Synthesis, characterization and low field emission of CNx nanotubes

Aligned CN_x nanotubes were fabricated by pyrolyzing ethylenediamine on p-type Si(1 1 1) substrates using iron as the catalyst. Scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectrum (XPS) and Raman spectroscopy were used to characterize the CN_x nanotubes. The CN_x nanotubes with the average length of 20 μm and diameters in the range of 50–100 nm have the “bamboo-like” structure and worse crystalline order. The low-field emission measurements of the CN_x nanotubes indicated that 20 μA/cm² current densities were observed at an electric field of 1.4 V/μm and 1.280 mA/cm² were obtained at 2.54 V/μm. The CN_x nanotubes exhibit better field emission properties than the carbon nanotubes and the BCN nanotubes. The emission mechanism of CN_x nanotubes is also discussed.     

Microwave-assisted functionalization of single-walled carbon nanotubes with 3-chloropropene

We have reported a highly efficient approach to functionalize single-walled carbon nanotubes by electrophilic addition polymerization of 3-chloropropene under microwave irradiation. Using Lewis acids as catalysts, 3-chloropropene can undergo polymerization followed by hydrolysis with alkaline methanol, and thus the reaction results in the attachment of polymer chains and hydroxyl groups to the surface of the nanotubes. The resulting nanotubes were characterized with Fourier transform infrared spectroscopy, thermogravimetric analysis, Raman spectroscopy, high-resolution transmission electron microscopy, and atomic force microscopy. The result shows that 30 min of irradiation time is enough to bring the reaction to the end and a longer time did not improve the degree of functionalization.     

Controlled synthesis, characterization and optical properties of CdS nanocrystalline thin films via chemical bath deposition (CBD) route

In this study, the CdS nanocrystalline thin films obtained from an ammonia-free chemical bath deposition process. The crystallites with a size range of 10–20 nm in diameter with zinc blend (cubic) and wurtzite (hexagonal) crystal structure and strong photoluminescence were prepared from the mixture solutions of: cadmium chloride dihydrate as a cadmium source, thiourea as a sulfur source and sodium citrate dihydrate as a complexing agent for cadmium ions. The well-cleaned glass used as a substrate for thin films deposition. The obtained samples were characterized by the techniques such as scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectra (XPS), atomic force microscopy (AFM) and fluorescence spectroscopy. Also, the effect of two parameters such as pH and temperature of reaction on the synthesis of CdS nanocrystals was studied. Finally, it was found the CdS nanocrystals showed sharp excitation features and strong “band-edge” emission.     

Fabrication of stable, transparent and superhydrophobic nanocomposite films with polystyrene functionalized carbon nanotubes

Stable, transparent and superhydrophobic carbon nanotube (CNT) nanocomposite films were fabricated by one-step spray casting process using the polystyrene functionalized CNTs, which were prepared by “living” free-radical polymerization and analyzed by means of infrared spectroscopy and thermal gravimetric analysis. The CNT film has a high water contact angle of 160° and a sliding angle of less than 3°. The surface topography of the fabricated film was characterized by field emission scanning electron microscopy. The transparency of the CNT film was investigated by UV–vis spectroscopy. The result shows that the CNT film has light transmittance of about 78% in the visible light region.     

Functionalization of vertically aligned carbon nanotubes with polystyrene via surface initiated reversible addition fragmentation chain transfer polymerization

Here we demonstrate the covalent attachment of vertically aligned (VA) acid treated single-walled carbon nanotubes (SWCNTs) onto a silicon substrate via dicyclohexylcarbodiimide (DCC) coupling chemistry. Subsequently, the pendant carboxyl moieties on the sidewalls of the VA-SWCNTs were derivatized to acyl chlorides, and then finally to bis(dithioester) moieties using a magnesium chloride dithiobenzoate salt. The bis(dithioester) moieties were then successfully shown to act as a chain transfer agent (CTA) in the reversible addition fragmentation chain transfer (RAFT) polymerization of styrene in a surface initiated “grafting-from” process from the VA-SWCNT surface. Atomic force microscopy (AFM) verified vertical alignment of the SWCNTs and the maintenance thereof throughout the synthesis process. Finally, Raman scattering spectroscopy and AFM confirmed polystyrene functionalization.     

