Dispersion Of Single-walled Carbon Nanotubes Research Articles

Study on dynamic mechanism of controllable SWCNTs arrays prepared by self-assembly

Single walled carbon nanotubes (SWCNTs) are seamless hollow tubular structures formed by a layer of graphite curled along a specific spiral vector. Individual SWCNT is restricted by the inconvenient manipulation in its nanoscale, and unable to maximize its functionality in the macro field. As a result, the two-dimensional array is the most basic structure for manufacturing SWCNTs devices in practical application. However, the fidelity of the array pattern and the distribution morphology of individual SWCNT in the large-scale array directly affect its performance, which also poses a challenge to the research on assembly methods and their underlying mechanisms. In this paper, the dynamic mechanism of controllable SWCNTs arrays prepared by self-assembly method has been studied from molecular dynamics to hydrodynamic by a combination of experiments and simulations. Some key factors limiting the fidelity of the arrays and the distribution morphology of individual SWCNT in the array, such as the self-assembly template, the concentration of the SWCNTs dispersion, are investigated and optimized by experiments. Finally, inspired by the results of the mechanism research, a blade-coating procedure is applied in self-assembly process to improve the alignment of SWCNTs in the array. The improved alignment of SWCNTs arrays are verified through morphology analysis and volt-ampere (V-A) characteristics compared with the SWCNTs randomly distributed arrays. The explicitly results are not only helpful to understand dynamic phenomena during self-assembly process and the influencing factors of the self-assembly method but also will provide meaningful guidance in the design, fabrication of SWCNTs arrays to prevent distortion in large scale and further promote their industrial application in manufacturing next-generation micro-nano devices.

Improved Characterization of Aqueous Single-Walled Carbon Nanotube Dispersions Using Dynamic Light Scattering and Analytical Centrifuge Methods.

Aqueous dispersions of single-walled carbon nanotubes (SWCNTs) with a surfactant were studied by using a combination of differential sedimentation and dynamic light scattering methods. When applied to elongated particles like SWCNTs, the differential sedimentation method makes it possible to measure their diameters in dispersions, while the dynamic light scattering method allows to measure their lengths. Both methods have logarithmic dependence on the ratio between the length and diameter of the particles, and their simultaneous use improves the accuracy of measuring particles' dimensions. It was shown that sonication of dispersions leads not only to unbundling of agglomerates into individual nanotubes but also to a decrease in their lengths and the appearance of new defects detectable in increasing the D/G ratio in the Raman spectra. Unbundling into individual nanotubes occurs after exposure to 1 kWh/L energy density, and the single nanotube diameter with SDBS is ca. 3.3 nm larger than that of the naked nanotubes. Conductivity of thin SWCNT films made out of individual nanotubes demonstrates a power law dependence with the exponent close to the theoretical one for rigid rods.

Thin Film Transistors Incorporating Ultrapure Semiconducting Single-Walled Carbon Nanotubes and Green Dielectrics

