Decoration of carbon nanotubes with nearly monodisperse MFe2O4 (MFe2O4, M = Fe, Co, Ni) nanoparticles

Magnetic monodisperse ferrite MFe₂O₄ (M = Fe, Co, Ni) nanoparticles have been successfully deposited on carbon nanotubes (CNTs) by in situ high-temperature hydrolysis and inorganic polymerization of metal salts and CNTs in polyol solution. X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), energy-dispersive X-ray spectrometry (EDS) and vibrating sample magnetometer (VSM) investigations were used to characterize the final products. The influencing factors for formation of CoFe₂O₄ nanoparticles along CNTs have also been discussed briefly. The main advantage of this synthetic strategy is that it is beneficial for the fabrication of magnetic CNTs with a compact layer of nanoparticles and could be extended to prepare series of ferrite/CNTs nanocomposites via the substitution of metal cations.     

Structural modification and enhanced electron emission from multiwalled carbon nanotubes grown on Ag/Fe catalysts coated Si-substrates

Multiwalled carbon nanotubes and carbon nano-filaments were grown using Fe as the main catalyst and Ag as a co-catalyst by microwave plasma enhanced chemical vapour deposition. In this work we demonstrate the growth behaviour of carbon nanotubes (CNTs) grown on pure Fe-film and Ag–Fe films. We find that using Ag film beneath Fe film significantly abate the catalyst–substrate interactions by acting as a barrier layer as well as enhances the nucleation sites for the growth of CNTs due to the limited solubility with Fe and silicon. Scanning electron microscopy and transmission electron microscopy studies were carried out to image the microstructures of the samples. It was observed that the length of Fe catalyzed CNTs was ∼500 nm and Ag–Fe catalyzed CNTs varied from ∼600 nm to 1.7 μm. Micro Raman spectroscopy confirmed the improved crystalline nature of Ag–Fe CNTs. It was found that I_D/I_G ratio for Fe catalyzed CNTs was ∼1.08 and for Ag–Fe catalyzed CNTs was ∼0.7. The Ag–Fe catalyzed CNTs were found to be less defective as compared to Fe catalyzed CNTs. Field emission measurements using diode configuration, showed that electron emission from Ag–Fe catalyzed CNTs was much stronger as compared to Fe catalyzed CNTs. The threshold field for Ag–Fe catalyzed CNTs was (2.6 V μm⁻¹) smaller as compared to Fe catalyzed CNTs (3.8 V μm⁻¹) and thus shows better emission properties. This enhancement in electron emission mechanism as a result of introduction of Ag underlayer is attributed to the increased emitter sites and improved crystallinity.     

Facile synthesis of MnO2/CNT nanocomposite and its electrochemical performance for supercapacitors

A nanocomposite of manganese dioxide coated on the carbon nanotubes (MnO₂/CNTs) was synthesized by a facile direct redox reaction between potassium permanganate and carbon nanotubes without any other oxidant or reductant addition. The morphology, microstructure and crystalline form of this MnO₂/CNT nanocomposite were characterized by scanning electron microscopy (SEM), transition electron microscopy (TEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The electrochemical properties are characterized by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and galvanostatic charge/discharge (GCD). The results show that the facile prepared MnO₂/CNTs nanocomposite shows specific capacitance of 162.2 F g⁻¹ at the current density of 0.2 A g⁻¹ and excellent charge/discharge property with 90% of its specific capacitance kept after 2000 cycles at the current density of 5 A g⁻¹.     

Preparation and electrochemical performance of manganese oxide/carbon nanotubes composite as a cathode for rechargeable lithium battery with high power density

Manganese oxide/carbon nanotubes (MO/CNTs) composite was prepared by hydrothermally reducing KMnO₄ with CNTs, where the used CNTs are of dual role, i.e., they serve as reductant during reaction and the remaining CNTs act as conducting agent in the composite. This composite was characterized by X-ray diffraction and scanning electron microscopy techniques. In addition, the electrochemical performances of the composite were investigated, which suggested an excellent rate-capability of this material; e.g., it delivered a high discharge capacity as 131 mAh g^− 1 at a high current density of 4 A g^− 1 (20 C), and high capacity at low discharge current density, e.g., about 209 mAh g^− 1 at 0.2 C rate. Therefore, such a MO/CNTs composite is promising in high power application of lithium battery and electrochemical capacitor.     

