The influence of single-walled carbon nanotube functionalization on the electronic properties of their polyaniline composites

The “in situ” preparation and characterization of composites of polyaniline (PANI) and single-walled carbon nanotubes (SWCNTs) are reported. To improve the dispersion and compatibility with the polymer matrix the raw SWCNTs were modified following different routes. SWCNTs oxidized by chemical or thermal treatments (nitric acid and air oxidation, respectively) were subjected to covalent functionalization with octadecylamine (ODA). SWCNT/PANI composites were prepared either from just oxidized SWCNTs, or from ODA functionalized SWCNTs. Temperature-programmed desorption, elemental analyses, ultraviolet-visible (UV-vis), UV-vis with near infrared and Raman spectroscopy, X-ray diffraction, scanning and transmission electron microscopy and conductivity measurements were used to characterize the functionalized SWCNT materials, dispersions and composites. The PANI composite prepared from air oxidized SWCNTs showed the best electrical conductivity indicating a better interaction with polyaniline than ODA functionalised SWCNTs. The improvement of conductivity is attributed to the doping effect or charge transfer of quinoide rings from PANI to SWCNTs.     

The synthesis of covalent bonded single‐walled carbon nanotube/polyvinylimidazole composites by in situ polymerization and their physical characterization

Single‐walled carbon nanotube (SWCNT) polyvinylimidazole (PVI) composites have been prepared by in situ emulsion polymerization. Dispersion of raw SWCNTs in the PVI matrix was improved by surface modification of the SWCNTs using nitric acid treatment and air oxidation. The carbonyl‐terminated SWCNTs were covalently bonded to PVI by in situ polymerization and the SWCNT/PVI composite was thus obtained. The morphological and structural characterizations of the surface‐functionalized SWCNTs and SWCNT/PVI composites were carried out by Fourier transform infrared spectroscopy, X‐ray diffraction, conductivity measurements, scanning, and transmission electron microscopy. Thermograms of the materials were determined by the differential scanning calorimetry technique. The characterization results indicate that PVI was covalently bonded to SWCNTs and a new material was then obtained. The functionalized SWCNTs showed homogenous dispersion in the composites, whereas purified SWCNT resulted in poor dispersion and nanotube agglomeration. SWCNT/PVI composites exhibited chemical stability enhancement in many common solvents. I–V curves of the samples exhibit an ohmic character. Conductivity values for pure SWCNTs, pure PVI and SWCNT/PVI composite were measured to be 3.47, 2.11 × 10⁻⁹, and 2.3 × 10⁻³ S/m, respectively. Because of resonance, a large dielectric constant is obtained for SWCNT/PVI composite, which is not observed for ordinary materials. POLYM. COMPOS., 2012. © 2012 Society of Plastics Engineers     

Ionomer covalent functionalization of single‐walled carbon nanotubes by radical polymerization of zirconium acrylate

A facile and efficient covalent functionalization of single‐walled carbon nanotubes (SWCNTs) via peroxide‐mediated free radical covalent attachment and polymerization of zirconium acrylate is reported. The resulting covalently functionalized SWCNTs exhibit improved solubility in organic solvents. The covalently functionalized SWCNTs are characterized by cross polarization magic angle spinning ¹³C NMR, differential scanning calorimetry, thermogravimetric analysis, x‐ray diffraction, Raman, and infrared spectroscopy. Infrared spectroscopy reveals that carboxylate groups of covalently attached ionomers chelate with zirconium ions and the participating carboxylate groups may be from different ionomer chains leading to cross‐linking the chains. The SWCNT topology, ionic clustering, and π‐electron clouds were explored by transmission electron microscopy. © 2014 American Institute of Chemical Engineers AIChE J, 60: 820–828, 2014     

Tailored dielectric and mechanical properties of noncovalently functionalized carbon nanotube/poly(styrene‐b‐(ethylene‐co‐butylene)‐b‐styrene) nanocomposites

The preparation of high‐dielectric poly(styrene‐b‐(ethylene‐co‐butylene)‐b‐styrene) (SEBS) composites containing functionalized single‐walled carbon nanotubes (f‐SWCNTs) noncovalently appended with dibutyltindilaurate are reported herein. Transmission electron microscopy and X‐ray photoelectron and Raman spectroscopy confirmed the noncovalent functionalization of the SWCNTs. The SEBS‐f‐SWCNT composites exhibited enhanced mechanical properties as well as a stable and high dielectric constant of approximately 1000 at 1 Hz with rather low dielectric loss at 2 wt% filler content. The significantly enhanced dielectric property originates from the noncovalent functionalization of the SWCNTs that ensures good dispersion of the f‐SWCNTs in the polymer matrix. The f‐SWCNTs also acted as a reinforcing filler, thereby enhancing the mechanical properties of the composites. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Dispersion of non-covalently functionalized single-walled carbon nanotubes with high aspect ratios using poly(2-dimethylaminoethyl methacrylate-co-styrene)