Probing Proteins in Solution by Xe NMR Spectroscopy

The interaction of xenon with different proteins in aqueous solution is investigated by ¹²⁹Xe NMR spectroscopy. Chemical shifts are measured in horse metmyoglobin, hen egg white lysozyme, and horse cytochrome c solutions as a function of xenon concentration. In these systems, xenon is in fast exchange between all possible environments. The results suggest that nonspecific interactions exist between xenon and the protein exteriors and the data are analyzed in term of parameters which characterize the protein surfaces. The experimental data for horse metmyoglobin are interpreted using a model in which xenon forms a 1:1 complex with the protein and the chemical shift of the complexed xenon is reported (Locci et al., Keystone Symposia “Frontiers of NMR in Molecular Biology VI”, Jan. 9–15, 1999, Breckenridge, CO, Abstract E216, p. 53; Locci et al., XeMAT 2000 “Optical Polarization and Xenon NMR of Materials”, June 28–30, 2000, Sestri Levante, Italy, p. 46).     

Effect of different microwave-based treatments on multi-walled carbon nanotubes

Three new methods for the functionalization of multi-walled carbon nanotubes (MWCNTs) are reported using microwave (MW) energy and water as a mild chemical agent. In the first method we reported the effect of MW irradiation on a dispersion of MWCNTs in deionized water, in the second method we studied the exposing of MWCNT to microwave irradiation in the presence of steam, and in the third method we used microwave oven-generated plasma for the functionalization of MWCNTs. We also performed thermal oxidation and acid treatment as two conventional methods for oxidative functionalization of carbon nanotubes, to compare their effect with our results. Transmission electron microscopy (TEM) and Raman spectroscopy results showed that although these microwave methods introduced some defects to the carbon nanotubes, the damage was less severe than conventional treatments. X-ray photoelectron spectroscopy (XPS) measurements confirmed that the functionalization of carbon nanotubes by these methods favored hydroxyl groups, which are useful when further functionalization is required.     

Rashba splitting of kinetically bound states in gated HgCdTe surface quantum wells

The Rashba spin–orbit splitting of 2D electron gas in gated HgCdTe surface quantum wells on n-HgCdTe is studied experimentally (by the magneto-capacitance spectroscopy of Landau level method) and theoretically with emphasis on the peculiarities of spectrum at surface densities N_s corresponding to the onset of 2D subbands occupancy, where the regime of kinetic binding is realized. Although the spin–orbit splitting in kinetic confinement regime is small, the “Rashba polarization” Δn/n can achieve 100% because of strong difference in values of cutoff wave vector k_c for different spin-split sub-subbands.     

Synthesis, characterization and electrochemical behavior of polypyrrole/carbon nanotube composites using organometallic-functionalized carbon nanotubes

Thorn-like, organometallic-functionalized carbon nanotubes were successfully developed via a novel microwave hydrothermal route. The organometallic complex with methyl orange and iron (III) chloride served as reactive seed template, resulting in the oriented polymerization of pyrrole on the modified carbon nanotubes without the assistance of other oxidants. Morphological and structural characterizations of the carbon nanotube/methyl orange-iron (III) chloride and polypyrrole/carbon nanotube composites were examined using transmission electron microscopy (TEM), energy dispersive spectroscopy (EDS), infrared spectroscopy and X-ray diffraction (XRD). The electrochemical property of the polypyrrole/carbon nanotube composite was elucidated by cyclic voltammetry and galvanostatic charge-discharge. A specific capacitance of 304 F g⁻¹ was obtained within the potential range of −0.5-0.5 V in 1 M KCl solution.     

Nanostructuring-induced modification of optical properties of p-GaAs (1 0 0)

A pulsed anodic etching method has been utilized for nanostructuring of p-type GaAs (1 0 0) surface, using HCl-based solution as electrolyte. The resulting porous GaAs layer is characterized by atomic force microscopy (AFM), room temperature photoluminescence (PL), Raman spectroscopy and optical reflectance measurements. AFM imaging reveals that the porous GaAs layer is consisted of a pillar-like of few nm in width distributed between more-reduced size nanostructures. In addition to the “infrared” PL band of un-etched GaAs, a strong “green” PL band is observed in the etched sample. The broad visible PL band of a high-energy (3.82 eV) excitation is found to compose of two PL band attributed to excitons confinement in two different sizes distribution of GaAs nanocrystals. The quantum confinement effects in GaAs nanocrystallites is also evidenced from Raman spectroscopy through the pronounced appearance of the transverse optical (TO) phonon line in the spectra of the porous sample. Porosity-induced a significant reduction of the specular reflection, in the spectral range (400–800 nm), is also demonstrated.     

