X-ray Diffraction Research Articles

Encapsulation of the vanadium substituted Keggin polyoxometalates [α-PVW11O40]4- and [α-PV2W10O40]5- in HKUST-1.

Two POM@MOF hybrid materials composed of a copper-based metal-organic framework (MOF) [Cu3(C9H3O6)2(H2O)3]n (HKUST-1) encapsulating vanadium-substituted Keggin polyoxometalates (POM), [α-PVW11O40]4- (PVW11) and [α-PV2W10O40]5- (PV2W10), were prepared and characterized. PVW11@HKUST-1 and PV2W10@HKUST-1 were synthesized hydrothermally by self-assembly of HKUST-1 in the presence of the preformed POMs, [α-PVW11O40]4- and [α-PV2W10O40]5-, respectively. The two POM@MOF composites were characterized by X-ray diffraction, TGA, BET surface area analysis and FT-IR and Raman spectroscopy. The electronic structure of the POM@MOF materials and their respective constituents is surveyed using solid state UV-vis reflectance spectroscopy. The UV-vis spectra order the oxidizing strength of the POM constituents ([α-PV2W10O40]5- > [α-PVW11O40]4-) and reveal the distinct electronic structure of the POM@MOF materials obtained by synthetic encapsulation of mono- and di-vanadium substituted Keggin polyoxotungstates in HKUST-1.

Investigation of Corrosion Behavior of Cenosphere reinforced Iron Based Composite Coatings

In the present study cenopshere was reinforced with FeCrNiC (Metco 42C) as matrix material and prepared four different feedstock powders such as FeCrNiC+0%Cenosphere, FeCrNiC+5%Cenosphere, FeCrNiC+10%Cenosphere and FeCrNiC+15%Cenosphere were coated by plasma spray technique on T22 substrate. Evaluation of the substrate and coatings potential under salt spray test was performed. Dense fog of 5% NaCl salt water was used to create a corrosive atmosphere within the chamber. The salt water's pH was kept constant at 6.5-7. The materials that underwent corrosion were examined using X-ray diffraction (XRD), and scanning electron microscopy (SEM). The FeCrNiC+15%Cenosphere and FeCrNiC+10%Cenosphere coatings exhibited reduced weight loss during a 168-hour corrosion test compared to the FeCrNiC+5%Cenosphere, FeCrNiC coatings, and substrate. The excellent chemical stability and corrosion resistance of Cr23C6, SiO2, NiO, and Cr2O particles contribute to gradually avoid the formation of red rust on Fe-based coated samples with exposure approaches to 52 and 130 hours.

Assessing Anticancer Properties of PEGylated Platinum Nanoparticles on Human Breast Cancer Cell lines using in-vitro Assays.

This study describes the in-vitro cytotoxic effects of PEG-400 (Polyethylene glycol-400)-capped platinum nanoparticles (PEGylated Pt NPs) on both normal and cancer cell lines. Structural characterization was carried out using X-ray diffraction and Raman spectroscopy with an average crystallite size 5.7 nm, and morphological assessment using Scanning electron microscopy (SEM) revealed the presence of spherical platinum nanoparticles. The results of energy-dispersive X-ray spectroscopy (EDX) showed a higher percentage fraction of platinum content by weight, along with carbon and oxygen, which are expected from the capping agent, confirming the purity of the platinum sample. The dynamic light scattering experiment revealed an average hydrodynamic diameter of 353.6 nm for the PEGylated Pt NPs. The cytotoxicity profile of PEGylated Pt NPs was assessed on a normal cell line (L929) and a breast cancer cell line (MCF-7) using the 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide (MTT) assay. The results revealed an IC50 of 79.18 µg/ml on the cancer cell line and non-toxic behaviour on the normal cell line. In the dual staining apoptosis assay, it was observed that the mortality of cells cultured in conjunction with platinum nanoparticles intensified and the proliferative activity of MCF-7 cells gradually diminished over time in correlation with the increasing concentration of the PEGylated Pt NPs sample. The in vitro DCFH-DA assay for oxidative stress assessment in nanoparticle-treated cells unveiled the mechanistic background of the anticancer activity of PEGylated platinum nanoparticles as ROS-assisted mitochondrial dysfunction.

