Synthesis of carbon nanotubes using pre-sintered oil fly ash via a reproducible process with large-scale potential.

Oil fly ash (OFA) is a byproduct generated by the burning of heavy crude oil in factories and power plants. Millions of tons of OFA is produced annually worldwide and is mostly treated as solid waste. Extensive efforts have been made to utilize OFA and reduce its environmental effects. Recently, OFA has been found to be a suitable catalyst and co-precursor for carbon nanotube (CNTs) production. However, the treatment methods used are expensive and time consuming. Here, we describe a new method for OFA treatment and provide optimized growth conditions for CNTs production. Pre-sintering of OFA at elevated temperatures (400-450 °C) in air or vacuum using a chemical vapor deposition (CVD) tube furnace (80-100 min) is a very effective treatment method for CNTs growth under optimum growth conditions. The optimum parameters for CNTs growth were growth temperature, gas pressure, gas flow rate, and growth time. Well-defined, thin nanotubes with diameters of 20-40 nm were produced. Bamboo-like nanotubes with zigzag curved walls were also observed in the produced CNTs. The weight percentage of the produced CNTs was approximately twice that of the treated OFA. Consequently, the pre-sintering method exhibited suitability for the mass production of CNTs. Thus, large quantities of the nanomaterial can be supplied for use in various applications, e.g., polymer composites, the rubber industry, construction materials, and lubricant additives.

Study of Electrospinning Parameters and Collection Methods on Size Distribution and Orientation of PLA/PBS Hybrid Fiber Using Digital Image Processing.

The Canny Edge-Based Distance Transform and Hough Transform algorithms were successfully implemented to analyze the size distribution and the orientation of the electrospun PLA/PBS hybrid fiber. The effect of polymer concentration, voltage, feed rate and needle-collector distance were studied. It was found that feed rate of 0.5 ml/h and needle-collector distance of 12 cm is required to generate smooth and uniform hybrid fibers in the smallest size electrospinning with 6 wt.% polymer at voltage of 20 kV. The stationary flat collector with a swaying needle and fast rotating drum disc with a stationary needle were used for the fiber alignment. In order to improve the size distribution and the orientation of the hybrid fibers it is proposed that the fibers should be collected on the rotary drum disc at 700 rpm or higher speed.

Size controlled ultrafine CeO2 nanoparticles produced by the microwave assisted route and their antimicrobial activity.

Cerium oxide (CeO2) nanoparticles (NPs) have a wide range of biological and biomedical applications. This work describes a new methodology for producing ultrafine, highly uniform NPs with controlled sizes using the chemical microwave assisted route. The size of CeO2-NPs decreased from 10 to 5 nm by increasing the molar ratio of cerium nitrate Ce(NO3)3.(6H2O) to that of hexamethylenetetramine (C6H12N) from 1:20 to 20:20. Detailed information about their structural characterization was obtained from the XRD, UV-visible, photoluminescence, Raman spectroscopy, SEM, TEM and AFM. These CeO2-NPs were tested as antimicrobial agent against Gram-negative (Escherichia.coli), Gram-positive (Bacillus.subtilis) bacteria and yeast (Saccharomyces cerevisiae). The obtained results showed significant inhibition of these strain even at low concentration of CeO2-NPs. The CeO2-NPs with the molar ratio 5:20 had the most effective inhibition against E.coli (~70%) at a concentration of 20 µL. The CeO2-NPs with the ratio 12:20 were found to be the most effective against B.subtilis (inhibition ~68%). On the other hand, CeO2-NPs synthesized with the 20:20 molar ratio caused the highest inhibition for S. cerevisiae (~60%). It is observed that at higher NPs concentration (i.e., >20 µL) the inhibition of these strains decreased. The antimicrobial activity may be attributed to the penetrating power of CeO2-NPs size beside the generated oxygen species radicals that caused inhibition of bacterial growth.

Zinc Oxide-Multi Walled Carbon Nanotubes Nanocomposites for Carbon Monoxide Gas Sensor Application.

