Synthesis Of Graphene Materials Research Articles

Graphene-Based Nanocomposites as Antibacterial, Antiviral and Antifungal Agents.

Over the past decade, there have been many interesting studies in the scientific literature about the interaction of graphene-based polymeric nanocomposites with microorganisms to tackle antimicrobial resistance. These studies have reported variable intensities of biocompatibility and selectivity for the nanocomposites toward a specific strain, but it is widely believed that graphene nanocomposites have antibacterial, antiviral, and antifungal activities. Such antibacterial activity is due to several mechanisms by which graphene nanocomposites can act on cells including stimulating oxidative stress; disrupting membranes due to sharp edges; greatly changing core structure mechanical strength and coarseness. However, the underlying mechanisms of graphene nanocomposites as antiviral and antifungal agents remain relatively scarce. In this review, recent advances in the synthesis, functional tailoring, and antibacterial, antiviral, and antifungal applications of graphene nanocomposites are summarized. The synthesis of graphene materials and graphene-based polymeric nanocomposites with techniques such as pressurized gyration, electrospinning, chemical vapor deposition, and layer-by-layer self-assembly is first introduced. Then, the antimicrobial mechanisms of graphene membranes are presented and demonstrated typical in vitro and in vivo studies on the use of graphene nanocomposites for antibacterial, antiviral, and antifungal applications. Finally, the review describes the biosafety, current limitations, and potential of antimicrobial graphene-based nanocomposites.

Application of supercritical fluid in the synthesis of graphene materials: a review

The studies on the utilisation of supercritical fluids (SCFs) in processing chemicals and materials have garnered significant attention in the past two decades. SCFs possess both gas- and liquid-like properties that are tunable, rendering them as superior solvents for reactions and processes, for example in the delamination of graphite. SCF technologies are deemed to be potential alternatives to existing technologies for graphene production that are yet to be industrially scalable. This review features recent works on the production of graphene facilitated by SCFs, with emphasis on the conversion of graphite to graphene through exfoliation and reduction. The exfoliation processes report the yield of 6 to 27% of monolayer graphene and 3 to 25% of ≤ 5 layers of graphene, whilst the carbon-to-oxygen (C/O) ratio of graphene produced via different reduction processes ranges from 0.37 to 28.2 with interlayer spacing of 0.35 to 0.38 nm. Recent applications of gas-expanded solvents for the synthesis of graphene and the fabrication of functionalised graphene materials via SCF-aided processes are also described. In addition, a summary of the properties of common SCFs as well as the characterisation of graphene materials, such as the number of layers, C/O ratio, interlayer spacing, pore size and surface area, is included to provide insights on the process efficiency.

Distinctive Features of Graphene Synthesized in a Plasma Jet Created by a DC Plasma Torch.

Synthesis of graphene materials in a plasma stream from an up to 40 kW direct current (DC) plasma torch is investigated. These materials are created by means of the conversion of hydrocarbons under the pressure 350–710 Torr without using catalysts, without additional processes of inter-substrate transfer and the elimination of impurities. Helium and argon are used as plasma-forming gas, propane, butane, methane, and acetylene are used as carbon precursors. Electron microscopy and Raman imaging show that synthesis products represent an assembly of flakes varying in the thickness and the level of deformity. An occurrence of hydrogen in the graphene flakes is discovered by X-ray photoelectron spectroscopy, thermal analysis, and express-gravimetry. Its quantity depends on the type of carrier gas. Quasi-one-dimensional approach under the local thermodynamic equilibrium was used to investigate the evolution of the composition of helium and argon plasma jets with hydrocarbon addition. Hydrogen atoms appear in the hydrogen-rich argon jet under higher temperature. This shows that solid particles live longer in the hydrogen-rich environment compared with the helium case providing some enlargement of graphene with less hydrogen in its structure. In conclusion, graphene in flakes appears because of the volumetric synthesis in the hydrogen environment. The most promising directions of the practical use of graphеne flakes are apparently related to structural ceramics.

