Synthesis Of Carbon Nanotubes Research Articles

Diameter-Controlled Synthesis of Carbon Nanotubes Using [2n]Collarenes as Rigid Organic Templates.

An effective route to diameter-controlled single-walled carbon nanotubes (SWCNTs) remains elusive. The use of organic templates to precisely control the diameter of the resulting nanotubes holds great promise in this regard but has hitherto had very limited practical success. A main obstacle is the limited availability of suitable organic templates. Here, we report the diameter-controlled bottom-up synthesis of SWCNTs with elaborately designed [2n]collarenes, hydrocarbon belts consisting of alternating phenylene and 1,4-cyclohexadiene rings, as rigid organic templates. A new approach has been developed to construct these collarenes, which are then used as templates in the bottom-up growth of SWCNTs. The resulting SWCNTs exhibit narrow diameter distributions, matching the diameters of the employed collarene templates. This work greatly propels the synthesis of diameter-controlled SWCNTs.

Effect of nickel catalyst thickness on growth of carbon nanotubes on glass nonwoven mat using thermal chemical vapor deposition method

This study aimed to explore how varying the thickness of nickel catalyst affects the synthesis of carbon nanotubes on glass mats using the thermal chemical vapor deposition (TCVD) method. Nickel served as the catalyst, with acetylene as the hydrocarbon source and argon as the carrier gas. Initially, different thicknesses of nickel catalyst were applied to the glass mat via plasma-enhanced chemical vapor deposition (PECVD). Subsequently, these samples underwent TCVD plasma treatment. Electrical resistance measurements were conducted, and scanning electron microscopy (SEM), Raman spectroscopy, and transmission electron microscopy (TEM) were employed to analyze the presence, surface morphology, and quality of the nanotubes. The research revealed that the thickness of the nickel catalyst significantly influences the nanotube synthesis process on glass mat substrates. An optimal thickness of nickel catalyst yielded a glass mat with an electrical resistance of 2 Ω per unit area post-TCVD treatment.

Artificial Intelligence -Driven Insights into Bisphenol A Removal Using Synthesized Carbon Nanotubes

Water quality nowadays, under climate change, has become a risk and challenging problem to save water from deterioration. Advanced solutions such as nanomaterials and artificial intelligence for simulation have become some of the best and essential solutions. Therefore, this study assessed the artificial intelligence models' accuracy in simulating the elimination of Bisphenol A (BPA) using synthesized carbon nanotubes (CNTs). We concluded that the pseudo-second-order model's (R2) correlation coefficient is (0.999) significantly higher than the other models. Because the findings between the Model and Actual Values are so accurate, the adsorption of BPA on CNT could be modeled using the pseudo-second-order model, qe = 144.928(mg/g) and K2 = 0.0016. The correlation coefficient of Pseudo-First-Order model's (R2) is (0.825) qe = 27.107(mg/g) and K1 = 0.0161, and the Intraparticle diffusion model's (R2) is (0.821),qe = 151.98(mg/g) and Kd = 2.4. The Langmuir model performed the best in isothermal experiments, with correlation coefficients of R2=0.9441, qm=181.81, and RL= 0.0375. Based on the information provided, we may conclude that the Langmuir model accounts for more BPA adsorption than the other models. We employed the feedforward neural network (FFNN) and the recurrent neural network (RNN). The FFNN achieved a coefficient of 0.971, while the RNN obtained a higher correlation coefficient of 0.98.

Synthesis of polyaniline tannate-modified carbon nanotubes by oxidative copolymerization as highly efficient corrosion inhibitors for mild steel in HCl solution

Corrosion is a prevalent issue in industrial production, directly impacting the production process and causing severe damages. To mitigate this problem, corrosion inhibitors are highly desired. Herein, a novel type of nano corrosion inhibitor, referred to as PTCNT, was synthesized through an oxidative copolymerization method utilizing aniline, ammonium persulfate (APS), and tannic acid (TA)-modified multiwalled carbon nanotubes (MWCNTs). The results demonstrated that the PTCNT effectively inhibited the corrosion of mild steel in 1 M HCl solution, achieving the corrosion inhibition efficiency of 90.6 % at the concentration of 75 mg/L. Characterization results implied that the PTCNT adsorbed onto the surface of the mild steel, forming a protective shielding layer. Potentiodynamic polarization measurements proved that the PTCNT functioned as the hybrid corrosion inhibitor. Furthermore, the adsorption of PTCNT on the mild steel surface was investigated using adsorption isotherm and adsorption kinetic modeling. Quantum chemical calculations were used to elucidate the adsorption mechanism of PTCNT. These findings raise new avenues for the development of highly efficient corrosion inhibitors for the mild steel in HCl solutions.