Zinc oxide (ZnO)/multi walled carbon nanotubes (MWCNTs) composites based sensors with different ZnO concentrations were fabricated to improve carbon monoxide (CO) gas sensing properties in comparison to the sensors based on bare MWCNTs. To study the structure, morphology and elemental composition of the resultant products, X-ray diffraction (XRD), Field emission scanning electron microscopy (FESEM) and Energy dispersive X-ray spectroscopy (EDS) were carried out. It has been observed that as the concentration of ZnO is increased more and more ZnO nanoparticles in the form of nodes get attached to MWCNTs resulting the reduction in average diameter of MWCNTs. The typical response of ZnO/MWCNTs composites based gas sensors for different CO concentrations (40, 100, 140 and 200 ppm) was studied by using very advanced sensing setup attached to I-V measurement system. Different sensing parameters such as: resistive response, sensitivity and response time were estimated at room temperature for all the fabricated sensors. The results indicated that the sensor based on nanocomposite which has 30 mg ZnO dispersed on 20 mg MWCNTs showing highest sensitivity and fastest response. All the sensors showed response times ranging from 8 to 23 seconds. The sensing mechanism behind the sensors based on ZnO/MWCNTs nanocomposites for CO gas at room temperature is also discussed in the present report.

Photocatalytic activity of V doped ZnO nanoparticles thin films for the removal of 2- chlorophenol from the aquatic environment under natural sunlight exposure.

Vanadium doped ZnO powders were used as precursors to deposit thin films of V(5+) incorporated ZnO nanoparticles on glass substrates by the pulsed laser deposition technique. The observed variations in Raman signals, visible region shift in the diffuse reflectance spectra along with a small shift in the (101) reflections of the X-ray diffraction (XRD) confirmed the insertion of V(5+) ions in ZnO lattice. No other additional reflection in the XRD results other than ZnO further endorsed the occupation of lattice positions by V entities rather than independent oxide formation. The asymmetric XPS peaks of Zn2p and V2p core levels confirmed the existence of both in the vicinity. The existence of minimal proportion of V(3+) along with V(5+) states varied the alteration of the oxidation states V in the synthetic route. The SEM images at various resolutions displayed the uniform distribution identical nanoparticles without the presence of additional phases in the deposited films. The SEM cross-section measurements revealed the uniform thickness of ∼90 nm of each film, whereas the surface studies of the films were performed by AFM. The as-synthesized films were tested for photocatalytic activity in sunlight illumination for the removal of 2-chlorophenol. The unique feature of the study was the estimation of the photocatalytic activity 20 ppm of 2-chlorophenol by exposing the low exposed area. The degradation of the substrate was measured by liquid phase UV-vis spectroscopy, whereas total organic carbon measurement revealed the mineralization of the substrate. The released Cl(-) ions were also measured by ion chromatography. The estimated flatband potentials and pHzpc values of the V doped materials, by Mott-Schottky analysis and zeta potential measurements respectively, were correlated with the photocatalytic activity. The kinetics of the photocatalytic degradation/mineralization process was estimated and results were correlated with the plausible mechanism.

Carbon dioxide-activated mesoporous date palm fronds carbon integrated with MnO2/polyaniline for highly efficient capacitive deionization of water.

The continuous population growth and drying up the freshwater reservoirs around the world are increasing the demand for fresh water. Therefore, there is an urgent need to explore newer technologies able to purify water on large scales for human usage. Capacitive deionization is one of the most promising approaches to generate fresh water by the removal of salt ions from brackish water. In this work, we prepared three different capacitive deionization electrodes using carbonized palm tree fronds (PFC). These PFC activation was achieved using CO2 at 900°C. To generate the deionization electrodes, PFC activated carbon was combined with either polyaniline (PANI), MnO2, or both (PFC-PANI, PFC-MnO2, and PFC-MnO2-PANI). The MnO2 and PANI provided additional functionality and enhanced electrical conductivity, which resulted in much higher Na+ and Cl- ions adsorption. The BET surface area of PFC-MnO2-PANI was estimated to be 208.56 m2/g, which is approximately three times that of PCF-PANI and PFC-MnO2 alone. The morphological analysis showed that the PANI and MnO2 nanorods were well dispersed throughout the PFC network. Although PANI and MnO2 is largely embedded inside the PFC network, some remnants are visible on the surface of the electrodes. The cyclic voltammetry (CV) curves showed capacitive behavior of all electrodes in which PFC-MnO2-PANI showed highest specific capacitance of 84 F/g, while the PFC-MnO2 and PFC-PANI showed 42 and 43 F/g, respectively. Owing to its enhanced functionality and CV characteristics, the PFC-MnO2-PANI showed maximum salt adsorption capacity of 10.5 mg/g in contrast to 3.72 and 5.64 mg/g for PFC-MnO2 and PFC-PANI, respectively. Moreover, the measured contact angle for PFC-MnO2-PANI was ~51°, which indicates the hydrophilic nature of electrode that improved ions adsorption. PRACTITIONER POINTS: Date tree fronds were converted into mesopores carbon using CO2 as activation agent. Three composites were prepared with PANI, MnO2, and date palm fronds activated carbon (PFC-MnO2, PFC-MnO2-PANI, and PFC-PANI). Surface area, pore profile, surface morphology, electrochemical behavior, desalination performance, and hydrophilicity of all the electrodes were investigated. The PFC-MnO2-PANI showed maximum salt adsorption capacity of 10.5 mg/g in contrast to 3.72 and 5.64 mg/g for PFC-MnO2 and PFC-PANI, respectively.

