Graphene Quantum Dots (GQDs), zero-dimensional nanoparticles which are derived from carbon-based sources owned the new pavement for the energy storage applications. With the varying synthesis routes, the in-built properties of GQDs are enhanced in different categories like quantum efficiency, nominal size range, and irradiation wavelength which could be applied for the several of energy and optoelectronics applications. GQDs are especially applicable in the specific energy storage devices such as super capacitors, solar cells, and lithium-ion batteries which were demonstrated in this work. This paper critically reviews about the synthesis techniques used for the GQDs involving energy storage applications with increased capacitance, energy conversion, retention capability, and stability.
Abstract Activated carbon from the shell of the cashew of Para (SCP) was produced by chemical activation with ZnCl using the ratio of SCP: ZnCl2 1.0:1.5 at 700 °C. The prepared activated carbon (SCP700) was used for the removal of two emerging contaminants, 4-bromophenol (4-BrPhOH) and 4-chloroaniline (4-ClPhNH2) that are primarily employed in the industry. Different analytical techniques were used to characterize the activated carbon. From the N2 adsorption–desorption isotherms were obtained the specific surface area of 1520 m2 g− 1 and total pore volume of 0.492 cm3 g−1. The functional groups were identified by the FTIR technique and quantified by modified Boehm titration. The results revealed the bearing of several functional groups on the SCP700 surface, which may utterly influence the removal of the emerging contaminants. The equilibrium experiments showed that the maximum uptaken capacities (Qmax) achieved at 45 °C were 488.2 (4-BrPhOH) and 552.5 mg g−1 (4-ClPhNH2). The thermodynamic parameters demonstrated that the processes of 4-BrPhOH and 4-ClPhNH2 adsorption are exothermic, spontaneous, energetically suitable, and the magnitude of ΔH° is compatible with physisorption. The mechanism of the adsorption of the emerging contaminants onto the carbon surface is dominated by microporous filling, hydrogen bonds, π-stacking interactions, and other Van der Waals interactions. The use of activated carbon for the treatment of industrial synthetic wastewater with several inorganic and organic molecules commonly found in industrial effluents showed a very high percentage of uptaking (up to 98.64%).
Biomass porous carbons derived from Laminaria japonica were prepared by KOH and H3PO4 activation methods, respectively. The results indicated that the chemical activation had an apparent effect on the molecular framework and space of materials. To enhance the selective adsorption for organic acids, biomass carbons were modified by dopamine combined with N-(2-aminoethyl)-3-aminopropyltrimethoxysilane. The SEM and BET results illustrated the effect of the chemical activation approach on the morphology and porous texture. The biomass porous carbon using KOH activation method had the highest surface area (up to 1558 m2/ g). Compared with unmodified materials, the modified materials showed higher adsorption capacity for organic acids (27.90 μg/mL for chlorogenic acid and 25.47 μg/mL for caffeic acid). It was suggested that modification of porous carbons might be a viable pathway to increase the specific adsorption affinity and efficiency for organic acids in dried jujube samples.
We report on the one-step synthesis of luminescent carbon nanodots (C-dots) via an electrical discharge between two graphite electrodes submerged into organic solvent (octane). This is a simple approach for the fabrication of C-dots with tunable photoluminescence (PL) that differs from the other preparation methods, as no post-passivation step is required. The synthesized carbon nanoparticles are of spherical shape and their size is distributed in the range of 2–5 nm and exhibit luminescence sensitive to excitation wavelength.
This paper presents a Raman spectroscopy study of the influence of methane flow on the micro-tribological behavior of diamond-like carbon coatings deposited with an industrial plasma-enhanced chemical vapor deposition system. Results have shown a direct relationship between the methane flow and thickness of the coatings. The analysis of the Raman spectra and deposition parameters allowed establishing the influence of H content with the methane flow, the disorder level and estimation of the sp3 fraction on the carbon coatings. The micro-tribology tests showed a strong dependence of the wear resistance and hardness with Raman parameters. The coating deposited at 72-sccm methane flow presented a thickness of 1.7 μm and a sp3 fraction of 0.33. This sp3 fraction gave rise to a hardness of 24 GPa and an excellent wear resistance of 3.3 × 10–6 mm3 N−1 mm−1 for this DLC coating. Wear tests showed a swelling in the wear profiles on this coating, which was associated with the occurrence of a re-hybridization process.