Electron-emission properties of carbon nanotube micro-tips coated by amorphous carbon nitride films

An approach to the preparation of a tip-type of field emitter that is made up of carbon nanotubes (CNTs) coated with amorphous carbon nitride (a-CN_x) films is presented for the purpose of enhancing its electron emission property. CNTs were directly grown on nano-sized conical-type tungsten tips via the inductively coupled plasma-chemical vapor deposition system, and a-CN_x films were coated on the CNTs using an radio frequency magnetron sputtering system. The morphologies and microstructures of the a-CN_x-coated CNTs were analyzed via field emission scanning electron microscopy, energy-dispersive x-ray spectroscopy, high-resolution transmission electron microscopy, and x-ray photoelectron spectroscopy. The electron emission properties of the a-CN_x/CNT hetero-structures were measured using a high-vacuum field emission measurement system. The best field emission properties, such as a very low turn-on voltage of 500 V and a maximum emission current of 176 μA were achieved for the CNT emitter coated with the 5 nm-thick a-CN_x film. In addition, this emitter showed a highly stable behavior in long-term (up to 25 h) electron emission.     

Facile synthesis of boron nitride coating on carbon nanotubes

Boron nitride (BN) coating on the surface of carbon nanotubes (CNTs) was synthesized by the direct reaction of NaBH₄ and NH₄Cl in the temperature range of 500–600 °C. X-ray diffraction, field emission scanning electron microscopy (FESEM), high-resolution transmission electron microscopy (HRTEM) and X-ray photoelectron spectroscopy (XPS) confirm the formation of BN coating. It is revealed that the BN coating follows the shape of CNTS without damaging the surface of CNTs, and the elements B and N distribute homogenously along the whole CNTs without chemical bonds between carbon and BN layers. Besides, the oxidation resistance of the CNTs improved a lot after being coated with BN.     

Enhanced electron emission from titanium coated multiwalled carbon nanotubes

Enhanced field emission properties and improved crystallinity of titanium (Ti) coated multiwalled carbon nanotubes (MWCNTs), prepared by microwave plasma enhanced chemical vapour deposition have been observed. Ti films of extremely low thicknesses (0.5 nm, 1.0 nm and 1.5 nm) were coated over carbon nanotubes (CNTs) and their field emission behaviour was investigated. The turn on field of Ti coated CNTs was found to be low (~ 0.8 V/μm) as compared to pristine CNTs (~ 1.8 V/μm). The field enhancement factor for Ti coated CNTs was quite large (~ 1.14 × 10⁴) as compared to pristine CNTs (~ 6 × 10³). This enhancement in electron emission is attributed to the passivation of defects and improved crystallinity of CNTs. Surface morphological and microstructural studies were carried out to investigate the growth of pristine and Ti coated CNTs. It was observed that Ti nanoclusters adsorb on the edges of MWCNTs and increase their crystallinity. This increase is directly correlated with the thickness of Ti film deposited. Micro Raman spectroscopy confirmed the improved crystallanity of Ti coated CNTs.     

PEG-300 assisted hydrothermal synthesis of 4ZnO·B2O3·H2O nanorods

4ZnO·B₂O₃·H₂O is commonly used as a flame-retardant filler in composite materials. The microstructure of the powder is of importance in its applications. In our study, for the first time, one-dimensional (1D) nanostructure of 4ZnO·B₂O₃·H₂O with rectangle rod-like shape has been synthesized by a hydrothermal route in the presence of surfactant polyethylene glycol-300 (PEG-300). The nanorods have been characterized by X-ray powder diffraction (XRD), inductively coupled plasma with atomic emission spectroscopy (ICP-AES), thermogravimetry (TG) and differential thermal analysis (DTA), scanning electron microscopy (SEM), transmission electron microscopy (TEM) equipped with selected area electron diffraction (SAED) as well as high-resolution transmission electron microscopy (HRTEM). These nanorods are about 70 nm in thickness, 150-800 nm in width and have lengths up to a few microns. 4ZnO·B₂O₃·H₂O nanorods crystallize in the monoclinic space group P2₁/m, a = 6.8871(19) Å, b = 4.9318(10) Å, c = 5.7137(16) Å, β = 98.81(21)° and V = 191.779(71) Å³.     