Highly Uniform Nanodiamond-Graphene Composites Microspheres for Electrocatalytic Hydrogen Evolution.

To progress the clean hydrogen-gas-based energy economy, there is a demand for cost-effective, highly efficient catalysts to facilitate the hydrogen evolution reaction process (HER). Due to the amazing catalytic capabilities of two-dimensional materials, extensive research has been done on these structures. However, most of the described syntheses take a lot of time, are challenging, and are ineffective. The present work demonstrates the performance of the recently reported nanodiamond/graphene composite microsphere ND-GCSs as a catalyst for HER. These spheres were produced via the microwave-irradiation approach. A modified process was adopted to improve the particle size uniformity and yield. The prepared composite spheres showed very interesting catalytic activity for the HER when assembled on a screen-printed carbon electrode. The prepared ND-GCSs@SPCE showed a significant shift of the onset potential to ca. -450 mV and a small Tafel slope value of ca. 85 mV/decade. The electron transfer was drastically enhanced with a tremendous decrease in charge transfer resistance to ca. 265 Ω. The electrocatalyst showed excellent long-term stability for the HER application. Additionally, this novel composite structure might be beneficial for diverse applications including batteries, supercapacitors, catalyst supports, and more.

Highly luminescent material based on Alq3:Ag nanoparticles.

Tris (8-hydroxyquinoline) aluminum (Alq3) is an organic semiconductor molecule, widely used as an electron transport layer, light emitting layer in organic light-emitting diodes and a host for fluorescent and phosphorescent dyes. In this work thin films of pure and silver (Ag), cupper (Cu), terbium (Tb) doped Alq3 nanoparticles were synthesized using the physical vapor condensation method. They were fabricated on glass substrates and characterized by X-ray diffraction, scanning electron microscope (SEM), energy dispersive spectroscopy, atomic force microscope (AFM), UV-visible absorption spectra and studied for their photoluminescence (PL) properties. SEM and AFM results show spherical nanoparticles with size around 70-80 nm. These nanoparticles have almost equal sizes and a homogeneous size distribution. The maximum absorption of Alq3 nanoparticles is observed at 300 nm, while the surface plasmon resonant band of Ag doped sample appears at 450 nm. The PL emission spectra of Tb, Cu and Ag doped Alq3 nanoparticles show a single broad band at around 515 nm, which is similar to that of the pure one, but with enhanced PL intensity. The sample doped with Ag at a concentration ratio of Alq3:Ag = 1:0.8 is found to have the highest PL intensity, which is around 2 times stronger than that of the pure one. This enhancement could be attributed to the surface plasmon resonance of Ag ions that might have increased the absorption and then the quantum yield. These remarkable result suggest that Alq3 nanoparticles incorporated with Ag ions might be quite useful for future nano-optoelectronic devices.

Thermoelectric and power generation of 2D structured pieces of graphene-nanodiamonds nanocomposite.

