C — Journal of Carbon Research

Trace elements such as cobalt (Co), molybdenum (Mo), and zinc (Zn) play necessary roles in different biological functions. Co is a microelement that influences the vascular system. Mo works as an enzymatic cofactor of three enzymes (aldehyde oxidase, sulfite oxidase, and xanthine oxidase dehydrogenase). However, these elements are difficult to detect, since the analytical methods developed have a high cost, which restrict their applicability. In this sense, fluorescent sensors are an alternative for detecting trace elements, such as Mo⁴⁺ ions. Herein, a new multichannel trace elements sensor has been proposed to detect Mo entities. In this sense, two different N-CQDs were synthesized and fully characterized. The N-CQDs presented quantum yield values of 25.93% and 6.02% and excellent solubility in water. Also, a mixture of these two carbon-based nanoparticles was used to identify and to quantify Mo in water between seven different trace elements. The method was found to reach 1.28 and 3.88 ppm for limit of detection (LOD) and quantification (LOQ), respectively. To further verify the potential of the detection platform, the multichannel sensor was applied to identify the different concentrations of metal ions (Fe²⁺, Co²⁺, Mn²⁺, Cu²⁺, Zn²⁺, Mg²⁺, and Mo⁴⁺) in water. The data matrix was treated using different algorithms, such as K-Means and Discriminant Analysis (DA). The detection strategy has successfully identified the molybdenum ions at 5 ppm. This result shows the potential application of a multichannel sensor toward the detection of Mo entities, since it is comparable with the molybdenum test already available on the market. Full article

Pesticides pose a significant threat to nontargeted organisms, and their pervasive use makes avoidance challenging. We employed nitrogen-doped carbon cryogels for the removal of organophosphate pesticides. The materials were synthesized and characterized using SEM, Raman spectroscopy, XPS, and BET analysis. Results revealed mesoporous cryogels with pore diameters ranging from 3 to 13 nm. Interestingly, the specific surface area did not change systematically with increasing nitrogen content. All investigated materials have similar composition and structural disorder. Dimethoate, malathion, and chlorpyrifos removal was investigated under stationary and dynamic conditions. Stationary conditions demonstrated successful removal of aliphatic dimethoate and malathion by all investigated materials. Conversely, the materials with the lowest and highest nitrogen content proved ineffective with aromatic chlorpyrifos. Under dynamic conditions, all materials effectively removed malathion and chlorpyrifos while exhibiting suboptimal performance for dimethoate adsorption. Application of nitrogen-doped carbon cryogels to tap water spiked with pesticides yielded successful results under the same conditions. Toxicity testing of treated samples revealed a consistent decrease in toxicity, indicating that contact with cryogels reduces the initial solution’s toxicity. This result also confirms that material–pesticide interaction does not lead to the formation of more toxic byproducts. The demonstrated efficacy suggests the potential application of these materials in water treatment. Full article

In this study, we carried out an electrochemical investigation of the palladium electrodeposition process at pH 5 and 8, evaluating the kinetic parameters related to its nucleation and growth processes on a Highly Oriented Pyrolytic Graphite (HOPG) electrode from a plating bath containing 1 mM of Pd and 1 M NH₄Cl. The voltammetric study allowed us to identify the potential values at which palladium can be electrodeposited, along with the adsorption and desorption processes of hydrogen absorbed on the deposited Pd. Analysis of the peak currents of the deposited Pd indicated diffusional control at both pH values. The evaluation of kinetic parameters, such as the number of active nucleation sites (N₀), the nucleation rate (A), and the rate constant of the proton reduction process (k_PR), was determined via potentiostatic studies, revealing their dependence on the applied potential to the electrode. The number of active nucleation sites predicted by the nucleation model correlated well with the number of nuclei observed via Scanning Electron Microscopy (SEM). SEM images revealed that at pH 5, the Pd clusters had an average diameter of 27 nm and a height of 39 nm, while at pH 8, the clusters had an average diameter of 12.8 nm and a height of 16.6 nm. At pH 5, homogeneous and dispersed Pd clusters were obtained, while at pH 8, agglomeration of Pd clusters was observed. Full article