Synthesis of well-crystallized birnessite using ethylene glycol as a reducing reagent

Well-crystallized birnessite sheets containing K⁺ in the interlayers have been prepared using KMnO₄, ethylene glycol and KOH by microwave heating at 90 °C for 10 min. Ethylene glycol was used as a reducing agent. The effect of KOH concentration on the formation of birnessite was studied. The products were characterized by X-ray powder diffraction (XRD), transmission electron microscopy (TEM), thermogravimetric analysis (TG), differential scanning calorimetric analysis (DSC) and Fourier transform infrared (FTIR). Birnessites were converted to cryptomelane upon heating at 400-800 °C and completely collapsed to form Mn₃O₄ at 1000 °C.     

Fabrication of transparent conductive carbon nanotubes/polyurethane-urea composite films by solvent evaporation-induced self-assembly (EISA)

Transparent and conductive carbon nanotubes (CNTs)/polyurethane-urea (PUU) composite films were prepared by solvent evaporation-induced self-assembly (EISA). Pristine CNTs were treated with acids (H₂SO₄/HNO₃ = 3:1, v:v), acylated with thionyl chloride, and purified after filtration. These acylated CNTs (0.05 wt.% in dimethylformamide, DMF) were deposited onto the 3-aminopropyl triethoxysilane (APTES)-modified glass substrate by DMF EISA at 100 °C with the withdrawal rate of 3 cm/h. The CNT layers of 200–400 nm thicknesses were transferred to the PUU films by solution casting or resin transfer molding (RTM) at ambient temperature. Optical transmittances of the composite films were 60–75% at 550 nm wavelength and their sheet resistances were 5.2 × 10⁰–2.4 × 10³ kΩ/square, and which varied significantly with type of CNTs and the transferring methods of CNT layers.     

Synthesis and characterization of NiFe2O4 nanosheet via polymer assisted co-precipitation method

Nickel ferrite (NiFe₂O₄) nanosheet has been synthesised by the polymer assisted co-precipitation method. The synthesised nanosheet was characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), high-resolution scanning electron microscopy (HRSEM), thermal analysis and vibrating sample magnetometry (VSM). The results showed that the as synthesised NiFe₂O₄ has sheet like morphology with good crystalline nature. The nanosheet was formed through random aggregation of magnetic nanoparticles. Ferromagnetic property was exhibited by the nanosheet with saturation magnetization M_s = 35 emu/g, remanent M_r = 8.6 Oe and coercive force H_c = 192 emu/g.     

X-ray images obtained from cold cathodes using carbon nanotubes coated with gallium-doped zinc oxide thin films

X-ray imaging data obtained from cold cathodes using gallium-doped zinc oxide (GZO)-coated CNT emitters are presented. Multi-walled CNTs were directly grown on conical-type (250 μm-diameter) tungsten-tip substrates at 700 °C via inductively coupled plasma-chemical vapor deposition (ICP-CVD). GZO films were deposited on the grown CNTs at room temperature using a pulsed laser deposition (PLD) technique. Field-emission scanning electron microscopy (FESEM) and high-resolution transmission electron microscopy (HRTEM) were used to monitor the variations in the morphology and microstructure of the CNTs before and after GZO coating. The formation of the GZO layers on the CNTs was confirmed using energy-dispersive X-ray spectroscopy (EDX). The CNT-emitter that was coated with a 10-nm-thick GZO film displayed an excellent performance, such as a maximum emission current of 258 μA (at an applied field of 4 V/μm) and a threshold field of 2.20 V/μm (at an emission current of 1.0 μA). The electric-field emission characteristics of the GZO-coated CNT emitter and of the pristine (i.e., non-coated) CNT emitter were compared, and the images from an X-ray system were obtained by using the GZO-coated CNT emitter as the cold cathode for X-ray generation.     

