Crystalline Morphology Research Articles

Dual‐Site Anchors Enabling Vertical Molecular Orientation for Efficient All‐Perovskite Tandem Solar Cells

AbstractAll‐perovskite tandem solar cells (TSCs) are gaining increasing attention due to their potential to surpass the efficiency limit of single‐junction solar cells. However, as the bottom low‐bandgap subcells, tin‐lead (Sn‐Pb) perovskites suffer from severe nonradiative recombination at the interfaces due to their susceptibility to oxidation and poor crystalline morphology. Here a surface modifier 4‐(trifluoromethyl)benzhydrazide (TFH) is reported to construct a reductive chemical environment on the surface of perovskite films and protect them from water and oxygen erosion. TFH anchors onto the Sn‐Pb perovskites in a preferred vertical orientation through dual‐site binding, forming interface dipoles that facilitate charge extraction. The reductive hydrazine groups of TFH can effectively inhibit the oxidation of Sn2+ and I−, thereby reducing the defect density and energy disorder of Sn─Pb perovskites. Consequently, the TFH‐treated devices achieved a champion PCE of 22.88%, maintaining over 93% of the initial efficiency after continuous one‐sun illumination for 500 h. Combined with a 1.79 eV wide‐bandgap subcell, it has demonstrated a PCE of 28.17% in all‐perovskite TSCs.

Low-cost bacterial cellulose production from agricultural waste for antibacterial applications

Various carbon sources can be utilized for the biosynthesis of bacterial cellulose (BC), with agricultural wastes being explored as sustainable options. In this study, glucose was extracted from bamboo dust via mild acid hydrolysis to prepare a modified medium combining extracted glucose with Hestrin-Schramm (HS) medium for BC biosynthesis using Acetobacter xylinus NCIM 2526. Chitosan, a biopolymer, was incorporated into the BC synthesis medium at concentrations of 0.2%, 0.6%, and 1% (w/v) after 2 days of shaking incubation, producing chitosan-incorporated BC membranes through in situ synthesis. Fourier transform infrared (FTIR) spectroscopy confirmed cellulose in the BC produced from the modified medium and chitosan in BC membranes with 0.2% and 0.6% (w/v) chitosan. Changes in physical and crystalline morphology were further characterized by scanning electron microscopy (SEM) and X-ray diffraction (XRD) analysis. The purity of cellulose was validated through chemical solubility tests, while energy-dispersive X-ray (EDX) analysis confirmed the presence of chitosan in the BC membranes. The average yields were 5.8 ± 0.21 g/l for pure BC, 5.2 ± 0.21 g/l for BC with 0.2% (w/v) chitosan, and 4.6 ± 0.21 g/l for BC with 0.6% (w/v) chitosan after 7 days. The medium with 1% (w/v) chitosan did not produce BC membranes. BC synthesized with 0.2% chitosan exhibited similar physical and chemical properties to pure BC and demonstrated good antimicrobial properties, suggesting its potential use in bandages and wound dressings.

Effects of Al doping on structural, optical, morphological, and low-concentration CO2 gas sensing properties of ZnO nanoparticles synthesized by sol-gel method

Abstract This work examines the morphological, structural, optical, and gas-sensing characteristics of ZnO thin films doped with Al that were created by the sol-gel spin coating technique. The thin films, doped with varying aluminum concentrations (0%, 2%, and 5%), were characterized using XRD, UV-visible spectroscopy, and FE-SEM to assess their crystallinity, band gap, and surface morphology. XRD analysis confirmed the incorporation of Al into the ZnO lattice without forming secondary phases, while UV-visible spectroscopy revealed an increase in transmittance and band gap with higher Al doping. FE-SEM images showed a transition from agglomerated grains to smoother surfaces with increased Al content. Gas sensing performance was evaluated using low-concentration CO2 as the target gas. The results demonstrated that Al doping significantly enhances the CO2 sensing response, with the 5% Al-doped ZnO exhibiting the optimal sensitivity due to increased carrier concentration and improved surface interaction. These findings suggest that Al-doped ZnO thin films are promising candidates for efficient CO2 gas sensors, combining enhanced structural and optical properties with superior gas sensing capabilities.