Printed electronics is a burgeoning field that has received intense research interest and is beginning to experience commercial successes. Single-walled carbon nanotubes (SWNTs) are a unique and promising building block for incorporation into next generation superfast electronic devices. SWNTs have very high carrier mobilites, with band gaps compatible for integration into logic circuits. Their excellent mechanical flexibility allows for potential incorporation into flexible printed electronics, enabling fully-printed transistors and circuits with performances that support low cost, large area fabrication. Progress in incorporating SWNTs into commercial devices has been hindered by the presence of metallic SWNTs, which are produced alongside semiconducting SWNTs during synthesis, and negatively impact device performance. Fabrication of ambipolar SWNT organic thin film transistors (OTFTs) with high carrier mobilities and high on/off ratios remains particularly challenging; many examples in the literature required high temperature, expensive and energy-demanding processes.Since the initial discovery of conjugated polymer-assisted dispersion and purification of SWNTs in 2008, several polymer families have been successfully shown to selectively disperse semiconducting SWNTs. However, only a relatively small number of these supramolecular complexes have been incorporated into OTFTs. We used a novel conjugated polymer to exclusively disperse semiconducting SWNTs. The dispersal procedure requires a simple sonication and centrifugation, during which the metallic SWNTs sediment out. Solution purity was evaluated using UVVis- NIR and Raman spectroscopies. The resulting dispersions are amenable to solution processing techniques such drop casting and spin coating, allowing for the potential for large area device fabrication at room temperature. Ambipolar OTFTs were fabricated under ambient conditions using this solution and tested in both air and under inert atmosphere. The presence of excess conjugated polymer, solution deposition techniques, SWNT density, surface treatment, and post-fabrication treatment were all investigated to determine which parameters facilitated the production of OTFTs with high mobilities (>20 cm2V-1s-1), high on/off ratios (10^6-10^8), negligeble hysteresis, controlled threshold voltages, and high bias stability.[1] Protocols for sorting and dispersing ultrapure sc-SWNTs with conjugated polymers for thin-film transistor (TFT) applications have been well refined. Conventional wisdom dictates that removal of excess unbound polymer through filtration or centrifugation is necessary to produce high- erformance TFTs. However, this is time-consuming, wasteful, and resource-intensive. We challenge this paradigm and demonstrate that excess unbound polymer during semiconductor film fabrication is not necessarily detrimental to device performance.[2] With focus on further improving device performance, we look to green, compostable dielectrics to pair with SWCNTs. We report a tri-layer dielectric using poly (lactic acid) (PLA), poly(vinyl alcohol)/cellulose nanocrystals (PVAc) and toluene diisocyanate terminated poly(caprolactone) (TPCL) which we integrated into SWCNT based TFTs in a top gate bottom contact architecture. The PVA provides a high dielectric constant due to the hydroxy groups, the cellulose is used to optimize the viscosity, the TPCL layer provides a robust hydrophobic surface[3], and the PLA eliminates the interfacial charge traps present in the PVAc. This leads to a decrease in leakage currents and reduced the polarity at the dielectric/semiconductor interface. The TFTs fabricated using tri-layer dielectrics led to air stable and balanced hole and electron mobilities which was not observed for the PVAc/TPCL bilayer systems with supressed hole mobility. These TFTs were then used to study the impact of electrochemical doping on the performance of sc-SWCNT TFTs when switching from n-type, where an electrical double layer is formed, to p-type, where the TFSI anions are free to interact with the sc-SWCNTs.[4]The following presentation will focus on the engineering of sc-SWNTs based electronic devices. The choice of conjugated wrapping polymer, dielectric and processing conditions on film formation and the TFT device performance.

Laser Fluence Dependent Modulation of Single Walled Carbon Nanotube Photoluminescence

Single-walled carbon nanotubes (SWCNT) have a unique, non-photobleaching, bandgap photoluminescence (PL) that has been of interest for sensor development. Take advantage of these properties, colloidal dispersions of single SWCNTs in aqueous solvents are often formed by creating a surface corona phase (CP) using amphiphilic materials. As SWCNT PL emission following photoexcitation can be significantly dependent on its local environment, the CP can be used to tune its photophysical properties, often as a design parameter for sensor development. Recent sensor experiments have shown that reporting and controlling laser excitation can be a method to significantly reduce measurement variability. In this work, we study this phenomenon of excitation fluence (EF) (mW/area) dependent PL modulation for aqueous dispersed SWCNTs. By using a continuously stirred chamber excited at a single location, the stirring rate can be a means of controlling SWCNT excitation exposure. SWCNT wrapped in both DNA and SDS SWCNT CPs showed a decreased quantum yield of nearly 40% with increasing EF while those with sodium cholate and phospholipid-PEG CPs remain invariant. Through spectroscopy and heat transfer modeling, we determined that the observed effect is unlikely to have a significant direct local solution heating contribution from SWNCT photoabsorption. Finally, we used previously studied SWCNT sensor constructs, for ascorbic acid and dopamine, to show how EF can affect calibration and eventual sensor applications. This work highlights the importance of measuring, testing, reporting and controlling for EF while developing SWCNT based photophysical sensors. This newly characterized property can also serve as a unique parameter to tune optical responsivity.

