Highly elastic and transparent multiwalled carbon nanotube/polydimethylsiloxane bilayer films as electric heating materials

Highly elastic and transparent bilayer films composed of MWCNT and polydimethylsiloxane (PDMS) layers were fabricated by spin-coating of MWCNT aqueous solution on glass plates and following curing of PDMS applied on the MWCNT layer. Morphological feature, optical transparency, tensile property, electrical property, and electric heating behavior of the bilayer films with different MWCNT layer thicknesses of 65–185 nm were investigated. SEM images confirmed that pristine MWCNTs were uniformly deposited on glass substrates and the PDMS layer was combined well with the MWCNT layer, resulting in high structural stability of the bilayer films to high elongational or twisting deformations. With the increase of the thickness of the MWCNT layer, the sheet resistance of the bilayer films decreased substantially from ~ 10⁵ Ω/sq to ~ 10³ Ω/sq, in addition to the change of the optical transmittance from ~ 75% to ~ 40% at a 550 nm wavelength. The electric heating behavior of MWCNT/PDMS bilayer films was strongly dependent on the thickness of the MWCNT layer as well as the applied voltage. Even under high twisting by 540° or continuous stepwise voltage changes for long periods of time, the MWCNT/PDMS bilayer films retained stable electrical heating performance in aspects of temperature responsiveness, steady-state maximum temperature, and electric power efficiency.     

Synthesis of multi-walled carbon nanotube/silica nanoparticle/polystyrene microsphere/polyaniline based hybrids for EMI shielding application

Novel polystyrene microsphere (PSMS)-based PSMS/Si and polystyrene/silica nanoparticle/multi-walled carbon nanotube (PS/Si/MWCNT) nanocomposite has been prepared using in situ sol-gel and chemical amalgamation methods. Aniline monomer was introduced by in situ route to form PSMS/PANI, PSMS/PANI/Si and PSMS/PANI/Si/MWCNT nanocomposite. FESEM of nanocomposite indicated core-shell spherical and tubular morphology. Glass transition temperature (T_g) and maximum decomposition temperature (T_max) of PSMS/PANI/Si/MWCNT nanocomposite were found as 295°C and 524°C, respectively, which were higher than the PSMS/PANI (T_g = 245°C; T_max = 387°C) and PSMS/PANI/Si (T_g = 257°C; T_max = 388°C) nanocomposite. For nanocomposite dispersion, tetrahydrofuran was studied as fine solvent. XRD depicted amorphous nature of PSMS/Si and PSMS/PANI/Si; however MWCNT reduced amorphous character of PSMS/PANI/Si/MWCNT. Electromagnetic interference (EMI) shielding effectiveness improved from 0.1 dB (PSMS) to 12.3 dB (PSMS/PANI/Si) to 24.5 dB (PSMS/PANI/Si/MWCNT). The increase in EMI shielding effectiveness was also observed with variation in log of conductivity from ?14 mho m^?1 (PSMA) to 1.17 mho m^?1 (PSMS/PANI/Si/MWCNT).     

Polyazomethine/carbon nanotube composites

Composites were synthesized by “in-situ” polymerization of polyazomethine, a liquid crystal polymer (LCP), in presence of multi-walled carbon nanotubes (MWNTs) previously dispersed in one of the employed monomers. Fiber processing was carried out by extrusion from the composites containing 1 and 10 wt.% of MWNTs at the mesophase temperature. We have observed that the typical highly oriented internal fibrillar structure can be significantly disrupted by increasing the nanotube content in the composite fibers. Evidences of MWNT alignment were found in the studied LCP/MWNT composites.     

Supported lipid bilayer formation and lipid-membrane-mediated biorecognition reactions studied with a new nanoplasmonic sensor template

This paper presents the use of the localized surface plasmon resonance (LSPR) sensor concept to probe the formation of macroscopic and laterally mobile supported lipid bilayers (SLBs) on SiOx-encapsulated nanohole-containing Au and Ag films. A comparison between Au- and Ag-based sensor templates demonstrates a higher sensitivity for Au-based templates with respect to both bulk and interfacial refractive index (RI) changes in aqueous solution. The lateral mobility of SLBs formed on the SiOx-encapsulated nanohole templates was analyzed using fluorescence recovery after photobleaching (FRAP), demonstrating essentially complete (>96%) recovery, but a reduction in diffusivity of about 35% compared with SLBs formed on flat SiOx substrates. Furthermore, upon SLB formation, the temporal variation in extinction peak position of the LSPR active templates display a characteristic shape, illustrating what, to the best of our knowledge, is the first example where the nanoplasmonic concept is shown capable of probing biomacromolecular structural changes without the introduction of labels. With a signal-to-noise ratio better than 5 x 10(2) upon protein binding to the cell-membrane mimics, the sensor concept is also proven competitive with state-of-the-art label-free sensors.     