Synthesis of carbon-mineral composites and graphene

С/Al2O3 and C/MgO carbon-mineral composites were synthesized by propane decomposition over Al2O3 at 600–650 °C and MgO carbonization in 1,3-butadiene at 600 °C. The synthesized carbon-mineral composites were studied by EPR, XRD and transmission electron microscopy. It was found that a mosaic structure of carbon clusters was formed on the internal surface of the oxides and gradually grew until it covered its whole surface. A method for synthesis of graphene materials by using MgO as a template followed by its dissolution in hydrochloric acid was suggested. A maximum was observed on the dependence of the graphene surface area on the carbon concentration in the composites. The highest specific surface area of the synthesized graphene about 1800–1900 m2/g was observed for the samples obtained from C-MgO composites containing 8–10 wt.% C.

Tuning the Multifunctional Surface Chemistry of Reduced Graphene Oxide via Combined Elemental Doping and Chemical Modifications.

The synthesis of graphene materials with multiple surface chemistries and functionalities is critical for further improving their properties and broadening their emerging applications. We present a simple chemical approach to obtain bulk quantities of multifunctionalized reduced graphene oxide (rGO) that combines chemical doping and functionalization using the thiol-ene click reaction. Controllable modulation of chemical multifunctionality was achieved by simultaneous nitrogen doping and gradual chemical reduction of graphene oxide (GO) using ammonia and hydrazine, followed by covalent attachment of amino-terminated thiol molecules using the thiol-ene click reaction. A series of N-doped rGO (N-rGO) precursors with different levels of oxygen groups were synthesized by adjusting the amount of reducing agent (hydrazine), followed by subsequent covalent attachment of cysteamine via the thermal thiol-ene click reaction to yield different ratios of mixed functional groups including N (pyrrolic N, graphitic N, and aminic N), S (thioether S, thiophene S, and S oxides), and O (hydroxyl O, carbonyl O, and carboxyl O) on the reduced GO surface. Detailed XPS analysis confirmed the disappearance of unstable pyridinic N in cys-N-rGO and the reduction degree threshold of N-rGO for effective cysteamine modification to take place. Our study establishes a strong correlation between different reduction degrees of N-rGO with several existing oxygen functional groups and addition of new tunable functionalities including covalently attached nitrogen (amino) and sulfur (C–S–C, C=S, and S–O). This simple and versatile approach provides a valuable contribution for practical designing and synthesis of a broad range of functionalized graphene materials with tailorable functionalities, doping levels, and interfacial properties for potential applications such as polymer composites, supercapacitors, electrocatalysis, adsorption, and sensors.

Synthesis of graphene materials by electrochemical exfoliation: Recent progress and future potential

AbstractSynthesis of structurally controlled graphene materials is critical for realizing their practical applications. The electrochemical exfoliation of graphite has emerged as a simple method to produce graphene materials. This review examines research progress in the last 5 years, from 2015 to 2019. Graphene material synthesis methods generally have a trade‐off between increasing production yield and achieving better material property control. The synthesis conditions for synthesizing pristine graphene, graphene oxide (GO), and graphene composites are significantly different. Thus, in this review, we first discuss synthesis methods for graphene materials with high C/O ratios from four aspects: graphite electrodes, equipment engineering, electrolytes, and additional reduction methods. Next, we survey synthesis methods for GO and examine how the pretreatment of the graphite electrodes, electrolytes, and operation parameters, such as applied voltages, electrolyte temperatures, and mechanical forces, affect the quality of GO. Further, we summarize electrochemical exfoliation methods used to dope graphene materials, introduce covalent functional groups, incorporate various nanoparticles, and assembly of graphene architectures. For all synthesis methods, we compare the properties of resulting graphene materials such as C/O ratios, lateral size, layer numbers, and quality characterized by Raman spectroscopy. Lastly, we propose our perspectives on further research. We hope this review stimulates more studies to realize the on‐demand production of graphene materials with desired properties using electrochemical exfoliation methods.

The effect of reactor geometry on the synthesis of graphene materials in plasma jets

The possibility of synthesis of graphene and graphane (hydrogenated graphene) using the decomposition of hydrocarbons by thermal plasma has been investigated. Investigations of the influence of the plasma-forming gas on the efficiency of synthesis and the morphology of graphene materials were carried out. The synthesis products have been characterized by the methods of scanning microscopy, Raman spectroscopy and thermal analysis. It is found that the morphology of graphene materials is affected by the geometry of the reactor. It was demonstrated that the obtained graphene materials are uniformly distributed in the volume of plastic based on cyanate ester resins under mixing.