Amount Of Doping Research Articles

Improving the Mechanical Properties and Microstructure of 12 mol% Ceria-Stabilized Tetragonal Zirconia Polycrystal Ceramics with Low-Content Nd2O3

In this study, 12 mol% ceria-stabilized tetragonal zirconia polycrystal ceramics with xNd2O3 (where x equals 0, 0.1, 0.2, 0.3, 0.4, 0.5, and 0.7) were synthesized via the solid-state method, and the effects of Nd2O3 doping amounts on the mechanical properties and microstructure were studied. The results show that with an increase in the Nd2O3 doping amount, the grain size of the ceramics was reduced from 2.93 μm to 0.69 μm. The hardness and strength of the ceramics increased significantly, while the fracture toughness decreased. The reduction in fracture toughness was attributed to the reduction in tetragonal grain size, which suppressed the tetragonal–monoclinic phase transformation caused by stress. Additionally, as the content of Nd2O3 increased, the formation of cubic zirconia accelerated, but no second phase was observed. Most importantly, when the doping amount of Nd2O3 reached 0.3 mol%, the comprehensive mechanical characteristics of the ceramics were optimal. This provides a research basis for the preparation of nanoscale 12 mol% ceria-stabilized tetragonal zirconia polycrystal ceramics.

Yttrium doped barium titanate nanocrystals synthesis using inverse miniemulsion and their properties

This paper highlighted in preparation and their properties of Y3+ doped barium titanate (BaTiO3) nanocrystals using inverse miniemulsion. The yttrium (Y) element dopant as the earlier utilized rare earth was used for barium titanate (BaTiO3) modification. The cubic structure of Y3+ doped BaTiO3 nanocrystals were successfully incubated in stable droplets of inverse miniemulsion under the solvent-thermal treatment condition. The suitable Y3+ doping amount in nanocrystals had positively attributed to reduce the value of bandgap (Eg ), to prolong the fluorescence lifetime, and to improve the photoelectric properties. The photodegradation mechanism and the schematic diagram of fluorescence emission and radical production were suggested for explanation the relation between photoelectric characteristics and photocatalytic properties. The selected 1.0% Y3+ doped nanocrystal provided an excellent photocatalysis candidate for organic compound photodegradation.

Ideal Co-NiO solid solution with excellent low-temperature propene catalytic combustion performance

Doping engineering of transitional metal oxides offers a great opportunity to further optimize the performance of corresponding catalysts. Here, we presented a solid-state co-precipitation routine to synthesize the Co-NiO ideal solid solution, where Co atoms achieved nearly atomically isolation in the NiO lattice matrix. Remarkably a clear correlation was established between the reactivity for propene combustion and the Co dopant amounts, with the propene combustion rate increasing proportionally to the Co dopant amounts. The homogeneously dispersed Co single atoms or tiny CoOx nanoclusters ensure this linear relationship. More importantly, due to the emergence of Co single atoms and CoOx nanoclusters with a lower coordination number, significant propene adsorption and subsequent C = C bond dissociation were observed in this Co-doped NiO, which improved the propene combustion reaction rate. Therefore, this solid-state co-precipitation strategy provides an effective doping route for building an ideal doped solid solution.

Effect of variable valence elements Se on Ti and P sites of LATP solid electrolyte

The NASICON solid electrolyte Li1.3Al0.3Ti1.7(PO4)3 (LATP) has garnered significant attention owing to its low cost, excellent air stability, and high ionic conductivity. However, it exhibits low density and elevated grain boundary resistance due to suboptimal sintering performance. In order to improve the sintering performance and further increase the ionic conductivity, LATP solid electrolyte was synthesized by introducing Se4+ ion doping by solid phase method. The effects of different doping amounts of Se4+ ions on the structure and properties of solid electrolyte were systematically studied. It was observed that a low doping amount of Se4+ ion replaces Ti4+ ion which increases the crystal density and inhibits the formation of secondary phase LiTiPO5. While the doping amount is high, part of Se4+ ion transforms into Se6+ ion and replaces P5+ ion, causing lattice distortion and broadening the Li+ ion migration channel, but at the same time, it also promotes the precipitation of secondary phase LiTiPO5 and impedes the Li + transfer. The prepared sample with 2 wt% of SeO2 exbihits the total ionic conductivity of 0.41 mS/cm at room temperature and an improved bulk density of 2.93 g/cm3.