The porous carbons with high specific surface area and excellent electrochemical properties were prepared using three types of green needle coke as raw materials. Electrochemical performances of the porous carbons derived from different microstructure green needle coke were investigated. The XRD and Raman spectra demonstrated that the content of the ordered carbon microcrystals were decreased and the content of amorphous and cross-linked structure were increased in the porous carbons with comparison to the raw materials. The results of N2 adsorption–desorption analysis verified that the content of ordered microcrystalline structure in the raw materials evidently influence the specific surface area and pore size distribution of the porous carbons. The porous carbon with 1665 m2 g−1 specific surface area and 2.89 nm average pore size has shown that the specific capacitance was 288 F g−1 at the current density 1 A g−1. Furthermore, the capacity retention was 94.93% and the Coulombic efficiency was 92.87% after 5000 charge/discharge cycles.
In this study, we developed a facile and template-free strategy for the preparation of activated porous carbon beads (APCBs) from polyacrylonitrile. The chemical activation with KOH was found to enhance the pore properties, such as specific surface area (SSA), pore volume, and pore area. The APCBs exhibited a large SSA of 1147.99 m2/g and a pore area of 131.73 m2/g. The APCB-based electrodes showed a good specific capacitance of 112 F/g at 1 A/g in a 6 M KOH electrolyte, and excellent capacitance retention of 100% at a current density of 5 A/g after 1000 cycles. Therefore, the APCBs prepared in this study can be applied as electrode materials for electric double-layer capacitors.
Starting materials are very significant to produce activated carbons because every starting material has a different chemical structure; hence they affect the surface functional groups and surface morphologies of obtained activated carbons. In this study, sycamore balls, ripe black locust seed pods, and Nerium oleander fruits have been used as starting materials by ZnCl2 chemical activations for the first time. Firstly, activated carbons were obtained from these starting materials with ZnCl2 chemical activation by changing production conditions (carbonization time, carbonization temperature, and impregnation ratio) also affecting the structural and textural properties of the resultant activated carbons. Then, the starting materials and resultant activated carbons were characterized by utilizing diverse analysis techniques, such as TGA, elemental analysis, proximate analysis, BET surface areas, pore volumes, pore size distributions, N2 adsorption–desorption isotherms, SEM, FTIR spectra, and H2 adsorption isotherms. The highest surface areas were determined to be 1492.89, 1564.84, and 1375.47 m2/g for the activated carbons obtained from sycamore balls, ripe black locust seed pods, and N. oleander fruits, respectively. The yields of these activated carbons with the highest surface areas were calculated to be around 40%. As the carbonization temperature increased with sufficient ZnCl2 amount, N2 adsorption–desorption isotherms began to turn into Type IV isotherms given by mesoporous adsorbents with its hysteresis loops. Also, their hysteresis loops resembled Type H4 loop generally associated with narrow slit-like pores. Moreover, hydrogen uptakes under 750 mmHg at 77 K were determined to be 1.31, 1.48, and 1.24 wt% for the activated carbons with the maximum surface areas produced from sycamore balls, ripe black locust seed pods, and N. oleander fruits, respectively. As a result, the highest surface areas of the activated carbons with different structural properties produced in this study were obtained with different production conditions.
Lightweight and flexible electromagnetic interference (EMI) shielding materials are in great demand for wearable EMI device. In the present work, lightweight and flexible carbon nanotube (CNT)/ferroferric oxide ( Fe3O4) composite film was made through a feasible chemical vapor deposition process for CNT film synthesis, followed by a hydrothermal reduction process for Fe3O4 coating. In the as-prepared composite, CNT film and Fe3O4 particles work as conductive skeleton and strong magnetic particle, respectively. The as-prepared composite film shows a novel EMI shielding effectiveness (SE) of 91 dB in the X-band, a small thickness of 0.09 mm and a low density of 0.86 g/cm3, which is superior to most of the carbonbased EMI materials.