Biochar has gained significant interest in the agroforestry sector, mainly because of its ability to improve soil quality and sequester carbon in the atmosphere. Among the feedstocks of possible use for biochar production is biomass, understood as products and residues of plant origin from agriculture and forestry. The quality of the biomass used for biochar production is important because the physicochemical characteristics of the final product depend on it. This review examines the use of biochar produced from forest wastes and its impact on agriculture, forest ecosystems and the environment in general. This work demonstrates that the use of biochar not only improves agricultural productivity and production, but also that the sustainable management of the environment and forests and contributes to forest fire risk mitigation. The authors, examining the physico-chemical properties of biochar produced by forest waste, noted that the most critical variable is the process (pyrolysis temperature, residence time and heating rate), but the type of biomass used as a raw material and the forest species used also have a significant impact in determining the characteristics of the final product. Full article

Biochar and carbon adsorbents from citrus waste have been prepared by thermal and chemical treatments; they have been used in the aqueous phase adsorption of acetaminophen (ACE) as a model emerging pollutant. These materials were fully characterized by elemental analysis, X-ray fluorescence (TXRF), adsorption/desorption of nitrogen, X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), point of zero charge (pH_pzc), scanning electron microscopy (SEM), and thermogravimetric analyses (TGA/DTG/DTA). A magnetic carbon adsorbent was obtained by FeCl₃ activation under an inert atmosphere, giving rise to the best results in ACE adsorption. Adsorption equilibrium data were obtained at 298, 318, and 338 K and fitted to different models, corresponding to the best fitting to the Redlich–Peterson model. The maximum adsorption capacity at equilibrium resulted in 45 mg ACE·g⁻¹ carbon at 338 K. The free energy values were calculated, and values between −21.03 and −23.00 kJ·mol⁻¹ were obtained; the negative values confirmed the spontaneity of the process. The enthalpy and entropy of the adsorption process were obtained, giving rise to −6.4 kJ·mol⁻¹ and 49 J·mol⁻¹·K⁻¹, respectively, indicating a slightly exothermic process and an increase in the randomness at the solid–liquid interface upon adsorption, respectively. The adsorption kinetics were also studied, with the Elovich model being the one that gave rise to the best-fitting results. Full article

Modifying the polymer matrix by nanoparticles can be a promising approach to improve the performance of fiber-reinforced polymer (FRP) composites. Organic solvents are usually used for dispersing graphene oxide (GO) well in the polymer matrix. In this study, a green, facile, and efficient approach was developed to prepare epoxy/GO nanocomposites. In situ polymerization is used for synthesizing nanocomposites, eliminating the need for organic solvents and surfactants. By loading just 0.6 wt% of GO into the epoxy resin, Young’s modulus, tensile strength, and toughness improved by 38%, 46%, and 143%, respectively. Fractography analysis indicates smooth fracture surfaces of pure resin that changed to highly toughened fracture surfaces in this nanocomposite. Plastic deformation, crack pinning, and deflection contributed to improving the toughness of the nanocomposites. FTIR investigations show that amide bonding was created by the reaction of the carboxylic acid groups in GO with some amine groups in the curing agent during the dispersion processes. Full article

With the worldwide awareness of sustainability, biomass-derived carbon electrode materials for supercapacitors have attracted growing attention. In this research, for the first time, we explored the feasibility of making use of the carbon byproduct from hydrothermal liquefaction (HTL) of microalgae, termed herein as algae-derived carbon (ADC), to prepare sustainable carbon electrode materials for high-performance supercapacitor development. Specifically, we investigated carbon activation with a variety of activating reagents as well as N- and Fe-do** of the obtained ADC with the intention to enhance its electrochemical performance. We characterized the structure of the activated and doped ADCs using scanning electron microscope (SEM), Raman spectroscopy, Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), and BET surface area and pore analysis, and correlated the ADCs’ structure with their electrochemical performance as evaluated using cyclic voltammetry (CV), galvanostatic charge/discharge (GCD), impedance, and cycle stability through an assembled symmetric two-electrode cell with 1 M H₂SO₄ as electrolyte. It was found that the ADC that is activated using KOH (KOH-ADC) showed the best electrochemical performance, and its specific capacitance was 14.1-fold larger with respect to that of the raw ADC and reached 234.5 F/g in the GCD test at a current density of 0.5 A/g. The KOH-ADC also demonstrated excellent capacitance retention (97% after 10,000 cycles at a high current density of 10 A/g) for stable long-term operations. This research pointed out a promising direction to develop sustainable electrode materials for supercapacitors from the carbon byproduct produced after HTL processing of algae. Full article

