Porous Carbon Foam with Carbon Nanotubes as Cathode for Li-CO2 Batteries.

With the extensive use of fossil fuels, the ever-increasing greenhouse gas of mainly carbon dioxide emissions will result in global climate change. It is of utmost importance to reduce carbon dioxide emissions and its utilization. Li-CO2 batteries can convert carbon dioxide into electrochemical energy. However, developing efficient catalysts for the decomposition of Li2 CO3 as the discharge product represents a challenge in Li-CO2 batteries. Herein, we demonstrate a carbon foam composite with growing carbon nanotube by using cobalt as the catalyst, showing the ability to enhance the decomposition rate of Li2 CO3 , and thus improve the electrochemical performance of Li-CO2 batteries. Benefiting from its abundant pore structure and catalytic sites, the as-assembled Li-CO2 battery exhibits a desirable overpotential of 1.67 V after 50 cycles. Moreover, the overpotentials are 1.05 and 2.38 V at current densities of 0.02 and 0.20 mA cm-2 , respectively. These results provide a new avenue for the development of efficient catalysts for Li-CO2 batteries.

Thermophysical Investigation of Multiform NiO Nanowalls@carbon Foam/1-Octadecanol Composite Phase Change Materials for Thermal Management.

Multiform NiO nanowalls with a high specific surface area were constructed in situ on carbon foam (CF) to construct NiO@CF/OD composite phase change materials (CPCMs). The synthesis mechanism, microstructures, thermal management capability, and photothermal conversion of NiO@CF/OD CPCMs were systematically studied. Additionally, the collaborative enhancement effects of CF and multiform NiO nanowalls on the thermal properties of OD PCMs were also investigated. NiO@CF not only maintains the porous 3D network structure of CF, but also effectively prevents the aggregation of NiO nanosheets. The chemical structures of NiO@CF/OD CPCMs were analyzed using XRD and FTIR spectroscopy. When combined with CF and NiO nanosheets, OD has high compatibility with NiO@CF. The thermal conductivity of NiO@CF/OD-L CPCMs was 1.12 W/m·K, which is 366.7% higher than that of OD. The improvement in thermal conductivity of CPCMs was theoretically analyzed according to the Debye model. NiO@CF/OD-L CPCMs have a photothermal conversion efficiency up to 77.6%. This article provided a theoretical basis for the optimal design and performance prediction of thermal storage materials and systems.

Carbonaceous Shape-Stabilized Octadecane/Multi-Walled Carbon Nanotube Composite Materials for Enhanced Energy Storage and Electromagnetic Interference Shielding.

Developing materials for efficient energy storage and effective electromagnetic interference (EMI) shielding is crucial in modern technology. This study explores the synthesis and characterization of carbonaceous shape-stabilized octadecane/MWCNT (multi-walled carbon nanotube) composites, utilizing activated carbon, expanded graphite or ceramic carbon foam, as shape stabilizers for phase change materials (PCMs) to enhance thermal energy storage and EMI shielding, for energy-efficient and advanced applications. The integration of octadecane, a phase change material (PCM) with carbonaceous stabilizers ensures the material's stability during phase transitions, while MWCNTs contribute to improved thermal storage properties and EMI shielding capabilities. The research aims to develop novel composites with dual functionality for thermal storage and EMI shielding, emphasizing the role of carbon matrices and their MWCNT composites. SEM and CT microtomography analyses reveal variations in MWCNT incorporation across the matrices, influenced by surface properties and porosity. Leaching tests, infrared spectroscopy (FT-IR) and differential scanning calorimetry (DSC) confirm the composite's stability and high latent heat storage. The presence of nanotubes enhances the thermal properties of octadecane and ΔH values almost reached their theoretical values. EMI shielding effectiveness measurements indicate that the composites show improved electric properties in the presence of MWCNTs.

Highly-Exposed Co-CoO Derived from Nanosized ZIF-67 on N-Doped Porous Carbon Foam as Efficient Electrocatalyst for Zinc-Air Battery.