Elucidation of crystalline morphology, crystallinity and mechanical properties of carbon fibre/PEEK composites under different cooling rates

Elucidation of crystalline morphology, crystallinity and mechanical properties of carbon fibre/PEEK composites under different cooling rates

Breaking New Grounds: solid-state synthesis of TiO2 – La2O3 – CuO Nanocomposites for degrading Brilliant Green dye under Visible Light

Environmental pollution, particularly from industrial dyes and chemicals, poses a significant threat to ecosystems and human health. Traditional pollution mitigation methods are often inefficient and costly. Photocatalysis has emerged as a promising solution for degrading pollutants using light energy. Titanium dioxide (TiO2) is a widely studied photocatalyst due to its stability, non-toxicity, and strong oxidative power. However, its efficiency is limited by a wide bandgap, restricting absorption to the UV region, and rapid electron-hole recombination. To address these limitations, doping TiO2 with materials like La2O3 and CuO has been explored to enhance its photocatalytic activity under visible light. This study investigates the enhancement of TiO2 nanocomposites by incorporating La2O3 and CuO. X-ray diffraction (XRD) revealed that the nanocomposites retained TiO2's anatase and rutile phases with improved crystallinity. Scanning electron microscopy (SEM) displayed spherical nanoparticles forming agglomerates, typically due to high surface energy. Energy-dispersive X-ray spectroscopy (EDS) and X-ray photoelectron spectroscopy (XPS) confirmed the presence of La and Cu in the TiO2 matrix. Fourier-transform infrared (FTIR) spectroscopy identified characteristic vibrational modes of Ti–O, La–O, and Cu–O bonds, suggesting strong chemical interactions between dopants and TiO2 lattice. Ultraviolet-visible (UV-Vis) spectroscopy showed a red shift in absorption spectra with La2O3 and CuO addition, reducing the bandgap energy from 3.23 eV (pure TiO2) to 2.27 eV for the TiO2–0.1La2O3–0.2CuO composite. Photoluminescence (PL) spectroscopy indicated improved charge separation and reduced electron-hole recombination rates in the synthesized nanocomposites. Photocatalytic performance was evaluated by degrading Brilliant Green (BG) dye under visible light. The TiO2–0.1La2O3–0.2CuO (TLC0.2) nanocomposite achieved a maximum dye degradation of over 95% after 204 minutes under optimal conditions (C0 = 17 mg/L and a S/L ratio of 1 g/L). Adding the inorganic agent Na2SO4 to this process significantly enhanced photocatalytic activity, increasing degradation from 56% to 95% after 180 min of visible light irradiation under C0 = 20 mg/L and S/L = 0.5 g/L conditions, as it shows a high stability after six reuse cycles. In conclusion, La2O3 and CuO doping significantly enhance TiO2 nanocomposites' crystalline structure, morphology, optical properties, and photocatalytic efficiency, demonstrating their potential for environmental remediation and solar energy conversion.

Exploring the Structural and Optical Properties of MoSe2 for Solar Cell Performance

Abstract Efficient energy absorption is critical in perovskite solar cells (PSCs) for effective electron collection and mitigation of hole migration. Molybdenum diselenide (MoSe2) was produced using a simple hydrothermal process and subsequently studied for its structural and optical properties using various techniques, including XRD, RAMAN, FESEM, EDX, UV-Visible, BET, and XPS. The results show that the enhanced crystalline morphology, size, optical band gap, and surface area demonstrate promising attributes for solar cell applications. Furthermore, the I-V investigation reveals that MoSe2-based PSCs achieve a notable efficiency of electricity conversion is 7.97%. The increased performance is because of the greater surface area of MoSe2. which facilitates increased light absorption, and its ability to accelerate charge transfer within the electron transport layer. Moreover, the structural integrity of MoSe2 contributes significantly to its efficacy in converting solar energy into electrical energy. These findings underscore MoSe2 as a compelling candidate for advancing solar cell technologies, offering potential pathways for achieving higher efficiency and reliability in future solar energy systems.