Novel nano-Y2O3/myristic acid nanocomposite PCM for cooling performances of electronic device with various fin designs

Effective thermal management is critical for enhancing the longevity and operational efficiency of electronic devices. This research introduces a novel cooling approach by incorporating Yttrium Oxide (Y2O3) nanoparticles into Phase Change Materials (PCMs) to improve thermal management in electronic devices. This study focuses on developing nanocomposite PCMs with Y2O3 nanoparticles embedded in a myristic acid (MA) matrix through melting and physical mixing. Nanoparticles were added to MA at various mass fractions: 0.5 %, 1 %, 1.5 %, and 2 %. Structural and morphological analyses were conducted using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), and field emission scanning electron microscopy combined with energy dispersive X-ray spectroscopy (FE-SEM-EDX). Thermophysical properties were characterized using differential scanning calorimetry (DSC) and thermal conductivity measurements with the KD2-Pro device. The inclusion of Y2O3 nanoparticles significantly enhanced the thermal conductivity of the PCM, reaching up to 0.229 W/m·K in the solid phase and 0.177 W/m·K in the liquid phase, representing improvements of 43.125 % and 18 %, respectively, over the base PCM. The highest average specific heat capacity (Cp) values in the solid and liquid phases were 1.98 J/g·°C and 2.69 J/g·°C, respectively, for the 2 % nanoparticle-additive sample. DSC analysis indicated slight shifts in phase transition temperatures and a noticeable reduction in latent heat values, from 215 J/g to 202 J/g for solidification and from 209 J/g to 201 J/g for melting. Computational analysis using ANSYS-FLUENT software validated the enhanced thermal dissipation properties of the nanocomposite PCM. Additionally, an examination of fin configurations within the PCM containers revealed that rectangular fins provided superior cooling efficacy compared to trapezoidal ones. This study demonstrates that the development of nano- Y2O3 enhanced MA nanocomposite PCMs presents a promising avenue for applications in electronic device thermal management and thermal energy storage.

Interactions between gamma-aminobutyric capped silver nanoparticles and large unilamellar vesicles (LUVs) and their antimicrobial activities

Multidrug-resistant bacteria (MDR) and bacterial virulence pose significant challenges to global health. Nanotechnology offers exciting possibilities for developing innovative strategies to combat these issues. This study investigates the synergistic effects of silver nanoparticles (AgNPs) and gamma-aminobutyric acid (GABA) to address antibiotic resistance and bacterial virulence. We report the synthesis and characterization of GABA-coated AgNPs (GABAAgNPs) using UV–VIS and infrared spectroscopies, zeta potential, X-ray diffraction, and transmission electron microscopy. The interaction between GABAAgNPs and model membranes (large unilamellar vesicles, LUVs) was assessed, revealing the formation of liposomal-bound GABAAgNPs (LPGABAAgNPs). Antimicrobial activity against E. coli ATCC 25922 demonstrated that LPGABAAgNPs exhibit enhanced antibacterial efficacy compared to free GABAAgNPs. These findings suggest that liposomal delivery of GABAAgNPs is a promising approach for optimizing their antibacterial properties. Moreover, incorporating GABA into the nanoparticle system offers the potential to modulate bacterial virulence, providing a multifaceted strategy to combat infection.