Non-precious-metal based electrocatalysts with highly-exposed and well-dispersed active sites are crucially needed to achieve superior electrocatalytic performance for oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) toward zinc-air battery (ZAB). Herein, Co-CoO heterostructures derived from nanosized ZIF-67 are densely-exposed and strongly-immobilized onto N-doped porous carbon foam (NPCF) through a self-sacrificial pyrolysis strategy. Benefited from the high exposure of Co-CoO heterostructures and the favorable mass and electron transfer ability of NPCF, the Co-CoO/NPCF electrocatalyst exhibits remarkable performance for both ORR (E1/2  = 0.843 V vs RHE) and OER (Ej = 10 mA cm-2  = 1.586 V vs RHE). Further application of Co-CoO/NPCF as the air-cathode in rechargeable ZAB achieves superior performance for liquid-state ZAB (214.1 mW cm-2 and 600 cycles) and flexible all-solid-state ZAB (93.1 mW cm-2 and 140 cycles). Results from DFT calculations demonstrate that the electronic metal-support interactions between Co-CoO and NPCF via abundant C-Nx sites is favorable for electronic structure modulation, accounting for the remarkable performance.

Dense NiCo2 O4 Nanoneedles Grown on Carbon Foam Showing Excellent Electrochemical and Microwave Absorption Properties.

Electromagnetic pollution could harm sensitive electronic equipment due to the rising use of electronic devices and communication infrastructure. The supercapacitor's electrochemical performance should be enhanced, and electromagnetic damage should be prevented. This study proposes NiCo2 O4 /CF composites for supercapacitors and microwave absorption. They are made by combining hydrothermal and annealing processes. Dense NiCo2 O4 nanoneedles were uniformly grown on the outer layer of carbon foam (CF) as a growth skeleton, preventing the agglomeration of NiCo2 O4 . The composite had a specific capacitance of 537.5 F/g at 1 A/g. When the current density was set to 1 A/g, the supercapacitor that used NiCo2 O4 /CF as the cathode had a specific capacitance of 70.7 F/g, and when the current density was increased to 10 A/g, the original specific capacitance of 87.2 % could still be maintained after 5000 charge-discharge cycles. At a power density of 3695.5 W/kg, an energy density of 22.1 Wh/kg could be maintained. Furthermore, we performed a microwave absorption test and determined its reflection loss curve for various sample thicknesses. Recombination enhanced the composite material's microwave absorption capability by greatly reducing the dielectric loss and the magnetic loss.

Novel photoelectrochemical 3D-system for water disinfection by deposition of modified carbon nitride on vitreous carbon foam.

Graphitic carbon nitride (GCN) is an optical semiconductor with excellent photoactivity under visible light irradiation. It has been widely applied for organic micropollutant removal from contaminated water, and less investigated for microorganisms' inactivation. The photocatalytic degradation mechanism using GCN is attributed to a series of reactions with reactive oxygen species and photogenerated holes that can be boosted by modifying its physical-chemical structure. This work reports a successful improvement of the overall photocatalytic and electrocatalytic activities of the pristine material by thermal and chemical modification by a copolymerisation synthesis method. The copolymerisation of dicyandiamide as a precursor with barbituric acid strongly reduced photoluminescence due to the enhanced charge separation thus improving the catalyst efficiency under visible light irradiation. The material with 1.6 wt% of barbituric acid showed the best photocatalytic performance and electrochemical properties. This photocatalyst was selected for immobilisation on a conductive carbon foam, which promotes a higher electrochemical active surface area and enhanced mass transfer. This three-dimensional metal-free electrode was employed for the photoelectrochemical inactivation of two different microorganisms, Escherichia coli, and Enterococcus faecalis, obtaining removals below the detection limit after 30 min in simulated faecal-contaminated waters. This photoelectrochemical reactor was also applied to treat polluted river and urban waste waters, and the faecal contamination indicators were vastly reduced to values below the detection limit in 60 min in both cases, showing the wide applicability of this innovative photoelectrode for different types of polluted aqueous matrices.

Preparation and Testing of a Palladium-Decorated Nitrogen-Doped Carbon Foam Catalyst for the Hydrogenation of Benzophenone.

Catalytic activity of a palladium catalyst with a porous carbon support was prepared and tested for benzophenone hydrogenation. The selectivity and yields toward the two possible reaction products (benzhydrol and diphenylmethane) can be directed by the applied solvent. It was found that in isopropanol, the prepared support was selective towards diphenylmethane with high conversion (99% selectivity and 99% benzophenone conversion on 323 K after 240 min). This selectivity might be explained by the presence of the incorporated structural nitrogens in the support.

Synthesis of Iron on Carbon Foam for Use in the Removal of Phenol from Aqueous Solutions.