Recently, the ultrafine 2D structured nanocomposite of graphene (Gr)-nanodiamonds (NDs) produced by a microwave-assisted chemical route was found to have attractive structural properties. This new 2D structured nanocomposite may be employed for a wide spectrum of applications including thermoelectricity (TE) applications. It is well established that TE materials should be highly effective to be used for designing operative devices for powering or cooling small devices. To fulfill such an objective, the functional TE material should possess a high-power factor and low thermal conductivity. In this study, NDs were successfully integrated into Gr with a magnificent structural alteration to the Gr layers/sheets. This structural modification was found to impact the TE final outcome above and below room temperature (RT). The obtained results showed that at 215 K the power factor value was increased from 4 µW m-1 K-2 for the pure Gr to ∼20 µW m-1 K-2 for the Gr-NDs nanocomposite. At higher T, e.g. 365 K, these values slightly decreased, but with clear superiority for the Gr-NDs nanocomposite. The thermal conductivity of the Gr-NDs nanocomposite was significantly reduced to ∼12% of that of the pure Gr, which could reflect a significant enhancement in the value of the figure of merit by >45 times. Furthermore, the output power generated by a single small leg module made of the Gr-NDs nanocomposite was measured and found to be measurable. The obtained values are still relatively low for practical application, but this newly produced material has great potential to be further developed for TE applications.

Thermoelectric Power Generation of TiS2/Organic Hybrid Superlattices Below Room Temperature.

Recently, the n-type TiS2/organic hybrid superlattice (TOS) was found to have efficient thermoelectric (TE) properties above and near room temperature (RT). However, its TE performance and power generation at the temperature gradient below RT have not yet been reported. In this work, the TE performance and power generation of the TOS above and below RT were investigated. The electrical conductivity (σ) and Seebeck coefficient (S) were recorded as a function of temperature within the range 233-323 K. The generated power at temperature gradients above (at ΔT = 20 and 40 K) and below (at ΔT = -20 and -40 K) RT was measured. The recorded σ decreased by heating the TOS, while |S| increased. The resulting power factor recorded ~100 µW/mK2 at T = 233 K with a slight increase following heating. The charge carrier density and Hall mobility of the TOS showed opposite trends. The first factor significantly decreased after heating, while the second one increased. The TE-generated power of a single small module made of the TOS at ΔT = 20 and 40 K recorded 10 and 45 nW, respectively. Surprisingly, the generated power below RT is several times higher than that generated above RT. It reached 140 and 350 nW at ΔT = -20 and -40 K, respectively. These remarkable results indicate that TOS might be appropriate for generating TE power in cold environments below RT. Similar TE performances were recorded from both TOS films deposited on solid glass and flexible polymer, indicating TOS pertinence for flexible TE devices.

Oil fly ash as a promise larvicide against the Aedes aegypti mosquitoes.

Two environmental problems exist in some tropical and subtropical areas: the Aedes aegypti (L.) (Ae. aegypti) mosquito and thousands of tons of heavy oil fly ash (HOFA) from power plants. Herein, micro/nanoparticles of HOFA have been utilized as a larvicide against Ae. aegypti without any chemical or biological additive materials. We estimated the accumulative mortalities in the third instar after 24/48 h (h). We found that after 24 h of exposing the larvae to the HOFA microsized, the LC50 and LC90 were 0.55 and 4.87 mg/ml, respectively, while they were 0.10 and 0.36 mg/ml after 48 h. At the same time, the LC50 and LC90 were respectively 0.12 and 0.60 mg/ml after 24 h exposing the larvae to the HOFA nanosized, and they were 0.06 and 0.23 mg/ml after 48 h. These results showed that the HOFA nanoparticles as larvicides were more effective than HOFA microparticles. The microscopy images also revealed deformations such as pigmentations, segment shrinkage, larva swelling, segment body contraction, siphon swelling, intermediate stage, head deformations, and thorax swelling in the larvae exposed to the HOFA. These deformations could indicate alterations in the hormones that control the biochemistry of the larvae body. The findings of this study could suggest the possibility of using HOFA, particularly in nanosized, as a promising larvicide against the Ae. aegypti mosquito.

Epoxy Flooring/Oil Fly Ash as a Multifunctional Composite with Enhanced Mechanical Performance for Neutron Shielding and Chemical-Resistance Applications.