Fabrication, characterization, and fat substitution application in chocolate spreads of methyl cellulose and xanthan gum foam-templated oleogels.

Food-grade oleogels were prepared by lyophilizing the foam-template of methyl cellulose (MC) and xanthan gum (XG). The cryogels prepared using MC exhibited low density, high porosity and firmness, as well as high oil absorption capacity (OAC) and oil binding capacity (OBC). Furthermore, the addition of XG improved properties of cryogels. As the concentrations of MC and XG were incremented, notable enhancements in the cryogels' density and firmness were observed, accompanied by a corresponding decrease in porosity. Upon attaining MC concentration of 1.2 % and XG concentration of 0.3 %, the OBC of the cryogels surpassed 90 %. SEM images revealed that the cryogels possessed a dense and highly uniform porous network structure. Furthermore, oleogels formulated using the higher viscosity variant of MC (designated as MC3) exhibited greater firmness and apparent viscosity, resulting in the formation of a robust network structure that demonstrated excellent thermal stability. The incorporation of oleogels into chocolate spreads significantly enhanced textural and rheological characteristics, while simultaneously decreasing their enthalpy of crystallization. Notably, the partial substitution of these oleogels in the spreads yielded a crystalline morphology that was indistinguishable from those prepared solely with saturated fats, indicating a successful integration and preservation of desirable structural attributes.

Biochar as a UV Stabilizer: Its Impact on the Photostability of Poly(butylene succinate) Biocomposites.

In the present study, biocomposite materials were created by incorporating biochar (BC) at rates of 1, 2.5, and 5 wt.% into a poly(butylene succinate) (PBSu) matrix using a two-stage melt polycondensation procedure in order to provide understanding of the aging process. The biocomposites in film form were exposed to UV irradiation for 7, 14, and 21 days. Photostability was examined by several methods, such as Fourier transform infrared spectroscopy (FTIR), which proved that new carbonyl and hydroxyl groups were formed during UV exposure. Moreover, Differential Scanning Calorimetry (DSC) measurements were employed to record the apparent UV effect in their crystalline morphology and thermal transitions. According to the molecular weight measurements of composites, it was apparent that by increasing the biochar content, the molecular weight decreased at a slower rate. Tensile strength tests were performed to evaluate the deterioration of their mechanical properties during UV exposure, while Scanning Electron Microscopy (SEM) images illustrated the notable surface alternations. Cracks were formed at higher UV exposure times, to a lesser extent in PBSu/BC composites than in neat PBSu. Furthermore, the mechanism of the thermal degradation of neat PBSu and its biocomposites prior to and upon UV exposure was studied by Pyrolysis-Gas Chromatography/Mass Spectrometry (Py-GC/MS). From all the obtained results it was proved that biochar can be considered as an efficient UV-protective additive to PBSu, capable of mitigating photodegradation.

Investigating the influence of RF power on the surface morphological and optical properties of sputtered TiO2 thin films

Thin films of titanium dioxide (TiO2), with thicknesses ranging from 105 to 231 nm, were deposited on glass substrates using radio-frequency (RF) magnetron sputtering in an argon atmosphere at four distinct RF power levels: 40, 70, 100, and 130 W, with the deposition time kept constant. The crystalline structure, surface morphology and optical and semiconductor properties of the obtained films were analyzed using X-ray diffraction (XRD), Atomic Force Microscopy (AFM) and UV–visible transmittance spectroscopy. These analyses revealed that the crystallinity of the films improves with increasing RF power, corresponding to an increase in film thickness. Consequently, the samples transition from poorly crystalline or amorphous structure to a monocrystalline rutile phase with a (110) texture. However, at the highest RF power studied, this texture is partially disrupted by the formation of nanocrystals with different orientations. The surface roughness exhibited multifractal characteristics, with complexity systematically decreasing and surface stiffness reducing as RF power increased. Refractive indices and optical band gap energies were determined using the Swanepoel and Tauc plot methods, respectively. The films exhibited a notable increase in the refractive index and a decrease in the optical band gap, from 3.81 eV to 3.52 eV, as the RF power was increased. This underscores the influence of RF power on the optical and semiconductor properties of TiO2 films.