Non-impregnated small-pore graphite (NSPG), which has a compact microstructure and is used in molten salt reactors (MSRs), was prepared by a novel process. The pore diameter of NSPG was reduced to ~800 nm. The irradiation evaluation of NSPG was carried out by 7 MeV Xe²⁶⁺ ion irradiation. The microstructural changes of NSPG were investigated with IG-110 as a comparison. The graphitization degree of NSPG was higher than that of IG-110, though it was not subjected to an impregnation process. Under low-dose ion irradiation (<2.5 dpa), the microscopic morphology of the NSPG changes in a small magnitude, and the lamellar structure of graphite remains within the scale of more than a dozen nanometers, which exhibits a better resistance to irradiation. With the increase in irradiation dose, the accumulation of defects leads the graphite toward amorphization, which shows consistency with IG-110. This study provides an efficient and low-cost method for the preparation of graphite for MSR, and investigates the damage behavior of graphite, which is of great significance in accumulating data for the development of MSR nuclear graphite and the optimal design of graphite materials. Full article

Metal-doped carbonaceous materials have garnered significant attention in recent years due to their versatile applications in various fields, including catalysis, energy storage, environmental remediation, electronics, and sensors, as well as reinforcement. This study investigates the synthesis and characterization of a composite material featuring a carbonaceous matrix doped with copper, focusing on the thermolysis of glycine as a precursor. The synthesis methodology involved utilizing glycine and copper acetate monohydrate in varying ratios, with the mixture subjected to heating in ceramic crucibles at temperatures ranging from 450 to 550 °C, with pyrolysis yields over the 5 to 39% interval. The pristine and Cu-doped samples obtained at 500 °C underwent characterization using a diverse array of techniques, including scanning and transmission electron microscopies, multi-elemental analysis by energy dispersive X-ray spectroscopy, CHNS elemental analysis, X-ray photoelectron spectroscopy, X-ray powder diffraction, infrared and Raman spectroscopies, ultraviolet-visible spectroscopy, and terahertz time-domain spectroscopy, along with conductivity measurements. Under optimized conditions, copper (at 6.5%) was present primarily in the free metallic form, accompanied by traces of tenorite (CuO) and cuprite (Cu₂O). The carbonaceous matrix exhibited a 6:1 ratio of graphitic carbon to a carbon-nitrogen compound with the formula C₂H₂N₂O₂, such as isomers of diazetidinedione, according to multi-elemental analysis results. Conductivity measurements disclosed a significant increase in conductivity compared to the product of glycine thermolysis, showcasing the enhanced electrical properties of the new composite. Additionally, terahertz measurements showed the potential of the material as a broadband absorber for the fabrication of terahertz devices and provided compelling evidence of a significant improvement in radiation absorption upon copper do**. In conclusion, this research sheds light on the promising properties of copper-doped carbonaceous composites obtained by glycine pyrolysis, offering insights into their potential applications in emerging technological domains. Full article

Based on recent interest and on the importance of the ongoing climate change catastrophe, this article provides the basics of global carbon cycle modelling as required for the assessment of the degree of carbon neutrality of biomass energy, and its underlying dynamics. It is aimed at clarifying the question “Are biomass fuels carbon neutral?”. The “Combined Energy and Biosphere Model” (CEBM) computes annual carbon flows including growth and decay of plants on 2.5 × 2.5° grid elements of the continents’ surface and offers detailed results on the changes of after implementation of large-scale biomass energy strategies worldwide. The main (and possibly unexpected) effect is the long-term depletion of the soil organic compartment after extraction of biomass fuels. When comparing CEBM model runs using (i) biomass energy sources and (ii) carbon-free energy sources (such as solar or wind), it becomes quantitatively clear already on the theoretical level (i.e., even without taking into account efficiency losses) that biomass is only “half as carbon neutral” as ideally assumed, to express a rule of thumb—mainly because of soil carbon depletion. Still, biomass energy will play an important role when fighting global warming, even if efforts to lower energy demand are preferable as a fundamental strategy. Full article

