Iranian Journal of Materials Science and Engineering

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This study investigates the synthesis of Al/MoS₂ nanocomposite coating by the electro spark deposition (ESD) method for its lubricating properties. ESD method was selected because it is a very easy, rapid, and cost-saving method and the resulting coating has a strong bonding with the substrate. As a substrate, a Ti-6Al-4V alloy sheet containing 6.12 % Al, 4.06 % V, 0.19% Fe, and 0.05 % Ni was used. For coating, an aluminum-molybdenum disulfide composite electrode in the form of a cylindrical rod was employed. Three frequencies of 5, 8, and 11 kHz, three current limits of 15, 25, and 35 amps, and three duty cycles of 50, 60, and 70% were used in the coating operation. AFM analysis was used to study the topography, morphology, and calculate roughness. The samples were then subjected to hardness tests. To determine the wear resistance of the samples, pin on disk tests were performed. XRD analysis was performed to identify the phases on the surface of the coated samples. SEM was used to examine the microstructure of the coating before and after wear testing, in order to determine the wear mechanism. The results indicated that the Al/MoS2 nanocomposite coating was synthesized on the substrate surface. The hardness of the reference sample is 353 Vickers, and that of the coated samples is about 200 Vickers. For the reference sample, the roughness was measured at 15.7 nm, and for the coated sample at 268.1 nm. As spark energy increased, the coefficient of friction increased by approximately 0.09. As spark energy increased, the wear rate increased by 27%. A significant increase in the Lancaster coefficient occurred around 5 joules of energy. According to the wear rate results, the sample with the lowest thickness wears 4% less than the sample with the highest thickness. The wear rate of sample 351170 is 78% lower than that of sample 150550.

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The present study used a hydrothermal technique to synthesize undoped and Mn2+ doped CdS/Zn3(PO4)2 semiconducting nanocomposite materials. Powder X-ray diffraction, scanning electron microscopy, UV-Vis diffuse reflectance spectrometer, Fourier transform-Infrared Spectroscopy-FT-IR, and photoluminescence techniques were employed to study structural, optical, and luminescence properties of produced nanocomposites. The hexagonal structure of CdS and the monoclinic structure of Zn3(PO4)2 are both reflected in the powder X-ray diffraction spectra. When Mn2+ ions are present in the host lattice, a lattice distortion occurs, causing a phase change from the phase of γ-Zn3(PO4)2 to the β-phase of Zn3(PO4)2, without affecting the hexagonal phase of CdS. The average crystallite size of produced nanocomposites was 22-25 nm, and also calculated the lattice strain and dislocation density to better understand internal deformation of the samples. The FT-IR spectra were used to investigate the molecular vibrations and functional groups in the samples. The surface morphology of the nanocomposites is hexagonal spheres on rectangular shaped nano-flakes, and the interatomic distance between the hexagonal spheres is decreased as the doping concentration increases, forming a rod-like structure on the flakes. EDAX results confirm the presence of various relevant elements in the prepared samples. The quantum confinement of produced samples reduces as the Mn2+ doping concentration in the host lattice increases. The photoluminescence results demonstrate shallow trapped states due to the transition: d-d (4T1 → 6A1) of the tetrahedrally coordinated Mn2+ states and the impact of Mn2+ ions exhibiting several peaks in the UV-Visible region (365-634 nm) generating RGB (Red, Green, Blue) luminescence. Color coordinates and CCT values were calculated using the CIE diagram, and color correlated temperatures in the range of 2513–7307 K were discovered, which might be used in solid state lighting applications.

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Considering the widespread use of aluminum composites in various industries and the emergence of nanomaterials such as graphene and boron nitrite (BN) with their unique properties, aluminum-based nanocomposite reinforced by the graphene-BN hybrid was fabricated at different percentages. For this purpose, the graphene-BN hybrid was prepared and subjected to wet milling along with the aluminum powder. The mechanical properties of the final nanocomposite which was consolidated using the spark plasma sintering (SPS) method were examined. Aluminum-based composite specimens containing 1 wt.% graphene–0 wt.% BN (AGB1), 0.95 wt.% graphene–0.05 wt.% BN (AGB2), 0.90 wt.% graphene–0.1 wt.% BN (AGB3), and 0.85 wt.% graphene–0.15 wt.% BN (AGB4) were fabricated and compared with non-reinforced aluminum (AGB0). The hardness values of 48.1, 51.1, 56.2, 54.1, and 43.6 Hv were obtained for AGB0, AGB1, AGB2, AGB3, and AGB4, respectively. Additionally, tensile strengths of these specimens were 67.2, 102.1, 129.5, 123.7, and 114.7 MPa, respectively. According to the results of the hardness and tensile tests, it was revealed that the AGB2 specimen had the highest tensile strength (93% higher than AGB0 and 27% higher than AGB1) and hardness (17% higher than AGB0 and 10% higher than AGB1).