Influence of substrate temperature and Mn/Y co-doping concentration on the morphological, structural and optical properties of CuO nanostructured film deposited by the spray pyrolysis method

In this work, the effect of substrate temperature (ST) during deposition and dopant amount of Mn (1,3,5, and 7 %) and Y(3 %), (Mn/Y), on the physical properties of copper oxide (CuO) the nanostructured film were analyzed using different diagnostic tools. The pure and (Mn, Y) co-doped CuO thin films were deposited by the spray pyrolysis method, which is effective and easy to apply for any substrate. Deposited pure and (Mn,Y) co-doped CuO nanostructured films were investigated by X-ray diffraction (XRD), UV–Vis spectroscopy, and Field emission scanning electron microscopy (FESEM) techniques to analyze the influence of ST and co-doping on the structural, morphological, and optical properties of prepared films. The FESEM is used to visualize nanostructures on the surface of the film. Also, it is observed that the surface morphology of CuO film changes from a spherical-like to a nanocloumnar-like structure with increasing substrate temperature. The XRD diffractograms confirm the monoclinic crystal structure of CuO, in polycrystalline nature for all deposited films. UV–Vis spectra suggest changing the optical absorbance and the band gap of the pure and Mn/Y co-doped CuO nanostructured films. In the first investigation of this study, the better substrate temperature was obtained as 400 °C according to results. In the second part, the effect of Y and Mn doping with different content was analyzed for the CuO film deposited at the chosen ST of 400 °C. There is no observable crystalline structure variation in the XRD pattern, but the size of nanostructure and dislocation density are varied with Mn/Y co-doping. FESEM micrographs confirm the impact of the co-doping concentration on the size, shape, and surface properties of CuO nanostructured film. In addition, the optical band gap increases with Mn doping up to 3 % of Mn content and it was determined as 2.69 eV for the sample 3Mn/Y@CuO nanostructured film. The obtained results suggest that the substrate temperature has an important impact on the physical properties of the spray deposited CuO nanostructured film, and the structural, optical, and surface properties of the CuO nanostructured films may be engineered by Mn/Y doping concentration.

The X-Direction Scanning of Atomic Force Microscopy to Analyze Porous Silicon P-Type Si(100) Fabricated by Electrochemical Anodization Method

This work only investigated the x-direction scanning of atomic force microscopy, which can accurately measure porous silicon's width, depth, and roughness. Pores on p-type Si (100) surfaces fabricated by electrochemical anodization method with the variation of resistivity and current density, i.e., 0.001-0.005 Ω.cm (high dopant) and 1-10 Ω.cm (low dopant), and 4, 6, 8, and 10 mA/cm2, respectively. Macroporous silicon was obtained for both high and low dopants. Pore width, pore depth, and roughness of silicon increase with increasing the current density. Characteristics of porous silicon for high dopants are smaller than that for low dopants. It indicates that large amounts of dopant in silicon can slow the etching process.

The mysterious magnetic ground state of Ba14MnBi11 is likely self-doped and altermagnetic

Magnetism in the Zintl compound Ba14MnBi11 is rather poorly understood. Experimental claims are largely inconsistent with ab initio calculations, much beyond typical errors of the latter. We revisit this old problem, assuming that the root of the problem may be in nonstoichiometry of existing samples. Our key finding is that the magnetic ground state is indeed very susceptible to charge doping (band filling). Calculations for stoichiometric Ba14MnBi11 give a rather stable ferromagnetic metallic state, in agreement with previous publications. However, by adding exactly one electron per Mn, the system becomes semiconducting as expected, and becomes weakly antiferromagnetic (AF). On the other hand, upon small amount of hole doping, the system transitions to a special type of AF state known as altermagnetism. Furthermore, hole and electron doping-induced phase transitions result from different underlying mechanisms, influencing different exchange pathways. We propose that the inconsistency between experiment and theory is not a failure of the latter, but results from a nontrivial ramification of nonstoichiometry. The possibility of doping-stabilized altermagnetism is exciting.