Glucose-derived carbon hybrids were synthesized by hydrothermal treatment in the presence of oxidized carbon nanotubes. Additionally, iron and nitrogen functionalities were incorporated into the carbon structure using different methodologies. The introduction of iron and nitrogen in a single step under a H₂ atmosphere favored the formation of quaternary nitrogen and oxidized nitrogen, whereas the incorporation of nitrogen under an N₂ atmosphere after do** the hybrids with iron mainly produced pyridinic nitrogen. The samples were characterized by scanning electron microscopy, X-ray spectroscopy, adsorption isotherms, inductively coupled plasma optical emission spectrometry, and Raman spectroscopy. The presence of iron and nitrogen in the carbons increases the onset potential toward oxygen reduction in KOH 0.1 mol L⁻¹ by 130 mV (0.83 V), in comparison to carbonized glucose, whereas the reaction mechanism shifts closer to a direct pathway and the formation of HO₂⁻ decreases to 25% (3.5 electrons). The reaction rate also increased in comparison to the carbonized glucose, as observed by the decrease in the Tafel slope value from 117 to 61 mV dec⁻¹. Furthermore, the incorporation of iron and nitrogen in a single step enhanced the short-term performance of the prepared electrocatalysts, which may also be due to the higher relative amount of quaternary nitrogen. Full article

In this work, passive cooling systems for the revam** of existent silicon photovoltaic (PV) cells were developed and analysed in order to mitigate the efficiency loss caused by temperature rise in the hot season. For this purpose, expanded graphite (EG) was used to stabilize a phase change material (PCM) with a melting temperature close to 53 °C in order to realize thermal management systems (TMSs) able to store heat at constant temperature during melting and releasing it in crystallization. In particular, stearic and palmitic acid mixture (PA-SA) was shape-stabilized in EG at different concentrations (10, 12 and 14 part per hundred ratio) under vacuum into a rotary evaporation apparatus followed by cold compaction; PA-SA leakage was reduced due to its intercalation between the graphite lamellae, and the thermal conductivity necessary to maximize the heat transfer to a bulk TMS was improved via powder cold compaction, which minimizes voids and creates preferential thermal conductive patterns. The composite materials, stable till 150 °C, were tested by differential scanning calorimetry (DSC) at 1 °C/min to precisely determine the phase transition temperatures and the enthalpic content, which was only slightly reduced from 196 J/g of the neat PCM to 169 J/g due to the very low EG fraction necessary for the stabilization. Despite only the 14:100 EG-to-PA-SA ratio, the system’s thermal conductivity was enhanced 40 times with respect to the neat PCM (from 0.2 to 8.3 W/(m K), value never reached in works present in the literature), with a good convergence of the values evaluated through hot disk tests and laser flash analysis (LFA), finding correlation with both graphitic content and density. In order to completely avoid leaking with the consequent dispersion of PCM in the environment during the final application, all the samples were encapsulated in a PE-made film. The mechanical properties were evaluated with compression tests at 30 °C and 80 °C simulating a possible compressive stress deriving from the contact needed to maintain the TMS position on the rear of the PV cells. Finally, the material response was simulated by imposing thermal cycles into a climatic chamber and reproducing the three hottest and coldest days of summer 2022 of two Italian locations, Verona (Veneto, 45° N, 11° E) and Gela (Sicily, 37° N, 14° E), thus highlighting the thermal management effects with delays in temperature increase and daily peak temperature smoothing. The role of EG is strategic for the processing and the properties of the resulting composites in order to realize a proper compromise between the melting enthalpy of PCM and the thermal conductivity enhancement given by EG. Full article