Heavy-oil fly ash (HOFA) is a graphitic carbon powder extracted in vast amounts as a waste material from burning crude oil in power plants. This HOFA has attractive structural properties besides its high amount of pure carbon (∼90 wt %). This powder exists in spherical, highly porous micron-sized particles, which implies its great potential as a mechanical reinforcement for different polymers. In this work, HOFA has been utilized to enhance the mechanical properties of epoxy flooring at HOFA weight fractions of 0, 1, 1.6, and 3.2 wt %. The obtained results revealed that the prepared epoxy-flooring/HOFA composites at a HOFA content of 1.6 wt % showed significant mechanical improvements compared with the pristine polymer. The tensile strength and Young's module values were enhanced by ∼17 and 11%, respectively. Furthermore, the neutron-shielding performance was investigated. The composite with 1.6 wt % showed better neutron attenuation and lower transmittance than the pristine epoxy. The chemical resistance was also extensively studied against sodium hydroxide, nitric acid, and sulfuric acid. The changes in morphology, chemical elements, mass, volume, and molecular structures were investigated rigorously for pristine epoxy and its composite with HOFA at 1.6 wt %. After exposure to these chemicals for 21 days, the tested properties of the epoxy-flooring/HOFA composite showed better chemical resistance than that of the pristine epoxy. Where the epoxy-flooring/HOFA composite showed a surface with low cracks and blistering, it showed lesser changes in mass and volume and fewer molecular structure changes. These results indicated that it is possible to use this multifunctional composite for several applications, including the petrochemical industry, radiation shielding, construction, and automobiles.

Freestanding Activated Carbon Nanocomposite Electrodes for Capacitive Deionization of Water.

Freshwater reserves are being polluted every day due to the industrial revolution. Man-made activities have adverse effects upon the ecosystem. It is thus the hour of need to explore newer technologies to save and purify water for the growing human population. Capacitive deionization (CDI) is being considered as an emerging technique for removal of excess ions to produce potable water including desalination. Herein, cost-effective activated carbon incorporated with carbon nanotubes (CNT) was used as a freestanding electrode. Further, the desalination efficiency of the designed electrodes was tuned by varying binder concentration, i.e., polyvinylidene difluoride (PVDF) in the activated carbon powder and CNT mixture. PVDF concentration of 5, 7.5, 10, and 12.5 wt% was selected to optimize the freestanding electrode formation and further applied for desalination of water. PVDF content affected the surface morphology, specific surface area, and functional groups of the freestanding electrodes. Moreover, the electrical conductivity and specific surface area changed with PVDF concentration, which ultimately affected the desalination capacity using the freestanding electrodes. This study paves the way to produce cost effective carbon-based freestanding electrodes for capacitive deionization and other applications including battery electrodes.

Antibacterial activity of the micro and nanostructures of the optical material tris(8-hydroxyquinoline)aluminum and its application as an antimicrobial coating.

Although tris(8-hydroxyquinoline)aluminum (Alq3), a fluorescent optical organometallic material, is known for its applications in optoelectronics, it has only few and limited applications in the biological field. In this study, the antibacterial activity of Alq3 micro and nanostructures was investigated. We prepared Alq3 nanostructures. We prepared nanosized Alq3 as rice-like structures that assembled into flower shapes with an α-crystal phase. Then, Alq3 micro and nanostructure antibacterial activities were estimated against seven human pathogenic bacterial strains. Besides, we compared their antibacterial activities with those of standard antibiotics. The minimal inhibitory concentration (MIC), minimum bactericidal concentration (MBC), and IC50 were evaluated. Alq3 micro and nanostructure antibacterial activity showed considerable values compared to standard antibiotics. Besides, the obtained data revealed that the antibacterial activity of Alq3 in nanostructures with a new morphology is more than that in microstructures. The antibacterial activity of Alq3 nanostructures was attributed to their more surface interactions with the bacterial cell wall. The molecules of 8-hydroxyquinoline in the Alq3 structure could play crucial roles in its antibacterial activity. To apply the achieved results, Alq3 was incorporated with polystyrene (PS) in a ratio of 2% to fabricate a PS/Alq3 composite and used to coat glass beakers, which showed inhibition in the bacterial growth reduced to 65% compared with non-coated beakers. The finding of this study showed that Alq3 could be used as a promising antimicrobial coating.

Development of Nanocoated Filaments for 3D Fused Deposition Modeling of Antibacterial and Antioxidant Materials.