Molecular Dynamics of Catalyst-Free Edge Elongation of Boron Nitride Nanotubes Coaxially Grown on Single-Walled Carbon Nanotubes.

Recent advances in low-dimensional materials have enabled the synthesis of single-walled carbon nanotubes encapsulated in hexagonal boron nitride (BN) nanotubes (SWCNT@BNNT), creating one-dimensional van der Waals (vdW) heterostructures. However, controlling the quality and crystallinity of BNNT on the surface of SWCNTs using chemical vapor deposition (CVD) remains a challenge. To better understand the growth mechanism of the BNNT in SWCNT@BNNT, we conducted molecular dynamics (MD) simulations using empirical potentials. The simulation results suggest that spontaneous BN nucleation is unlikely to occur on the outer surface of the SWCNT when we assume only vdW interaction between the BN and SWCNT layers. However, we observe the elongation of the BNNT when a short BNNT is provided as a seed nucleus on the SWCNT. This grown BNNT structure, with its sharply cut edges, aligns with experimental observations made using transmission electron microscopy (TEM). Moreover, the edge-reconstruction process favors zigzag B edges, which exhibit low edge energy according to the ReaxFF potential. Our simulation successfully provides insights into the catalyst-free growth process of this one-dimensional vdW heterostructure.

A Double-walled Noncovalent Carbon Nanotube by Columnar Packing of Nanotube Fragments.

Herein, we report the synthesis of double-walled noncovalent carbon nanotubes (CNTs) through host-guest complexation of nanotube fragments and tube-forming crystal engineering. As the smallest fragment of double-walled CNTs, a host-guest complex of perfluorocycloparaphenylene (PFCPP) and carbon nanobelt (CNB) was synthesized by mixing them in solvents. The immediate complexation of the PF[12]CPP⊃(6,6)CNB complex with a remarkably high association constant (Ka) of 2×105 L/mol was observed. Time-dependent 1H NMR and thermogravimetry measurements revealed that the stability of (6,6)CNB was significantly improved by encapsulation. X-ray crystallography confirmed the robust belt-in-ring structure of this complex. As indicated by the short distance between PF[12]CPP and (6,6)CNB (2.8 Å), intermolecular orbital interactions exist between the belt and the ring, which were further supported by theoretical calculation and phosphorescence quenching experiments. While the PF[12]CPP⊃(6,6)CNB complex adopts various crystal packing structures, chloroform was discovered to be a magic "glue" solvent inducing one-dimensional alignment of the PF[12]CPP⊃(6,6)CNB complex to build an unprecedented double-walled noncovalent CNT structure.

Machine Learning as a "Catalyst" for Advancements in Carbon Nanotube Research.

The synthesis, characterization, and application of carbon nanotubes (CNTs) have long posed significant challenges due to the inherent multiple complexity nature involved in their production, processing, and analysis. Recent advancements in machine learning (ML) have provided researchers with novel and powerful tools to address these challenges. This review explores the role of ML in the field of CNT research, focusing on how ML has enhanced CNT research by (1) revolutionizing CNT synthesis through the optimization of complex multivariable systems, enabling autonomous synthesis systems, and reducing reliance on conventional trial-and-error approaches; (2) improving the accuracy and efficiency of CNT characterizations; and (3) accelerating the development of CNT applications across several fields such as electronics, composites, and biomedical fields. This review concludes by offering perspectives on the future potential of integrating ML further into CNT research, highlighting its role in driving the field forward.

