Search Results (48)

In chemical vapor deposition (CVD)-mediated graphene growth, copper foil serves as both a catalyst for methane decomposition and as a substrate for graphene nucleation and growth. Due to the low solubility of carbon in copper and the ease of transferring graphene from its surface, copper—particularly the Cu(111) facet—is widely favored for high-quality, monolayer graphene synthesis. In this article, the thermodynamic processes involved in methane dissociation and graphene nucleation on the Cu(111) surface were investigated using density functional theory (DFT). Molecular dynamics simulations were performed for structural optimization and to evaluate the reaction energies. Additionally, the average adsorption energies (ΔEad) of carbon clusters with varying atomic numbers on the Cu(111) surface were calculated. The graphene growth process was further modeled using the kinetic Monte Carlo (KMC) method to simulate carbon atom migration and nucleation dynamics. Thermodynamic analysis based on equilibrium component data was conducted to examine the influence of key operational parameters—temperature, pressure, and the CH₄/H₂ partial pressure ratio—on the graphene deposition rate. Full article

The sodium super ionic conductor (NASICON) structured LiTi₂(PO₄)₃ (LTP) has been developed as electrode material for Li-ion batteries (LIBs) with promising electrochemical performance, owing to its outstanding structural stability and rapid lithium-ion diffusion. Nevertheless, challenges still exist, especially the rapid capacity fading caused by the low electronic conductivity of LTP-NASICON material. Recently, the hydrothermal method has emerged as an important technique for the production of diverse nano-electrode materials due to its low preparation temperature, high phase purity, and well-controlled morphology and crystallinity. Herein, we report, for the first time at low-moderate temperatures, an advanced hydrothermal synthesis of LTP-coated reduced graphene oxide (LTP@rGO) particles that includes the growth of LTP particles while simultaneously coating them with rGO material. The LTP offers a discharge specific capacity of 84 mAh/g, while the LTP@rGO delivers a discharge capacity of 147 mAh/g, both with a coulombic efficiency of 99.5% after 100 cycles at a 1C rate. Full article

Chemical vapor deposition (CVD) is a highly adaptable manufacturing technique used to fabricate high-quality thin films, making it essential across numerous industries. As materials fabrication processes progress, CVD has advanced to enable the precise deposition of both inorganic 2D materials, such as graphene and transition metal dichalcogenides, and high-quality polymeric thin films, offering excellent conformality and precise nanostructure control on a wide range of substrates. Conjugated conducting polymers have emerged as promising materials for next-generation electronic, optoelectronic, and energy storage devices due to their unique combination of electrical conductivity, optical transparency, ionic transport, and mechanical flexibility. Oxidative CVD (oCVD) involves the spontaneous reaction of oxidant and monomer vapors upon their adsorption onto the substrate surface, resulting in step-growth polymerization that commonly produces conducting or semiconducting polymer thin films. oCVD has gained significant attention for its ability to fabricate conjugated conducting polymers under vacuum conditions, allowing precise control over film thickness, doping levels, and nanostructure engineering. The low to moderate deposition temperature in the oCVD method enables the direct integration of conducting and semiconducting polymer thin films onto thermally sensitive substrates, including plants, paper, textiles, membranes, carbon fibers, and graphene. This review explores the fundamentals of the CVD process and vacuum-based manufacturing, while also highlighting recent advancements in the oCVD method for the fabrication of conjugated conducting and semiconducting polymer thin films. Full article

Here, crystalline SiO₂ quantum dots (QDs) of 3–5 nm size were grown within the layers of reduced graphene oxide (rGO) by a solution mode chemical growth process at a relatively low temperature (100 °C). The composite was applied as a negative electrode in a Li-ion half-cell battery and the electrochemical investigation confirmed a distinct first-cycle discharge/charge capacity (~865 mAhg⁻¹/387 @ 51 mAg⁻¹). The battery could retain a capacity of 296 mAhg⁻¹ after 60 charge/discharge cycles with 99% coulombic efficiency. Furthermore, at a high current rate of 1.02 Ag⁻¹, the battery was able to display an apparent rate capability (214.47 mAhg⁻¹), indicating the high chemical and mechanical stability of the composite at a high current rate. A structural analysis revealed clear distinct diffraction peaks of SiO₂ and high-resolution transmission electron microscopy images showed discrete atomic planes, thereby confirming the growth of crystalline SiO₂ QDs within the layers of rGO. Full article