The potential use of magnetic nanopowder for phenol adsorption mobilised on natural grain carbon foam from an aqueous solution was studied. Phenolic compounds are priority pollutants with high toxicity even at low concentrations. A magnetic nanopowder was synthesised by dissolving an iron sponge in nitric acid to produce iron nitrate, which was added to a natural grain mixture with flour as the main ingredient. The synthesised carbon foam was investigated for the effects of initial concentration, time, and TEM (transmission electron microscopy) characterisation. The phenol adsorption increased as the iron content of the carbon foam and the initial concentration increased. A kinetic study showed that the phenol adsorption data adequately covered all the carbon foam samples tested using an equation corresponding to a pseudo-first order chemical reaction. The Freundlich, Langmuir, and Temkin equations were tested for modelling the adsorption isotherms at equilibrium, and it was concluded that the Temkin model fit the experimental data adequately. Due to its exceptional physical and chemical properties, carbon magnetic nanopowder is regarded as an outstanding pollutant absorber in environmental investigations. R2 values derived from the pseudo-first-order model exceed 0.99. R2 > 0.94 indicates that the Freundlich isotherm provides the best fit to the equilibrium data.

Melamine Foam-Derived Carbon Scaffold for Dendrite-Free and Stable Zinc Metal Anode.

Aqueous Zn-ion batteries (AZIBs) are one of the most promising large-scale energy storage devices due to the excellent characteristics of zinc metal anode, including high theoretical capacity, high safety and low cost. Nevertheless, the large-scale applications of AZIBs are mainly limited by uncontrollable Zn deposition and notorious Zn dendritic growth, resulting in low plating/stripping coulombic efficiency and unsatisfactory cyclic stability. To address these issues, herein, a carbon foam (CF) was fabricated via melamine-foam carbonization as a scaffold for a dendrite-free and stable Zn anode. Results showed that the abundant zincophilicity functional groups and conductive three-dimensional network of this carbon foam could effectively regulate Zn deposition and alleviate the Zn anode's volume expansion during cycling. Consequently, the symmetric cell with CF@Zn electrode exhibited lower voltage hysteresis (32.4 mV) and longer cycling performance (750 h) than the pure Zn symmetric cell at 1 mA cm-2 and 1 mAh cm-2. Furthermore, the full battery coupling CF@Zn anode with MnO2 cathode can exhibit a higher initial capacity and better cyclic performance than the one with the bare Zn anode. This work brings a new idea for the design of three-dimensional (3D) current collectors for stable zinc metal anode toward high-performance AZIBs.

Regulation pore size distribution for facilitating malachite green removal on carbon foam.

Malachite green (MG) is widely used as a textile dye and an aquacultural biocide, and become a serious pollution of drink water, but effectually isolating and removing it from wastewater are still a challenge. Here we report a new strategy to prepare a carbon foam with tunable pore size distribution by a one-pot lava foam process. We find that uniform micropore size is beneficial to the formation of C-OH coordination on the pore surface, increasing MG adsorption rates via H+ ionization. As a result, carbon foam with uniform pore size distribution demonstrates an optimum MG removal efficiency of 1812 mg g-1 and a higher partition coefficient of 3.02 mg g-1 µM-1, which is twice that of carbon foams with irregular pore size distribution. The adsorption of MG onto these adsorbents was found to be an endothermic monolayer chemical adsorption process, and the Gibbs free energy of adsorption process was decreased obviously by regulating micropore size distribution. The experiment results are in good agreement with pseudo-second-order kinetic and Langmuir isotherm models. Revealed the pore size distribution was the critical factor of MG removal by carbon foam. It should be and inspiration for the design and development of highly efficiency adsorbents for dyes removal.

Facile preparation of robust dual MgO-loaded carbon foam as an efficient adsorbent for malachite green removal.

