Carbon Foam Research Articles

Tuning Work Function of Fe2N@C Nanosheets by Co Doping for Enhanced Lithium Storage.

Transition metal nitrides (TMNs) with high theoretical capacity and excellent electrical conductivity have great potential as anode materials for lithium-ion batteries (LIBs), but suffer from poor rate performance due to the slow kinetics. Herein, taking the Fe2N for instance, Co doping is utilized to enhance the work function of Fe2N, which accelerates the charge transfer and strengthens the adsorption of Li+ ions. The Fe2N nanoparticles with various Co dopants are anchoring on the surface of honeycomb porous carbon foam (named Cox-Fe2N@C). Co-doping can enlarge the work function of pristine Fe2N and thereby optimize the charging/discharging kinetics. The work function can be increased from 5.23eV (pristine Fe2N) to 5.67eV for Co0.3-Fe2N@C and 5.56eV for Co0.1-Fe2N@C. As expected, the Co0.1-Fe2N@C electrode exhibits the highest specific capacity (673mA h g-1 at 100mA g-1) and remarkable rate capability (375mA h g-1 at 5000mA g-1), outperforming most reported TMNs electrodes. Therefore, this work provides a promising strategy to design and regulate anode materials for high-performance and even commercially available LIBs.

Highly thermally conductive and shape-stabilized phase change materials with desirable solar/electric-to-thermal conversion performance based on high-modulus graphite/PVA foam

The widespread utilization of phase change materials (PCMs) has been impeded by challenges such as leakage, low thermal/electrical conductivity, and inadequate light absorption. Although constructing interconnected three-dimensional (3D) carbon networks within PCMs can mitigate these issues, their complex and energy-intensive fabrication processes, coupled with insufficient mechanical strength causing significant leakage and collapse of liquefied PCMs under external loads or impacts, hinder their practical application. Herein, we present a novel approach for the preparation of 3D graphite/polyvinyl alcohol foam (GPF) through a simple vacuum foaming combined with air-drying method. The obtained GPF-5 exhibits impressive compression strength (4.46 MPa) and compression modulus (93.1 MPa) at low density of 0.30 g/cm3. Upon impregnation with polyethylene glycol (PEG), GPF-5/PEG exhibits notable mechanical strength (7.62 MPa), contributing to its thermal shape stability and resistance to leakage. Even when subjected to temperatures above the melting point of PEG under external loads, GPF-5/PEG maintains its original shape without any liquid leakage. Due to the efficient construction of 3D thermal conductivity pathways within GPF, GPF-5/PEG demonstrates a high thermal conductivity of up to 3.48 W/m K−1 with graphite contents of 21.1 wt%, representing an increase of 136 % and 1640 % compared to graphite/PEG (with equivalent graphite content) and pure PEG, respectively. Additionally, GPF-5/PEG displays high latent heat of melting (136.8 J/g) and superior thermal cycling stability. Moreover, GPF-5/PEG demonstrates high solar-to-thermal and electric-to-thermal energy conversion capabilities, highlighting their potential for diverse applications. The work offers a rational strategy for fabricating high-modulus carbon foam, which can be used for PCMs-based multi energy conversion and storage systems with high thermo-mechanical properties.

Preparation and Characterization of Lightweight Carbon Foam Derived From Silicon‐Containing Arylacetylene Resin With Antioxidant Properties and Excellent Electromagnetic Interference Shielding Performance

ABSTRACTIn this study, carbon foam derived from silicon‐containing arylacetylene resin (CFPSA) was prepared by using silicon‐containing arylacetylene (PSA) resin as the carbon precursor and polyurethane (PU) foam as the organic sacrificial template. CFPSAs with diverse apparent densities were prepared through the simple impregnation of PU foam with PSA resin solutions of varying concentrations. Their structures, such as the pore morphology; chemical composition; thermal stability; compression properties, and electromagnetic interference (EMI) shielding effectiveness (SE), were characterized. The results indicate that with an increase in the PSA resin concentration, the skeleton of CFPSA becomes thicker, the pore size slightly increases, the apparent density increases, the compressive strength increases, and the EMI SE slightly reduces. CFPSA‐10's apparent density is 0.032 g/cm3, its 5% thermal weight loss temperature (Td5) in an air atmosphere is 642°C, its thermal conductivity is 38.1 mW/m K, its specific compression strength is 2.45 MPa/g cm3, and its specific EMI SE divided by thickness (SSE/t) is 2367 dB cm2/g. CFPSA exhibits lightweight and antioxidant properties, as well as excellent electromagnetic interference shielding performance, presenting great potential for application in aerospace and other fields.