This paper presents a comparative analysis of ausferritic ductile cast iron matrix obtained through heat treatment and in its raw state. Ausferrite without heat treatment was achieved by modifying the chemical composition, while nodular graphite was produced using Inmold technology. The presence of compacted graphite in the as-cast ausferritic cast iron was attributed to elements that impede the crystallization of nodular graphite. This study demonstrates that an ausferritic matrix in ductile cast iron can be achieved by incorporating molybdenum in conjunction with nickel or copper. Thermal and derivative analysis (TDA) revealed a minor thermal effect during the transformation of austenite into bainitic ferrite in as-cast ausferritic cast iron. Furthermore, the transformation of austenite in cast iron containing nickel was observed to occur at a temperature of approximately 60 °C higher than in cast iron with copper. The structure of bainitic ferrite platelets in as-cast ausferritic ductile cast iron resembled that of Austempered Ductile Iron (ADI). It was revealed that the amount of austenite in as-cast ausferritic ductile cast iron is more than double that in ADI. The carbon content of austenite was estimated theoretically, revealing that alloying additives in the as-cast ausferritic ductile cast iron reduce the solubility of carbon in austenite, thereby significantly influencing the properties of the cast iron. Full article

We explore the possibility of attaining valley-dependent tunnelling and confinement using proximity-induced spin-orbit couplings (SOCs) in graphene-based heterostructures. We consider gate-tunable asymmetric quantum dots (AQDs) on graphene heterostructures and exhibiting a $C_{3v}$ and/or $C_{6v}$ symmetry. By employing a tight-binding model, we explicitly reveal a pure valley confinement and valley signal in AQDs by streaming the valley local density, leading to valley-charge separation in real space. The confinement of the valley quasi-bound states is sensitive to the locally induced SOCs and to the spatial distribution of the induced AQDs; it is also robust against on-site disorder. The adopted process of attaining a pure valley-Hall conductivity and confinement with zero charge currents is expected to provide more options towards valley-dependent electron optics. Full article

Activated carbon (AC) serves as extensively researched adsorbents, with numerous established methods for their preparation. This study originated from the hypothesis that compressing a hydrocarbon substance to create a densely compacted pellet, known as pelletizing, would enhance the development of porous features of the resulting AC. The anticipated enhancement is attributed to the rise in spatial proximity amidst HEC polymer chains within the bulk of the pellet, which facilitates aromatization both in extent and functionality. 2-Hydroxyethyl cellulose (HEC) pellets were prepared by adjusting the duration of load holding, aiming to increase the packing density of HEC polymer chains via cree**. The BET analysis of the resulting AC samples demonstrates the efficacy of compression on HEC pellets in enhancing their porous properties. The FE-SEM study revealed diverse AC surface morphologies that are associated with a set of specific pelletizing conditions. The ¹³C NMR spectroscopy for carbon skeletons, FT-IR spectroscopy for organic functionality, and XPS spectroscopy for surface composition collectively report the leverage of compression treatment before pyrolyzing HEC pellets. Furthermore, the assessment of hydrogen sulfide adsorption by the resulting AC samples revealed distinctive breakthrough curves, providing validation for the proposed compression effect. Full article

Carbon-based materials have garnered significant attention since the groundbreaking synthesis of graphene. The exploration of novel 2D carbon allotropes has led to the discovery of materials with intrinsic properties distinct from graphene. Within this context, the biphenylene network (BPN) was successfully synthesized. In this study, we used molecular dynamics (MD) simulations with the Reactive Force Field (ReaxFF) to delve into the thermomechanical properties and fracture patterns of biphenylene-based nanotubes (BPN-NTs) exhibiting armchair (AC-BPN-NT) and zigzag (ZZ-BPN-NT) chiralities. Throughout the longitudinal deformation process, we observed significant morphological transformations preceding the structural fracture of the system. These transformations unfolded in distinct inelastic phases. In both cases, AC- and ZZ-BPN-NT, stress accumulation in four-membered rings led to the creation of octagonal structures; however, in AC, this occurs in the fracture region, subsequently causing the presence of nanopores. On the other hand, for ZZ-BPN-NT, stress accumulation in the rectangular rings occurred in bonds parallel to the deformation, with elongated octagonal structures. The Young’s modulus of these nanotubes ranged from 746 to 1259 GPa, with a melting point of around 4000 K. Our results also explore the influence of diameter and curvature, drawing comparisons with BPN monolayers. Full article