This study developed a facile approach for the fabrication of dual MgO-loaded carbon foam (DMCF) via carbonization of a cured MgO/cyanate ester resin mixture, which underwent self-foaming of the resin followed by the carbothermal reduction of MgO. The features of the prepared DMCF prepared were characterized by FESEM, TEM, XRD, FTIR, XPS and so on, and the effects of adsorption conditions, adsorption isotherms, kinetics, and thermodynamics on malachite green (MG) removal using the DMCF as adsorbents were investigated through batch adsorption experiments. Results demonstrate that the DMCF possesses a unique dual loading of MgO particles which are not only loaded onto its foam walls but also filled within the walls with a graphene-wrapped core-shell structure. The experimental maximum adsorption capacity of MG reaches up to 1874.18 mg/g with a partition coefficient of 10.87 mg/g/µM. The adsorption process can be better described with Langmuir, pseudo-second-order, and intraparticle diffusion models. Moreover, the DMCF exhibits a removal percentage of 84.85% after five reuses, indicating that it is an efficient and promising adsorbent for MG adsorption.

Sodiophilically Graded Gold Coating on Carbon Skeletons for Highly Stable Sodium Metal Anodes.

Metallic sodium (Na) is an appealing anode material for high-energy Na batteries. However, Na metal suffers from low coulombic efficiencies and severe dendrite growth during plating/stripping cycles, causing short circuits. As an effective strategy to improve the deposition behavior of Na metal, a 3D carbon foam is developed that is sputter-coated with gold nanoparticles (Au/CF), forming a functional gradient through its thickness. The highly porous Au/CF host is proven to have gradually varying sodiophilicity, which in turn facilitates initially preferential Na deposition on the gold-rich, sodiophilic region in a "bottom-up growth" mode, leading to uniform plating over the entire Au/CF host. This finding contrasts with dendrite formation in the pristine CF host, as proven by in situ microscopy. The Na-predeposited Au/CF (Na@Au/CF) composite anode operates steadily for 1000 h at a low overpotential of ≈20 mV at 2 mA cm-2 in a symmetric cell. When the composite anode is coupled with a Na3 V2 (PO4 )2 F3 cathode, the full cell has a high capacity of 102.1 mAh g-1 after 500 cycles at 2 C. The sodiophilicity gradient design that is explored in this study offers new insight into developing porous Na metal hosts with highly stable plating/stripping performance for next-generation Na batteries.

A stiff ZnO/carbon foam composite with second-level macroporous structure filled ZnO particles for heavy metal ions removal.

A stiff zinc oxide/carbon foam (ZnO/CF) composite as a desirable adsorbent for heavy metal ions was innovatively designed and fabricated by loading ZnO particles into a carbon foam with capsule-like second-level macropores. The features of the resulting composite were characterized by FESEM, XRD, BET, FTIR, and XPS. The effects of adsorption parameters on the Pb(II), Cr(III), and Cu(II) ions removal were studied through batch experiments. Results show that the ZnO/CF composite possesses a second-level macroporous structure filled ZnO particles, which has both mesoporous structure and Zn-O-C bond with the strongly synergistic effect. And meanwhile, it has a relatively high compression strength of 2.18 MPa at a density of 0.18 g cm-3. The experimental maximum adsorption capacities for Pb(II), Cr(III), and Cu(II) ions reach 170.85 mg g-1, 168.74 mg g-1, and 104.61 mg g-1 with relatively high partition coefficients of 5.803 mg g-1 µM-1, 1.169 mg g-1 µM-1, and 0.648 mg g-1 µM-1, respectively. The experimental data are in accordance with Langmuir isotherm and pseudo-second-order kinetic model. Moreover, the composite still exhibits a good adsorption performance even after five cycles.

General and Scalable Fabrication of Core-Shell Metal Sulfides@C Anchored on 3D N-Doped Foam toward Flexible Sodium Ion Batteries.

Flexible self-standing transitional metal sulfides (TMSs)/carbon nanoarchitectures have attracted widespread research interests for sodium ion batteries (SIBs), thanks to their enormous capability to address intrinsic issues of TMSs for SIBs applications. However, controllable synthesis of hierarchical hybrid structures is always laborious and involves complicated procedures. Herein, a simple yet general and scalable adsorption-annealing strategy is first devised to finely construct core-shell carbon-coated TMSs (TMSs@C, including Co9 S8 @C, FeS@C, Ni3 S2 @C, MnS@C, and ZnS@C) nanoparticles anchored on 3D N-doped carbon foam (3DNCF) via the coordination and hydrogen-bond adsorption. Benefiting from synergistic contributions from strong chemical affinity between nanodimensional TMSs and 3DNCF, efficient electronic/ionic transport channels, as well as a uniform carbon accommodating layer, the resulted self-standing TMSs@C/3DNCF electrodes exhibit distinguished sodium storage performances, including large reversible capacities, high rate behaviors, and exceptional long-span cycle stability in both half cells and flexible full devices. More significantly, the smart methodology developed holds huge promise for commercialization of binder-free TMSs@C/3DNCF anodes toward advanced flexible SIBs.