Microwave plasma conversion of food waste using carbon foam: Production of heteroatom-doped graphene and combustible gas

The mass production of food waste (FW) has a terrible impact on the environment, but with proper treatment, FW can be transformed into a new resource. Currently, thermal conversion (especially incineration) has been the most common and efficient means of handling FW, but it also entails negative impacts, such as high carbon emissions and lower added value. In this study, a new high-efficiency thermal conversion process is proposed that uses carbon foams to induce the formation of microwave plasma (MP), which generates very high final temperatures to enable the direct conversion of FW into combustible gases and high-value-added heteroatom-doped microwave plasma graphene (HMPG) in 5–20 s. This work investigated the optimal carbonization temperature of the melamine sponge (carbon foam precursor) and the effect of microwave plasma reaction duration on the distribution of the gas products and the properties of HMPG, and HMPG was characterized in detail by Raman spectroscopy, X-ray diffraction, scanning electron microscope, etc. Ultimately, HMPG was tested in potassium ion battery anodes for evaluation of its energy storage potential, and the results showed that the capacities were able to reach ∼270 mAh g−1 at 50 mA g−1 after 60 cycles.

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.

MXene quantum dots modified pitaya peel-based composite phase change material with excellent thermal properties for building energy efficiency applications

Bio-based materials have attracted much attention because their application in the construction field is conducive to energy saving and emission reduction. In this paper, a bio-based composite phase change material (CPCM) was prepared by utilizing pitaya peel as a bio-based material, MXene quantum dots (MQDs) as a modified material, and polyethylene glycol (PEG) as a phase change medium. MXene quantum dots dispersed in the pitaya peel-based porous carbon skeleton enhanced the three-dimensional thermal conductivity network of the porous carbon skeleton somewhat improved the thermal conductivity (0.676 W/mK) of the polyethylene glycol/MXene quantum dots-modified pitaya peel-based porous carbon foam (PPF) composite phase change material (PEG/PPF@M). It is worth noting that PEG/PPF@M has excellent thermal stability and its enthalpy is basically unchanged after 100 cycles, which proves the recyclable stability of PEG/PPF@M in practical applications. PEG/PPF@M has great potential for thermal management of buildings and electronic components. Overall, a novel multifunctional CPCM was prepared in this study using a simple process method, which can not only be applied in electronic products to improve the service life of electronic components, but also in the field of construction to realize energy saving and emission reduction, as well as the recycling and reuse of waste.

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.

Colossal Barocaloric Effect in Encapsulated Solid‐Liquid Phase Change Materials

AbstractBarocaloric cooling as an emerging cooling technology offers an eco‐friendly alternative to traditional vapor compression refrigeration. Research on barocaloric materials primarily concentrates on solid–solid phase change materials (PCMs), among which plastic crystals exhibit colossal barocaloric effect. Solid‐liquid PCMs such as paraffin also exhibit giant barocaloric effect, however, their potential is often overshadowed by leakage issues. In this work, a strategy is demonstrated by encapsulating solid‐liquid PCMs into porous carbon matrixes to generate a large family of colossal barocaloric materials. In practice, by orthogonally combining paraffins with encapsulation matrixes like graphene foam, carbon nanotube foam, and carbon foam, it can be obtained composites that work without leakage issues. The significant advantage is their colossal barocaloric effect with the highest entropy value up to 570 J K−1 kg−1 in paraffin‐20@graphene foam. Moreover, the composites possess thermal conductivity up to 89.9 W m−1 K−1 in paraffin‐20@carbon foam, and tunable working temperature in the range of 270—330 K. Most importantly, this strategy, demonstrated with 5 solid‐liquid PCMs and 3 encapsulation matrixes in this work, is just the beginning. Further exploration with more materials can develop a huge family of encapsulated solid‐liquid PCMs with colossal barocaloric performance for modern cooling technology.