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In this study, an epoxy-based nanocomposite reinforced with copper oxide-graphene oxide hybrid was investigated. Initially, the hybrid powder of CuO–GO with a weight ratio of 9:1 was prepared. The hybrid filler with different weight percentages ranging from 0.1–0.5 was used to reinforce the epoxy resin. The prepared samples were analyzed using XRD, FTIR, FESEM, TEM, and tensile testing. According to the XRD results and SEM images, the hybrid powder was successfully prepared, and the mechanical testing results showed an improvement in tensile strength in the composite samples. The best composite sample in terms of tensile strength was the one containing 0.3 wt% of hybrid reinforcement, which exhibited a 73% increase in strength compared to the neat resin sample.

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The present work deals with the effect of Multi-walled Carbon Nanotube (MWCNT) and functionalized (carboxyl and amine) MWCNT on the mechanical properties of the PAEK (Poly Aryl Ether Ketone) polymer composite. The MWCNT and functionalized (carboxyl and amine) MWCNT concentration varied as 0.25, 0.5 and 0.75 weight percentages. Compositeswere prepared by using a melt compounding method using a twin-screw extruder and all testing samples were prepared using an injection molding machine as per American Society for Testing and Materials (ASTM) standards. Samples were tested for tensile strength, impact strength, flexural strength, heat deflection temperature, hardness, and density. There is an increase in the tensile strength, impact strength, flexural strength, and heat deflection temperature, with percentage increase in filler loading up to 0.5 %, followed by decrease in it with higher filler loading. The increase is maximum for amine functionalized MWCNT.

 

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With increasing energy demand and depletion of fossil fuel resources, it is pertinent to explore the renewable and eco-friendly energy resource to meet global energy demand. Recently, perovskite solar cells (PSCs) have emerged as plausible candidates in the field of photovoltaics and considered as potential contender of silicon solar cells in the photovoltaic market owing to their superior optoelectronic properties, low-cost and high absorption coefficients. Despite intensive research, PSCs still suffer from efficiency, stability, and reproducibility issues. To address the concern, the charge transport material (CTM) particularly the electron transport materials (ETM) can play significant role in the development of efficient and stable perovskite devices. In the proposed research, we synthesized GO-Ag-TiO₂ ternary nanocomposite by facile hydrothermal approach as a potential electron transport layer (ETL) in a regular planar configuration-based PSC. The as synthesized sample was examined for morphological, structural, and optical properties using XRD, and UV-Vis spectroscopic techniques. XRD analysis confirmed the high crystallinity of prepared sample with no peak of impurity. The optimized GO-Ag-TiO₂ ETL exhibited superior PCE of 8.72% with J_sc of 14.98 mA.cm^-2 ,V_oc of 0.99 V, and a fill factor of 58.83%. Furthermore, the efficiency enhancement in comparison with reference device is observed which confirms the potential role of doped materials in enhancing photovoltaic performance by facilitating efficient charge transport and reduced recombination. Our research suggests a facile route to synthesize a low-cost ETM beneficial for the commercialization of future perovskite devices.
 