A novel hierarchical stiff carbon foam with graphene-like nanosheet surface as the desired adsorbent for malachite green removal from wastewater.

A novel hierarchical stiff carbon foam (HSCF) was successfully prepared via a carbothermal reduction between the carbon foam with two-level pore structure and the Al2O3 from aluminum sulfate, and used as a bulk adsorbent for removing malachite green (MG) dye. The structures of the HSCF were characterized using SEM, XRD, FTIR, BET, and XPS, and the effects of adsorption condition on the MG removal were studied through batch adsorption experiments. Results show that large-sized and complex-shaped HSCF can be easily fabricated with a high compression strength of 1.58 MPa at a low bulk density (0.10 g cm-3). The HSCF possesses a fluffy graphene-like nanosheet surface with a mesoporous structure and meanwhile exhibits good hydrophilicity loaded with aluminum hydroxide. The experimental maximum adsorption capacity for MG reaches 425.2 mg g-1 with a relatively high partition coefficient of 9.38 mg g-1 µM-1 at the optimal condition. The experimental data are in good agreement with Langmuir isotherm and pseudo-second-order kinetic model, and meanwhile, the adsorption of MG onto the HSCF is a spontaneous and endothermic process. Also, the HSCF still exhibits good adsorption ability and stability after seven regeneration cycles.

Bacterial-Derived, Compressible, and Hierarchical Porous Carbon for High-Performance Potassium-Ion Batteries.

Hierarchical-structured electrodes having merits of superior cycling stability and high rate performance are highly desired for next-generation energy storage. For the first time, we reported a compressible and hierarchical porous carbon nanofiber foam (CNFF) derived from a sustainable and abundant biomaterial resource, bacterial cellulose, for boosting the electrochemical performance of potassium-ion batteries. The CNFF free-standing electrode with a hierarchical porous three-dimensional structure demonstrated excellent rate performance and outstanding cyclic stability in the extended cycling test. Specifically, in the long-term cycling-stability test, the CNFF electrode maintained a stable capacity of 158 mA h g-1 after 2000 cycles at a high current density of 1000 mA g-1, which has an average capacity decay of 0.006% per cycle. After that, the CNFF electrode maintained a capacity of 141 mA h g-1 at a current density of 2000 mA g-1 for another 1500 cycles, and a capacity of 122 mA h g-1 at a current density of 5000 mA g-1 for an additional 1000 cycles. The mechanism for the outstanding performance is that the hierarchical porous and stable CNFF with high surface area and high electronic conductivity provides sufficient sites for potassium-ion storage. Furthermore, quantitative kinetics analysis has validated the capacitive- and diffusion-controlled charge-storage contributions in the carbon-foam electrode. This work will inspire the search for cost-effective and sustainable materials for potassium electrochemical energy storage.

Myoglobin immobilized on mesoporous carbon foam in a hydrogel (selep) dispersant for voltammetric sensing of hydrogen peroxide.

Mesoporous carbon foam (MCF) was prepared by via the Pechini method which is facile and template-free. The MCF was characterized by field emission scanning electron microscopy, transmission electron microscopy, X-ray diffraction and BET surface area analysis. Afterwards, the MCF was dispersed in the natural hydrogel salep to give a composite. Finally, myoglobin was immobilized on the composite and then placed on a glassy carbon electrode (GCE). The modified GCE gives a distinct quasi-reversible redox peak during electroreduction of hydrogen perxide (H2O2). The estimated electron transfer coefficient (α) and the heterogeneous electron transfer rate constant (ks) for redox process of Mb are 0.54 and 2.25 s-1, respectively. The sensor, best operated at -0.2 V (vs. Ag/AgCl), responds to H2O2 in the 1.0 to 80 µM H2O2 concentration range, with a 180 nM limit of detection (at S/N ratio of 3). The technique was applied to the determination of H2O2 in spiked fetal bovine serum samples. Graphical abstract Mesoporous carbon foam (MCF) synthesis, dispersion in Salep solution, preparing the Salep-MCF composite (S-MCF), immobilizing the Mb at S-MCF and preparing Mb/S-MCF composite, Casting the Mb/S-MCF on electrode surface to prepare Mb/S-MCF/GCE and electrochemical behavior of biosensor.