Hybrid Pd0.1Cu0.9Co2O4 nano-flakes: a novel, efficient and reusable catalyst for the one-pot heck and Suzuki couplings with simultaneous transesterification reactions under microwave irradiation.

We report the fabrication of a novel spinel-type Pd₀.₁Cu₀.₉Co₂O₄ nano-flake material designed for Mizoroki-Heck and Suzuki coupling-cum-transesterification reactions. The Pd₀.₁Cu₀.₉Co₂O₄ material was synthesized using a simple co-precipitation method, and its crystalline phase and morphology were characterized through powder XRD, UV-Vis, FESEM, and EDX studies. This material demonstrated excellent catalytic activity in Mizoroki-Heck and Suzuki cross-coupling reactions, performed in the presence of a mild base (K₂CO₃), ethanol as the solvent, and microwave irradiation under ligand-free conditions. Notably, the Heck coupling of acrylic esters proceeded concurrently with transesterification using various alcohols as solvents. The catalyst exhibited remarkable stability under reaction conditions and could be recycled and reused up to ten times while maintaining its catalytic integrity.

Rapid Thermal-Driven Crystal Growth and Defect Suppression in Antimony Selenide Thin Film for Efficient Solar Cells.

Antimony selenide (Sb2Se3) has demonstrated considerable potential and advancement as a light-absorbing material for thin-film solar cells owing to its exceptional optoelectronic characteristics. However, challenges persist in the crystal growth, particularly regarding the nucleation mechanism during pre-selenization process for Sb2Se3. The defects originating from this process significantly impact the quality of the absorber layer, leading to the degradation in the power conversion efficiency (PCE) of the device. Herein, the evolution of pre-selenization using rapid thermal processing (RTP) on the crystallization quality of Sb2Se3 film is systematically investigated. By optimizing the initial nucleation process during pre-selenization, resulting in a reduction of grain boundaries and nucleation centers, the Sb2Se3 thin films demonstrate enhanced crystallinity and pinholes-free morphology. It is found that the improved quality of the grain interior and interfaces of the Sb2Se3 absorber can mitigate intrinsic defects within the bulk layer, and passivate interfacial defect recombination. As a result, the short circuit current density (JSC) is elevated to 28.97mA cm-2, and a competitive efficiency of 9.03% is achieved in Sb2Se3 device. This study provides comprehensive insight into the process of crystal growth and the mechanism for defect suppression, which holds guiding significance for advancing photovoltaic performance.

Novel Al/CoFe/p-Si and Al/NiFe/p-Si MS-type photodiode for sensing

CoFe and NiFe are used in the construction of Si-based metal-semiconductor-type photodiodes. Thin film layers are sputtered onto thep-Si surface where Al metal contacts are deposited using the thermal evaporation technique. Film characteristics of the layers are investigated with respect to the crystalline structure and surface morphology. Their electrical and optical properties are investigated using dark and illuminated current-voltage measurements. When these two diodes are compared, Al/NiFe/p-Si exhibits better rectification properties than Al/CoFe/p-Si diode. There is also a high barrier height where these values for both diodes increase with illumination. According to the current-voltage analysis, the existence of an interlayer causes a deviation in diode ideality. In addition, the response to bias voltage, the derivation of electrical parameters, and the light sensitivity of diodes are evaluated using current-voltage measurements under different illumination intensities and also transient photosensitive characteristics.