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Hybrid photocatalysts, comprising both inorganic and organic polymeric components, are the most promising photocatalysts for the degradation of organic contaminants. The nanocomposite, Titania-Polyaniline (TiO₂-PANI) was synthesized using the chemical oxidative polymerization method. Various characterization techniques were employed to assess the properties of the catalysts. The ultraviolet diffuse reflectance spectroscopy (UV-DRS) analysis revealed that the TiO₂ absorbs only UV light while the TiO₂-PANI nanocomposite absorbs light from both UV and visible regions. The X-ray diffraction (XRD) results confirmed the presence of TiO₂ (anatase) in both TiO₂ nanoparticles and TiO₂-PANI (Titania-Polyaniline)  nanocomposite. The phases of the catalysts were verified through Raman, TEM, and SAED techniques where all results are in good agreement with each other. The average crystallite size of TiO₂ nanoparticle and TiO₂-PANI nanocomposite were 13.87 and 10.76 nm. The thermal stability of the catalysts was assessed by the Thermal gravimetric analysis (TGA) technique. The order of the thermal stability is TiO₂ > TiO₂-PANI > PANI.  The crystal lattice characteristics were confirmed using Transmission electron microscopy (TEM). The surface area measurements were confirmed from the Brunauer-Emmett-Teller (BET) study and were employed for the evaluation of the photocatalytic efficiency of both, TiO₂ nanoparticles and TiO₂-PANI nanocomposite catalysts. The energy dispersive spectroscopy (EDS) study was employed for elemental detection of the fabricated materials. While Raman spectroscopy was employed for the chemical structure and the phase characteristics of the materials. The standard conditions for the degradation of the CF dye were 8 g/L of catalyst dosage, 20 mg/L of dye concentration, and a pH of 7. The TiO₂-PANI nanocomposite exhibited superior efficiency as compared to pure TiO₂ nanoparticles, achieving almost 100 % degradation in just 40 minutes.  

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Silver/polyvinyl alcohol (Ag/PVA) nanocomposites were fabricated via an electrochemical method. Silver nanoparticles (AgNPs) with varying grain sizes were directly synthesized within PVA polymer matrices at deposition times of 15, 30, 45, 60, and 120 minutes. The integration of AgNPs within the PVA matrix was confirmed through Transmission Electron Microscopy (TEM) and optical absorbance measurements. X-ray Diffraction (XRD) analysis demonstrated the face-centered cubic structure of AgNPs. Furthermore, these prepared nanocomposites exhibited significant antibacterial properties against Bacillus subtilis and Pseudomonas pneumonia, as well as antifungal activity against Alternaria alternata. Remarkably, the AgNPs/PVA nanocomposite exhibited outstanding antifungal efficiency, resulting in an impressive inhibition zone of up to 47 mm.
 

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Dual nanocomposites based on metal sulfide nanomaterials with a narrow band gap are favorable candidates for future optoelectronic applications and ionizing ray sensors. In this study, novel silver-doped zinc sulfide/ cadmium sulfide (ZnS/CdS: Ag) nanocomposites were synthesized using the cost-effective solvothermal approach. For the first time, the radiation sensitivity of the newly developed nanocomposite was assessed using a ²⁴¹Am alpha source and ion beam-induced luminescence (IBIL) measurements. The ZnS/CdS: Ag nanocomposite demonstrated significant light emission in the blue-green spectrum when measured at room temperature. When exposed to alpha irradiation, the ZnS/CdS: Ag nanocomposite film displayed exceptional sensitivity compared to pure ZnS or CdS films. The FESEM images revealed a uniform distribution of semi-spherical and rod-shaped nanoparticles, with an average particle size measuring 180 nm. The results from XRD and EDX demonstrated distinct peaks corresponding to ZnS, CdS, and associated elements within the nanocomposite. The existence of several groups within the nanocomposite was confirmed through Fourier transform infrared spectroscopy. Evaluations revealed that the optical quality of the ZnS/CdS: Ag nanocomposite showed enhancement in comparison to pure ZnS and CdS. The results suggest that the ZnS/CdS: Ag nanocomposite film holds great promise for applications in optoelectronic devices and detection technologies.
 

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Hybrid asymmetric supercapacitors using distinct cathode/anode materials offer enhanced energy density by expanding operational potential windows compared to symmetric configurations. In this work rGO/α-Fe₂O₃ and rGO/TiO₂ nanocomposites were synthesized via hydrothermal method for hybrid asymmetric supercapacitors applications. Field emission scanning electron microscope (FESEM) revealed uniform distribution of spherical α-Fe₂O₃ and TiO₂ nanoparticles on rGO sheets. The X-ray diffractometry (XRD) analysis confirmed the presence of the hematite and anatase in the rGO/α-Fe₂O₃ and rGO/TiO₂ nanocomposites, respectively. Additionally, in the XRD spectra of both nanocomposites, a broad peak corresponding to the (002) crystalline planes of rGO was observed. Electrochemical testing showed specific capacities of 130 F/g (rGO/α-Fe₂O₃) and 253 F/g (rGO/TiO₂) at 5 mV/s in 1M KOH. The assembled hybrid asymmetric supercapacitors (rGO/α-Fe₂O₃//rGO/TiO₂) achieved a 1.6 V operational potential window. Power density and energy density of 1066 W kg^-1 and 9.7 Wh kg^-1 were achieved at a current density of 1 A/g, respectively.
 