Single-walled carbon nanotubes (SWCNTs) with high aspect ratios were well dispersed in organic solvents to form stable suspensions using poly(2-dimethylaminoethyl methacrylate-co-styrene) (poly(DMAEMA-co-St)). The polymeric dispersant poly(DMAEMA-co-St) was synthesized in various compositions by atom transfer radical polymerization. The structures and the compositions of the poly(DMAEMA-co-St) were confirmed by ¹H NMR spectroscopy. The stability and dispersion of the functionalized SWCNTs with high aspect ratios in suspension were observed by dispersion stability analysis, transmission electron microscopy, scanning electron microscopy, and atomic force microscopy. The existence of unbundled SWCNTs was confirmed by Raman and ultraviolet/visible/near-infrared spectroscopy. Finally, SWCNT transparent conductive films with high transmittances and low sheet resistances were prepared on a poly(ethylene terephthalate) substrate using a spin-coating method.     

Selective deposition of semiconducting single-walled carbon nanotubes onto amino-silane modified indium tin-oxide surface for the development of poly(3-hexylthiophene)/carbon-nanotube photovoltaic heterojunctions

A method is described to obtain separation of single-walled carbon nanotubes (SWCNTs) on an indium tin-oxide (ITO) substrate by modifying the conducting surface of ITO with amino-silane functional groups. Scanning electron microscopy confirmed that the amino-silane functionalization of the substrate is a critical parameter for the immobilization of separated nanotubes. In particular spin coating the SWCNT solution onto the amino-silane modified ITO surface results in a lower nanotube density with respect to the reference sample obtained on pure ITO together with the immobilization of semiconducting carbon nanotubes onto the substrate. The possibility of using these SWCNT thin films to obtain polymer/nanotube heterojunctions for the development of organic solar cells is considered.     

Optical absorption response of chemically modified single-walled carbon nanotubes upon ultracentrifugation in various dispersants

Arc discharge single-walled carbon nanotubes (SWCNTs) were modified through different oxidative treatments and functionalization reactions. The modified SWCNT powders were dispersed in four different aqueous media and purified by ultracentrifugation. Extinction coefficients of the modified SWCNTs depended on the SWCNT type but did not depend on the dispersion medium. According to visible/near infrared spectroscopy, the purity of all the modified SWCNT dispersions substantially improved after ultracentrifugation; however, the spectrum profile, the degree of purity and the centrifugation yield were influenced by the SWCNT type, the surface functional groups and the dispersion medium. Semi-quantitative purity indexes calculated from optical absorption spectra were supported by transmission electron microscopy observations. Contents in metal impurities were analyzed by energy dispersive X-ray spectroscopy. SWCNT samples processed by oxidative acid treatments and ultracentrifugation showed metal contents of lower than 0.5 wt%.     

Surfactant-free assembling of functionalized single-walled carbon nanotube buckypapers

The electrical and textural properties of single-walled carbon nanotube buckypapers were tunned through chemical functionalization processes. Single-walled carbon nanotubes (SWCNTs) were covalently functionalized with three different chemical groups: Carboxylic acids (-COOH), benzylamine (-Ph-CH₂-NH₂), and perfluorooctylaniline (-Ph-(CF₂)₇-CF₃). Functionalized SWCNTs were dispersed in water or dimethylformamide (DMF) by sonication treatments without the addition of surfactants or polymers. Carbon nanotube sheets (buckypapers) were prepared by vacuum filtration of the functionalized SWCNT dispersions. The electrical conductivity, textural properties, and processability of the functionalized buckypapers were studied in terms of SWCNT purity, functionalization, and assembling conditions. Carboxylated buckypapers demonstrated very low specific surface areas (< 1 m²/g) and roughness factor (R_a = 14 nm), while aminated and fluorinated buckypapers exhibited roughness factors of around 70 nm and specific surface areas of 160-180 m²/g. Electrical conductivity for carboxylated buckypapers was higher than for as-grown SWCNTs, but for aminated and fluorinated SWCNTs it was lower than for as-grown SWCNTs. This could be interpreted as a chemical inhibition of metallic SWCNTs due to the specificity of the diazonium salts reaction used to prepare the aminated and fluorinated SWCNTs. The utilization of high purity as-grown SWCNTs positively influenced the mechanical characteristics and the electrical conductivity of functionalized buckypapers.     