Facile synthesis of polyester-polyether block copolyols for the sustainable high-performance polyurethane reactive hot melt adhesives

The presence of polyols with both polyester and polyether structures in polyurethane enhances bonding strength and facilitates easy curing. In this study, polyester-polyether block polyols with varying molecular weights (2500–3500) were synthesized through ring-opening polymerization (ROP) using l-lactide (LA) and ε-Caprolactone (CL). The chemical structure of the polyols was characterized using 1H nuclear magnetic resonance (1H NMR), Fourier transform infrared (FTIR), and gel permeation chromatography (GPC). Differential scanning calorimetry (DSC) and polarized optical microscopy (POM) were employed to examine the crystalline morphology of the polyols. Subsequently, the synthesized polyols were combined with 4,4′-diphenylmethane diisocyanate (MDI) and other additives to prepare polyurethane reactive hot melt adhesives. It was observed that, in PCL-based polyurethane reactive hot melt adhesives, increasing the molecular weight of the polyols resulted in improved crystalline morphology, increased lap shear strength and tensile strength, and enhanced thermal stability. On the other hand, PLA-based polyurethane reactive hot melt adhesives exhibited low bonding strength and lacked practical application value due to the poor toughness of PLA. Interestingly, the bonding strength and tensile strength of PLA-based polyurethane reactive hot melt adhesives improved when physically blended with PCL-based polyurethane reactive hot melt adhesives. These polyols offer a novel approach for utilizing LA and CL in adhesive applications.

Innovative upcycling cigarette filters into high-performance cellulose nanofiber-epoxy composites

This research introduces a novel upcycling method for transforming cigarette filters—an abundant and persistent environmental waste—into high-performance epoxy composites reinforced with cellulose nanofibers. The innovation lies in extracting cellulose acetate nanofibers from used cigarette butts via a multi-step purification and electrospinning process, followed by their conversion into regenerated cellulose nanofibers through alkaline hydrolysis. This dual-fiber approach allows us to fabricate four distinct epoxy composites, each reinforced by different nanofiber types: recycled cellulose acetate nanofibers, regenerated cellulose nanofibers from recycled cigarette filters, and their commercial counterparts. Notably, this is the first time regenerated nanofibers derived from waste cigarette filters have been utilized for epoxy composite reinforcement, demonstrating a sustainable, high-value use for a major pollutant. Comprehensive characterizations, including FTIR, XRD, SEM, and contact angle measurements, confirmed the successful regeneration of cellulose nanofibers, showing improved hydrophilicity, reduced crystallinity, and uniform nanofiber morphology with diameters between 200 and 300 nm. The innovation further extends to the mechanical performance of these composites: tensile tests revealed that those reinforced with regenerated cellulose nanofibers exhibited superior tensile strength (49.5–53.8 MPa), significantly outperforming both cellulose acetate nanofiber composites (40.1–42.6 MPa) and neat epoxy resin (31.4 MPa). This marked improvement is attributed to enhanced nanofiber dispersion and interfacial adhesion within the epoxy matrix, an essential advancement over traditional composites. In addition, thermal analysis showed that all composites maintained thermal stability in the 300–400 °C range, comparable to commercial alternatives. The regenerated nanofiber-reinforced composites also displayed enhanced optical transparency due to reduced light scattering, making them ideal candidates for applications requiring both mechanical strength and optical clarity. By pioneering the use of cigarette filter waste for fabricating advanced cellulose nanofiber composites, this study presents an eco-friendly approach to addressing environmental pollution while creating sustainable materials with superior mechanical, thermal, and optical properties.