Lattice Distortion Creates Enhancements in Photocatalytic and Electrocapacitive Performance of Sol–Gel‐Derived Cu‐Doped NiTiO3

A remarkable 35% enhancement in the photocatalytic and electrocatalytic abilities of an ilmenite nickel titanate (NiTiO3) material is reported. This boost in catalytic performance is achieved by simply creating a static distortion in the rhombohedral unit cell by replacing a small proportion of a small‐size nondegenerate Ni (69 pm) with a large‐size degenerate Cu (73 pm). The materials are synthesized by using a simple sol–gel method. The appropriate doping amount of Cu facilitates the better separation of intrinsic charge carrier pairs by inhibiting their recombination. The photocatalytic and electrochemical activities of durable materials in aqueous MB dye (10 ppm) and KOH (1 molar) electrolyte solutions are found to be directly associated with this improvement in inherent charge carrier transfer characteristics. The enhanced photodissociation of MB dye (42–56%) and specific capacitance (381–450 F g−1) in a KOH (1 molar) electrolyte are in full accord with the investigations carried out using crystallographic and optoelectronic analysis, charging–discharging measurements, and electrochemical impedance (EIS) spectroscopy investigations. Same material with high textural surface areas or controllable particle morphologies might show a far better photo/electrocatalytic performance in a variety of practical applications.

Strong Grain Boundary Passivation Effect of Coevaporated Dopants Enhances the Photoemission of Lead Halide Perovskites.

Herein, we demonstrate that coevaporated dopants provide a means to passivate buried interfacial defects occurring at perovskite grain boundaries in evaporated perovskite thin films, thus giving rise to an enhanced photoluminescence. By means of an extensive photophysical characterization, we provide experimental evidence that indicate that the codopant acts mainly at the grain boundaries. They passivate interfacial traps and prevent the formation of photoinduced deep traps. On the other hand, the presence of an excessive amount of organic dopant can lead to a barrier for carrier diffusion. Hence, the passivation process demands a proper balance between the two effects. Our analysis on the role of the dopant, performed under different excitation regimes, permits evaluation of the performance of the material under conditions more adapted to photovoltaic or light emitting applications. In this context, the approach taken herein provides a screening method to evaluate the suitability of a passivating strategy prior to its incorporation into a device.

Iron–Cobalt Bimetallic Metal–Organic Framework-Derived Carbon Materials Activate PMS to Degrade Tetracycline Hydrochloride in Water

Organic pollutants entering water bodies lead to severe water pollution, posing a threat to human health. The activation of persulfate advanced oxidation processes using carbon materials derived from MOFs as substrates can efficiently treat wastewater contaminated with organic pollutants. This research uses NH2-MIL-101(Fe) as a substrate, doped with Fe2+ and Co2+, to prepare Fe/Co-CNs through a one-step carbonization method. The surface morphology, pore structure, and chemical composition of Fe/Co-CNs were investigated using characterization techniques such as XRD, SEM, TEM, XPS, FT-IR, BET, and Raman. A comparative study was conducted on the performance of catalysts with different Fe/Co ratios in activating PMS for the degradation of organic pollutants, as well as the effects of various influencing factors (the dosage of Fe/Co-CNs, the amount of peroxymonosulfate (PMS), the initial pH of the solution, the TC concentration, and inorganic anions) on the catalyst’s activation of persulfate for TC degradation. Through radical quenching experiments and post-degradation XPS analysis, the active radicals in the FeCo-CNs/PMS system were investigated to explain the possible mechanism of TC degradation in the Fe/Co-CNs/PMS system. The results indicate that Fe/Co-CNs-2 (with a Co2+ doping amount of 20%) achieves a degradation rate of 93.34% for TC (tetracycline hydrochloride) within 30 min when activating PMS, outperforming other Co2+ doping amounts. In addition, singlet oxygen (1O2) is the main reactive species in the reaction system.

Novel Co and Cr free, high-temperature black ceramic pigment based on (Ni, Mn) co-doping (CuFe)Fe4O8

Novel Co and Cr free, high-temperature (Ni, Mn) co-doping (CuFe)Fe4O8 black ceramic pigment was synthesized. The results indicate that the brightness (L*) values of the synthesized pigments decrease first, then reach an optimal value, and then increase with the doping amounts increasing of both Ni2O3 and MnO2. The optimized Ni2O3 and MnO2 doping amounts are 0.20 (molar ratio to (CuFe)Fe4O8) and 0.75 (molar ratio to (CuFe)Fe4O8), respectively. L*, a* and b* values of the optimized pigment (0.20Ni, 0.75Mn) co-doping (CuFe)Fe4O8 are 21.36, 1.10 and −0.24, respectively. The crystal phase of the optimized pigment is (CuFe)Fe4O8 (JCPDS73–2314). The crystal size of the pigment is 0.8–1.5μm with excellent dispersivity. The glazing temperatures have little effect on the coloration of the pigment when used at 1000℃, 1150℃ and 1300℃. The results show that the pigments have excellent high-temperature resistance and are expected to be widely used in high-temperature glazing coloration.