Single-electron transfer living radical copolymerization of SWCNT-g-PMMA via graft from approach

The sidewall functionalization of single-walled carbon nanotubes (SWCNTs) was established by poly (methyl methacrylate) (PMMA) using controlled radical polymerization (CRP) method. A bromide functionalized SWCNT (SWCNT-Br) has been used as an initiator for the synthesis of SWCNT-graft-PMMA (SWCNT-g-PMMA). The efficiency of the sacrificial initiator (S) was monitored during the polymerization process. The obtained polymers possess a uniform distribution of molecular weight with a lower polydispersity index of 1.36. The SWCNTs-based initiator acts as an efficient medium for the controlled growth of polymer on the SWCNTs surfaces. The presence of bimodal gel permeation chromatographic (GPC) curve for the SWCNT-g-PMMA(S) obtained through sacrificial initiator (S) confirms uncontrolled behavior. However, the clear sharp peak for SWCNT-g-PMMA obtained without sacrificial initiator shows its well-controlled process of polymerization, which acts as a mimic to bone cement. The efficiency of the functionalization of SWCNT and the controlled formation of SWCNT-g-PMMA composites were characterized by TGA, Raman, TEM, NMR, XPS and dispersion measurements.     

Electrical conductivity and tensile properties of block‐copolymer‐wrapped single‐walled carbon nanotube/poly(methyl methacrylate) composites

Poly(methyl methacrylate) (PMMA) composites containing raw or purified single‐walled carbon nanotubes (SWCNTs) are prepared by in situ polymerization and solution processing. The SWCNTs are purified by centrifugation in a Pluronic surfactant, which consists of polyethyleneoxide and polypropyleneoxide blocks. Both the effects of SWCNT purity and non‐covalent functionalization with Pluronic are evaluated. Electrical conductivity of PMMA increases by 7 orders of magnitude upon the integration of raw or purified SWCNTs. The best electrical properties are measured for composites made of purified SWCNTs and prepared by in situ polymerization. Strains at fracture of the SWCNT/PMMA composites are nearly identical to those of the neat matrix. A certain decrease in the work to fracture is measured, particularly for composites containing purified SWCNTs (?31.6%). Fractography and Raman maps indicate that SWCNT dispersion in the PMMA matrix improves upon the direct addition of Pluronic, while dispersion becomes more difficult in the case of purified SWCNTs. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41547.     

Raman spectroscopic evidence for interfacial interactions in poly(bithiophene)/single-walled carbon nanotube composites

Electrochemical polymerization of 2,2′-bithiophene (BTh) on single-walled carbon nanotube (SWCNT) films has been studied by Raman scattering and infrared absorption spectroscopy. Covalent functionalization of SWCNTs with poly(bithiophene) (PBTh) in its un-doped and doped states is demonstrated. The occurrence of a charge transfer process at the interface of PBTh and SWCNTs, is shown by: (i) an up-shift of the Raman lines associated with the radial breathing modes of SWCNTs that reveals both a doping process and an additional twisting together as a rope with the conducting polymer as binding agent; (ii) a new Raman band in the range 1430-1450 cm⁻¹ indicating the functionalization of SWCNTs with PBTh in doped and un-doped states; (iii) strong absorption bands situated in the interval 600-800 cm⁻¹ resulting from steric hindrance produced by the nanotube binding to the polymeric chain. Treatment of the PBTh/SWCNT composite with aqueous NH₄OH solution forms un-doped PBTh covalently functionalized SWCNTs. At the resonant excitation of the metallic tubes, an additionally enhanced Raman process is generated by plasmon excitation in the metallic nanotubes. It is evidenced by a particular behavior in the Stokes and anti-Stokes branch of the PBTh Raman line at 1450 cm⁻¹.     