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Nanomaterials have significantly transformed multiple scientific and technological fields due to their exceptional properties, which result from their quantum confinement effects and high surface-to-volume ratios. Among these materials, zinc oxide (ZnO) and titanium dioxide (TiO₂) nanoparticles have attracted considerable interest because of their diverse applications.
In this study, TiO₂-ZnO nanocomposites were synthesized using varying calcination times of 1, 1.5, 2, 2.5, and 3 hours. Characterization of fabricated samples through X-ray diffraction (XRD)‌ spectroscopy, Fourier transform infrared (FTIR) spectroscopy, field emission scanning electron microscopy (FESEM), and energy-dispersive X-ray spectroscopy (EDXS) confirmed the successful fabrication of the nanocomposites. In this regard, XRD analysis revealed anatase TiO₂ and hexagonal wurtzite ZnO phases. Raman spectroscopy also supported these findings, identifying characteristic peaks of both TiO₂ and ZnO.
The calcination time had a minimal effect on the crystal structures and also morphology of the nanocomposites, which gave rise to its negligible impact on optical properties and biological activities of the samples. Optical properties assessed by means of UV-visible and photoluminescence (PL) spectroscopy showed consistent band gap absorption and emission profiles across all samples, among which the nanocomposite calcined for 1 hour exhibited the best optical properties.

The sample prepared at 1 hour not only showed the most favorable optical properties, but also demonstrated significant antibacterial, antifungal, and cytotoxic activities, which make it suitable for various applications. In this regard, a reduction of more than 99.9% occurred in the number of Escherichia coli and Staphylococcus aureus bacteria and also Candida albicans fungus by using TiO₂-ZnO nanocomposite. Besides, addition of 500 µg/ml of nanocomposite decreased the cell viability to 34.47%, which signifies its high cytotoxicity activity.

 

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 Poly(2-aminobenzothiazole) (PAT) is a relatively new heterocyclic conducting polymer having a sulfur and nitrogen-rich chemical structure. During the past decade or so, there have been notable advances on the development of PAT. Especially, PAT and PAT-based composites have shown great potential for their applications in photovoltaic cells, solar cells and anti-corrosion organic coatings.   In this study, 2-aminothiazole was successfully prepared as pure polymer and as composite materials with multi-wall carbon nanotubes (MWCNTs). FTIR, X-ray diffraction and SEM images were investigated, showing that the composite of poly 2-aminobenzothiazole: MWCNTs was successfully synthesized. The electrical features of the pure polymer and the composite thin films were examined. The findings show that the conductivity of the pure polymer and composite thin films are about 1.67x10^-6  (S/cm) and 4.1x10^-2 (S/cm), respectively, exhibiting a significant enhancement by a factor of 2.5x10⁴ times as a results of doping the pure polymer by 1% wt MWCNTs.
 

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In this study, we investigated the antimicrobial, bioactivity, and in vitro cytotoxicity of a nanocomposite made of copper oxide (CuO) and aluminum oxide (Al₂O₃) with two different morphologies of copper oxide (Spherical-sCuO and Nanoplate-pCuO), which was made using the Spark Plasma Sintering (SPS) process on a titanium substrate as an orthopedic implant. Two different weight percents of copper oxide nanostructures of sCuO NP (10 wt%, 20 wt%) and pCuO NP (10 wt%, 20 wt%) have been used in this research. Synthesized nanocomposites were investigated by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR), and field emission scanning electron microscope (FESEM). Based on the obtained results, the XRD pattern and XPS confirmed that the nanocomposites were successfully synthesized without impurity. FESEM images showed that CuO nanoparticles and nanoplates were distributed on the alumina matrix homogeneously. The antibacterial activity of synthesized nanocomposites was investigated using Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus), gram-negative and gram-positive bacteria, respectively. Antibacterial activity results showed that CuO nanoparticles had high antibacterial activity, and the effect of CuO nanostuctures depended not only on their morphology and size, but also on the type of microorganisms. Furthermore nanocomposite with nanoplate copper oxide exhibited more bioactivity properties than the spherical shape. S. aureus showed greater resistance to CuO nanostructure, while E. coli was more susceptible to them (15%). In addition, toxicity tests showed that nanoplate copper oxide exhibited greater toxicity due to its high surface reactivity than spherical nanoparticles. This study provides new insights into the role of copper oxide nanoparticle morphology in the properties of nanocomposites for use as orthopedic implants.