Semi-quantitative analysis of the structural evolution of mesophase pitch-based carbon foams by Raman and FTIR spectroscopies

Semi-quantitative analysis of the structural evolution of mesophase pitch-based carbon foams by Raman and FTIR spectroscopies

High Capacitance Performance N, O Codoped Carbon Foams Synthesized via an All-In-One Step Carbonization of Molecular Salt Strategy.

The preparation of porous carbon is constrained by the extensive use and detrimental impact of activators and dopants. Therefore, developing green and efficient strategies that leverage the intrinsic properties and pretreatment of the materials to achieve self-activation and self-doping is particularly crucial for porous carbon materials. Herein, potassium histidine was utilized as the molecular salt precursor, attaining the efficient and streamlined preparation of porous carbon through a one-step carbonization process that enables self-activation, self-doping, and self-templating. More interestingly, the carbonization temperature significantly impacts the porous structure of the molecular salt precursors, the properties of the heteroatoms, and electrochemical performance. The designed electrodes exhibit high accessibility to electrolyte ions and effective ion-electron transport channels. Therefore, the optimal carbon material (KHis800) has an excellent mass-specific capacitance of 305.2 F g-1 at 0.2 A g-1, and a high capacitance retention rate of 115.6% (50,000 cycles at 5 A g-1). Notably, KHis800 also shows a maximum energy density of 19.6 Wh kg-1. This research is dedicated to exploring a more efficient preparation method for porous carbon material via molecular salts, offering insights for the sustainable development of carbon materials.

Designing a Microstructure of NiCo-LDH@CNTs@Carbon Foam for Efficient Electromagnetic Wave Absorption and Excellent Environmental Tolerance.

The constantly evolving environment imposes increasingly stringent demands on the mechanical qualities of materials employed for absorbing electromagnetic waves (EMWs). Therefore, there is an urgent need for advanced materials capable of efficiently absorbing EMWs and withstanding harsh electromagnetic conditions. In this study, the electrodeposition method was effectively used to synthesize nickel-cobalt layered double hydroxides (NiCo-LDHs) in a controlled manner on a composite structure of carbon nanotubes and carbon foam, creating an exquisite construction. The manipulation of the electrodeposition time facilitated the regulation of the density of the layered structure within the composite material, thereby significantly enhancing its polarization relaxation performance. Increased defect sites and interface polarization enhance impedance matching and the attenuation constant, resulting in greatly improved absorption performance. The optimized sample demonstrated exceptional wave-absorbing performance in comparative experimental analysis, attaining a maximum reflection loss of -58.18 dB. It also has an effective absorption bandwidth of 5.36 GHz at a wavelength of 2.28 mm. The exceptional isolation effect of LDH, coupled with the outstanding insulation ability of the porous carbon skeleton, confers remarkable corrosion resistance and thermal insulation performance on the composite material. Hence, this discovery offers novel insights into designing environmentally tolerant absorbent materials.

Polyurethane Foam and Algae-Based Activated Carbon Biocomposites for Oil Spill Remediation.

This study investigates the incorporation of algae-based activated carbon into polyurethane foam to improve a biocomposite for gasoil sorption. The biocomposites were thoroughly analyzed using various techniques to examine the properties of both the blank foam and the algae activated carbon foam with a carbon content of 4.41 mass% and particle diameter of 500 µm. These techniques included Scanning Electron Microscopy (SEM), thermogravimetric analysis (TGA), and density analysis. The TGA analysis revealed that the biocomposites had an impact on the onset temperature (Tonset) of the foams. Higher concentrations of the biocomposites resulted in a decrease in Tonset from approximately 310 °C in the blank foam (PUF0) to 300 °C in the composite (PUF3B). The final residue percentage also decreased from around 20% in PUF0 to 10% in PUF3B. Density analysis showed that the apparent density of the foam increased from 0.016 g/cm3 in the blank foam to 0.020 g/cm3 in the biocomposite (PUF3B), while the real density slightly decreased from 0.092 g/cm3 to 0.076 g/cm3, indicating a reduction in overall porosity from 82.5% to 74.4%. All foams that were modified showed an increase in their ability to absorb gasoil in a PUF/gasoil/water system. The optimized biocomposite (PUF1B), with 1.14 mass% of 500 µm algae carbon, displayed the highest sorption capacity, starting at approximately 50 g/g at 1.5 h and increasing to 53 g/g over 72 h. The analysis of adsorption kinetics revealed that by utilizing adsorption isotherms, particularly the Langmuir isotherm, a more accurate fit to the data was achieved. This allowed for the prediction of the maximum gasoil adsorption capacity. This study aims to further develop, analyze, and utilize biocomposites made from algae-based activated carbon and polyurethane. These materials offer a sustainable and environmentally friendly approach to cleaning up oil spills.