Titanate Nanotubes Coated with Ag Nanoparticles: Effects of Annealing Temperature on Crystalline Structure, Morphology, and Photocatalytic Activity

Titanate Nanotubes Coated with Ag Nanoparticles: Effects of Annealing Temperature on Crystalline Structure, Morphology, and Photocatalytic Activity

Cross‐referenceable microscopic and micro‐spectroscopic analysis of fiber reinforced thermoplastics

AbstractThis study aims at the assessment of damage on crystallinity of fiber reinforced thermoplastic (FRTP) composites resulting from mechanical polishing to demonstrate a novel methodology enabling comprehensive crystalline structural characterization. Investigating the crystalline structure is relevant for understanding the relationship with the mechanical properties. In a previous study, FRTPs have successfully been processed to the thickness of 5 μm or below via an innovative polishing strategy, which for the first time visualized the crystalline morphologies by polarized optical microscopy. Analyzing these sections via micro‐Raman and micro‐infrared spectroscopies facilitate the quantification of these structure. However, no study reports on the correct interpretation of FRTP data appropriately considering the damage resulting from mechanical polishing to date. Herein, we report fundamental knowledge on this aspect via detailed Raman micro‐spectroscopic investigations to demonstrate our novel strategy. Four types of FRTPs with major matrix resins (GF/PBT, CF/PA6, CF/PEEK and GF/PP) were analyzed and the damage on both polished cross‐sections, prepared by traditional process, and the thin sections was confirmed to be approx. 1%–2% crystallinity, which solidified the credibility of the obtained analytical data. Then, the newly established methodology of ‘cross‐referenceable microscopic and micro‐spectroscopic analyses for FRTPs’ was applied for comprehensive crystalline structural characterization.Highlights Cross‐sectioning and thin‐sectioning of FRTPs. Evidencing of damage on the crystallinity resulting from mechanical polishing. Equations to convert Raman spectral data into crystallinity. Strategy for considering the anisotropy of Raman measurements. Practical application of novel microscopic and micro‐spectroscopic strategies.

Improved in-situ characterization for the scaling-induced wetting in membrane distillation: Unraveling the role of crystalline morphology

Despite being recognized as a promising technique for treating high salinity water, membrane distillation (MD) has been plagued by the scaling of sparingly soluble salts. The growth of crystals can not only create additional resistance to evaporating water at the feed-membrane interface, but also alter the hydrophobic network to bridge the feed and distillate (i.e., result in the phenomenon of wetting). When recognizing the uncertain behaviors of calcium sulfate (CaSO4) scaling in MD, this study was motivated to ascertain whether the crystal-membrane interactions could be dependent on the variation in crystalline morphology. In particular, optical coherence tomography (OCT) was employed to characterize the scaling-induced wetting via a direct-observation-through-the-membrane (DOTM) mode, which mitigated the effects of developing an external scaling layer on resolving the crystal-membrane interactions. The improved in-situ characterization suggests that the crystalline morphology of CaSO4 could be effectively regulated by varying the stoichiometry of crystallizing ions; the richness of calcium in the aqueous environment for crystallization would be in favor of weakening the crystal-membrane interactions. The stoichiometry-dependent growth of CaSO4 crystals can be exploited to develop an effective strategy for preventing the hydrophobic network from being wetted or irreversibly damaged.

Facile synthesis of transition metal-selenides@CNTs for electrochemical oxygen evolution reactions

The fabrication of carbon based efficient electrocatalysts for hydrogen production during electrochemical water splitting could be a great achievement to fulfill the future renewable energy demand. In this study, one-step hydrothermal process was used to develop composites of multi-metal selenides with carbon nanotubes (MnSe@CNTs, MnCuSe@CNTs, MnCoNiSe@CNTs) as electrocatalysts for OER during electrolytic water splitting. XRD and SEM with EDS analysis confirm the successful fabrication of proposed catalyst and their crystalline morphology. Among the synthesized functionalized CNTs composites, bimetallic selenide composite gives a better electrocatalytic activity with the reduce overpotential, lower Tafel slope and reduced charge transfer resistance in 1 M KOH. By using this catalyst, water oxidation starts at 1.4 V onset potential with a very low overpotential of 245 mV and the Tafel slope was only 107 mV dec−1. Metal based selenides composites with CNTs introduces a lot of active sites, subsequent nanoparticles of MnSe, MnCuSe, & MnCoNiSe, causes to boost the surface area and electrocatalysis towards oxygen evolution reactions.