Preparation and characterization of amphiphilic multi-walled carbon nanotubes

Multiwalled carbon nanotubes (MWCNTs, average diameter 8 nm) functionalized by N-vinyl pyrrolidone (NVP) were synthesized by radical polymerization and characterized by Fourier transform infrared and Raman spectroscopies, thermogravimetric analysis and transmission electron microscopy. These NVP–MWCNTs exhibit remarkable solubility in water, ethanol and dimethyl formamide. The polyvinyl pyrrolidone can be attached onto the surface of the MWCNTs and the degree of functionalization is affected by NVP content. The functionalization causes possible grafting reaction and solid physical coating between MWCNTs and PVP.     

Filling of single-walled carbon nanotubes by CuI nanocrystals via capillary technique

The present study is focused on the synthesis and investigation of the nanocomposite CuI@SWNT obtained by the filling of metallic single-walled carbon nanotubes (SWNTs) (inner diameter 1–1.4 nm) by wide-gap semiconducting CuI nanocrystals using so-called capillary technique. The method is based on the impregnation of pre-opened SWNTs by molten CuI in vacuum with subsequent slow cooling to room temperature. SWNTs and CuI@SWNT nanocomposites were studied by nitrogen capillary adsorption method, EDX microanalysis, HRTEM microscopy and Raman spectroscopy. The changing of electronic properties of CuI@SWNT as compare to row nanotubes was observed.     

An efficient route towards the covalent functionalization of single walled carbon nanotubes

A simple and efficient method of chemical functionalization of both single and multiwalled carbon nanotubes has been discussed to give enhanced water solubility by rapidly and efficiently generating an appreciable amount of hydrophilic functional groups using microwave radiation. Surface functionalization containing more than 30 wt% of oxygen has been achieved, resulting into solubility of 2–5 mg/mL. Further covalent functionalization of such soluble SWNTs provides a remarkable degree of aniline functionalization through amidation, where the formation of polyaniline has been avoided. Functionalization of SWNTs is confirmed by techniques like electron microscopy, Fourier transform infrared spectroscopy, thermogravimetry, Raman spectroscopy, cyclic voltammetry and impedance spectroscopy. Electrochemical analysis suggests an enhanced double layer capacitance (110 F/g) of nanotubes after microwave treatment. Aniline functionalization of SWNTs shows possible variations on the nanotube topography with concomitant formation of a dynamic polymer layer on the nanotube surface.     

Covalent attachment of polystyrene on multi-walled carbon nanotubes via nitroxide mediated polymerization

A new method to attach polymers on carbon nanotubes has been studied. We used nitroxide mediated polymerization (NMP) to graft polystyrene from multi-walled carbon nanotubes (MWNTs). Carboxyl groups on MWNTs were activated with thionyl chloride (SOCl₂) to give acyl chloride derivative (MWNT-COCl). NMP initiator was introduced to MWNT by esterification of 1-hydroxy-2-phenyl-2-(2′,2′, 6′, 6′-tetramethyl-1′-piperidinyloxy)ethane (HO-PE-TEMPO) with acyl chloride groups of MWNTs. The obtained MWNT-PE-TEMPO was used for initiation of bulk polymerization of styrene, yielding polystyrene-grafted MWNTs (MWNT-g-pSt). The resulting composites of MWNT-g-pSt were analyzed by TEM, SEM, FT-IR and TGA.     

Photoresponsive conductance switching of multi-walled carbon nanotubes bearing covalently linked spironaphthoxazine

Multi-walled carbon nanotubes functionalized with a photochromic spironaphthoxazines (MWCNTs-SPO) were synthesized by the reaction between the hydroxyl group of SPO and the carbonyl chloride groups on the surface of MWCNTs. The functional spirooxazine photochromic groups on the surface of MWCNTs were identified by the X-ray photoelectron spectroscopy. As a novel derivative of MWCNTs, photoresponsive conductance switching of the MWCNTs-SPO was demonstrated under a 365 nm UV light irradiation. A simple photoinduced resistance measurement following the cyclic irradiation of UV light shows a very reversible response. The effect of the electron injection in the SPO is rationalized in terms of the HOMO–LUMO energy levels of both spiro and merocyanine forms.     