An easy method for direct metal coordination reaction on unoxidized single-walled carbon nanotubes

The transition metal copper (II) ion (Cu²⁺) was effectively coordinated with a single-walled carbon nanotube (SWCNT) to produce a SWCNT–Cu²⁺ complex by a metal coordination reaction. Since the complex was very reactive towards the carboxylic acid group, the chemical functionalization of SWCNTs was easy to accomplish. This approach was used to functionalize the surface of the SWCNTs with stearic acid or ethylenediaminetetraacetic acid for tuning of the relative hydrophobicity and hydrophilicity of the surface, respectively. The mild reaction conditions used for metal coordination of the SWCNTs minimized the defects that result from chemical modification of SWCNT. Thus, the electrical properties of unmodified SWCNTs were preserved. Various analytical techniques, including Fourier transform infrared spectroscopy, thermal gravimetric analysis, ultraviolet–visible spectroscopy, and water sorption isotherm measurements, were used to characterize the surface properties of the functionalized SWCNTs. Functionalization of SWCNTs by metal coordination reaction effectively modified the SWCNT surface, while conserving the excellent physical properties of the SWCNTs. The surface properties of the SWCNTs were easily tuned by introduction of the functional groups required for specific applications.     

Grafting of 4-(2,4,6-Trimethylphenoxy)benzoyl onto Single-Walled Carbon Nanotubes in Poly(phosphoric acid) via Amide Function

Single-walled carbon nanotubes (SWCNTs), which were commercial grade containing 60–70 wt% impurity, were treated in a mild poly(phosphoric acid) (PPA). The purity of PPA treated SWCNTs was greatly improved with or without little damage to SWCNTs framework and stable crystalline carbon particles. An amide model compound, 4-(2,4,6-trimethylphenoxy)benzamide (TMPBA), was reacted with SWCNTs in PPA with additional phosphorous pentoxide as “direct” Friedel–Crafts acylation reaction to afford TMPBA functionalized SWCNTs. All evidences obtained from Fourier-transform infrared spectroscopy, Raman spectroscopy, thermogravimetric analysis, scanning electron microcopy, and transmission electron microscopy strongly supported that the functionalization of SWCNTs with benzamide was indeed feasible.     

Effect of montmorillonite and shear stress on the orientation of single walled carbon nanotubes in polypopylene composite fiber

The effect of montmorillonite and shear stress on the orientation of single walled carbon nanotubes and properties of SWCNT/MMT/polypropylene composite was investigated. The effect of functionalization of SWCNT on the orientation was also investigated. Polarized Raman spectroscopy was used to analyze the orientation of the SWCNTs. Orientation of SWCNTs was dependent on the experienced shear stress and functionalization of SWCNTs. The addition of MMT also improved the orientation of functionalized SWCNTs, while its effect was not significant for pristine SWCNTs. The existence of critical shear stress was observed for the orientation of the SWCNTs and the orientation of SWCNTs was found to occur more efficiently above this critical shear stress. Melt viscosity and heat of fusion data also confirmed that the addition of MMT‐induced improved orientation and dispersion of SWCNTs, especially for functionalized SWCNTs. POLYM. ENG. SCI., 54:2455–2459, 2014. © 2013 Society of Plastics Engineers     

Deposition of functionalized single wall carbon nanotubes through matrix assisted pulsed laser evaporation

Single-wall carbon nanotubes (SWCNTs) functionalized with oxygen-containing groups were deposited onto glass substrates by matrix assisted pulsed laser evaporation (MAPLE). The experiments were performed by subjecting ultraviolet laser pulses (KrF¹ excimer laser, 248 nm wavelength) to frozen SWCNT-toluene targets placed in a parallel plane a few cm in front of the substrate. The morphology, structure, and chemical composition of the deposited materials were studied through atomic force microscopy, high resolution transmission electron microscopy, Raman spectroscopy and X-ray photoelectron spectroscopy. The influence of the laser fluence on the material structure was investigated. The results indicate that the functionalized SWCNTs can be transferred by MAPLE at low laser fluences without the alteration of the structure of the initial material used as targets in MAPLE experiments. An increase of the fluence leads to the decomposition of the functional groups, mainly carboxylic acid groups, without degradation of the SWCNT structure whereas, at the highest fluences, the amorphization and even coalescence of the carbon nanotubes takes place.     