Raman Characterization of Guanine Functionalized SWCNTs

Single-walled carbon nanotubes (SWCNTs) have unique photophysical properties that render them an important class of materials for future nanoelectronics and bio-nano sensor applications. A method was recently discovered for making spatially patterned modifications to SWCNT band gaps and thereby modulating their electronic and optical properties in a controlled manner. The reaction used for this is called guanine functionalization.1 It is achieved by generating singlet oxygen in a dispersion of SWCNTs coated with single-stranded DNA, resulting in covalent bond formation between the guanine nucleobases in the DNA coatings and the nanotube sidewalls. Each of the many covalently bonded guanine sites acts as a weak exciton trap, causing red-shifted SWCNT emission and absorption spectra. Fluorescence spectroscopy shows that the extent of guanine functionalization can depend strongly on SWCNT structure, but spectral broadening can hamper the precise deconvolution of emission features of different (n,m) species. To track such covalent functionalization through Raman scattering, the D to G band ratios are commonly used as a measure of sp3 defect density and therefore of the functionalization extent. However, this conventional Raman method cannot show which (n,m) species in unsorted samples have been functionalized, because they all contribute to the D and G band signals. We will describe a novel Raman analysis based on the relative intensities of bands that have shifts located between the RBM and D regions. These Raman features are found to be diameter-specific, allowing estimation of (n,m)-resolved functionalization extents in unsorted SWCNT samples. In addition, we will present an assignment and interpretation of the relevant Raman features. Zheng, Y.; Bachilo, S. M.; Weisman, R. B., Controlled patterning of carbon nanotube energy levels by covalent DNA functionalization. ACS Nano 2019, 13, 8222-8228.

Influence of Excess Conjugated Wrapping Polymer in Semiconducting Single-Walled Carbon Nanotube Dispersions

Single-walled carbon nanotubes (SWNTs) are promising nanomaterials for incorporation into organic electronic devices (OEDs), with the potential to fabricate flexible devices while exploiting inexpensive solution-processing techniques. As-synthesized SWNTs are insoluble and comprised of a mixture of metallic and semiconducting SWNTs (sc-SWNTs), necessitating dispersal and purification before integration into OEDs. Refinement of conjugated polymer extraction techniques has allowed for the isolation of sc-SWNTs from metallic in a reproducible and scalable manner. The availability of highly-pure sc-SWNT materials has facilitated the production of thin-film transistors (TFTs) with very high charge carrier mobilities, outperforming organic small molecule and polymer semiconductors. However, the realization of commercial OED applications of polymer-sorted sc-SWNTs have not yet been achieved, partially due to the prohibitive time and materials costs associated with purifying sc-SWNTs.Current protocols for dispersing sc-SWNTs with conjugated polymers involve three broad steps: (1) dispersion of bulk SWNT material, (2) removal of non-dispersed carbonaceous materials, and (3) removal of excess polymer through filtration or centrifugation. The final step of removal of excess polymer is time-consuming and wasteful, but viewed as necessary for preparing high-performing TFTs, as the conjugated polymer has much lower performance compared to SWNTs.In this study we performed the first systematic investigation of the effect of excess polymer on SWNT TFT performance. Three SWNT concentrations were investigated, with varying ratios of excess polymer added to each. TFT device performance was monitored using several metrics, including: mobility, threshold voltage, on/off ratios and hysteresis. Characterization of large numbers of replicate TFT devices determined that below a threshold amount of excess polymer the presence of excess polymer did not have a negative impact on device performance. Detailed analysis of the sc-SWNT films through Raman spectroscopy and atomic force microscopy (AFM) confirmed that a simple rinsing step was sufficient to remove all the unbound conjugated polymer from the substrate surface without affecting the sc-SWNT network. The volume of solvent required for the rinsing step was substantially lower than that required for filtration or centrifugation steps. Furthermore, at higher SWNT concentrations the excess polymer prevented nanotube bundling, resulting in moderate improvements in both mobility and on/off ratios. Our results were reproducible for two different conjugated polymer sc-SWNT systems, demonstrating the versatility of this procedure.