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The development of polymer composite materials for gear applications has gained significant attention due to the growing need for lightweight, corrosion-resistant, and high-performance alternatives to traditional metallic gears. This literature review consolidates key findings and insights from numerous studies, highlighting the advancements, challenges, and potential of polymer composites in gear applications. High-performance polymers such as poly ether ether ketone (PEEK), poly ether ketone(PEK), poly ether ketone ketone (PEKK) and poly aryl ether ketone (PAEK) especially when reinforced with multi-walled carbon nanotubes (MWCNTs) and functionalized MWCNTs, exhibit superior mechanical, thermal, and tribological properties. These enhancements include improved strength-to-weight ratios, wear resistance and load transfer capabilities. The review also examines the influence of various parameters on gear performance. The necessity for standardized testing methods and benchmarks to evaluate wear, surface temperature, roughness and environmental exposure is emphasized to ensure reliability and consistency. This study focuses on study of development of high performance polymer composite materials for gear applications and performance analysis of these gears.

 

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In the current study, titanium dioxide (TiO₂) nanoparticles were synthesized and subsequently combined with chitosan (CS) and silver (Ag) to augment their antimicrobial effectiveness. The synthesized TiO₂, TiO₂-CS, and TiO₂-CS-Ag nanocomposites were subjected to various characterization analyses in order to thoroughly assess their structural, morphological, and compositional attributes. XRD analysis substantiated the phase transition from anatase to rutile consequent to incorporation of chitosan and silver, accompanied by a diminution in nanoparticle dimensions. FTIR spectra corroborated the existence of functional groups linked to chitosan and silver, while FESEM illustrated morphological modifications, notably the emergence of polygonal nanostructures within the TiO₂-CS-Ag composite. The antibacterial efficacy of the synthesized nanocomposites was evaluated against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus). Although pure TiO₂ demonstrated minimal antibacterial properties, the TiO₂-CS and TiO₂-CS-Ag composites exhibited substantial inhibition zones, with the most pronounced efficacy recorded for the TiO₂-CS-Ag composite attributable to the synergistic interaction between chitosan and silver nanoparticles. BET analysis revealed that the augmented antimicrobial activity was associated with the increased surface area of the TiO₂-CS-Ag nanocomposite.
 

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  Fe₃O₄/ZnO/CuO nanocomposites with various molar ratios of CuO were successfully synthesized. Sol-gel method was used to syntehesize nanocomposite materials at a low temperature. A set of experiments, including X-ray diffraction (XRD), Dynamic Light Scattering (DLS), scanning electron microscopy (SEM), and UV-Vis spectroscopy, was used to confirm the successful synthesis of Fe₃O₄/ZnO/CuO nanocomposites in crystalline form.
The photocatalytic activity of the samples was investigated via the degradation of methylene blue (MB) dye
from synthetic wastewater under three distinct conditions: visible light, ultraviolet light, and a combination of visible light with ultrasonic treatment. Fe₃O₄/ZnO/CuO nanocomposite with a molar ratio of 1:1:0.5 showed the highest photocatalytic activity when irradiated with either visible or ultraviolet light. Furthermore, when visible light was combined with ultrasonic treatment, complete (100%) removal of methylene blue was achieved within 120 minutes. The results demonstrate that these nanocomposites are efficient catalysts for wastewater treatment through the removal of organic pollutants Fe₃O₄/ZnO/CuO nanocomposites with various molar ratios of CuO were successfully synthesized. Sol-gel method was used to syntehesize nanocomposite materials at a low temperature. A set of experiments, including X-ray diffraction (XRD), Dynamic Light Scattering (DLS), scanning electron microscopy (SEM), and UV-Vis spectroscopy, was used to confirm the successful synthesis of Fe₃O₄/ZnO/CuO nanocomposites in crystalline form.
The photocatalytic activity of the samples was investigated via the degradation of methylene blue (MB) dye
 from synthetic wastewater under three distinct conditions: visible light, ultraviolet light, and a combination of visible light with ultrasonic treatment. Fe₃O₄/ZnO/CuO nanocomposite with a molar ratio of 1:1:0.5 showed the highest photocatalytic activity when irradiated with either visible or ultraviolet light. Furthermore, when visible light was combined with ultrasonic treatment, complete (100%) removal of methylene blue was achieved within 120 minutes. The results demonstrate that these nanocomposites are efficient catalysts for wastewater treatment through the removal of organic pollutants