Impact of raw material on thermo‐physical properties of carbon foam

AbstractCarbon foam materials are currently used in several industrial and engineering applications due to their outstanding properties. The properties of carbon foam can be altered through the manufacturing processes applied in specific applications. In this paper, we collected and analyzed four samples manufactured by CFOAM and one sample developed by Ohio University (OU) to understand the behaviour of this material and determine its properties. We utilized advanced techniques to experimentally measure and determine the following properties: pore size and volume, porosity, specific surface area, mass, density, and thermal conductivity. Among the samples, the low‐porosity CFOAM (CF35) and the OU sample exhibited higher specific surface areas and densities compared to the others. However, CF35 demonstrated the highest thermal conductivity, while OU displayed the lowest. As a result, CF35 emerges as the optimal choice for applications requiring high‐rate heat transfer, while the remaining CFOAM samples are well‐suited for lightweight applications. Thus, OU foam proves to be a highly suitable candidate for insulation applications such as building sidewalls.

Highly graphitized carbon foam to construct phase change materials composites for multiple solar−thermal energy conversion

Nowadays, converting and storing solar energy is crucial in contemporary society. Thermal energy storages (TESs) can be vital in harnessing solar energy effectively. Phase change materials (PCMs) are favorable candidates for TESs owing to the smoothing outcome and, thus, increasing reliability. However, these materials suffer from limited thermal conductivity, inadequate light absorption, and high leakage during phase transition. In the present study, a facile and scalable graphitized carbon foam/Ni nanoparticles composite with exciting properties such as excellent light adsorption and high thermal conductivity was prepared as a platform to overcome the PCMs challenges. To obtain this composite, the coated commercial melamine foams (CMF) with an ethanolic solution containing the phenolic resin and NiCl2.6H2O were pyrolyzed at 900 °C. The composite foam (CNiF) was utilized as a framework for paraffin (PA), which was soaked in melted PA at 75 °C under the vacuum drying oven for 50 min (CNiF/PA). The prepared black and magnetic composites exhibited high photo-to-thermal energy efficiency of 66, 80, and 92 % under light intensities of 900, 1000, and 1100 W/m2, respectively. In addition, the composite controls voltage fluctuations and prevents voltage drops in thermoelectric generators (TEGs) in solar thermal systems. The output voltages were 0.51, 0.63, and 0.81 V under light intensities of 1500, 1800, and 2100 W/m2, respectively. Moreover, the magnetically moving magnetic carbon foam solar absorber within the molten PA along the solar illumination path dramatically enhances the speed of solar-thermal energy storage. The set-up was subjected to light with an intensity of 1500 W/m2, which revealed a decrease in melting time, with the PA melting in 86 min. The PA melting time decreased by 37 % under solar irradiation.

A Green Slurry Electrolysis to Recover Valuable Metals from Waste Printed Circuit Board (WPCB) in Recyclable pH-Neutral Ethylene Glycol

The continuous growth of e-waste necessitates an efficient method to recover their metal contents to improve their recycling rate. The successful recovery of the metallic component from Waste Electrical and Electronic Equipment (WEEE) can generate great economic benefits to incentivize the industrial recycling effort. In this study, we report the use of slurry electrolysis (SE) in pH-neutral ethylene glycol (EG) electrolyte to extract and recover the metallic component from waste printed circuit broad (WPCB) powder. The system operates at room temperature and atmospheric pressure, and the electrolyte can be recycled multiple times with no signs of chemical degradation. The EG electrolyte system can oxidize the metallic component without triggering anodic gas evolution, which allowed us to incorporate a reticulated vitreous carbon (RVC) foam anode to maximize the capture and oxidation of the metal content. The system demonstrated up to 99.1% Faraday efficiency for the cathodic metal deposition and could recover Cu from the WPCB powder in a selective manner of 59.7% in the presence of 12 other metals. The SE reaction system was also scalable and displayed no compromises on the Cu recovery selectivity. With the ability to leach and recover metallic content from WPCB in a mild and chemically benign condition, the SE system displayed much promise to be adapted for industrial-scale metal recovery from WPCB. Reference Liu, K., Lam, JCH. et al. "A green slurry electrolysis to recover valuable metals from waste printed circuit board (WPCB) in recyclable pH-neutral ethylene glycol." J. Hazard. Mater. 2022433: 128702.Liu, K., Lam, JCH. et al. "Teaching Electrometallurgical Recycling of Metals from Waste Printed Circuit Boards via Slurry Electrolysis Using Benign Chemicals." J. Chem. Educ. 2023 100(2): 782-790. Figure 1