Facile synthesis of nitrogen-containing multiwalled carbon nanotubes as a worth metal-free electrocatalyst for hydrogen evolution reaction and semicarbazide oxidation

Studies of metal-free carbon nanostructures prove effective in energy and environmental applications due to their molecular tunability and vast chemical space. Herein, we synthesize nitrogen-containing multi-walled carbon nanotubes (N-MWCNTs) via. acid-catalysed incorporation of 3, 4-diaminopyridine into multi-walled carbon nanotubes (MWCNTs), and demonstrating their efficacy in electrocatalytic hydrogen evolution reaction (HER) and semicarbazide (SCB) oxidation for energy and environmental waste management, respectively. Successful synthesis is further confirmed by analysis techniques, i.e. Fourier transform infrared (FTIR) spectral analysis shows the diminishing OH frequency around 3250 cm−1 in MWCNTs after functionalization and the formation of an OC–NH bond in N-MWCNTs at 1710 cm−1. X-ray diffraction (XRD) confirms the incorporation of N-species, while Raman spectroscopic analysis indicates an increase in the ID/IG ratio MWCNTs (∼1) to N-MWCNTs (∼1.25), suggesting more defective sites in the N-MWCNTs nanocomposite. X-ray photoelectron spectroscopy (XPS) reveals peaks at 399.38, 400.49, and 402.05 eV, attributed to pyridinic-N, aromatic amide-N, and protonated amine groups, respectively. N₂ adsorption-desorption studies shows a high Brunauer-Emmett-Teller (BET) surface area for N-MWCNTs (119.22 m2/g) compared to MWCNTs (74.94 m2/g). Linear sweep voltammetry (LSV) profiles demonstrate enhanced activity of N-MWCNTs for both HER and SCB oxidation at an ultralow potential of E = −0.55 V vs RHE at 10 mA/cm2, with a lower Tafel slope of 108 mV.dec−1. Moreover, the electrochemical sensing studies indicates on N-MWCNTs were demonstrating an efficient electron transfer to SCB with the lower detection limit of 0.004 μmol. This work provides carbon-based metal-free electrocatalysts for energy harvesting and environmental management.

CARBON NANOTUBES AS EFFECTIVE REMEDY FOR THIN OIL-WATER FILMS REMOVAL

This article describes the process of synthesis of multi-walled carbon nanotubes (MWCNTs) as well as the results of their use as adsorbents for removing the oil contaminants from the surface of water. SEM and TEM analyses were employed to characterize the synthesized MWCNTs. The sorption capacity of MWCNTs for crude oil was 3–4 ml/g, and with an increase in the specific gravity of the petroleum product, this value also increased. Keywords: oil-water films, environmental pollution, multi-walled carbon nanotubes, renewable adsorbents.

Effects of Ni Loadings on the Structure and Morphology of Carbon Nanotubes Using Nickel Doped Iron Oxide Catalysts

AbstractIron oxide and their different doped iron oxide catalyst have been used for decades and are considered as efficient catalysts in several synthesis schemes including synthesis of carbon nanotubes. The iron oxide of the catalyst is abundant in nature, high catalytic activity at low over potentials, stability in basic media and low cost, making it environmentally and economically attractive. Nickel doped iron oxide catalyst have not been reported in the literature. Doping of nickel over iron oxide catalyst, different percentage 1 %, 5 %, 10 % and 20 % were done by impregnation method. The samples were characterized by X‐Ray powder Diffraction (XRD), Fourier‐Transform Infrared Spectroscopy (FTIR), Scanning Electron Microscope (SEM), Energy Dispersive X‐ray (EDX) and Thermo Gravimetric Analysis (TGA). Nickel doped iron oxide was used as catalyst for the synthesis of carbon nanotubes (CNTs) and doping changed the morphology of carbon nanotube (CNTs). FTIR results confirmed the doping and presence of different functional groups. Chemical vapor deposition (CVD) was carried out for the synthesis of multiwall carbon nanotubes (MWCNTs) on nickel doped iron oxide catalyst for different percentage (1 %, 5 %, 10 % and 20 %) separately. CVD assembly was carried in tube furnace and the reaction was checked at two different temperature i.e 700 °C and 750 °C and using methane and compressed natural gas (CNG) as precursors. The catalyst was activated in the furnace at 800 °C for an hour. Methane and argon were used in proportion 2 : 1 inside the furnace. SEM showed formation of CNTs at 750 °C with CNG precursor. Formation of CNTs increased with increasing doping with this CNTs was confirmed by SEM.