Orientation of carbon nanotubes in polypropylene melt

The correlation between shear stress and the orientation of single‐walled carbon nanotubes (SWCNTs) in an SWCNT/polypropylene composite during the melt process was investigated. Highly oriented composite fibers were produced by extruding the polypropylene melt using a capillary rheometer. The experimental range of shear rates covered those of common polymer melt‐shaping processes. The effect of functionalization of the SWCNTs on orientation was also investigated. Polarized Raman spectroscopy was used to analyze the orientation of the SWCNTs. A high degree of SWCNT orientation was observed under high shear stress, and the functionalized SWCNTs induced a higher degree of orientation than did pristine SWCNTs. The existence of a critical shear stress was observed for the orientation of the SWCNTs, and their orientation was found to occur more efficiently above this critical shear stress. The crystallization temperature and heat of fusion were characterized using a differential scanning calorimeter, and both parameters were observed to increase with the incorporation of SWCNTs. © 2012 Society of Chemical Industry     

A comprehensive scenario for commonly used purification procedures of arc-discharge as-produced single-walled carbon nanotubes

The purification of single-walled carbon nanotube (SWCNT) samples was analysed using a multi-technique approach, with structural as well as spectroscopic probes, in order to characterize the samples and to identify important factors for improvement of SWCNT sample quality. The first dry oxidation step (air at 365 °C) is shown to have only a weak selectivity for the removal of the amorphous carbon or weakly organized graphitic species as well as resulting in a partial consumption of the SWCNTs. The functionalization of the SWCNTs is highly specific with formation of carboxyl, hydroxyl and carbonyl groups. On the other hand this oxidation step is highly efficient for the oxidation of the catalytic impurities (Ni, Y) which can be easily removed by subsequent acid treatment. A final high temperature treatment indicates some incomplete restoration of the quality of the SWCNT surface.     

High-crystallization polyoxymethylene modification on carbon nanotubes with assistance of supercritical carbon dioxide: Molecular interactions and their thermal stability

As a typical engineering plastic and high-crystallization polymer, polyoxymethylene (POM) has been successfully wrapped on single-walled carbon nanotubes (SWCNTs) using a simple supercritical carbon dioxide (SC CO₂) antisolvent-induced polymer epitaxy method. The characterization results of scanning electron microscopy (SEM) and transmission electron microscopy (TEM) reveal that the SWCNTs are coated by laminar POM with the thicknesses of a few nanometers. The polymer adsorption on CNTs via multiple weak molecular interactions of CH groups with CNTs has been identified with FTIR and Raman spectroscopy. The experimental results indicate that the decorating degree of POM on the surface of CNTs increases significantly with the increase of SC CO₂ pressure, and accordingly the dispersion of SWCNT modified by POM at higher pressure are more excellent than that of obtained at lower pressure. Further the processing stability of POM/CNTs composites are investigated by differential scanning calorimetry and thermogravimetric analysis. The experimental results obtained show that their thermal stability behavior is closely related to surface properties of CNTs. Apparently, the composites with POM-decorating SWCNTs as the filler shows higher melting points compared to the POM composites with pristine SWCNTs as the filler. Therefore, we anticipate this work may lead to a controllable method making use of peculiar properties of SC CO₂ to help to fabricate the functional CNTs-based nanocomposites containing highly crystalline thermoplastic materials such as POM.     

Design of carbon nanotube-polymer frameworks by electropolymerization of SWCNT-pyrrole derivatives

Single-walled carbon nanotubes (SWCNTs) have been functionalized by electropolymerizable pyrrole groups following covalent and non-covalent strategies. The covalent pyrrole grafting was carried out by ester formation between pyrrole alcohol and chemically oxidized SWCNT. The strong π-interactions between pyrene and SWCNT were exploited for the non-covalent adsorption of a new pyrene-pyrrole derivative on the pristine nanotube surface. The pyrrole-ester-SWCNT was solubilized in THF and electropolymerized by controlled potential electrolysis at 0.95 V. The pyrene-pyrrole SWCNT was spread on an electrode surface and electropolymerized in its adsorbed state at 0.95 V in CH₃CN. The reinforced nanostructured polypyrrole SWCNT-framework was investigated with scanning electron microscopy.     

Modification of fluorinated single-walled carbon nanotubes with aminosilane molecules

Single-walled carbon nanotubes (SWCNTs) modified with amino groups were prepared via chemical addition of fluorine on the carbon nanotube surface by plasma treatment. The amino termination makes possible to realize hybrid nanostructures made out of SWCNTs and alkoxy-silane (3′-(aminopropyl)tri-ethoxysilane (APTES)) molecules. The functionalization of the SWCNTs was evidenced by transmission electron microscopy, infrared spectroscopy and thermogravimetric measurements. It was found that the application of a dc electric field enhances the assembly of APTES modified SWCNTs into ordered films with rectifying diode behavior.