Coal tar, a by-product of the pyrolysis of coal, is rich in aromatic compounds that have the potential to facilitate the synthesis of graphene, a high-quality carbon material, via low-temperature chemical vapor deposition (CVD). This approach offers a promising avenue for the cost-effective and large-scale industrial production of graphene while minimizing energy consumption. Nevertheless, there is a paucity of research focused on the low-temperature synthesis mechanisms of graphene derived from aromatic compounds in the context of graphene growth. To achieve high-quality graphene synthesis from coal tar and its aromatic constituents at reduced temperatures, a comprehensive investigation into the reaction pathways of these aromatic compounds is essential. In this study, we meticulously simulate the pyrolysis of benzene, a key aromatic component of coal tar, across various temperature settings utilizing reactive force field (ReaxFF) methodology. Furthermore, we apply density functional theory (DFT) calculations, executed through the Vienna Ab initio Simulation Package (VASP), to assess the dehydrogenation energy associated with the adsorption of benzene on vapor-deposited copper foils. Our molecular dynamics simulations, enhanced by a mixed force field approach, revealed that the dehydrogenated benzene ring (C₆ intermediate) acts as a critical precursor for graphene synthesis. This research significantly elucidates the reaction pathways of aromatic benzene in coal tar through molecular simulations conducted at different temperatures, both in the gas phase and on solid copper foil substrates. Full article

This study explores the low-temperature synthesis of graphene using plasma-enhanced chemical vapor deposition (PECVD), emphasizing the optimization of process parameters to achieve controlled growth of pristine and hydrogenated graphene. Graphene films were synthesized at temperatures ranging from 700 °C to as low as 400 °C by varying methane (25–100 sccm) and hydrogen (25–100 sccm) gas flow rates under 10–20 mBar pressures. Raman spectroscopy revealed structural transitions: pristine graphene grown at 700 °C exhibited strong 2D peaks with an I(2D)/I(G) ratio > 2, while hydrogenated graphene synthesized at 500 °C showed increased defect density with an I(D)/I(G) ratio of ~1.5 and reduced I(2D)/I(G) (~0.8). At 400 °C, the material transitioned to a highly hydrogenated amorphous carbon film, confirmed by photoluminescence (PL) in the Raman spectra. Atomic force microscopy (AFM) showed pristine graphene with a root mean square roughness (R_q) of 0.37 nm. By carefully adjusting PECVD synthesis parameters, it was possible to tune the surface roughness of hydrogenated graphene to levels close to that of pristine graphene or to achieve even smoother surfaces. Conductive AFM measurements revealed that hydrogenation could enhance graphene’s contact current under specific conditions. The findings highlight the role of PECVD parameters in tailoring graphene’s structural, morphological, and electronic properties for diverse applications. This work demonstrates a scalable, low-temperature approach to graphene synthesis, offering the potential for energy storage, sensing, and electronic devices requiring customized material properties. Full article

Recent observations of superconductivity in low-dimensional systems composed of twisted, untwisted, or rhombohedral graphene have attracted significant attention. One-dimensional moiré superlattices and flat bands have interestingly been identified in collapsed chiral carbon nanotubes (CNTs), opening up new avenues for the tunability of the electronic properties in these systems. The nucleation of hexagonal moiré superlattices and other types of stacking faults has also been demonstrated in partially collapsed and uncollapsed carbon nano-onions (CNOs). Here, we report a novel investigation on the dynamics of stacking fault nucleation within the multilayered lattices of micrometer-scale vertically oriented films of multiwall CNTs (MWCNTs), resulting from the pyrolysis of molecular precursors consisting of ferrocene or dimethyl ferrocene, at low vapor flow rates of ~5–20 mL/min. Interestingly, local nucleation of moiré-like superlattices (as stacking faults) was found when employing dimethyl ferrocene as the pyrolysis precursor. The morphological and structural properties of these systems were investigated with the aid of scanning and transmission electron microscopies, namely SEM, TEM, and HRTEM, as well as X-ray diffraction (XRD) and Raman point/mapping spectroscopy. Deconvolution analyses of the Raman spectra also demonstrated a local surface oxidation, possibly occurring on defect-rich interfaces, frequently identified within or in proximity of bamboo-like graphitic caps. By employing high-temperature Raman spectroscopy, we demonstrate a post-growth re-graphitization, which may also be visualized as an alternative way of depleting the oxygen content within the MWCNTs’ interfaces through recrystallization. Full article

This study investigates the carbon products generated by melamine under various heat-treatment temperatures with the catalysis of calcium carbonate. We discovered that the cost-effective precursor melamine readily self-assembles and curls into graphene tubes when catalyzed by the alkaline earth salt CaCO₃ at elevated temperatures. Under heat-treatment conditions of 1100 °C and 1200 °C, the growth morphology of graphene tubes with open structures and exceptionally large diameters was observed, and the diameters reached the micron level. These products exhibit a high degree of carbonization and an extremely low nitrogen content, as low as 1.7%. Further, the intensity ratio (ID/IG) of the D band and the G band is as low as 0.79 in Raman characterization. The results show that the products have a certain graphite structure, which proves the catalytic activity of CaCO₃. This is attributed to the incorporation of CaCO₃ into the raw material system, which impedes the complete thermal decomposition of melamine. On the other hand, the resulting CaO particles are evenly distributed along the tubular products, providing certain support for their self-assembly and growth, thereby achieving the efficient growth of graphene tubes. Full article