Enhancing bone tissue engineering with nanocomposites based on NiO nanoparticles/graphene oxide

Through the creation and characterization of novel poly (L-lactic acid) (PLLA)-based nanocomposites containing graphene oxide (GO), nanocrystalline hydroxyapatite (nano-HAP), and nickel oxide (NiO) nanoparticles, this study seeks to improve the performance of bone tissue scaffolds. Utilizing a casting procedure to create nanocomposites, wet chemical methods were used to synthesize nano-HAP. X-ray diffraction, transmission electron microscopy, and Fourier transform infrared spectroscopy were used to characterize the materials. The nanocomposite comprising 5 % GO + 5 % NiO + 10 % nano-HAP showed a 110 % increase in tensile modulus, a 38 % increase in extension, and a 29 % increase in load-bearing capacity compared to plain PLLA. The results showed a considerable increase in mechanical strength. On the surfaces of the nanocomposite, osteoblast adhesion and proliferation increased by 185 %, according to biological tests. Studies on degradation revealed regulated rates that matched bones' natural mending process while preserving a pH environment that was steady. According to these results, adding nanostructures to PLLA scaffolds improves their mechanical and biological properties considerably, which may lead to therapeutic uses in bone tissue engineering in the future.

Optical and structural transformations in polyethylene terephthalate (PET) films subjected to Ag[formula omitted]-ion implantation and subsequent Au[formula omitted]-ion irradiation

We report on the dual effects of ion implantation and swift heavy ion on the optical and structural characteristics of polyethylene terephthalate (PET) films using UV–Vis spectrophotometry, FTIR and X-ray diffraction measurements. Samples were first implanted with 150 keV Ag+-ions at different fluences of 1 ×1016, 5 ×1016, and 1 ×1017 ions/cm2, and thereafter irradiated with 30 MeV Au7+-ions at different fluences, while analysing elemental depth profile in situ on the Time of Flight Heavy Ions Elastic Recoil Detection (ToF-Hi-ERDA) instrument. The elemental depth profile measurements showed considerable atomic depletion of hydrogen from 36% down to below 6% and oxygen from 18% to about 5%. The proportion of carbon increased from 45% to over 87%. The optical bandgap decreased with increasing ion implantation fluence and reduced even further on irradiation with 30 MeV 197Au7+-ions. The most notable outcome of the implantation was the onset of the precipitation of gold nanoparticles (Au-NPs) in the PET matrix, marked by Localised Surface Plasmon Resonance effects, coincided with a relatively significant drop in the bandgap energy. This latter effect could only be best explained as the result of these Au-NPs in the PET. This suggests that optical bandgap tuning in polymer films, usually achievable through high fluence implantation at low energy (i.e., keV), could also be realized through low fluence irradiation with MeV energy ions. It is surmised that, for the noble metals, NP-induced bandgap modification in PET precludes the need for high fluence to achieve the same. This has the obvious advantage of bandgap alterations at much lower structural damage to the target polymer. As reported by FTIR results, one can observe structural changes with the formation of new chemical bonds on thin films. X-ray diffraction results exhibited one prominent peak corresponding to the (100) plane, which varies in intensity with increased implantation fluence, suggesting a change in the crystallinity of the PET. The decrease in (100) peak or crystallinity was well connected with the presence and decrease of 847, 970, and 1471 cm−1 peaks, which were assigned to the ethylene glycol molecular groups.

Enhanced Propylene/Propane Separation via Aniline-Decorated ZIF-8 Membrane: Lattice Rigidity Adjustment and Adsorption Site Introduction.

Metal-organic framework (MOF)-based membranes excel in molecular separation, attracting significant research interest. The crystallographic microstructure and selective adsorption capacity of MOFs closely correlate with their gas separation performance. Here, aniline was added to the ZIF-8 synthesis in varying concentrations. Aniline, encapsulated within ZIF-8 cavities, interacts strongly with the 2-methylimidazole linker, resulting in both a shift in crystallographic phase from I_43m to Cm in Rietveld refinement of X-ray diffraction (XRD) patterns and the selective adsorption behavior between propylene and propane. Consequently, an aniline decorative ZIF-8 (Anix-ZIF-8) membrane was prepared using a fast current-driven synthesis method, which exhibits good propylene/propane separation selectivity of up to 85. Calculation of the interaction energy between aniline and the various crystallographic phases of ZIF-8 using density functional theory (DFT) further verifies that aniline not only promotes the formation of crystallographic Cm phase, but also enhances the adsorption selectivity of propylene over propane.Aniline modification effectively tunes the crystallographic microstructure of ZIF-8, thereby, improving molecular sieving capabilities.

