Dispersion Of Single-walled Carbon Nanotubes Research Articles

Preparation and performances of conductive, wear-resistant, and anti-corrosion coatings based on low content monodisperse SWCNTs

Single-walled carbon nanotubes (SWCNTs) are considered an ideal candidate material for multifunctional coatings because of their excellent electrical, thermal and mechanical properties. However, achieving uniform dispersion of SWCNTs while maintaining their structure and performance remains a significant challenge. The monodisperse SWCNTs (m-SWCNTs) can be obtained using a non-covalent PVP dispersant under the graded homogenization method. PVP acted as steric hindrance due to the π-π conjugate, thereby hindering the agglomeration and preventing the damage of SWCNTs. We incorporate low amounts of m-SWCNTs into fluorocarbon (FC) coatings to fabricate m-SWCNTs/FC composite coatings. We also investigate the effect of m-SWCNTs content on the electrical conductivity, corrosion resistance and wear resistance of the composite coating. Our results indicate that when the content of m-SWCNTs reaches at 0.25 wt%, the electrical resistivity of the m-SWCNTs/FC composite coating is 1.67 × 10−2 Ωm, significantly decreased by 9 orders of magnitude compared to FC coating. The conductive network would be formed by the high aspect ratio and non-damaged of m-SWCNTs to improve the conductivity. Additionally, the wear rate containing 0.15 wt% m-SWCNTs decreased by 50.1 % due to the improved strength and heat conduction to inhibit the adhesive wear. Furthermore, in comparison to bare steel, the corrosion current density of 0.15 wt% m-SWCNTs/FC composite coating is reduced by two orders of magnitude due to zigzag the corrosive path. Our studies suggest that the m-SWCNTs/FC composite coatings have a broad prospect in preparing large-scale, high-performance, and low-cost functional coatings.

Exploring the reactivity and interactions of a poly(fluorene‐co‐tetrazine)‐conjugated polymer with Single‐walled Carbon Nanotubes

AbstractConjugated tetrazine‐containing polymers that undergo inverse electron demand Diels‐Alder (IEDDA) reactions with trans‐cyclooctenes are interesting not only for their intrinsic optoelectronic properties, but also their interactions with π‐conjugated surfaces. Here, we prepared a series of poly(fluorene‐co‐tetrazine) polymers and carried out IEDDA reactions to decorate them with hydroxyl, hexadecyl, or triethylene glycol side chains. The polymers were investigated pre‐ and post‐IEDDA coupling in terms of their ability to disperse single‐walled carbon nanotubes (SWNTs) in organic solvent. It was found that polymer molecular weight, side chain structure, and degree of conjugation all impacted the quality of SWNT dispersions. While the starting poly(fluorene‐co‐tetrazine) polymer produced concentrated dispersions, the post‐IEDDA polymer containing dihydropyridazine groups did not produce dispersions of equal concentration. However, upon oxidation to the fully aromatic pyridazines, the polymers regained their ability to form concentrated dispersions. Furthermore, the post‐IEDDA polymers exhibited increased selectivity toward metallic SWNTs relative to the starting polymer. Due to the efficiency of the IEDDA reaction, it was also possible to use this chemistry to derivatize the nanotube complex with poly(fluorene‐co‐tetrazine) post‐dispersion. Overall, this work demonstrates the first use of reactive polytetrazines to disperse SWNTs, allowing rapid modification of polymer‐nanotube complexes.

The Influence of Molecular Weights on Dispersion and Thermoelectric Performance of Alkoxy Side-Chain Polythiophene/Carbon Nanotube Composite Materials.