A novel composite consisting of fluorine-doped carbon and graphene double-coated LiMn_0.6Fe_0.4PO₄ (LMFP) nanorods was synthesized via a facile low-temperature solvothermal method that employs a hybrid glucose and polyvinylidene fluoride as carbon and fluorine sources. As revealed by physicochemical characterization, F-doped carbon coating and graphene form a ‘point-to-surface’ conductive network, facilitating rapid electron transport and mitigating electrochemical polarization. Furthermore, the uniform thickness of the F-doped carbon coating alters the growth of nanoparticles and prevents direct contact between the material and the electrolyte, thereby enhancing structural stability. The strongly electronegative F⁻ can inhibit the structural changes in LMFP during charge/discharge, thus reducing the Jahn–Teller effect of Mn³⁺. The distinctive architecture of the LMFP/C-F/G cathode material exhibits excellent electrochemical properties, exhibiting an initial discharge capacity of 163.1 mAh g⁻¹ at 0.1 C and a constant Coulombic efficiency of 99.7% over 100 cycles. Notably, the LMFP/C-F/G cathode material achieves an impressive energy density of 607.6 Wh kg⁻¹, surpassing that of commercial counterparts. Moreover, it delivers a reversible capacity of 90.3 mAh g⁻¹ at a high current rate of 5 C. The high-capacity capability and energy density of the prepared materials give them great potential for use in next-generation lithium-ion batteries. Full article

Understanding the interactions in hybrid systems based on graphene and functional oxides is crucial to the applicability of graphene in real devices. Here, we present a study of the structural defects occurring on graphene during the early stages of the growth of CoO, tailored by the electronic coupling between graphene and the substrate in which it is supported: as received pristine graphene on polycrystalline copper (coupled), cleaned in ultra-high vacuum conditions to remove oxygen contamination, and graphene transferred to SiO₂/Si substrates (decoupled). The CoO growth was performed at room temperature by thermal evaporation of metallic Co under a molecular oxygen atmosphere, and the early stages of the growth were investigated. On the decoupled G/SiO₂/Si samples, with an initial low crystalline quality of graphene, the formation of a CoO wetting layer is observed, identifying the Stranski-Krastanov growth mode. In contrast, on coupled G/Cu samples, the Volmer-Weber growth mechanism is observed. In both sets of samples, the oxidation of graphene is low during the early stages of growth, increasing for the larger coverages. Furthermore, structural defects are developed in the graphene lattice on both substrates during the growth of CoO, which is significantly higher on decoupled G/SiO₂/Si samples mainly for higher CoO coverages. When approaching the full coverage on both substrates, the CoO islands coalesce to form a continuous CoO layer with strip-like structures with diameters ranging between 70 and 150 nm. Full article

Silver nanoparticles (Ag NPs) have been produced by low-dose (1–20 kGy) gamma irradiation of silver nitrate in the presence of graphene-based material (graphene oxide or electrochemically exfoliated graphene). The large surface area of those graphene-based materials combined with the presence of oxygen-containing functional groups on the surface provided successful nucleation and growth of Ag nanoparticles, which resulted in a uniformly covered graphene surface. The obtained Ag nanoparticles were spherical with a predominant size distribution of 10–50 nm for graphene oxide and 10–100 nm for electrochemically exfoliated graphene. The photothermal efficiency measurement showed a temperature increase upon exposure to a 532 nm laser for all samples and the highest photothermal efficiency was measured for the graphene oxide/Ag NP sample prepared at 5 kGy. Electromagnetic interference (EMI) shielding efficiency measurements showed poor shielding for the composites prepared with graphene oxide. On the other hand, all composites prepared with electrochemically exfoliated graphene showed EMI shielding to some extent, and the best performance was measured for the samples prepared at 5 and 20 kGy doses. Full article