Synthesis of Carbon Nanotubes Using Microwave Radiation to Modify Elastomer with Improved Electrical and Thermal Conductivity

Synthesis of Carbon Nanotubes Using Microwave Radiation to Modify Elastomer with Improved Electrical and Thermal Conductivity

Silver Oxide Nanoparticle Decorated Carbon Nanotube as Efficient Electron Gun

AbstractAlthough there have been numerous great field emission reports of pure and hybrid carbon nanotubes (CNTs) with ultra‐low turn‐on field and ultra‐high emission stability, practically all of the reports indicate concern about CNT manufacture on a large scale. This is due to the fact that CNT experiments require high pressure, temperature, metal catalysis, and an inert environment, and even after meeting all of these perfect conditions, the yield is quite low. Furthermore, as CNT is relatively inert in nature, it is nearly hard to make it reactive with any other metal without adequate functionalization. Keeping this in mind, this work reports the synthesis of CNT in amorphous form by a simple low‐temperature solid‐state reaction between ammonium chloride and ferrocene. The as‐synthesized CNT is further functionalized by silver oxide nanoparticle without additional functionalization. X‐ray diffraction (XRD) confirms the proper phase formation as well as the successful functionalization of the pure and hybrid sample, electron microscopic images confirm the successful functionalization of the as‐prepared CNT whereas Fourier transformed infrared (FTIR) spectroscopic analysis gives the ideas about different bonding present in all the samples. It has been found that the hybrid sample gives much better field emission performance compare to the pure CNT with betterment in both turn‐on field and enhancement factor more than 100%. The betterment is believed to be due to the favorable band bending, larger number of emission sites, and sharp curvature of the silver particles.

A Cycloparaphenylene Acetylene as Potential Precursor for an Armchair Carbon Nanotube.

The bottom-up synthesis of carbon nanotubes (CNTs) is a long-standing goal in synthetic chemists. Producing CNTs with defined lengths and diameters would render these materials and thus their fascinating properties accessible in a controlled way. Inspired by a recently reported synthesis of armchair graphene sheets that relied on a benzannulation and Scholl oxidation of a poly(p-phenylene ethynylene), the same strategy is applied on a cyclic substrate with a short, but well defined CNT as target structure. Herein we report the synthesis of a derivatized [12]cyclo-para-phenylene acetylene ([12]CPPA) that was accessible employing a Sonogashira macro-cyclization. The obtained macrocycle is the largest [n]CPPA reported to date and displays bright turquoise fluorescence with a large quantum yield of 77%. The [12]CPPA can be transformed by a 12-fold benzannulation that converts each alkyne to a naphthalene and therefore allows formation of an armchair [12,12] CNT precursor. The final 72-fold Scholl oxidation to the [12,12] CNT turned out to be challenging and its optimization requires an improved synthetic strategy to produce large quantities of the final precursor. The developed approach poses a potential break through strategy for the production of CNTs and certainly incentivizes synthetic chemists to apply the same methodology for various conjugated macrocycles.

Synthesis of magnetic multi-walled carbon nanotubes with layered double hydroxide (M-MWCNTs@MnAl-LDH) nanocomposite as an adsorbent for lead extraction

MnAl layered double hydroxide hybrid with magnetic-multiwalled carbon nanotubes was synthesized by a hydrothermal method and used for the extraction of Pb(II) (lead) from spices and water samples in the dispersive solid phase microextraction (dSPμE) technique using FAAS. The as-prepared adsorbent MMWCNTs@MnAl-LDH was characterized by XRD, FTIR, EDX, and SEM techniques. Various analytical parameters were optimized, including pH 8, adsorbent dosage of 5 mg, HNO3 eluent concentration of 1 mol L−1, eluent volume of 3 mL, eluent time of 60 s, and sample volume of 20 mL, for quantitative lead recoveries, with an LOD of 0.314 μg L−1, an LOQ of 1.048 μg L−1, and PF of 11.53. Under the optimized conditions, the linearity ranges from 0.5 to 500 μg L−1 (R2 = 0.9997). For the validation test of the established dSPμE procedure, Certified reference materials (CRMs) were used, yielding satisfactory recovery results ranging from 97.8 to 102.7 %. The method was applied to determine lead in turmeric, tap water, and industrial water samples.

Synthesis and Characterization of Magnetic Nanoparticle-Decorated Multiwalled Carbon Nanotubes.