In the development of wearable electronic devices, the composite modification of conductive polymers and single-walled carbon nanotubes (SWCNTs) has become a burgeoning research area. This study presents the synthesis of a novel polythiophene derivative, poly(3-alkoxythiophene) (P3(TEG)T), with alkoxy side chains. Different molecular weight variants of P3(TEG)T (P1-P4) were prepared and combined with SWCNTs to form composite materials. Density functional theory (DFT) calculations revealed a reduced bandgap for P3(TEG)T. Raman spectroscopy demonstrated π-π interactions between P3(TEG)T and SWCNTs, facilitating the dispersion of single-walled carbon nanotubes and the formation of a continuous conductive network. Among the composite films, P4/SWCNTs-0.9 exhibited the highest thermoelectric performance, with a power factor (PF) value of 449.50 μW m-1 K-2. The fabricated flexible thermoelectric device achieved an output power of 3976.92 nW at 50 K, with a tensile strength of 59.34 MPa for P4/SWCNTs. Our findings highlight the strong interfacial interactions between P3(TEG)T and SWCNTs in the composite material, providing an effective charge transfer pathway. Furthermore, an improvement in the tensile performance was observed with an increase in the molecular weight of the polymer used in the composite, offering a viable platform for the development of high-performance flexible organic thermoelectric materials.

Low-Temperature Synthesis of Linear Carbon Chain inside Single-Walled Carbon Nanotubes

Linear carbon chain (LCC) has attracted much interest concerning its structure and applications. It has been reported that LCC possesses higher strength, elastic modulus, and stiffness than any known material, which provides a possibility for LCC as a new composite material, yet its chemical stability remains an issue [1]. Therefore, finding a method to efficiently synthesize LCC has become a meaningful research topic in recent years. A landmark study on LCC synthesis was given by using double-walled carbon nanotubes (DWCNTs) as the template combined with a high-temperature annealing treatment at 1460°C to acquire long chains composed of more than 6,000 carbon atoms [2]. Except for DWCNTs, LCC synthesis starting from single-walled carbon nanotubes (SWCNT) as templates was also reported. However, given the instability of SWCNTs at higher temperature [2] the synthesis efficiency is not as good as for DWCNTs. As far as we know, there is still no report on an efficient LCC synthesis inside SWCNTs. Herein, we report the low-temperature (400°C) efficient LCC synthesis starting from a SWCNT template.To this end, a SWCNT dispersion [3] underwent a surfactant exchange process and was fabricated into a SWCNT film by the filtration method. The SWCNT film was annealed under 400°C in an argon atmosphere to synthesize LCC. Raman spectroscopy (laser wavelength 532 nm) was used to characterize the efficiency of the LCC synthesis. A strong peak at 1863 cm-1 appeared after annealing, originating from the well-known C-mode of the linear carbon chain [4] thereby confirming its existence inside SWCNTs. SWCNTs synthesized by a low-pressure alcohol catalytic chemical vapor deposition (ACCVD) method [5] were also adopted for the LCC synthesis template, resulting in a similar LCC Raman peak at 1863 cm-1. We attribute this successful low-temperature LCC synthesis to the appropriate surfactant which could be encapsulated inside CNTs and converted to LCC during the annealing process.Keywords: Linear Carbon Chain, Single-walled Carbon Nanotubes, Surfactants

(Invited) Probing Charge Carrier-Induced Changes in the Complex Dielectric Function in Carbon Nanotube Dispersions

The injection of charge carriers into pi-conjugated semiconductors, whether by electrochemical injection or chemical charge transfer, is a powerful approach to tune their electrical conductivity. Recently, the concept of dielectric catastrophe, where the charge carrier density is sufficiently large to significantly alter the intrinsic dielectric properties, has been demonstrated at high doping levels in organic semiconductor thin films. The observed increase in the dielectric constant leads to reduced coulombic interactions between charge carriers and the associated counterions, promoting enhanced free carrier generation and transport.Here, we employ a combination of steady state optical spectroscopy, quantitative 19F NMR studies, and microwave dielectric loss spectroscopy to probe charge carrier density and transport in doped single-walled carbon nanotube dispersions. We demonstrate that a similar dielectric catastrophe phenomenon can be observed even in isolated single-walled carbon nanotubes dispersed in a low dielectric constant solvent AND, perhaps more surprisingly, at carrier densities less than one carrier per nanotube. The precise details of the observed changes in complex dielectric function are dependent on the chemical structure of the charge-transfer dopant, with a near-instantaneous increase in the dielectric constant and electrical conductivity observed for low carrier densities using bulky benzyloxy-substituted icosahedral dodecaborane cluster dopants, DDBs. We attribute the observations to weak coulombic interactions between the injected charge carrier and the dopant counterion, along with the large polarizability afforded by the unique physicochemical properties of single-walled carbon nanotubes. If time permits, we will show results from recent studies where we extend this approach to the doping of other nanocarbons.

