Pt0 and PtO2 phases, indicating stability and constutient's interactions. ToF-SIMS also validated the uniform distribution of Pt nanoparticles within the ZnO thin film, confirming the effectiveness of the sol-gel method. As a result of Pt doping, PL studies revealed a large quenching effect on band edge emission in the UV and visible emission region of ZnO thin film, which is due to Pt acting as a recombination center for photogenerated carriers. Overall, our results highlight the influence of annealing and Pt incorporation on the optical and structural properties of ZnO thin films and highlight their potential applications for photonics and catalysis.

Sodium polyacrylate hydrogel electrolyte: Flexible rechargeable supercapacitor using thermally reduced graphene oxide nanosheets

The alternative source of the gel polymer electrolyte (GPE) is introduced by developing the sodium polyacrylate (S-PANa) solid hydrogel electrolyte, which is the front runner in the recent flexible and wearable electronic devices due to their excellent mechanical property, high ionic conductivity, and electrochemical stability. In this work, we synthesized the S-PANa solid hydrogel electrolyte and utilized it for the flexible symmetric supercapacitor using thermally reduced graphene oxide nanosheets (TRGO) coated on carbon cloth as an electrode. The prepared S-PANa hydrogel is of a highly porous nature and has better surface roughness, as examined by the Field Emission Scanning Electron Microscopy (FE-SEM) and 3D nano profiler analysis. The electrochemical characterization of the assembled flexible solid-state hydrogel supercapacitor (FSHSC) reveals the electric double-layer capacitive behavior with an excellent device capacitance of 45.77 mF/cm2. The significant role of diffusion charge re-distribution, overcharging issues, ohmic drop, and leakage current of the FSHSC is studied, followed by self-discharge and leakage current analysis. Moreover, the FSHSC device delivers the maximum energy density of 5.15 μWh/cm2 with a remarkable retention capacitance of 99 % over 10,000 continuous cycles. Further, in practical utilization, the solar-charged FSHSC device can effectively power the electronic LED for a long duration and enhance its efficiency for the development of a sustainable backup power system. Overall, these experimental results demonstrated the significant use of the S-PANa hydrogel-based flexible device, which can be an alternative source in future energy storage systems instead of using gel electrolyte-based flexible devices.