Multiwalled carbon nanotubes find applications in many fields due to their extraordinary properties. However, depending on their synthesis method, they show no or a poor response to the presence of a magnetic field. This limits their usability in magnetic applications. In this study, the maximum induced magnetization of multiwalled carbon nanotubes was increased by deposition of magnetic nanoparticles, which were produced by nanosecond pulsed laser deposition under inert low-pressure conditions using iron (Fe), magnetite (Fe3O4), cobalt (Co), and nickel (Ni) targets. Extensive chemical and physical characterization of the added nanoparticles was performed. It was found that for the same synthesis conditions, Fe and Fe3O4 targets resulted in the formation of larger, asymmetrical magnetic Fe nanoparticles with a Fe3O4 shell (Fe@Fe3O4) (3.2-8.6 nm) and Fe3O4 (6.0-12.4 nm) nanoparticles, respectively. Smaller, more spherical Co@CoO (2.1-5.0 nm) and Ni@NiO (1.4-3.5 nm) nanoparticles were obtained from the Co and Ni targets, respectively. The highest increase in maximum induced magnetization was observed for multiwalled carbon nanotubes with Fe@Fe3O4 (5.37 ± 0.15 emu/g) or Co@CoO nanoparticles (4.29 ± 0.01) compared to pristine multiwalled carbon nanotubes (2.46 ± 0.08 emu/g) and nanotubes with Fe3O4 (3.79 ± 0.38 emu/g) or Ni@NiO nanoparticles (2.85 ± 0.06 emu/g). Finally, superior adhesion of the Fe@Fe3O4 and Fe3O4 nanoparticles to multiwalled carbon nanotubes compared to the Ni@NiO and Co@CoO nanoparticles was identified.

Enhanced charge storage in supercapacitors using carbon nanotubes and N-doped graphene quantum dots-modified (NiMn)Co2O4

The integration of ternary metal oxides into carbon materials is anticipated to significantly boost the electrochemical performance of supercapacitor electrodes. This article synthesized carbon nanotubes (CNT)/(NiMn)Co2O4 composite materials using a straightforward hydrothermal method and subsequently prepared composite thin films of CNT/P-(NiMn)Co2O4@NGQD by phosphating and incorporating nitrogen-doped graphene quantum dots (NGQD). These films served as the functional electrode material for supercapacitors, enhancing their performance capabilities. The specific capacity of CNT/P-(NiMn)Co2O4@NGQD was measured at 2172.0 F g−1 at a current density of 1 A g−1, maintaining a capacitance of 1954.0 F g−1 at 10 A g−1, thus demonstrating excellent rate performance. Electrochemical impedance spectroscopy (EIS) further revealed enhancements in electrolyte flow dynamics and capacitance behavior post-NGQD introduction. The energy density of the composite material reached 94.4 Wh kg−1 at power density of 800 W kg−1, demonstrating superior electrochemical performance. The enhancement in these electrochemical properties is attributed to the high specific surface area and active sites of CNT/P-(NiMn)Co2O4@NGQD films, along with the synergistic effects of NGQD and metal ions facilitating rapid electrons and charge transfer. This work provides new insights into developing high-performance supercapacitors.

Synthesis of Ultrahigh-Purity (6,5) Carbon Nanotubes Using a Trimetallic Catalyst.

Chirality-controlled synthesis of carbon nanotubes (CNTs) is one of the ultimate goals in the field of nanotube synthesis. At present, direct synthesis achieving a purity of over 90%, which can be called single-chirality synthesis, has been achieved for only two types of chiralities: (14,4) and (12,6) CNTs. Here, we realized an ultrahigh-purity (∼95.8%) synthesis of (6,5) CNTs with a trimetallic catalyst NiSnFe. Partial formation of Ni3Sn crystals was found within the NiSnFe nanoparticles. The activation energy for the selective growth of (6,5) CNTs decreased owing to the formation of Ni3Sn crystals, resulting in the high-purity synthesis of (6,5) CNTs. Transmission electron microscopy (TEM) reveals that one-dimensional (1D) crystals of periodic strip lines with 8.8 Å spacing are formed within the as-grown ultrahigh-purity (6,5) CNTs, which are well-matched with the simulated TEM image of closely packed 37 (6,5) CNTs with 2.8 Å intertube distance, indicating the direct formation of chirality-pure (6,5)-CNT bundle structures. The photoluminescence (PL) lifetime increases more than 20 times by the formation of chirality-pure bundle structures of (6,5) CNTs compared to that of isolated (6,5) CNTs. This can be explained by exciton delocalization or intertube excitons within bundle structures of chirality-pure (6,5) CNTs.