High-precision alignment techniques for realizing an ultracompact electromagnetic calorimeters using oriented high-z scintillator crystals

Electromagnetic calorimeters used in high-energy physics and astrophysics rely heavily on high-Z inorganic scintillators, such as lead tungstate (PbWO4 or PWO). The crystalline structure and lattice orientation of inorganic scintillators are frequently underestimated in detector design, even though it is known that the crystalline lattice strongly modifies the features of the electromagnetic processes inside the crystal. A novel method has been developed for precisely bonding PWO crystals with aligned atomic planes within 100 μrad, exploiting X-ray diffraction (XRD) to accurately measure miscut angles. This method demonstrates the possibility to align a layer of crystals along the same crystallographic direction, opening a new technological path towards the development of next-generation electromagnetic calorimeters.

NaZr2(PO4)3 - a cubic langbeinite-type sodium-ion solid conductor.

The synthesis of langbeinite-type phosphates with small cations such as Li+ or Na+via a high-temperature solid-state reaction is a challenging task due to the predominant formation of a related NaSICON-type phase. This work reports on the synthesis route, crystal structure, thermal behavior, and Na-conductive properties of the langbeinite-type NaZr2(PO4)3 prepared by a mechanochemically activated ion-exchange reaction between hydrothermally prepared NH4Zr2(PO4)3 and NaNO3. The crystal structure of NaZr2(PO4)3 is refined based on X-ray diffraction data and validated by Fourier-transformed infrared spectroscopy. NaZr2(PO4)3 is found to be stable up to 730 °C, undergoing a transformation into the NaSICON phase with further heating. Notably, in the 25-500 °C range, the material shows negative thermal expansion. The Na+ conductivity within the range of 50-225 °C amounts to 1.7 × 10-8 S cm-1 at 50 °C and 1 × 10-6 S cm-1 at 225 °C with an activation energy of 0.44 eV, accompanied by a sufficiently low (∼10-12 S cm-1) electronic conductivity. The bandgap of 4.44 eV and the electrochemical stability window covering the 1.39-4.18 V vs. Na/Na+ range are calculated using density functional theory. The obtained results open up opportunities for designing langbeinite-structured phosphates as potential solid electrolytes for Na-ion batteries.

Green synthesis of polyethylene glycol coated, ciprofloxacin loaded CuO nanoparticles and its antibacterial activity against Staphylococcus aureus

Antibacterial resistance requires an advanced strategy to increase the efficacy of current therapeutics in addition to the synthesis of new generations of antibiotics. In this study, copper oxide nanoparticles (CuO-NPs) were green synthesized using Moringa oleifera root extract. CuO-NPs fabricated into a form of aspartic acid-ciprofloxacin-polyethylene glycol coated copper oxide-nanotherapeutics (CIP-PEG-CuO) to improve the antibacterial activity of NPs and the efficacy of the drug with controlled cytotoxicity. These NPs were charachterized by Fourier transform infrared spectroscopy (FTIR), x-rays diffraction spectroscopy (XRD), scanning electron microscopy (SEM) and energy-dispersive spectroscopy (EDS). Antibacterial screening and bacterial chemotaxis investigations demonstrated that CIP-PEG-CuO NPs show enhanced antibacterial potential against Gram-positive and Gram-negative clinically isolated pathogenic bacterial strains as compared to CuO-NPs. In ex-vivo cytotoxicity CIP-PEG-CuO-nano-formulates revealed 88% viability of Baby Hamster Kidney 21 cell lines and 90% RBCs remained intact with nano-formulations during hemolysis assay. An in-vivo studies on animal models show that Staphylococcus aureus were eradicated by this newly developed formulate from the infected skin and showed wound-healing properties. By using specially designed nanoparticles that are engineered to precisely transport antimicrobial agents, these efficient nano-drug delivery systems can target localized infections, ensure targeted delivery, enhance efficacy through increased drug penetration through physical barriers, and reduce systemic side effects for more effective treatment.