Use of non-covalently modified SWCNTs for enhancing the properties of BMI composites with a low loading

The properties of polymer nanocomposites depend greatly on the dispersion of nanoparticles in the polymer matrix. To improve the dispersion of single-walled carbon nanotubes (SWCNTs) in bismaleimide (BMI) resin, this paper developed a feasible method for non-covalent modification of SWCNTs by using polyvinylpyrrolidone (PVP). Moreover, the effect of functionalized SWCNTs on the properties of BMI composites was systematically investigated. The results showed that it was very effective for PVP as a surface modifier for the dispersion of SWCNTs in BMI resin. As a consequence, the electrical conductivity and mechanical properties of the SWCNT/BMI composites were all improved by the incorporation of SWCNTs at a low content. The study also presented that the heat resistance and thermal stability of SWCNT/BMI composites were simultaneously enhanced.

Enhancing the Electrical Conductivity and Strength of PET by Single-Wall Carbon Nanotube Film Coating.

Single-wall carbon nanotubes (SWCNTs) with excellent physicochemical properties are considered a promising candidate for the electrical and mechanical reinforcements of polymers. However, the poor dispersion of SWCNTs in plastics seriously limits their application and their achieved performance enhancement. Here, we coat a freestanding, highly conductive SWCNT film onto the surface of a polyethylene terephthalate (PET) film by a hot-pressing method. Due to the uniform SWCNT network structure and strong interfacial interaction, the SWCNT/PET hybrid film showed notably enhanced electrical and mechanical properties even though with a very low SWCNT weight fraction of 0.066%. The surface square resistance of the SWCNT/PET film decreased to 120-140 Ω/□ from 1016 Ω. In addition, Young's modulus and tensile strength of the SWCNT/PET film reached 4.6 GPa and 148 MPa, which are 31.3 and 24.4%, respectively, higher than the pure PET film. The SWCNT/PET film shows excellent mechanical durability and thermal stability, demonstrating its potential use as an antistatic material.

The effects of single-walled carbon nanotubes dispersion and agglomeration in aluminum matrix: Fabrication and finite element simulation

This paper provides novel research on the effect of full dispersion and agglomeration of single-walled carbon nanotubes (SWCNT) in the Aluminum (AL) matrix. The effect was investigated using the representative volume element (RVE) and finite element method (FEM). The acquired findings were compared to the experimental method (EXP) to assess the correctness of the employed method. In the investigation to anticipate the SWCNT rule in AL/SWCNT mechanical properties, RVE and FEM approach focused on two primary conditions: SWCNT complete dispersion and via agglomeration. Al/SWCNT was manufactured using powder technology. SEM images revealed that there were local SWCNT agglomerations within the composites at greater carbon nanotube concentrations, resulting in a decrease in the specimens' elastic modulus and mechanical strength. Based on RVE and EXP methods, the elastic modulus was increased until dispersed SWCNTs were added up to 2 wt%, after which the modulus was decreased as more SWCNTs were added. The elastic modulus with EXP was compared to the RVE curve cylinder SWCNT full dispersion and curve cylinder with SWCNT agglomeration results under periodic boundary conditions (PBC). The comparison demonstrated that EXP and RVE were in an acceptance agreement. In addition, AL-SWCNT RVEs were studied under damage condition.

Electromagnetic Shielding Enhancement of Butyl Rubber/Single-Walled Carbon Nanotube Composites via Water-Induced Modification.

Electromagnetic properties of polymer composites strongly depend on the loading amount and the completeness of the filler's dispersive structure. Improving the compatibility of single-walled carbon nanotubes (SWCNTs) with isobutylene butyl rubber (IIR) is a good solution to mitigate aggregation. The change in configuration of poly-oxyethylene octyl phenol ether (OP-10) was induced using water as the exposed hydrophilic groups linking with water molecules. The SWCNT and IIR/SWCNT composites were then prepared via wetly-melt mixing at a relatively high temperature to remove water, and they were then mixed with other agents after vacuum drying and cured. The SWCNTs were dispersed uniformly to form a good network for a lower percolation threshold of the wave-absorbing property to 2 phr from 8 phr. With 8 phr SWCNTs, the tensile strength of the material improved significantly from 7.1 MPa to 15.1 MPa, and the total electromagnetic shielding effectiveness of the material was enhanced to 23.8 dB, a 3-fold increase compared to the melt-mixed material. It was demonstrated that water-induced modification achieved good dispersion of SWCNTs for electromagnetic shielding enhancement while maintaining a wide damping temperature range from -55 °C to 40 °C with a damping factor over 0.2.