Three-dimensional (3D) printing is one of the most futuristic manufacturing technologies, allowing on-demand manufacturing of products with highly complex geometries and tunable material properties. Among the different 3D-printing technologies, fused deposition modeling (FDM) is the most popular one due to its affordability, adaptability, and pertinency in many areas, including the biomedical field. Yet, only limited amounts of materials are commercially available for FDM, which hampers their application potential. Polybutylene succinate (PBS) is one of the biocompatible and biodegradable thermoplastics that could be subjected to FDM printing for healthcare applications. However, microbial contamination and the formation of biofilms is a critical issue during direct usage of thermoplastics, including PBS. Herein, we developed a composite filament containing polybutylene succinate (PBS) and lignin for FDM printing. Compared to pure PBS, the PBS/lignin composite with 2.5~3.5% lignin showed better printability and antioxidant and antimicrobial properties. We further coated silver/zinc oxide on the printed graft to enhance their antimicrobial performance and obtain the strain-specific antimicrobial activity. We expect that the developed approach can be used in biomedical applications such as patient-specific orthoses.

Structural, morphological, and optical properties of carbon nanoparticles unsheathed from date palm fronds.

Several studies have reported the synthesis of carbon nanoparticles (CNPs) by various methods. In this study, an easy one-step process to unsheathe CNPs from date palm fronds through a top-down ball milling method has been reported. The CNPs were characterized using various spectroscopic and microscopic methods to determine their structural and morphological features, optical properties, crystallinity, physicochemical properties, and particle stability. Transmission electron microscopy (TEM) revealed that the obtained CNPs' size ranged from 4 to 22 nm in a crystalline form. Scanning electron microscopy (SEM) confirmed their spherical shape, while the maximum photoluminescence (PL) intensity was recorded at 464 nm when excited at 375 nm. The unsheathed CNPs produced a good quantum yield (QY) of 3.24%. Furthermore, the CNPs exhibited high Raman ratios of I D/I G and I 2D/I G with values of 0.59 and 0.04, respectively, verifying their multilayer crystalline graphitic nature. These Raman ratios also agree with the X-ray diffractometry (XRD) results. The CNPs' sp2 and sp3 carbon bonds were confirmed by X-ray photoelectron spectroscopy (XPS), with oxygen on the surface forming carboxyl and carbonyl groups with no other observable impurities. Furthermore, the extracted CNPs showed excellent PL properties for up- and down-conversion. These properties are exemplary for low-cost biomass with potential applications in biomedicine. Therefore, the extracted CNPs reported in this study have potential applications in optical imaging.

Carbon Nanoparticles Extracted from Date Palm Fronds for Fluorescence Bioimaging: In Vitro Study.

Numerous studies have been reported on single- and multicolored highly fluorescent carbon nanoparticles (FCNPs) originating from various sources and their potential applications in bioimaging. Herein, multicolored biocompatible carbon nanoparticles (CNPs) unsheathed from date palm fronds were studied. The extracted CNPs were characterized via several microscopic and spectroscopic techniques. The results revealed that the CNPs were crystalline graphitic and hydrophilic in nature with sizes ranging from 4 to 20 nm. The unsheathed CNPs showed exemplary photoluminescent (PL) properties. They also emitted bright blue colors when exposed to ultraviolet (UV) light. Furthermore, in vitro cellular uptake and cell viability in the presence of CNPs were also investigated. The cell viability of human colon cancer (HCT-116) and breast adenocarcinoma (MCF-7) cell lines with aqueous CNPs at different concentrations was assessed by a cell metabolic activity assay (MTT) for 24 and 48 h incubations. The results were combined to generate dose-response curves for the CNPs and evaluate the severity of their toxicity. The CNPs showed adequate fluorescence with high cell viability for in vitro cell imaging. Under the laser-scanning confocal microscope, the CNPs with HCT-116 and MCF-7 cell lines showed multicolor fluorescence emissions, including blue, green, and red colors when excited at 405, 458, and 561 nm, respectively. These results prove that unsheathed CNPs from date palm fronds can be used in diverse biomedical applications because of their low cytotoxicity, adequate fluorescence, eco-friendly nature, and cheap production.

High Thermoelectric Power Generation by SWCNT/PPy Core Shell Nanocomposites.