Improved morphological stability of NiFe2O4 via Sr doping for chemical looping hydrogen production

As a new hydrogen production technology, chemical looping hydrogen production has the advantage of internal CO2 separation. NiFe2O4 is considered as promising oxygen carrier material for chemical looping hydrogen production due to the high oxygen carrying capacity and low cost. However, rapid redox performance fading caused by structure degradation and interface instability in successive redox reactions that led fto poor stability, and seriously limited the practical application of NiFe2O4 in chemical looping hydrogen production. Herein, we reported a method for improving the morphological stability of NiFe2O4 through Sr doping. NiFe2O4 samples containing different SrO contents (2 wt%, 5 wt% and 8 wt%) were prepared by a simple mechanical mixing method. A series of characterization analysis results showed that adding an appropriate amount of Sr could significantly improve the microstructure, increase the oxygen vacancy concentration and inhibit the phase segregation of NiFe2O4. The NiFe-5Sr presented the largest BET surface area (24.63 m2/g) and highest concentration of oxygen vacancies (77.49 %). NiFe-0Sr and NiFe-2Sr experienced severe phase segregation during continuous cyclic reactions, resulting in significant surface sintering and deactivation. During 20 redox cycles, NiFe-5Sr presented the highest hydrogen yield (around 10 mmol/g) and stable surface morphology. The research results indicated that the optimal doping amount for SrO was 5 %.

Electro-Optic Kerr Response in Optically Isotropic Liquid Crystal Phases

The results of an experimental investigation of the temperature and wavelength dependence of the Kerr constant (K) of mixtures with an increasing amount of chiral dopant in an isotropic liquid crystal phase are reported. The material was composed of a nematic liquid crystal (5CB) and a chiral dopant (CE2), which formed non-polymer-stabilized liquid crystalline blue phases with an exceptionally large value of K∼2 × 10−9 mV−2. The measurements were performed on liquid and blue phases at several concentrations covering a range of temperatures and using three wavelengths: 532 nm, 589 nm and 633 nm. The work focused on changes caused by concentration and their impact on the increase in the value of K, and it was found that in the case of the 5CB/CE2 mixture these changes were significant and quite systematic with temperature and wavelength. It is shown that the dispersion relation based on the single-band birefringence model described K well in isotropic liquid crystal phases at all of the measured concentrations. In an isotropic fluid, both temperature-dependent parameters in the dispersion relation had a simple linear form and, therefore, the K-surface could be described by only four constants. In the blue phase, the expression reproducing the temperature variation of K depended on concentration, which could vary from being almost linear to quasi-linear and could be represented well by an inverse exponential analytic expression.

Enhanced construction of 3D carbon skeleton through molten salt coupling activation effect for high efficiency capacitive deionization of lead (II) ions removal in wastewater

Efficiently eliminating of highly toxic ultra-dilute lead ions (Pb2+) from wastewater is a challenging task. Capacitive deionization (CDI) technology, based on the electrochemical capacitance mechanism, has emerged as a pivotal approach to address this challenge. In this work, a KNO3-mediated molten salt-coupled activation strategy was proposed to prepare nitrogen-doped hierarchical porous biomass carbon electrode material (3DCF-650-0.2) with a three-dimensional carbon skeleton, which was integrated into a symmetrical CDI device for Pb2+ removal. The 3DCF-650-0.2 electrode exhibited a high specific capacitance of 330.3 F g-1 at a current density of 1 A g-1, with a capacity retention rate of 98.45% after 10,000 cycles at 10 A g-1. Furthermore, the electrochemical adsorption capacity of the CDI device for Pb2+ reached 72.86 mg g-1 (1.2 V, 50 mg L-1), and the CDI device retained a high adsorption capacity of 91.14% after twenty adsorption/desorption cycles. These excellent adsorption properties are attributed to the in-situ activation and gas foaming of KNO3, which favors the production of reasonable pore structure (electric double-layer capacitance) and an appropriate pyrrolic nitrogen doping amount (selective adsorption) in the carbon materials. This work provides insight into the mechanism of the molten salt-coupled activation strategy, offering new ideas for the targeted design of high-performance CDI biomass carbon materials.