Strategically designed multiwalled carbon nanotube/bismuth ferrite/polyaniline nanocomposites and unlocking their potential for advanced supercapacitors

Bismuth ferrite (BF) serves a potential electrode-active material due to its peculiar characteristics such as wide voltage window and high specific capacitance, excellent stability, facile synthesis routes, etc. to name a few. Herein we report the strategic design and facile synthesis of multiwalled carbon nanotubes (MWCNT)/BF/polyaniline (PANI) nanocomposites, particularly for application in advanced supercapacitors. The MWCNT/BF/PANI nanocomposite architecture is a strategic design in which the maximum available surface area is utilized for the electrode nanostructure with increased porosity that allows easy movement of electrolyte-ions through it. The uniform arrangement of BF on MWCNTs helps in mitigating the possible agglomeration, further augmenting the surface area for an enhanced charge storage. The strategic layout of PANI on BF-decorated MWCNTs has given a coral-like structure for the nanocomposite electrode which significantly increased the surface area, reduced ion pathways and facilitating better access to electrolytic K+ ions. The MWCNT/BF/PANI nanocomposite electrode exhibits a specific capacitance of 3640 F g−1 at a current density of 5 A g−1. The innovative design as well as the synergy between the individual components of the nanocomposite electrode play a pivotal role in attaining the enhanced electrochemical performance.

Impact of nickel and alkaline earth metals interaction on sustainable carbon nanotubes generation from plastic face masks via catalytic pyrolysis

The one-pot synthesis of carbon nanotubes (CNTs) emerges as a promising approach for plastic valorization, owing to its simplicity and scalability. However, limited attention has been given to catalyst design for this method, particularly regarding the influence of Group 2 alkaline earth metal elements (X) on the Ni-based catalyst activity. This study investigates the impact of X on the catalytic activity of Ni towards sustainable CNTs synthesis using plastic face masks. The findings revealed that X influenced the carbon yield of NiMo-X catalysts and the morphology of the resultant carbon nanomaterials. Notably, NiMo-Ca demonstrated the highest carbon yield, whereas NiMo-Mg and NiMo-Ba exhibited the lowest. Furthermore, NiMo-Mg tends to produce clean and thin CNTs, while NiMo-Ba tends to yield carbon flakes with numerous irregular cokes. In addition to the effect of Ni crystallite size, which influences the transition from tubular to flake-like carbon structures, environmental factors are also considered. Specifically, NiMo-Mg generated a high CO2/CH4 environment, while NiMo-Ba exhibited slower catalytic cracking of polymeric chains from face masks, both of which were unfavorable for CNTs growth. Conversely, NiMo-Ca facilitated higher carbon recovery, likely due to its creation of a low CO2/CH4 environment via CO2 methanation. Optimization studies indicated that increasing pyrolysis temperatures and durations lead to reduced carbon yield, while cyclic pyrolysis of face masks up to five iterations enhances the reusability of NiMo-X catalysts with improved carbon recovery. Overall, this study provides valuable insights into the early pyrolytic gas formation and carbon nucleation phase, which are influenced by the surface Ni fraction and Ni polarization, as well as the later CNTs growth phase, which is related to the Ni crystallite size.

Simple pyrolysis synthesis of multi-walled carbon nanotubes as a highly stable electrode material for supercapacitor applications

We report the preparation of multi-walled carbon nanotubes (MWCNTs) by using a simple and cost-effective method for supercapacitor applications. The fabricated MWCNTs electrode shows a maximum specific capacitance of 278 F g−1 at 1 A g−1 and 257 F g−1 at 5 mV/s. Also, excellent retention has been achieved in the fabricated MWCNT electrode and 97 % capacitance is retained even after 10,000 cycles. The findings highlight the potential of pyrolysis-synthesized MWCNTs as a viable electrode material for supercapacitors, offering a pathway towards the development of efficient and durable energy storage devices for various applications.