Fiber-reinforced cement composites, particularly those incorporating natural fibers like cellulose, have gained attention for their potential towards more sustainable construction. However, natural fibers present inherent deficiencies in mechanical properties and can benefit from hybridization with carbon fibers. This study focuses on the incorporation of cellulose and carbon fibers, in varying contents, into fibrocement composites, employing a Response Surface Methodology (RSM) to optimize the material characteristics. The methodology involves testing, encompassing flexural tensile, compression, and fracture toughness tests. The results indicate an increasing trend in flexural strength for higher carbon fiber content, peaking near 5%. A plateau in flexural strength is observed between 1.2% and 3.6% carbon fiber content, suggesting a range where mechanical properties stabilize. Compressive strength shows a plateau between 1.2 and 3.6% and reaches its highest value (≈33 MPa) at a carbon fiber content greater than 4.8%, and fracture toughness above 320 MPa·m^1/2 is achieved with carbon fiber content above 3.6%. This study offers insights into optimizing the synergistic effects of cellulose and carbon fibers in fibrocement composites. Full article

The present work delineates the tailoring of the thermal effusivity and diffusivity of the novel class of heat transfer fluids—ionanofluids—by the incorporation of nanocarbons like diesel soot (DS), camphor soot (CS), carbon nanotubes (CN), and graphene (GR). When the thermal diffusivity delivers information on the thermal energy propagation, the thermal effusivity concerns the energy exchange at the interface, enabling energy-efficient thermal system design. The nanocarbons are subjected to morphological characterisation by field emission scanning electron microscopy. Fourier-transform infrared and Raman spectroscopic analyses confirm functional groups and vibrational bands. The microcrystalline size and graphiticity are also understood from the Raman spectrum. Ionanofluids prepared by dispersing nanocarbons into an ionic liquid base 1-Butyl-3-methylimidazolium methyl sulfate (BMMS) are analysed by nondestructive photopyroelectric calorimetry (PPE). The PPE analysis of ionanofluids demonstrates that nanocarbons influence thermal parameters in the base fluid, with soot ionanofluids exhibiting increased thermal effusivity and diffusivity due to their various carbon allotropic composition. This study underscores the importance of selecting the appropriate carbon allotrope for tailoring ionanofluids’ thermal properties, providing insights into manipulating these properties for enhanced performance across various industrial applications. Full article

Modern integrated circuits (ICs) take advantage of three-dimensional (3D) nanostructures in devices and interconnects to achieve high-speed and ultra-low-power performance. The choice of electrical insulation materials with excellent dielectric strength, electrical resistivity, strong mechanical strength, and high thermal conductivity becomes critical. Diamond possesses these properties and is recently recognized as a promising dielectric material for the fabrication of advanced ICs, which are sensitive to detrimental high-temperature processes. Therefore, a high-rate low-temperature deposition technique for large-grain, high-quality diamond films of the thickness of a few tens to a few hundred nanometers is desirable. The diamond growth rate by microwave plasma chemical vapor deposition (MPCVD) decreases rapidly with lowering substrate temperature. In addition, the thermal conductivity of non-diamond carbon is much lower than that of diamond. Furthermore, a small-grain diamond film suffers from poor thermal conductivity due to frequent phonon scattering at grain boundaries. This paper reports a novel MPCVD process aiming at high growth rate, large grain size, and high sp³/sp² ratio for diamond films deposited on silicon. Graphite paste containing nanoscale graphite and oxy-hydrocarbon binder and solvent vaporizes and mixes with gas feeds of hydrogen, methane, and carbon dioxide to form plasma. Rapid diamond growth of diamond seeds at 450 °C by the plasma results in large-grained diamond films on silicon at a high deposition rate of 200 nm/h. Full article