Expanding the Landscape of Phosphorous-Based Open Shell Species: Stable Mono-, Di-, and Trianionic Radicals Based on a Contorted Triphosphaalkene.

The stepwise reduction of the highly contorted truxene-based triphosphaalkene 1 using KC8 led to the isolation of mono-, di-and tri-anionic species. The solid-state molecular structures of mono- and diradical anionic species were elucidated by single crystal X-ray diffractions, revealing elongated P-C bonds and a pronounced "indene" aromatization compared to the parent system. All three radical species displayed distinct Electron Paramagnetic Resonance (EPR) spectra, providing compelling evidence for the open-shell electronic configuration of both the diradical and triradical species-an observation unprecedented in any previously reported phosphorous-based anionic polyradicals. Mulliken spin density calculations revealed a dominant localization of radical spin on a single phosphorous atom in the monoanion. In the dianion, spin localization is observed on two phosphorous atoms (~34% each), with a minor contribution from the third phosphorous (0.13%), while the trianion demonstrates a uniform distribution of spin density (~30%) across each phosphorous atom.

Research on high-strength and rapid-hardening magnesium phosphate as a novel bonding material for limestone artifacts

Due to natural erosion and human interference, limestone artifacts often suffer from cracks and gradual detachment. There is a critical need for new bonding materials that possess excellent aging resistance and high compatibility with the artifact substrates. This study investigates the effects of varying proportions of citric acid (CA) and borax (B) as composite retarders on the fundamental properties of magnesium phosphate cement (MPC). Through the application of X-ray diffraction techniques and cold field emission scanning electron microscopy, this research elucidates the mechanisms by which the retarders affect MPC. It was found that a 5 % addition of CA and B significantly reduces the hydration temperature during the early stages of MPC setting, enhances the unconfined compressive strength (reaching 44.3 MPa at 28 days), and allows for controllable setting times (17 minutes). Additionally, the presence of CA was found to delay crystal growth, resulting in an increased quantity of the amorphous phase and higher density of MPC. The optimal MPC formulation was selected as a bonding and repair material for limestone artifacts. For comparative analysis, traditional glutinous rice lime mortar (GL) and commercially available epoxy resin (EP) were tested under wet-dry cycling and UV aging conditions. Results indicated that EP materials demonstrated significant aesthetic incompatibilities and progressive cracking and detachment as aging tests progressed. GL materials exhibited significantly lower bonding strength compared to EP and MPC. In contrast, MPC displayed excellent aging resistance, moderate bonding strength, and a Shore hardness value closely matching that of the limestone substrates. Therefore, high-strength, rapid-hardening MPC represents a valuable and forward-looking solution for the conservation of limestone artifacts.

Evolution mechanism of coal chemical structure after supercritical CO2 transient fracturing

This study investigates the chemical structural evolution of coal during supercritical CO2 transient fracturing using a self-developed experimental platform. Coal samples with different metamorphic ranks were subjected to transient fracturing under different pressures. Characterization techniques, including X-ray diffraction, Raman spectroscopy, and Fourier transform infrared spectroscopy, analyzed the fractured coal samples. Initially, supercritical CO2 dissolved minerals and non-aromatic structures, rearranging organic compounds. As fracturing intensified, alkanes and substituents rapidly released, causing large aromatic rings to break into smaller ones. The breakage of small aromatic rings created pores and increased aromatic structure dimensions. Moreover, the interaction between fractured small aromatic rings and oxygen atoms in the C=O group facilitated the formation of new C–C bonds, promoting the connection of aromatic rings to form larger structures. In the early stages of fracturing, the molecular structure of coal relaxed, and subsequently, as the fracturing intensified, the hydrogen bonds initially broken could reconnect to aromatic structures to form OH-π interactions, enhancing intermolecular attraction. This promoted molecules to be more inclined to form stable, dense structures. Understanding this evolution mechanism aids in analyzing the transformation of fractured coal pores, thereby enhancing our understanding of the mechanism for improving coal seam permeability using this technology.