Visible Light-driven Effective Photocatalytic Degradation of the Persistent Organic Pollutant Using Cobalt-doped Strontium Titanate

Residual antibiotics in natural aquatic environments pose a critical threat to humans and other organisms. However, most sewage treatment plants fail to remove them. Photocatalytic nanomaterials can efficiently destroy these persistent organic pollutants in wastewater. In this study, we developed a series of cobalt-doped SrTiO3 (Co-STO) catalysts with different doping amounts (3, 5, 7, and 9 wt%) for the effective photocatalytic degradation of ciprofloxacin (CIP). The nanostructures were characterized using X-ray diffraction, field-emission scanning electron microscopy with energy dispersive X-ray analysis, transmission electron microscopy, X-ray photoelectron spectroscopy, UV-visible diffuse reflectance spectroscopy, and Brunauer–Emmett–Teller N2 adsorption isotherms. The Co-STO particles have a mesoporous diameter of ~30.8 nm, and the Co-doped nanostructures have a rhombohedral hopper-like shape. Co-doping decreased the bandgap of pure STO from 3.61 to 3.42 eV, which enabled it to absorb visible light. Among the catalysts, 7 wt% Co-STO showed the highest CIP degradation activity (90.6%) during 120 min of visible-light irradiation. Radical scavenging experiments revealed that superoxide (O2 •-) is the primary reactive species during degradation. These Co-doped nanostructures have potential applications in the remediation of hazardous pollutants in pharmaceutical wastewater. Moreover, the crystal and energy band structure, density of states, and Bader charge of these molecules were analyzed.

Enhancing magnetostriction in FeAl alloys via crystal growth orientation tuning by a trace amount of Pt doping

Iron-based cubic alloy systems opened the door to the development of magnetostrictive materials with moderate magnetostriction, low cost, and good mechanical properties. At the as-cast state, the grain growth orientation of these alloy systems is close to random, which deteriorates magnetostriction. Doping with certain elements can tune the growth orientation to enhance magnetostriction. However, the driving force for the crystal growth along preferential orientation is still not clear. Here in this work, revealed by density functional theory (DFT) calculation, Pt doping can tune the crystal growth direction of FeAl along <100> crystal direction (same as easy magnetization direction), which can be utilized to realize 90° domain-switching and thus magnetostriction is enhanced greatly. These are confirmed by experimental results. The magnetostriction increases from 29 ppm to 80 ppm, representing a 176% enhancement through doping with 0.4 at.% Pt. The maze magnetic domain structures, observed by magnetic force microscope, are also preferentially <100> oriented and feature stripes. In consideration of the similarity between this study and our previous study on FeGa alloy (C. Zhou et al., 2020), it can be expected that our methods can be extended to other magnetostrictive materials and help develop polycrystals with desired orientations.

LArRI — A new setup for Liquid Argon Refractive index measurement

Liquid argon (LAr), widely used as the active target in neutrino and dark matter experiments, is a scintillator with a light yield of approximately 40 photons/keV. The scintillation spectrum is centered at 128 nm, and the attenuation length is of the order of meters, depending on the purity. The addition of small amounts of dopants allows for shifting the scintillation peak simplifying the light detection and opening the possibility to the development of imaging systems. There is no precise knowledge of the optical properties of LAr in the VUV range, but it could be exploited to improve the performances of liquid argon-based experiments, especially when the involved mass is in the ton scale. LArRI (Liquid Argon Refractive Index) aims to directly measure the refractive index of LAr in the VUV spectrum, using an interferometric technique. The refractive index is obtained by comparing two interference patterns, created in vacuum and liquid, acquired with cryogenic silicon photomultipliers. This work primarily presents the methodology, the preliminary tests, and the analysis strategy, which are intended to be applied to real data shortly.