Optimizing Mid-Temperature Sodium Iodine Batteries for Sustainable Large-Scale Energy Storage: A Comprehensive Modeling Approach and Experimental Validation

The need for safe, eco-friendly, low-cost batteries for large scale implementation rises in the presence of the expansions of renewable energy sources. High-temperature liquid sodium batteries (e.g. sodium-sulfur) are a well-established technology for large-scale grid storage. Combining the molten sodium anode with an aqueous iodine cathode overcomes the problems of thermal loses and sealing by reducing the operating temperature to about 100°C. This leads to higher cost efficiency, energy density and a simplified cell design.Here we present a novel modelling approach for complex carbon-based cathode structures and its limits and abilities on enhancing the utilizable capacity. Due to their sustainability and high efficiency, which is comparable to Li-Ion –batteries, mid-temperature sodium-iodine batteries are a promising candidate for stationary energy storage applications. With a high specific energy of around 200 Wh kg-1, sodium-iodine batteries have the ability to meet the growing demand of short-term energy storage caused by the integration of renewable energy sources into the power grid. Up to this day, the detailed processes inside the battery are not well-understood. Quantities like initial species concentrations, C-rate, cell design and cathode geometry have large impacts on the overall battery performance. A deeper understanding of these processes is inevitable for enhancing the battery performance by choosing the optimal abovementioned quantities. We set up a fully resolved 3D Simulation model to gain insight into microstructural processes inside the battery, as experimental studies are limited to macroscopic quantities like electronic current and potential. The methodology is based on continuum hypothesis by using an open-source CFD software, which is rewritten accordingly. The proposed spatially resolved three-dimensional simulation model takes charge and mass transport, heterogeneous and homogeneous reactions as well as the electrochemical processes into account. Results show that transport limitations confine the utilizable capacity of the battery [1].This contribution focuses on enhancing the battery energy density and efficiency by including open-pored glassy carbon foam structures in the cathode half-cell [2, 3]. We state simulation predicted, optimal morphology properties of such a structure. Furthermore, we describe the evaluation of improved thermodynamic data of the aqueous iodine solution by refitting simulation results to polarization curves. We utilize a novel impedance spectroscopy simulation method for sodium iodine batteries to improve parameterization of the underlying electrochemical model by comparing the results with experimental data. References Gerbig, F., Cernak, S., Nirschl, H. (2021). 3D Simulation of Cell Design Influences on Sodium–Iodine Battery Performance. Energy Technology, vol. 9, no. 6, p. 2000857Gerbig, F., Cernak, S. and Nirschl H. (2021), Towards a Novel Sodium-Iodine Battery with an Aqueous Catholyte: Numerical Investigations of Complex Cathode Structures, ECS Trans., vol. 104, no. 1, pp. 123–130Gerbig, M. Holzapfel, and H. Nirschl, Simulating the Impact of Glassy Carbon Foam Electrodes on the Performance of Sodium Iodine Batteries, J. Electrochem. Soc., vol. 170, no. 4, p. 40517, 2023, doi: 10.1149/1945-7111/accab7. Figure 1

Continuous Direct Air Capture and Electrochemical Conversion of CO2 and H2O into Ethylene and Oxygen in Solid Electrolyte Reactor

Chemelectronics LLC has developed economical approach to use solar energy to convert CO2 directly captured from air using carbon dioxide capture conductive sorbent materials coated on carbon foam electrodes into chemical products (ethylene) and oxygen from nick foam electrodes separated with solid polyelectrolytes. We take advantage of commercial off-the-shelf solar panels as electricity to supply the electrochemical reduction of CO2 directly captured from air into chemical products with zero carbon emission.Based on the life cycle analysis, there is no CO2 emission from CO2 capture and conversion. The energy will be produced from solar panels.