Synchrotron Microfocus Wide-Angle X-ray Scattering Reveals the Evolution of Radial Microstructural Heterogeneity in γ-Irradiated/Heated Polyacrylonitrile Fibers

Synchrotron Microfocus Wide-Angle X-ray Scattering Reveals the Evolution of Radial Microstructural Heterogeneity in γ-Irradiated/Heated Polyacrylonitrile Fibers

Formation of Uranyl Peroxide Compounds via Dissolution of Studtite, [(UO2)(O2)(H2O)2](H2O)2, in Ionic Liquids.

Four uranyl peroxide compounds with novel structures were formed following the dissolution of studtite, [(UO2)(O2)(H2O)2](H2O)2, in imidazolium-based ionic liquids. The compounds were characterized using single crystal X-ray diffraction (SCXRD), powder X-ray diffraction (PXRD), Raman and infrared (IR) spectroscopy, and scanning electron microscopy (SEM) with energy-dispersive X-ray spectroscopy (EDS). The ionic liquids used in the experiments were 1-ethyl-3-methylimidazolium (EMIm) diethyl phosphate, EMIm ethyl sulfate, and EMIm acetate. Each of the four uranyl peroxide compounds contain components from the ionic liquids as terminal ligands on uranyl peroxide molecular units, bridging ligands in uranyl peroxide sheet structures, or charge balancing cations located in the interstitial space. The studtite dissolved in and reacted with the ionic liquids, producing unique crystal structures depending on the anionic component of the ionic liquid, the temperature at which the synthesis was performed, and the introduction of additional ionic species into the solution. This is the first report of studtite dissolving in and reacting with ionic liquids to form uranyl peroxide compounds, which has the potential to vastly increase the number of synthetic routes for the formation of uranyl peroxide clusters and uranyl peroxide cage clusters.

Evaluation of cytotoxic potential of silver nanoparticles biosynthesized using essential oils of Jasminum sambac against breast cancer and bacterial cells.

Essential oils (EOs) which cover about 91% whole biomolecules formulated from Jasminum sambac leaves based on Gas chromatography-mass spectrometry were employed to identify structures. EOs were observed as good agents in the preparation of Silver nanoparticles (AgNPs) through the proposed mechanism that was attempted to interpret the pathway of the bio-preparation process. The characterization of EOs-AgNPs carried via ultraviolet-visible to reveal surface plasmon resonance at 420nm, Fourier transform infrared to observe functional groups EOs compared to EOs-AgNPs. X-ray diffraction (XRD) revealed a broad chart owing to the small size of AgNPs in average size less than 10nm calculated relying on image J software, spherical AgNPs with a small dispersive size observed by transmission electron microscopy. Quasi near spherical surface morphology of EOs-AgNPs had detected by field emission scanning electron microscope. EOs-AgNPs were assessed for their antibacterial potential against both Gram-positive (Staphylococcus aureus) and Gram-negative (Escherichia coli) bacteria as suppressing bacterial agents. EOs-AgNPs had their anti-breast cancer MCF-7 cell line ability investigated by DNA fragmentation; cycle flow cytometry (apoptosis) at half maximal inhibitory concentration (IC50) was determined at 260µg/mL which has been stated by cytotoxicity (MTT) assay. EOs-AgNPs have antibacterial and anticancer therapeutic potential, and it is safe, inexpensive, and scalable in the nanoscale range.

Polyphosphate-Mediated Crystallographic and Colloidal Stabilization of CuS Nanoparticles: Enhanced NIR-Responsive Chemo-Photothermal Efficacy.