Processing and characterization of polyurethane nanocomposite foam reinforced with montmorillonite–carbon nanotube hybrids

This study investigates the effect of montmorillonite carbon nanotube hybrids on the final properties of polyurethane (PU) nanocomposite foams. The hybrids were fabricated by chemical vapour deposition and dispersed in rigid polyurethane foam by an in situ polymerization process. The resulting morphology and dispersion were evaluated by scanning electron microscopy, optical microscopy and transmission electron microscopy. PU nanocomposite foams have revealed the presence of cells of smaller size and an increase of cell density when compared to neat polymer foams. Thermogravimetric studies revealed that addition of the hybrids nanoparticles improve the thermal properties of the resulting nanocomposites. Addition of small amounts of montmorillonite carbon nanotube hybrids has enhanced the compressive properties of the resulting PU nanocomposite foams making it suitable for several applications.     

On the contribution of carbon nanotube deformation to piezoresistivity of carbon nanotube/polymer composites

The change in electrical resistance due to mechanical deformation of carbon nanotube (CNT)/polymer composites can be rationalized in terms of two effects: (i) changes in the composite electrical resistivity due to changes in the CNT network configuration and (ii) deformation of the CNTs themselves. The contribution of CNT dimensional changes (ii) to the piezoresistivity of CNT/polymer composites is investigated here. An analytical model based exclusively on dimensional changes which describes the CNT change of electrical resistance in terms of its mechanical deformation is proposed. A micromechanics approach and finite element analysis are performed to correlate the macroscale composite strain to the individual CNT strain. The CNT change of electrical resistance is quantified for different matrix elastic moduli and CNT weight fractions. The CNT/polymer composite is also modeled as an effective continuum material in terms of both its electrical and mechanical responses so that the effect of dimensional changes on the global piezoresistivity can be investigated. Based on the modeling predictions and previous experimental results, it is estimated that the CNT change of resistance due to the macroscale composite strain is marginal (∼5%) compared to the total composite change of resistance commonly measured in the laboratory, suggesting that the dominant effect in the piezoresistivity of CNT/polymer composites is the change in the CNT network configuration.     

碳纳米管／环氧树脂复合材料的研究

研究了碳纳米管（CNTs）／环氧树脂复合材料的分散性能及电性能。探讨了碳纳米管的含量、管径和稀释剂的用量对环氧树脂电学性能的影响，并用透射电子显微镜（TEM）和扫描电子显微镜（SEM）对其进行表征。结果表明，碳纳米管的分散和含量对环氧树脂的电性能影响很大，而加入碳纳米管能够使环氧树脂由绝缘体变为导体（电阻率〈^10mΩ·cm）。     

Superhydrophobic carbon nanotube/polydimethylsiloxane composite coatings

This paper reports a method for fabricating carbon nanotube (CNT)/polydimethylsiloxane (PDMS) composite superhydrophobic coatings. With toluene as a solvent, the coating is obtained directly by spray of CNT/PDMS/toluene suspension. The hydrophobicity and micro-/nanostructure of the coatings are studied with respect to the mass ratio (MR) of CNT to PDMS. Based on the multiscale morphology analysis, it is shown that the nanoscale roughness is essential for achieving superhydrophobicity. To form nanoscale rough surface and obtain a stable superhydrophobic coating, MR>0·3 is recommended. In addition, such coatings also show small slide angle, low adhesion strength and long term stability of the coated surface. The method reported in this study is low cost and especially suitable for engineering applications.     

纳米碳管结构差异对树脂炭包覆硅/纳米碳管复合材料电化学性能的影响

采用聚乙烯醇（PVA）树脂炭化的方法，制备了PVA树脂炭包覆硅／不同纳米碳管复合材料，通过X-射线、高分辩电镜观察和电化学性能测试等手段比较研究了单壁、双壁和多壁纳米碳管作为弹性导电网络缓解硅在充放电过程中体积变化方面的效果。结果表明，单壁纳米碳管和双壁纳米碳管比多壁纳米碳管能够更好地缓解硅在循环过程中产生的结构和体积变化，这主要是因为其长径比大，缠裹效果更好。单壁纳米碳管和双壁纳米碳管具有相近的直径、长径比及宏观分布形式，但在循环过程中，双壁纳米碳管的结构稳定性好于单壁纳米碳管，进而其缓解硅结构变化的效果更好。     