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Researchers have increasingly investigated hybrid nanocomposites that mix physical and chemical properties of carbonaceous materials and metal/metal oxides. In this work, a nanocomposite composed of reduced graphene oxide and silver (I) oxide, rGO@Ag₂O, was prepared using ascorbic acid as a green reducing agent. The Ag₂O nanoparticles were synthesized by means of a controlled precipitation process in water. The carbonaceous material of rGO was obtained through a modified Hummers' approach. After being combined with a solvent, the Ag₂O and rGO in ethanol were dried with heat. The resultant nanocomposite was structurally and optically examined using different characterization techniques.  
The results showed that GO has been successfully reduced, Ag₂O revealed a crystalline structure, and Ag₂O nanostructures were found on the surface of rGO sheets. Disk diffusion assay was adopted in order to evaluate antibacterial activity of nanocomposite against both Staphylococcus aureus (Gram-positive) and Escherichia coli (Gram-negative) bacteria. The Ag₂O nanostructures in the composite form exhibited inhibition zone with higher diameter compared to their uncomposited counterparts. Higher antibacterial activity of rGO@Ag₂O was attributed to the role of negatively charged oxygen-containing groups present on the surface of rGO in slightly improvement in the stability of Ag₂O nanostructures.
Our findings show that rGO@Ag₂O could be a useful antimicrobial material for biomedical surfaces, as a coating, and in systems that clean water. It could be a good option for future research in nano-enabled antimicrobial technology because it can destroy bacteria, is made in an environmentally benign way, and could be made on a larger scale.
 

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Today, the application of high‑performance thin‑film nanocomposites as impedance‑matching layers in telecommunication and military technologies has gained substantial importance. In this study, a multiphase nanocomposite comprising Fe₃O₄, ZnTiO₃, and multi‑walled carbon nanotubes (MWCNT) embedded within an epoxy resin matrix was designed and synthesized under carefully controlled laboratory conditions. Experimental data were analyzed using multiple regression analysis alongside error variance reduction techniques to identify the optimal composition among the four finalized sample variants. During the fabrication process, the samples underwent sequential mixing, heating, and sonication steps to ensure proper dispersion of the fillers, followed by casting into molds with dimensions corresponding to the rectangular waveguide test section used for the electromagnetic measurements.Topological and morphological characterizations of the fabricated composites were performed by Scanning Electron Microscopy (SEM), while crystal structure assessments employed X‑ray Diffraction (XRD) analysis. Furthermore, electromagnetic characterization was conducted using WR‑90 waveguide measurements over the frequency range of 8.2–12.4 GHz. Among the samples examined, specimen C4, containing an increased ZnTiO₃ content, demonstrated superior particle dispersion and consequently improved electromagnetic impedance‑matching performance. Numerical simulations carried out with the Frequency Domain Solver of CST Microwave Studio corroborated the experimental findings with considerable agreement. The results identified Fe₃O₄ as the dominant contributor to magnetic loss mechanisms, whereas MWCNTs served as conductive constituents within the composite matrix. The inclusion of ZnTiO₃ markedly enhanced impedance matching characteristics, resulting in a significant reduction of wave reflection and thereby facilitating improved wave energy transmission control across a broad bandwidth. Specifically, for the 1 mm thick C4 sample, the reflection coefficient was reduced to −17.85 dB, while the transmission parameter S₂₁ remained below −0.072 dB at 8.2 GHz, indicating excellent impedance matching and minimal reflective loss. Frequency‑dependent analysis further demonstrated a stable balance between dielectric and magnetic contributions, manifesting in consistent electromagnetic performance without substantial deviation across the measured spectrum. Accordingly, the investigated nanocomposite emerges as a promising candidate for lightweight, high‑performance absorber layers, impedance‑matching layers, and electromagnetic coatings in advanced telecommunication and defense applications.