Length-Dependent Enantioselectivity of Carbon Nanotubes by Gel Chromatography

High-purity enantiomer separation of chiral single-wall carbon nanotubes (SWCNTs) remains a challenge compared with electrical type and chirality separations due to the limited selectivities for both chirality and handedness, which is important for an exploration of their properties and practical applications. Here, we performed length fractionation for enantiomer-purified SWCNTs and found a phenomenon in which the enantioselectivities were higher for longer nanotubes than for shorter nanotubes due to length-dependent interactions with the gel medium, which provided an effective strategy of controlling nanotube length for high-purity enantiomer separation. Furthermore, we employed a gentler pulsed ultrasonication instead of traditional vigorous ultrasonication for preparation of a low-defect long SWCNT dispersion and achieved the enantiomer separation of single-chirality (6,5) SWCNTs with an ultrahigh enantiomeric purity of up to 98%, which was determined by using the linear relationship between the normalized circular dichroism intensity and the enantiomeric purity. Compared with all results reported previously, the present enantiomeric purity was significantly higher and reached the highest level reported to date. Due to the ultrahigh selectivity in both chirality and handedness, the two obtained enantiomers exhibited perfect symmetry in their circular dichroism spectra, which offers standardization for characterizations and evaluations of SWCNT enantiomers.

PMMA/SWCNT Composites with Very Low Electrical Percolation Threshold by Direct Incorporation and Masterbatch Dilution and Characterization of Electrical and Thermoelectrical Properties.

In the present study, Poly(methyl methacrylate) (PMMA)/single-walled carbon nanotubes (SWCNT) composites were prepared by melt mixing to achieve suitable SWCNT dispersion and distribution and low electrical resistivity, whereby the SWCNT direct incorporation method was compared with masterbatch dilution. An electrical percolation threshold of 0.05-0.075 wt% was found, the lowest threshold value for melt-mixed PMMA/SWCNT composites reported so far. The influence of rotation speed and method of SWCNT incorporation into the PMMA matrix on the electrical properties and the SWCNT macro dispersion was investigated. It was found that increasing rotation speed improved macro dispersion and electrical conductivity. The results showed that electrically conductive composites with a low percolation threshold could be prepared by direct incorporation using high rotation speed. The masterbatch approach leads to higher resistivity values compared to the direct incorporation of SWCNTs. In addition, the thermal behavior and thermoelectric properties of PMMA/SWCNT composites were studied. The Seebeck coefficients vary from 35.8 µV/K to 53.4 µV/K for composites up to 5 wt% SWCNT.

Green modification of single-walled carbon nanotubes dispersion with good dispersibility and long storage stability

Green modification of single-walled carbon nanotubes dispersion with good dispersibility and long storage stability

Sb2Te3 nanoparticle-containing single-walled carbon nanotube films coated with Sb2Te3 electrodeposited layers for thermoelectric applications

Single-walled carbon nanotubes (SWCNTs) are promising thermoelectric materials owing to their flexibility and excellent durability when exposed to heat and chemicals. Thus, they are expected to be used in power supplies for various sensors. However, their thermoelectric performances are inferior to those of inorganic thermoelectric materials. To improve the thermoelectric performance while maintaining the excellent characteristics of SWCNTs, a novel approach to form inorganic thermoelectric layers on the SWCNT bundle surfaces using electrodeposition is proposed. We synthesized Sb2Te3 nanoparticle-containing SWCNT films and coated them with electrodeposited Sb2Te3 layers. The Sb2Te3 nanoparticles were synthesized via a spontaneous redox reaction, which were then added to a SWCNT dispersion solution, and films were produced via vacuum filtration. At higher nanoparticle contents in the films, the Sb2Te3 electrodeposited layers completely covered the SWCNT bundles owing to the increase in the concentration of precursor ions near the SWCNT bundle surface, which in turn was the result of melted nanoparticles. The thermoelectric performance improved, and the maximum power factor at approximately 25 °C was 59.5 µW/(m K2), which was 4.7 times higher than that of the normal SWCNT film. These findings provide valuable insights for designing and fabricating high-performance flexible thermoelectric materials.