Ion channel behavior of supported bilayer lipid membranes on a glassy carbon electrode

A new kind of solid substrate, a glassy carbon (GC) electrode, was selected to support lipid layer membranes. On the surface of the GC electrode, we made layers of didodecyldimethylammonium bromide (a synthetic lipid). From electrochemical impedance experiments, we demonstrated that the lipid layers on the GC electrode were bilayer lipid membranes. We studied the ion channel behavior of the supported bilayer lipid membrane. In the presence of perchlorate anions as the stimulus and ruthenium(II) complex cations as the marker ions, the lipid membrane channel was open and exhibited distinct channel current. The channel was in a closed state in the absence of perchlorate anions.     

碳纳米管加载量对复合材料吸波性能的影响

将不同质量分数的碳纳米管和环氧树脂充分混合，制成复合吸波涂料并涂覆在铝板上制成吸波涂层。采用TEM对碳纳米管的形貌进行观察。使用反射率扫频测量系统HP8757E标量网络分析仪检测复合材料的吸波性能。结果表明，复合材料在2GHz～18GHz均有良好的吸波性能。碳纳米管加载质量分数为8％和10％时，复合材料吸波性能最佳。8％碳纳米管加载量，峰值最大，达到～22．55dB，波峰出现在12．32GHz，带宽分别为2．56GHz（R〈-8dB）和4．00GHz（R〈-5dB）。10％碳纳米管添加量，带宽最大，分别达到2．80GHz（R〈-8dB）和7．00GHz（R〈-5dB），波峰出现在13．67GHz，峰值为-14．59dB。     

Supported bilayer electrophoresis under controlled buffer conditions

A pH controlled flow cell device was constructed to allow electrophoretic movement of charged lipids and membrane associated proteins in supported phospholipid bilayers. The device isolated electrolysis products near the electrodes from the electrophoresis process within the bilayer. This allowed the pH over the bilayer region to remain within ±0.2 pH units or better over many hours at salt concentrations up to 10 mM. Using this setup, it was found that the electrophoretic mobility of a dye conjugated lipid (Texas Red 1,2-dihexadecanoyl-sn-glycero-3-phosphoethanolamine (TR-DHPE)) was essentially constant between pH 3.3 and 9.3. In contrast, streptavidin, which was bound to biotinylated lipids, shifted from migrating cathodically at acidic pH values to migrating anodically under basic conditions. This shift was due to the modulation of the net charge on the protein, which changed the electrophoretic forces experienced by the macromolecule. The addition of a polyethylene glycol (PEG) cushion beneath the bilayer or the increase in the ionic strength of the buffer solution resulted in a decrease of the electroosmotic force experienced by the streptavidin with little effect on the Texas Red-DHPE. As such, it was possible in part to control the electrophoretic and electroosmotic contributions to streptavidin independently of one another.     

Morphology and electrochemical properties of amphiphilic viologen functionalized multiwalled carbon nanotube hybrids in Langmuir-Blodgett films

Amphiphilic viologens were electrostatically adsorbed on the surface of multiwalled carbon nanotubes (MWCNT) to form viologen-MWCNT hybrids, in which the content of viologens was about 5-10% in weight. Although both viologens and MWCNT hardly dispersed in the water-insoluble organic solvents, the as-prepared viologen-MWCNT hybrids were well dispersed in them with a strong long-term stability, the features of which provided a possibility to prepare their insoluble monolayers at the air-water interface. The surface pressure-area isotherms of these hybrids revealed that they could form stable monolayers, which were transferred on the substrate surfaces by the Langmuir-Blodgett (LB) method. Morphologies of the LB films were characterized by using scanning electron microscopy and atomic force microscopy, the images of which revealed the formation of network two- or three-dimensional films of the functionalized MWCNT. Cyclic voltammograms of the LB films revealed one or two couples of one electron transfer process corresponding to the viologen-MWCNT hybrids with the cathodic and anodic potentials closely related to the alkyl chains of the viologens.     