Biological activity of MgO nanoparticle synthesis by plasma-assisted reduction method

In the current report, MgO nanoparticles are synthesized by the plasma-assisted reduction method. This method is eco-friendly due to its safety, not use of toxic reducing agents, low cost, and rapid synthesis. Several techniques were employed to determine the crystalline size, particle size, morphology, elemental analysis, and optical properties of the MgO NPs. MgO nanoparticles had a semi-spherical particle structure with diameters ranging from 30.40 to 39.57 nm. The average crystalline size was measured to be 23.7 nm. An analysis using a UV–vis spectrophotometer reveals that the absorbance of MgO nanoparticles results in a significant peak at 354 nm, indicating an energy band gap of 3.2 eV. Subsequent detailed analysis was performed utilizing Rietveld refinement to accurately determine the crystallographic parameters. Additionally, electron density mapping was scrutinized to provide further insights into the atomic arrangement. The antibacterial and antibiofilm activity of MgO NPs was assessed against Klebsiella pneumoniae, Escherichia coli (gram-negative), and Staphylococcus aureus (gram-positive) bacteria at a dose concentration of 10 mg l−1. The antibacterial activity (zone of inhibition) and inhibition biofilm rate of MgO NPs against S aureus were more effective than those of K peneumoniae and E. coli. Consequently, this investigation demonstrates that the MgO NPs exhibited strong antibacterial properties and exhibited significant potential for the inhibition of pathogenic bacteria.

Green synthesis of CaO nanoparticles from chicken eggshells: antibacterial, antifungal, and heavy metal (Pb2⁺, Cr2⁺, Cd2⁺ and Hg2⁺) adsorption properties

BackgroundChicken eggshells, a common poultry byproduct, are rich in calcium and provide a sustainable source for producing calcium oxide nanoparticles (CaO NPs). Their use in eco-friendly synthesis aligns with the growing emphasis on sustainable materials for environmental and biomedical applications. Objectives: This study develops an eco-friendly method for synthesizing CaO NPs from chicken eggshells, characterizes their physicochemical properties, and evaluates their antibacterial and antifungal activities. It also tests their effectiveness in removing heavy metal ions (Pb2⁺, Cr2⁺, Cd2⁺, and Hg2⁺) from aqueous solutions.MethodsCaO NPs were synthesized by calcining chicken eggshells at 700°C for 7 h. Comprehensive characterization included analysis of crystalline structure, morphology, optical properties, bandgap energy, chemical composition, and thermal stability. Antibacterial and antifungal activities were tested using the well-agar diffusion method. Batch adsorption experiments evaluated heavy metal ion removal under varying conditions of pH, temperature, stirring time, and adsorbent concentrationResultsThe synthesis produced spherical, single-crystal CaO NPs with diameters ranging from 5 to 30 nm and a crystalline size of approximately 20 nm. The nanoparticles had a bandgap energy of about 4.7 eV. Significant antibacterial activity was observed against Staphylococcus aureus, Klebsiella pneumoniae, and Escherichia coli, with increasing inhibition zones correlating with nanoparticle concentration. The CaO NPs also effectively inhibited Candida albicans. For efficient metal ion removal, the optimal conditions were found to be 30 min at pH 6 with 40 mg of CaO NPs at 25°C, achieving recovery rates of 98% for Pb2⁺, 97% for Cd2⁺, 97% for Cr2⁺, and 97% for Hg2⁺. For near-complete removal, extending the process to 70 min at pH 6 with 40 mg of CaO NPs at 45°C achieved the highest recovery rates: 99% for Pb2⁺, 98% for Cd2⁺, 99% for Cr2⁺, and 99% for Hg2⁺, though this approach involves higher energy and cost.ConclusionCaO NPs derived from chicken eggshells are effective antibacterial agents and adsorbents for heavy metal removal. These findings highlight their potential for sustainable applications in environmental and biomedical fields.