Feasible H2S Sensing in Water with a Printed Amperometric Microsensor.

Concern over pollution has led to an increase in wastewater treatment systems, which require constant monitorization. In particular, hydrogen sulfide (H2S) is a toxic gas, soluble in water, commonly found in industrial and urban effluents. For proper removal control, fast, durable, and easy-to-handle analytical systems, capable of on-line measurements, such as electrochemical sensors, are required. Moreover, for a proper monitoring of said treatment processes, analysis must be carried out through all steps, thus needing for an economic and highly reproducible method of sensor fabrication. Digital printing have risen in the last few years as technologies capable of mass producing miniaturized electronical devices, allowing for the fabrication of amperometric sensors. Here, a 2 mm2 graphite (Gr) electrode, modified with different dispersions of single-walled carbon nanotubes (SWCNTs), poly(vinyl alcohol), poly(diallyl dimethylammonium chloride), and polylactic acid (PLA), is presented as a H2S sensor. SWCNTs allow for lower oxidation potentials, higher sensitivity, and a reduced rate of sulfur poisoning, while polymer dispersion of PLA increases mechanical stability and as a result, electrochemical performance. This microsensor presents an optimal pH working range between 7.5 and 11.0, a limit of detection of 4.3 μM, and the capacity to operate on complex matrices for H2S contamination detection.

Influence of the chemical structure of aromatic dispersants on the dispersion of carbon nanotubes

The effect of the chemical structure of cationic dispersants on the dispersion of single-walled carbon nanotubes (SWCNTs) was investigated. Various aromatic compounds with quaternary ammonium cations were synthesized as dispersants for SWCNTs. The aqueous SWCNT dispersions were prepared using three types of SWCNTs and nine synthesized dispersants. UV–vis–NIR absorbance of the SWCNT dispersions was used to test the dispersing ability of the synthesized dispersants. This analysis showed that the dispersing ability of the synthesized dispersants was strongly dependent on their chemical structure. The dispersants possessing amide bonds showed higher dispersing ability than those with ester bonds. The increase in the number and size of the aromatic moieties also enhanced the dispersing ability. The dispersants that had a twisted-aromatic moiety and ether bonds interacted preferentially with small-diameter SWCNTs. However, dispersants with planar aromatic moieties dispersed SWCNTs of various diameters. The dispersions of the SWCNT/cationic complex had long-term stability (over 10 months at 20–30 °C), good thermal stability (1 h at 70 °C), and a wide pH range from 3 to 11.

Single‐walled Carbon Nanotubes Dispersed by CO2 Responsive Surfactants for Fabricating High Conductive Epoxy Composites

AbstractThe emerging nanomaterials single‐walled carbon nanotube (SWNTs) with large specific surface area, excellent electrical conductivity and high mechanical strength, has been used to fabricate electronic devices. However, the extremely strong π‐π interactions make SWNTs easy to agglomerate, thus limiting their application. In this work, a novel method was applied to disperse SWNTs by using rigid rosin‐based CO2 responsive surfactant rosin acid dimaleimide choline (R‐BMI‐C). When pH 10.4, SWNTs can be uniformly and stably dispersed, and at pH 6.3, SWNTs aggregated. The dispersed SWNTs was then integrated into diglycidyl ether of bis phenol A (DGEBA) to fabricate high conductive epoxy composites. Their properties were characterized by SEM, TG, high resistivity meters, etc.. The results showed that the modified SWNTs/DGEBA composites obtained an ultra‐low percolation threshold (0.025 wt.%). Compared with the original SWNTs/DGEBA composite, its tensile strength and elastic modulus were enhanced by 17 % and 96 %, respectively, when the SWNTs content was 0.5 wt.%.