The uCVD (microchemical vapor deposition) graphene growth system is an improved CVD system that is suitable for scientific research and experimental needs, and it is characterized by its rapid, convenient, compact, and low-cost features. The micro-hotplate based on an SOI wafer is the core component of this system. To meet the requirements of the uCVD system for the micro-hotplate, we propose a suspended multi-cantilever heating platform composed of a heating chip, cantilevers, and bracket. In this article, using heat transfer theory and thermoelectric simulation, we demonstrate that the silicon resistivity, current input cross-sectional size, and the convective heat transfer coefficient have a huge impact on the performance of the micro-heating platform. Therefore, in the proposed solution, we adopt a selective doping process to achieve a differentiated configuration of silicon resistivity in the cantilevers and heating chip, ensuring that the heating chip meets the requirements for graphene synthesis while allowing the cantilevers to withstand high currents without damage. Additionally, by adding brackets, the surfaces of the micro-hotplate have the same convective heat transfer environment, reducing the surface temperature difference, and improving the cooling rate. The simulation results indicate that the temperature on the micro-hotplate surface can reach 1050.8 °C, and the maximum temperature difference at different points on the surface is less than 2 °C, which effectively meets the requirements for the CVD growth of graphene using Cu as the catalyst. Full article

This work carried out research to determine the possibilities of using graphene oxide to provide wood with new functional features. With the saturation parameters used and working liquid with a concentration of 0.004% graphene oxide, the retention of the nanomaterial in wood was 0.25 kg/m³. The presence of graphene oxide increased the crystallinity of the wood to 64% (compared with 57% for unmodified wood). The TG/DTG spectra of wood impregnated with graphene oxide and the control wood indicated that the initial weight loss of the samples observed at a temperature of 100 °C was similar and amounted to less than 4%. A second mass loss was observed in a temperature range of 270 to 380 °C. The mass loss in this temperature range reached 70% and was similar in the test and control samples. Wood modified with graphene oxide showed increased thermal stability in a temperature range of 360 to 660 °C compared with native wood. Given the results obtained, there were no statistically significant differences in the water absorption of modified or control wood. The presence of low concentrations of graphene oxide in the culture medium did not inhibit the growth of the fungus Trichoderma viride; however, a decrease in the growth activity of mycelial hyphae was observed with an increasing concentration of nanomaterial in the medium. It has been reported that graphene oxide, as a stress factor, initiates changes at the cellular level, characterized by the formation of structures called chlamydospores by the body. Full article

Lithium–sulfur (Li–S) batteries have received extensive attention due to their numerous advantages, including a high theoretical specific capacity, high energy density, abundant reserves of sulfur in cathode materials, and low cost. Li–S batteries also face several challenges, such as the insulating properties of sulfur, volume expansion during charging and discharging processes, polysulfide shuttling, and lithium dendritic crystal growth. In this study, a composite of a porous multi-site diatomite-loaded graphene oxide material and a PAN fiber membrane is developed to obtain a porous and high-temperature-resistant GO/diatomite/polyacrylonitrile functional separator (GO/DE/PAN) to improve the electrochemical performance of Li–S batteries. The results show that the use of GO/DE/PAN helps to inhibit lithium phosphorus sulfide (LPS) shuttling and improve the electrolyte wetting of the separator as well as the thermal stability of the battery. The initial discharge capacity of the battery using GO/DE/PAN is up to 964.7 mAh g⁻¹ at 0.2 C, and after 100 cycles, the reversible capacity is 683 mAh g⁻¹ with a coulombic efficiency of 98.8%. The improved electrochemical performance may be attributed to the porous structure of diatomite and the layered composite of graphene oxide, which can combine physical adsorption and spatial site resistance as well as chemical repulsion to inhibit the shuttle effect of LPS. The results show that GO/DE/PAN has great potential for application in Li–S batteries to improve their electrochemical performance. Full article

Water pollution is a significant environmental issue that has emerged because of industrial and economic growth. Human activities such as industrial, agricultural, and technological practices have increased the levels of pollutants in the environment, causing harm to both the environment and public health. Dyes and heavy metals are major contributors to water pollution. Organic dyes are a major concern because of their stability in water and their potential to absorb sunlight, increasing the temperature and disrupting the ecological balance. The presence of heavy metals in the production of textile dyes adds to the toxicity of the wastewater. Heavy metals are a global issue that can harm both human health and the environment and are mainly caused by urbanization and industrialization. To address this issue, researchers have focused on developing effective water treatment procedures, including adsorption, precipitation, and filtration. Among these methods, adsorption is a simple, efficient, and cheap method for removing organic dyes from water. Aerogels have shown potential as a promising adsorbent material because of their low density, high porosity, high surface area, low thermal and electrical conductivity, and ability to respond to external stimuli. Biomaterials such as cellulose, starch, chitosan, chitin, carrageenan, and graphene have been extensively studied for the production of sustainable aerogels for water treatment. Cellulose, which is abundant in nature, has received significant attention in recent years. This review highlights the potential of cellulose-based aerogels as a sustainable and efficient material for removing dyes and heavy metals from water during the treatment process. Full article