Ultrasonically prepared polystyrene/multi-walled carbon nanotube nanocomposites

Polystyrene (PS) and multi-walled carbon nanotube (MWNT) nanocomposites were synthesized via an in situ bulk polymerization by employing an ultrasonicator without adding an initiator, in which the ultrasonication was found to do a favor in producing well-dispersed MWNT in the PS matrix. Morphology of the as-synthesized PS/MWNT nanocomposite was investigated by both scanning electron microscopy and transmission electron microscopy. Electrical conductivity of the PS/MWNT nanocomposite film fabricated by a solvent casting method was also examined to be enhanced with MWNT content, while average molecular weights of the synthesized PS in the PS/MWNT nanocomposites analyzed by a gel permeation chromatography increased and then saturated at 2 wt% MWNT. Rheological properties of MWNT containing PS were enhanced because of improved dispersion of the MWNT through an interaction between MWNT and PS.     

Super-long aligned TiO2/carbon nanotube arrays

5?mm long aligned titanium oxide/carbon nanotube (TiO(2)/CNT) coaxial nanowire arrays have been prepared by electrochemically coating the constituent CNTs with a uniform layer of highly crystalline anatase TiO(2) nanoparticles. While the presence of the TiO(2) coating was confirmed by scanning electron microscopy, transmission electron microscopy, Raman spectroscopy and x-ray diffraction, the resultant TiO(2)/CNT coaxial arrays were demonstrated to exhibit minimized recombination of photoinduced electron-hole pairs and fast electron transfer from the long TiO(2)/CNT arrays to external circuits. This, in conjunction with the aligned macrostructure, facilitates the fabrication of TiO(2)/CNT arrays for various device applications, ranging from photodetectors to photocatalytic systems. Thus, the millimeter long TiO(2)/CNT arrays represent a significant advance in the development of new macroscopic photoelectronic nanomaterials attractive for a variety of device applications beyond those demonstrated in this study.     

Fabrication of 3D carbon nanotube/porous carbon hybrid materials

Three dimensional hybrid carbon materials have been prepared using different biomass-derived porous carbons as catalyst supports for growing multi-walled carbon nanotubes (MWCNTs) via a chemical vapor deposition method. The nickel catalyst-loaded supports before and after growing MWCNTs were characterized by scanning and transmission electron microscopy, Fourier transform infrared spectroscopy spectra, and mercury porosimetry. The results show that the grown MWCNTs microstructures are closely related to the porous structures and surface conditions of the carbon supports. By using bamboo as template, a porous carbon support with a large total pore volume, appropriate pore size, and abundant favorable surface functional groups is obtained, which is found to be an ideal support for growing the MWCNTs. Investigation of growth mechanism demonstrated that the combination of appropriate porous structures and surface conditions plays an essential role in catalyst distribution and MWCNTs growth.     

定向碳纳米管/炭纳米复合材料形貌和显微结构

以CVD法定向碳纳米管(ACNTs)阵列为骨架,利用化学气相渗透(CVI)工艺制备了新型定向碳纳米管/炭(ACNT/C)纳米复合材料。通过偏光金相显微镜(PLM)、扫描电子显微镜(SEM)、高分辨透射电子显微镜(HRTEM)、X射线衍射(XRD)和Raman光谱等分析方法对其显微结构和热解炭沉积机理进行了研究。结果表明:所制ACNT/C纳米复合材料的热解炭结构主要为类粗糙层结构,围绕碳纳米管生长的热解炭石墨层片结构清晰,并且碳纳米管和热解炭之间具有良好的界面结合;而在相同工艺条件下围绕炭纤维生长的热解炭为典型的光滑层结构。这可能是由于在热解炭沉积过程中存在碳纳米管"诱导"沉积过程,即沿着碳纳米管径向的离域化共轭π键和具有类似结构的芳香族大分子通过π-π非共价键作用相结合,并在CNTs纳米尺寸的影响下,芳香族大分子按照"软取向"(Softepitaxy)围绕碳纳米管生成环形层片状类石墨结构的热解炭。该研究结果有望为热解炭的可控沉积起到一定的借鉴作用。     

Superhydrophobic carbon nanotube/silicon carbide nanowire nanocomposites

The composite film of carbon nanotubes and silicon carbide nanowires was synthesized directly on the silicon substrate by the catalyst-assisted method. The carbon nanotubes crimped together decorated with silicon carbide nanowires covering the whole substrate. The appropriate amount of aluminum powders is a crucial factor to achieve the composite film. The composite film exhibited excellent intrinsic superhydrophobicity without any further functionalization. By using the nano/micropillar composite structure model, the presence of silicon carbide nanowires is found to be the key factor that results in the superhydrophobicity of the films. The feasible synthesis of the superhydrophobic coating could have potential application in water-repelling devices, like biochemical sensors and microfluidic systems.