Diameter-Selective Sorting of Single-Walled Carbon Nanotubes Using π-Molecular Tweezers for Energy Materials

Single-walled carbon nanotubes (SWCNTs) have remarkable electrical properties, making them excellent candidate energy materials for applications, such as transistors and thermoelectric devices. However, as-prepared SWCNTs are mixtures of various chiral indices associated with different diameters, and this heterogeneity hinders their practical applications. Therefore, the development of a method for sorting SWCNTs according to the diameter is required. Here, we report one-pot diameter sorting of SWCNTs through noncovalent functionalization with π-molecular tweezers, which act as a structure-selective oligomeric dispersant for SWCNTs. The tweezers are capable of isolating (9,4) SWCNTs and (7,6) SWCNTs with diameters of ∼0.9 nm from as-prepared SWCNTs to a sorting ratio of 90%. This high-diameter selectivity originates from molecular wrapping of the π-molecular tweezers around the SWCNT sidewalls based on π–π and hydrophobic interactions. Our findings are promising not only in terms of developing a suitable SWCNT sorting methodology but also for understanding their molecular-level sorting mechanism.

Highly efficient oxidation of single-walled carbon nanotubes in liquid crystalline phase and dispersion for applications in Li-ion batteries

Single-walled carbon nanotubes (SWCNTs), which have high electrical conductivity, are promising candidates for enhancing the energy storage capability of lithium-ion batteries (LIBs). However, their usage in energy storage devices is limited due to the large bundle size and difficulties in dispersion. Here, we implement the debundling and mild oxidation of SWCNTs in the liquid crystalline phase paste (2 wt% solid content) with strong acid and co-intercalant (NaNO3). The thermal treatment successfully introduced carboxylic acid groups without requiring other oxidizing agents. The pretreated SWCNTs were dispersed in organic solvents such as N-methyl pyrrolidone (NMP) without dispersant molecules and were utilized as conductive additives for LIBs. Raman spectroscopy analysis showed that the D/G ratio of the SWCNT film changed from 0.012 to 0.023, implying that the oxidation method proposed herein is less defective and efficient. The filtrated 15 μm film of the SWCNTs exhibited a high electrical conductivity of 2384 S/cm. SWCNT dispersion in NMP was utilized to fabricate LIB cathode electrodes. Compared to the carbon black-applied electrodes, the SWCNT-applied LiNi0.8Co0.1Mn0.1O2 (NCM811) electrodes exhibited enhanced dispersity of conductive additive/binder networks, leading to improved electrode integrity. The capacity retention after 100 cycles for cells with SWCNTs was approximately 23.3 % better than that of the cells without SWCNTs.

Superior photodynamic effect of single-walled carbon nanotubes in aprotic media: a kinetic study

It has been confirmed that single-walled carbon nanotubes (SWCNTs) could generate reactive oxygen species in aprotic media by utilizing photon energy. However, the impact of photon irradiation on SWCNTs and the kinetics of the generation process in aprotic media are still unclear, which significantly limits the yield performance. In this work, the kinetics for photodynamic effects has been investigated by performing characterizations on ultraviolet-treated SWCNTs using Raman spectroscopy, conductive atomic force microscope (in-situ), kelvin probe force microscope, and X-ray photoelectron spectroscopy. It is found that ultraviolet-treated SWCNTs are observed to have more defects, lower conductivity, and less surface charge after energy conversion. Starting from the fundamental intrinsic properties of SWCNTs, the kinetics and formation of these changes are thoroughly discussed. It turns out that the dispersion, chirality, and structural integrity of SWCNTs are important for achieving high-performance photodynamic effects, which are validated using several different SWCNTs as well as other carbon nanomaterials. A type of (6,5) s-SWCNTs exhibited the highest energy efficiency among a variety of other carbon nanomaterials. The yield rate is 2.15 mM/h, and the energy consumption is determined to be 2.79 W·h/mM. This work is expected to help dramatically boost the energy efficiency of the photodynamic effect in aprotic media, and pave the way for designing high-performance carbon nanomaterial-based photoinduced devices.