Pt-modified carbon nanotube networked layers for enhanced gas microsensors

Carbon nanotubes (CNTs) networked films have been grown by chemical vapor deposition (CVD) technology onto miniaturized low-cost alumina substrates, coated by nanosized Co-catalyst for growing CNTs, to perform chemical detection of toxic gasses (NO₂ and NH₃), greenhouse gasses (CO₂ and CH₄) and domestic safety gasses (CO and C₂H₅OH) at an operating sensor temperature of 120 °C. The morphology and structure of the CNTs networks have been characterized by scanning electron microscopy (SEM). A dense network of bundles of multiple tubes consisting of multi-walled carbon nanostructures appears with a maximum length of 1-5 μm and single-tube diameter varying in the range of 5-40 nm. Surface modifications of the CNTs networks with sputtered Platinum (Pt) nanoclusters, at tuned loading of 8, 15 and 30 nm, provide higher sensitivity for significantly enhanced gas detection compared to un-decorated CNTs. This could be caused by a spillover of the targeted gas molecules onto Pt-catalyst surface with a chemical gating into CNTs layers. The measured electrical conductance of the functionalized CNTs upon exposures of a given oxidizing and reducing gas is modulated by a charge transfer model with p-type semiconducting characteristics. The effect of activated carbons as chemical filters to reduce the influence of the domestic interfering alcohols on CO gas detection has been studied. Functionalized CNT gas sensors exhibited better performances compared to unmodified CNTs, making them highly promising candidates for functional applications of gas control and alarms.     

Preparation of Fe3O4/PVA nanofibers via combining in-situ composite with electrospinning

A novel approach, combining in-situ composite method with electrospinning, was used to prepare high magnetic Fe₃O₄/poly(vinyl alcohol) (PVA) composite nanofibers. Fe₃O₄ magnetic fluids were synthesized by chemical co-precipitation method in the presence of 6 wt.% PVA aqueous solution. PVA was used as stabilizer and polymeric matrix. The resulting Fe₃O₄/PVA composite nanofibers were characterized with field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM) and X-ray diffractometer (XRD), respectively. These composite fibers showed a uniform and continuous morphology, with the Fe₃O₄ nanoparticles embedded in the fibers. Magnetization test confirmed that the composite fiber showed a high saturated magnetization (M_s = 2.42 emµ·g^-1) although only 4 wt.% content.     

Mechanical behavior of self-assembled carbon nanotube reinforced nylon 6,6 fibers

The versatile electrospinning technique was used to successfully align and disperse multiwalled carbon nanotubes (MWCNT) in nylon 6,6 matrix to obtain composite fibers. The morphology of the composite fibers and the dispersion of the CNTs within the fibers were analyzed using scanning electron microscopy (SEM) and transmission electron microscopy (TEM), respectively. TEM analysis revealed that the CNTs were well-dispersed, separated and aligned along the fiber axis. The thermal and mechanical properties of the composite fibers were characterized as a function of weight fraction of the CNTs. Incorporation of the CNTs in the fibers resulted in an increase in glass-transition temperature (T_g) by ∼7 °C, indicating that the addition of CNTs has restricted the mobility of the polymer chains and provided confinement to neighboring molecular chains. Tensile and nanoindentation experiments were performed to investigate the mechanical deformation behavior of the composite fibers. The results suggested that incorporation of high strength and high aspect ratio CNTs into the fiber matrix enhanced significantly the stiffness and strength of nylon 6,6 fibers. An understanding of the structure–property relationships can provide fruitful insights to develop electrospun fibers with superior properties for miniaturized and load-bearing applications.     