Influence of the electronic distribution of polymers in the spatial conformation of polymer grafted carbon nanotube composites

In this work we report the covalent functionalization of multiwalled carbon nanotubes (MWCNTs) with polyacrylonitrile (PAN) and polyvinylpyridine (PVP) by the graft from method. Differences in the electronic distribution of both polymers resulted in different interaction between polymers and the nanotubes. It was found that PVP chains wrapped the nanotubes while nanotubes functionalized with PAN presented PAN chains forming amorphous entanglements on the nanoscale linked to the MWCNTs. Differences in the conformation between both polymers and the MWCNTs can be attributed to interactions between the aromatic groups in PVP and the MWCNTs through π–π stacking. The absence of aromatic groups in the case of the PAN chains favours the interaction between them. The functionalization efficiency was characterized using Fourier transform infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA) and UV–vis spectroscopy, while morphological changes were characterized by high resolution transmission electron microscopy.     

Detonability limits in thin annular channels

In this paper, detonability limits in two-dimensional annular channels are investigated. Since the channel heights are small in comparison to the tube diameter, curvature effects can be neglected and the annular channels can be considered to be essentially two-dimensional. Mixtures that are highly diluted with argon are used since previous investigations seem to indicate that detonations in such mixtures are “stable” in that cellular instabilities play minor roles on the propagation of the detonation. For stable detonations where the ZND structure is valid, boundary layer effects can be modeled as a flow divergence term in the conservation of mass equation following the pioneering work of Fay [J.A. Fay, Phys. Fluids 2(3) (1959) 283–289]. Expansion due to flow divergence in the reaction zone results in a velocity deficit. There exists a maximum deficit when an eigenvalue detonation velocity can no longer be found, which can be taken as the onset of the detonability limits. Experimentally, it was found that unlike “unstable” detonations, the detonability limits for “stable” detonations are well-defined. No unstable near-limit phenomena (e.g., galloping detonations) was observed. Good agreement is found between the theoretical predictions and the experimentally obtained velocity deficits and limits in the two channel heights of 2.2 and 6.9 mm for hydrogen–oxygen and acetylene–oxygen mixtures diluted with over 50% argon. It may be concluded that at least for these special mixtures where the detonation is “stable,” the failure mechanism is due to flow divergence caused by the negative displacement thickness of the boundary layer behind the leading shock front of the detonation wave.     

Growth of carbon nanotubes by Fe-catalyzed chemical vapor processes on silicon-based substrates

In this paper, a site-selective catalytic chemical vapor deposition synthesis of carbon nanotubes on silicon-based substrates has been developed in order to get horizontally oriented nanotubes for field effect transistors and other electronic devices. Properly micro-fabricated silicon oxide and polysilicon structures have been used as substrates. Iron nanoparticles have been obtained both from a thin Fe film evaporated by e-gun and from iron nitrate solutions accurately dispersed on the substrates. Single-walled nanotubes with diameters as small as 1 nm, bridging polysilicon and silicon dioxide “pillars”, have been grown. The morphology and structure of CNTs have been characterized by SEM, AFM and Raman spectroscopy.     

Development of a novel high speed (electron-mobility) epi-n-ZnO thin films by L-MBE for III–V opto-electronic devices

Intrinsic epitaxial zinc oxide (epi-ZnO) thin films were grown by laser-molecular beam epitaxy (L-MBE), i.e., pulsed laser deposition (PLD) technique using Johnson Matthey “specpure”-grade ZnO pellets. The effects of substrate temperatures on ZnO thin film growth, electrical conductivity (σ), mobility (μ) and carrier concentration (n) were studied. As well as the feasibility of developing high quality conducting oxide thin films was also studied simultaneously. The highest conductivity was found for optimized epi-ZnO thin films is σ=0.06×10³ ohm⁻¹ cm⁻¹ (n-type) (which is almost at the edge of semiconductivity range), carrier density n=0.316×10¹⁹ cm⁻³ and mobility μ=98 cm²/V s. The electrical studies further confirmed the semiconductor characteristics of epi-n-ZnO thin films. The relationship between the optical and electrical properties were also graphically enumerated. The electrical parameter values for the films were calculated, graphically enumerated and tabulated. As a novelty point of view, we have concluded that without doping and annealing, we have obtained optimum electrical conductivity with high optical transparency (95%) for as deposited ZnO thin films using PLD. Also, this is the first time that we have applied PLD made ZnO thin films to iso-, hetero-semiconductor–insulator–semiconductor (SIS) type solar cells as transparent conducting oxide (TCO) window layer. We hope that surely these data be helpful either as a scientific or technical basis in the semiconductor processing.