4D-STEM and Eels Analysis of Complex C-Based Sensor Architectures

Transforming high-carbon precursors into open-porous carbon foams and coatings via thermal processes is gaining attention as a sustainable method for various applications, including catalysis, energy utilization, and sensing [1]. In this research, we adopt a one-step laser patterning approach to selectively pyrolyze doctor-bladed ink coatings on flexible PET substrates, thereby producing highly porous, intricately designed CO2 sensor structures with a thickness of about 50 µm. Our ink formulation includes glucose as a pore-forming agent and adenine as a nitrogen source to enhance sensing capabilities. Laser processing in an oxygen-rich setting results in flexible, highly porous sensor heterostructures characterized by distinct areas enriched with nitrogen and oxygen functionalities. The laser intensity’s attenuation with depth leads to the development of a distinctly porous graphitic surface layer (serving as the electrical transducer layer) and a denser nitrogen-enriched lower sensor layer, linked by a narrow transitional region [2]. To understand the formation and functionality of these sensors, we conducted an in-depth TEM analysis of cross-sections of the complete device, prepared through ultramicrotomy cross-sectioning. STEM-EELS elemental distribution maps distinctly show the chemical composition differences between the upper and lower layers of the sensor. Principal component analysis was utilized to separate the complex sensor structures into their constituent crystalline and amorphous carbon and nitrogen-containing phases. 4D-STEM analysis exposed the arrangement of the crystalline graphitic phase and the orientation of graphite basal planes adjacent to the pores of the open-porous sensor. Analyzing these structural parameters is essential for understanding the electrical performance of the sensor, as depicted in Figure 1 [3]. Figure 1: A (top)) SEM micrograph of sensor embedded in epoxy, (bottom) depth-dependent thermal laser intensity attenuation; B (left)) HA ADF-STEM micrograph showing different sensor layers, (middle) STEM-EELS nitrogen distribution map, (right) PCA bond analysis, C) HRTEM images of sensor from transducer (top) and sensor (bottom) layers with SAED image of respective ROIs (inset); D) 4D-STEM analysis depicting misalignment angle between graphitic carbon basal plane normal relative to the pore surface normalReferences[1] M. Hepp, et al. npj Flexible Electronics 6, 1-9 (2022)[2] H. Wang, et al. Advanced Functional Materials 32, 2207406 (2022)[3] C. Ophus, et al. Microscopy and Microanalysis 28, 390-403 (2022) Acknowledgements: We acknowledge use of the DFG-funded Micro-and Nanoanalytics Facility (MNaF) at the University of Siegen (INST 221/131-1). Figure 1

Advances in Inorganic Foam Materials Fabricated Via Blowing Strategy: A Comprehensive Review.

Two-dimensional (2D) materials with excellent properties and widespread applications have been explosively investigated. However, their conventional synthetic methods exhibit concerns of limited scalability, complex purification process, and incompetence of prohibiting their restacking. The blowing strategy, characterized by gas-template, low-cost, and high-efficiency, presents a valuable avenue for the synthesis of 2D-based foam materials and thereby addresses these constraints. Whereas, its comprehensive introduction has been rarely outlined so far. This review commences with a synopsis of the blowing strategy, elucidating its development history, the statics and kinetics of the blowing process, and the choice of precursor and foaming agents. Thereafter, we dwell at length on across-the-board foams enabled by the blowing route, like BxCyNz foams, carbon foams, and diverse composite foams consisting of carbon and metal compounds. Following that, a wide-ranging evaluation of the functionality of the foam products in fields such as energy storage, electrocatalysis, adsorption, etc. is discussed, revealing their distinctive strength originated from the foam structure. Finally, after concluding the current progress, we provide some personal discussions on the existing challenges and future research priorities in this rapidly developing method.

Graphene Reinforced Binary Resin-Based Carbon Foam Composites for Mechanical and Electromagnetic Interference Shielding Applications

Graphene Reinforced Binary Resin-Based Carbon Foam Composites for Mechanical and Electromagnetic Interference Shielding Applications