Ionic liquid assisted hydrothermal synthesis of hollow vesicle-like MoS2 microspheres

The preparation of MoS₂ microspheres with hollow vesicle-like structure was successfully achieved, which used hydrazine solution with (NH₄)₂MoS₄ as the precursor. The reaction process was assisted by a convenient ionic liquid (1-butyl-3-methylimidazolium chloride) with the hydrothermal method at 200 °C for 24 h. X-ray fluorescence (XRF), X-ray diffraction (XRD), scanning electron microscopy (SEM) and high-resolution transmission electron microscopy (HRTEM) techniques were used to characterize the samples. It was shown that the MoS₂ microspheres had uniform spherical morphology with the diameter of 1-2 μm. It was also indicated that the hollow vesicle monomers on the surface of microspheres were structured with multi-layer of MoS₂, whose d spacing was 1.0 nm. A tentative formation mechanism was proposed for the growth process of the MoS₂ microspheres with hollow vesicle-like structure.     

Hydrothermal synthesis of carbon nanotube/cubic Fe3O4 nanocomposite for enhanced performance supercapacitor electrode material

Carbon nanotube/Fe₃O₄ (CNT/Fe₃O₄) nanocomposite with well-dispersed Fe₃O₄ nano-cubes inlaid on the surfaces of carbon nanotubes, was synthesized through an easy and efficient hydrothermal method. The electrochemical behaviors of the nanocomposite were analyzed by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and chronopotentiometry in 6 M KOH electrolyte. Results demonstrated that CNT as the supporting material could significantly improve the supercapacitor (SC) performance of the CNT/Fe₃O₄ composite. Comparing with pure Fe₃O₄, the resulting composite exhibited improved specific capacitances of 117.2 F/g at 10 mA/cm² (3 times than that of pure Fe₃O₄), excellent cyclic stability and a maximum energy density of 16.2 Wh/kg. The much improved electrochemical performances could be attributed to the good conductivity of CNTs as well as the anchored Fe₃O₄ particles on the CNTs.     

Preparation of Eu-doped LaPO4 films using successive-ionic-layer-adsorption-and-reaction

Thin films of Eu-doped lanthanum orthophosphate (LaPO₄) were fabricated on glass substrates using the successive-ionic-layer-adsorption-and-reaction method and subsequent hydrothermal and furnace annealing. A monoclinic structure was observed to be present in LaPO₄:Eu films after hydrothermal annealing at 200 °C. Scanning electron microscopy and transmission electron microscopy images of LaPO₄:Eu films show the homogenously close-packed morphology of micro-sized nanofibers at around 10 to 20 nm in diameter. The red emission activated at 254 nm was obtained from LaPO₄:Eu films.     

A facile surfactant-free fabrication of single-crystalline truncated Fe3O4 cubes

Single-crystalline truncated Fe₃O₄ cubes with active basal facets have been successfully fabricated through a facile surfactant-free hydrothermal route. The presented materials were characterized by X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM), energy dispersive spectroscopy (EDS), dynamic light scattering (DLS), selection area electron diffraction (SAED) and magnetic property measurement system (MPMS). The results showed that all products are Fe₃O₄ with face-center-cubic (FCC) structure. The morphology of Fe₃O₄ depends on the contents of hydroxide ions, hydrazine hydrate and reaction time. The well-defined truncated Fe₃O₄ cubes with active basal facets {1 0 0} were fabricated when the pH value, the hydrazine hydrate content and reaction time are 10, 10 mL and 24 h, respectively. The as-prepared Fe₃O₄ cubes exhibit excellent magnetic properties, which endow the materials with great potential applications in many fields.     

Facile one-pot synthesis and luminescence of hexagonal TbPO4·nH2O hollow spheres

Monodisperse hexagonal TbPO₄·nH₂O hollow spheres were successfully obtained by utilizing Tb(OH)CO₃ colloidal spheres as the precursor and NH₄H₂PO₄ as the phosphorus source through the hydrothermal process. The obtained hollow spheres were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), respectively. They have the average diameter of 200 nm. There are a number of tiny nanorods with the length of about 60 nm on the surface of the spheres. The obtained TbPO₄ hollow spheres exhibit green color emission from ⁵D₄ − ⁷F_J (J = 6, 5, 4, 3) transitions of the Tb³⁺ ions, which are expected to be applied in display applications and biological applications.