Solid-State Lithium-Sulfur Batteries Operated at 37 °C with Composites of Nanostructured Li7La3Zr2O12/Carbon Foam and Polymer.

An all solid-state lithium-ion battery with high energy density and high safety is a promising solution for a next-generation energy storage system. High interface resistance of the electrodes and poor ion conductivity of solid-state electrolytes are two main challenges for solid-state batteries, which require operation at elevated temperatures of 60-90 °C. Herein, we report the facile synthesis of Al3+/Nb5+ codoped cubic Li7La3Zr2O12 (LLZO) nanoparticles and LLZO nanoparticle-decorated porous carbon foam (LLZO@C) by the one-step Pechini sol-gel method. The LLZO nanoparticle-filled poly(ethylene oxide) electrolyte shows improved conductivity compared with filler-free samples. The sulfur composite cathode based on LLZO@C can deliver an attractive specific capacity of >900 mAh g-1 at the human body temperature 37 °C and a high capacity of 1210 and 1556 mAh g-1 at 50 and 70 °C, respectively. In addition, the solid-state Li-S batteries exhibit high Coulombic efficiency and show remarkably stable cycling performance.

Facilitative capture of As(V), Pb(II) and methylene blue from aqueous solutions with MgO hybrid sponge-like carbonaceous composite derived from sugarcane leafy trash.

Enhancing the contaminant adsorption capacity is a key factor affecting utilization of carbon-based adsorbents in wastewater treatment and encouraging development of biomass thermo-disposal. In this study, a novel MgO hybrid sponge-like carbonaceous composite (HSC) derived from sugarcane leafy trash was prepared through an integrated adsorption-pyrolysis method. The resulted HSC composite was characterized and employed as adsorbent for the removal of negatively charged arsenate (As(V)), positively charged Pb(II), and the organic pollutant methylene blue (MB) from aqueous solutions in batch experiments. The effects of solution pH, contact time, initial concentration, temperature, and ionic strength on As(V), Pb(II) and MB adsorption were investigated. HSC was composed of nano-size MgO flakes and nanotube-like carbon sponge. Hybridization significantly improved As(V), Pb(II) and methylene blue (MB) adsorption when compared with the material without hybridization. The maximum As(V), Pb(II) and MB adsorption capacities obtained from Langmuir model were 157 mg/g, 103 mg/g and 297 mg/g, respectively. As(V) adsorption onto HSC was best fit by the pseudo-second-order model, and Pb(II) and MB with the intraparticle diffusion model. Increased temperature and ionic strength decreased Pb(II) and MB adsorption onto HSC more than As(V). Further FT-IR, XRD and XPS analysis demonstrated that the removal of As(V) by HSC was mainly dominated by surface deposition of MgHAsO4 and Mg(H2AsO4)2 crystals on the HSC composite, while carbon π-π* transition and carbon π-electron played key roles in Pb(II) and MB adsorption. The interaction of Pb(II) with carbon matrix carboxylate was also evident. Overall, MgO hybridization improves the preparation of the nanotube-like carbon sponge composite and provides a potential agricultual residue-based adsorbent for As(V), Pb(II) and MB removal.

Metal-Catalyzed Carbon Foams Synthesized from Glucose as Highly Efficient Electromagnetic Absorbers.

This paper introduces a novel method for preparing high-performance, metal-containing carbon foam wave-absorbing materials. The process involves foaming glucose through catalysis by transition metals followed by high-temperature pyrolysis. The resulting carbon foam materials exhibit a highly porous structure, which is essential for their wave-absorption properties. Notably, at a thickness of 2.0 mm, the glucose-derived carbon foam composite catalyzed by Fe and Co (GCF-CoFe) achieved a minimum reflection loss (RLmin) of -51.4 dB at 15.11 GHz, along with an effective absorption bandwidth (EAB) of 5.20 GHz, spanning from 12.80 GHz to 18.00 GHz. These impressive performance metrics indicate that this approach offers a promising pathway for developing low-density, efficient carbon foam materials for wave-absorption applications. This advancement has significant implications for fields requiring effective electromagnetic interference (EMI) shielding, stealth technology, and other related applications, potentially leading to more efficient and lightweight solutions.