Photothermal therapy (PTT) is an emerging treatment modality for cancer management. However, the photothermal agents (PTAs) used in PTT should have sufficient biocompatibility, water dispersibility, and good photoresponsive. In this aspect, water-dispersible and biocompatible linear polyphosphate (LP)-functionalized CuS nanoparticles (LP-CuS NPs) were developed using sodium tripolyphosphate (LP molecule) as a surface passivating agent. The successful formation of the green covellite CuS phase was confirmed by X-ray diffraction and TEM analyses, and its surface functionalization with the LP ligand was evident from X-ray photoelectron spectroscopy, Fourier transform infrared, thermogravimetric analysis, and light scattering measurements. It has been found that the use of LP not only stabilizes the crystallographic covellite CuS phase by overcoming the requirement of a soft ligand but also provides long-term aqueous colloidal stability, which is essential for PTT applications. The aqueous suspension of LP-CuS NPs showed excellent heating efficacy under near infrared (NIR) light irradiation (980 nm) and has a strong binding affinity towards anticancer drug, doxorubicin hydrochloride (DOX). The drug-loaded systems (DOX@LP-CuS NPs) revealed a pH-dependent drug release behavior with higher concentrations in a mild acidic environment. The in vitro studies showed substantial cellular uptake of DOX-loaded systems in cancer cell lines and enhanced toxicity towards them upon irradiation of NIR light through apoptotic induction, suggesting their potential application in chemo-photothermal therapy.

Synthesis and Characterization of Coconut-Derived Graphene Nano Sheet (GNS) and Its Properties in Nickel/GNS and Zinc/GNS Hybrid Electrodes

This study introduces a sustainable method of producing a graphene nano sheet (GNS) from coconut shells and investigates its application in GNS, Ni/GNS, and Zn/GNS electrodes for advanced energy storage devices. The GNS was synthesized in a scalable manner using a pyrolysis and impregnation technique, with its successful synthesis verified by X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDX), Raman spectroscopy, and electrical conductivity measurement characterizations. The study highlights the enhanced performance of Zn/GNS electrodes, which outperform both pure GNS and Ni/GNS variants. This superior performance is attributed to the smaller particle size of Zn (mean = 2.356 µm) compared to Ni (mean = 3.09 µm) and Zn’s more favourable electron configuration for electron transfer. These findings demonstrate the potential of bio-derived GNS composites as efficient, high-performance electrodes, paving the way for more sustainable and cost-effective energy storage solutions.

Thermoluminescence properties of β-ray irradiated LuAGG:Ce nanophosphors prepared by sol-gel method for potential applications in dosimetry

In this paper, Lu2.97Al5–xGaxO12:Ce0.03 (x = 0, 1, 2, 3) nanophosphors were synthesized using sol-gel method and calcined at 1100 °C for 3 h. The effect of Ga content on the structural, photoluminescence (PL), and notably thermoluminescence (TL) glow curve, dose response, repeatability and fading properties were investigated. X-ray diffraction (XRD) results indicated that all synthesized samples were crystallized in a pure garnet phase. The PL emission spectra exhibited a broad emission band corresponding to the 5 d → 4f (2F5/2, 2F7/2) transition of Ce3+ ions in the garnet lattice. Furthermore, a significant decrease in emission intensity was observed upon increasing Ga content. The TL characteristics of nanopowders irradiated with β-rays revealed a significant effect of Ga content on the peak position, shape and intensities of TL Glow curves, which can be explained by the reduction of the energy gap and the distribution of trap levels. The dose response linearity in the range of 0.125–100 Gy was examined for different Ga content, revealing a good linear behavior for x = 0 and 1 Ga. Additionally, samples prepared with x = 0, 1, and 2 Ga exhibited a high level of repeatability across a batch of 10 samples. Also, fading studies were performed for 128 h and revealed strong fading in samples synthesized with x = 0 and 1 Ga. These results suggest potential applications of Lu3Al5O12:Ce and Lu3Al4Ga1O12:Ce in ionizing radiation dosimetry.