Polypyrrole (PPy) is a conducting polymer with attractive thermoelectric (TE) properties. It is simple to fabricate and modify its morphology for enhanced electrical conductivity. However, such improvement is still limited to considerably enhancing TE performance. In this case, a single-wall carbon nanotube (SWCNT), which has ultrathin diameters and exhibits semi-metallic electrical conductivity, might be a proper candidate to be combined with PPy as a core shell one-dimensional (1D) nanocomposite for higher TE power generation. In this work, core shell nanocomposites based on SWCNT/PPy were fabricated. Various amounts of pyrrole (Py), which are monomer sources for PPy, were coated on SWCNT, along with methyl orange (MO) as a surfactant and ferric chloride as an initiator. The optimum value of Py for maximum TE performance was determined. The results showed that the SWCNT acted as a core template to direct the self-assembly of PPy and also to further enhance TE performance. The TE power factor, PF, and figure of merit, zT, values of the pure PPy were initially recorded as ~1 µW/mK2 and 0.0011, respectively. These values were greatly increased to 360 µW/mK2 and 0.09 for the optimized core shell nanocomposite sample. The TE power generation characteristics of the fabricated single-leg module of the optimized sample were also investigated and confirmed these findings. This enhancement was attributed to the uniform coating and good interaction between PPy polymer chains and walls of the SWCNT through π-π stacking. The significant enhancement in the TE performance of SWCNT/PPy nanocomposite is found to be superior compared to those reported in similar composites, which indicates that this nanocomposite is a suitable and scalable TE material for TE power generation.

Structural and Electrochemical Properties of Physically and Chemically Activated Carbon Nanoparticles for Supercapacitors.

The demand for supercapacitors has been high during the integration of renewable energy devices into the electrical grid. Although activated carbon materials have been widely utilized as supercapacitor electrodes, the need for economic and sustainable processes to extract and activate carbon nanomaterials is still crucial. In this work, the biomass waste of date palm fronds is converted to a hierarchical porous nanostructure of activated carbon using simple ball-milling and sonication methods. Chemical and physical activation agents of NaOH and CO2, receptively, were applied on two samples separately. Compared with the specific surface area of 603.5 m2/g for the CO2-activated carbon, the NaOH-activated carbon shows a higher specific surface area of 1011 m2/g with a finer nanostructure. Their structural and electrochemical properties are functionalized to enhance electrode-electrolyte contact, ion diffusion, charge accumulation, and redox reactions. Consequently, when used as electrodes in an H2SO4 electrolyte for supercapacitors, the NaOH-activated carbon exhibits an almost two-fold higher specific capacitance (125.9 vs. 56.8 F/g) than that of the CO2-activated carbon at the same current density of 1 A/g. Moreover, using carbon cloth as a current collector provides mechanical flexibility to our electrodes. Our practical approach produces cost-effective, eco-friendly, and flexible activated carbon electrodes with a hierarchical porous nanostructure for supercapacitor applications.

One-Dimensional Nanocomposites Based on Polypyrrole-Carbon Nanotubes and Their Thermoelectric Performance.

Conducting polymers have attracted significant attention due to their easy fabrication, morphology modification, and their electrical properties. Amongst them, polypyrrole (PPy) has attractive thermoelectric (TE) properties. Engineering of this polymer in one-dimensional (1D) nanostructured form is found to enhance its TE performance. This was achieved in the present work by using multi-walled carbon nanotubes (MWCNTs) as a core template to direct the self-assembly of PPy and also to further enhance its TE performance. The growth of PPy on the sidewalls of MWCNTs was performed in an acidic medium based oxidative in situ polymerization. Various concentrations of MWCNTs within the range 1.1-14.6 wt.% were used to form the MWCNTs/PPy nanocomposites in 1D core-shell structures. The morphology and microstructure results of the produced nanocomposite samples showed that this MWCNTs were successfully coated by thick and thin layers of PPy. At low concentrations of MWCNTs, thick layers of PPy are formed. While at high concentrations thin layers are coated. The formed 1D nanocomposites have enhanced TE performance, particularly those containing higher contents of MWCNTs. The power factor and figure of merit values for the formed 1D nanocomposites recorded around 0.77 µV/mK2 and 1 × 10-3 at room temperature (RT), respectively. This enhancement was attributed to the perfect coating and good interaction between PPy and MWCNT through π-π stacking between the polymer chains and these nanotubes. These results might be useful for developing future TE materials and devices.