Research on the Rheological Properties and Modification Mechanism of Epoxy Resin/SBS Composite-Modified Asphalt

Both epoxy resin (ER) and SBS are considered effective pavement materials for avoiding ruts. However, epoxy resin asphalt suffers from poor low-temperate performance and a high material cost in practical applications. Aiming to tackle these issues, a new type of composite asphalt modifier (ER-SBS) has been fabricated by combining epoxy resin with SBS. This work prepared modified asphalt with different doping amounts using the above composite asphalt modifier (ER-SBS), intending to explore the properties of composite-modified asphalt and the modification mechanism of the modifier. Furthermore, the effects of the composite modifier at different doping amounts on the viscoelastic property of asphalt were explored through rheological tests, and then the prepared composite-modified asphalt was compared with matrix asphalt and SBS-modified asphalt. In addition, the modification mechanism of the composite modifier was investigated by fluorescence microscopy and infrared spectroscopy. The difference in pavement performance between the composite-modified asphalt and SBS-modified asphalt was compared by a rut test and dynamic modulus test. The research results showed that the composite modifier improved the high- and low-temperature performances and viscoelastic property of matrix asphalt. When the doping amount was raised to 9%, the composite-modified asphalt exhibited better a modification effect than SBS-modified asphalt. The rut test results indicated that composite-modified asphalt demonstrated a stronger deformation resistance than SBS-modified asphalt. The dynamic modulus test showed that the composite-modified asphalt has better viscoelastic properties and temperature sensitivity. Fluorescence microscopy suggested that the crosslinking between the composite modifier and asphalt forms a mesh structure which greatly improves its resistance to deformation. From infrared spectroscopy, the composite modifier clearly functions as a physical modifier.

Investigating the efficacy of Palladium Doped Ceria for the Photodegradation of Azo Dyes

Ceria (CeO2) was prepared by microwave assisted precipitation method while sonothermal method was utilized for the synthesis of palladium doped ceria (Pd-CeO2) photocatalyst. HR-TEM analysis confirms the face centered cubic geometry (FCC) of CeO2. The particle size of Pd-CeO2 calculated from HR-TEM analysis (7.6±2.18 nm) is in close relation with XRD (8.25±0.25 nm). The SAED pattern of Pd-CeO2 shows the poly crystallinity where the d-spacing was 0.31 and 0.30 nm which corresponds to CeO2 and Pd crystal facets 111 and 100 respectively. The amount of dopant and existence of Pd, Ce and O was confirmed from EDX spectra and elemental mapping. BET surface area analysis of CeO2 (64.45 m2/g), Pd-CeO2 (60.20 m²/g) revealed that the decrease in the surface area of CeO2 due to Pd loading which is confirmed by pore volume (0.079 cm³/g) for CeO2 and pore volume for Pd-CeO2 (0.073 cm³/g). The photocatalytic activity of Pd-CeO2 was screened against a model azo dye Acid red-4 (AR-4). The fluctuation of the rate of photodegradation (PD) of AR-4 was observed under different reaction conditions. Therefore, the reaction parameters were optimized to achieve best catalytic activity up to PD; 98%. The kinetic study suggests that the PD of AR-4 follows 1st order kinetics with regression coefficient (R2=0.973) and rate constant (k=0.024/min). Recycling study revealed the prolong use of catalyst without significant loss of activity. DFT study and experiments revealed the synergism of Pd on the photo response of CeO2. Perhaps this synergistic effect due to metal support interaction, causes redistribution of charges and Fermi energy levels. The synthesized catalyst showed potential application for the treatment of textile industrial effluents.

One-step pyrolysis derived Fe and heteroatom co-doped biochar composites for efficient microwave absorption

Electromagnetic (EM) pollution frequently disrupts the regular operation of sophisticated electrical devices, necessitating the urgent development of lightweight EM wave absorbers that possess powerful absorption capability. Herein, we report a simple method for the preparation of Fe and heteroatom co-doped biochar composites (FeX-BC, where X = N, S) by directly carbonizing the precursors of anhydrous FeCl3, cherry kernel powder, and heteroatom dopants (melamine or Na2S2O3·5H2O). By adding different amounts of dopants during the synthesis of the precursors, it is possible to adjust the heteroatom content of the FeX-BC samples with precision. It is worth mentioning that the FeN0.1-BC composite delivers the best EM wave absorption performance with an effective absorption bandwidth of 4.8 GHz and a minimal reflection loss of −63.2 dB. Furthermore, the significant attenuation of EM wave can be attributed to the synergistic interplay of magnetic loss, dielectric loss and the enhanced impedance matching. This study introduces a simple methodology for the fabrication of EM wave absorbers, a significant contribution to the synthesis, advancement, and functional applications of biomass-derived materials.