Graphene is an unconventional material with a two-dimensional hexagonal crystalline array of elemental carbon atoms and outstanding properties; accordingly, a desirable objective in the line of research of graphene is the development of novel and more productive methods of synthesis, validating its properties and applications. In our exploratory research, we have effectively exfoliated graphene from graphite using supercritical fluids (water, ethanol and carbon dioxide). The exfoliated graphene was properly characterized; via scanning electron microscopy, the morphology of graphene was observed; Raman spectra confirmed the exfoliation of graphene depicting the characteristic shift towards smaller Raman number in the 2D band (2676 cm−1) compared to that of graphite (≈ 2700 cm−1); transmission electron microscopy analysis exhibited the crystalline structure of graphene attesting also the expected transparency of exfoliated layers. Graphene exfoliation from graphite by supercritical fluids promises to be a simple large-scale method for graphene production.
In this study, we report a controlled one-pot green synthesis of multiwalled carbon nanotubes (MWCNTs) via pyrolysis of sustainable agriculture waste (chickpea peel) at 400 °C in aqueous medium. These MWCNTs demonstrated 7.0 nm diameter, 0.28 nm graphitic spacing with carbonyl, hydroxyl, and carboxylic acid functionality. The D band (presence of sp3 defects) and G band ( E2g mode of graphite) at 1350 cm−1 and 1580 cm−1 originated in Raman spectrum, respectively. The prepared MWCNTs showed blue fluorescence with 10% fluorescence quantum yield in aqueous medium. The MWCNTs showed triple exponential decay characteristics with an average fluorescence lifetime of 4.7 ns. The synthesized MWCNTs revealed a consistent fluorescence in the cytoplasm of 22RV1 human prostate carcinoma cell line without exerting any sign of cytotoxicity. The MWCNTs also exhibited remarkable cytocompatibility in human immortalized prostate epithelial RWPE1 cells.
Processing and characterization of graphene (Gr)-reinforced aluminium alloy 7075 (AA7075) microcomposites and nanocomposites are reported in this work. Composites are fabricated by mechanical alloying process at wet conditions. The bulk composites are prepared by uniaxial die pressing to get higher densification and sintered in an inert atmosphere. Density of the nanocomposites is higher than the microcomposites due to the reduction of grain size by increased milling time. X-ray diffraction (XRD) analysis confirms graphene interaction with the AA7075 matrix lattice spaces. The effective distribution of graphene with aluminium alloy is further confirmed by the Transmission Electron Microscopy (TEM) analysis. The hardness of the composites proportionally increases with the graphene addition owing to grain refinement. Wear morphology is characterized using Scanning Electron Microscopy (SEM) and Atomic Force Microscopy (AFM). Microcomposites reveal abrasive and ploughing wear mechanism of material removal from the surface. Nanocomposites show adhesive wear with delamination and particle pull-out from the material surface.
Engineering the microstructure of the carbonaceous materials is a promising strategy to enhance the capacitive performance of supercapacitors. In this work, nanostructured Black Pearl (1500 BP) carbon which is a conductive carbon being commercially used in printing rolls, conductive packaging, conductive paints, etc. is analyzed for its feasibility as an electrode material for Electric Double-Layer Capacitors (EDLCs). To achieve that commercial Black Pearl (BP), carbon is treated with mild acid H3PO4 to remove the impurities and enhance the active sites by regulating the growth of agglomerates and creating micropores in the nano-pigments. Generally, the coalescence of nanoparticles owing to their intrinsic surface energy has tendency to create voids of different sizes that act like meso/micropores facilitating the diffusion of ions. The electrochemical performance of BP carbon before and after chemical activation is investigated in aqueous ( H2SO4, KOH and KCl) and a non-aqueous electrolyte (1 M TEMABF4 in acetonitrile) environment employing different electrochemical techniques such as Cyclic Voltammetry (CV), Galvanostatic charge/discharge (GCD) and Electrochemical Impendence Spectroscopy (EIS). The chemically activated BP carbon delivers the highest specific capacitance of ∼156 F g−1 in an aqueous electrolyte, 6 M KOH. The highest specific power, ~ 15.3 kW kg−1 and specific energy, 14.6 Wh kg−1 are obtained with a symmetric capacitor employing non-aqueous electrolyte because of its high working potential, 2.5 V.