Single-walled Carbon Nanotubes Wrapped with Charged Polysaccharides Enhance Extracellular Electron Transfer.

Microbial electrochemical systems (MESs) rely on the microbes' ability to transfer charges from their anaerobic respiratory processes to electrodes through extracellular electron transfer (EET). To increase the generally low output signal in devices, advanced bioelectrical interfaces tend to augment this problem by attaching conducting nanoparticles, such as positively charged multiwalled carbon nanotubes (CNTs), to the base carbon electrode to electrostatically attract the negatively charged bacterial cell membrane. On the other hand, some reports point to the importance of the magnitude of the surface charge of functionalized single-walled CNTs (SWCNTs) as well as the size of functional groups for interaction with the cell membrane, rather than their polarity. To shed light on these phenomena, in this study, we prepared and characterized well-solubilized aqueous dispersions of SWCNTs functionalized by either positively or negatively charged cellulose-derivative polymers, as well as with positively charged or neutral small molecular surfactants, and tested the electrochemical performance of Shewanella oneidensis MR-1 in MESs in the presence of these functionalized SWCNTs. By simple injection into the MESs, the positively charged polymeric SWCNTs attached to the base carbon felt (CF) electrode, and as fluorescence microscopy revealed, allowed bacteria to attach to these structures. As a result, EET currents continuously increased over several days of monitoring, without bacterial growth in the electrolyte. Negatively charged polymeric SWCNTs also resulted in continuously increasing EET currents and a large number of bacteria on CF, although SWCNTs did not attach to CF. In contrast, SWCNTs functionalized by small-sized surfactants led to a decrease in both currents and the amount of bacteria in the solution, presumably due to the detachment of surfactants from SWCNTs and their detrimental interaction with cells. We expect our results will help researchers in designing materials for smart bioelectrical interfaces for low-scale microbial energy harvesting, sensing, and energy conversion applications.

Dispersion of Single-Walled Carbon Nanotubes by Aromatic Cyclic Schiff Bases via Non-Covalent Interactions.

One of the challenging issues that hinders the application of single-walled carbon nanotubes (SWCNTs) is the poor solubility and the inevitable formation of bundles. Efforts still need to be made towards solving the problem. Herein, we report a non-covalent strategy to disperse aggregated SWCNTs by aromatic cyclic Schiff bases assisted by ultrasonic techniques. The aromatic cyclic Schiff base (OMM) was synthesized via Schiff base reactions, and the molecular structure was determined by ATR-FT-IR, solid-state 13C-NMR, and HRMS. Although the yielded product showed poor solubility in aqueous solution and organic solvents, it could interact with and disperse the aggregated SWCNTs in dimethyl formamide (DMF) under the condition of ultrasound. UV-vis-NIR, FL, Raman spectra, AFM, and TEM, along with computer simulations, provide evidence for the interactions between OMM molecules and SWCNTs and the dispersion thereof. The semiconductive (7,5), (8,6), (12,1), and (9,7)-SWCNTs expressed a preference for dissolution. The capability of dispersion is contributed by π-π, C-H·π, and lone pair (lp)·π interactions between OMM and SWCNTs based on the simulated results. The present non-covalent strategy could provide inspiration for preparing organic cyclic compounds as dispersants for SWCNTs and then facilitate their further utilization.

Molecular-level hybridization of single-walled carbon nanotubes and a copper complex with counterbalanced electrostatic interactions

Hybridization and wet processibility are highly desired development strategies for next-generation nanomaterials. In particular, the hybridization of carbon nanotubes (CNTs) and transition metals has been investigated for decades owing to the numerous advantages, such as high mechanical and electrical properties. However, manufacturing nano-hybridized CNTs/transition metals is complicated, and no studies have been reported on the dispersion and hybridization of transition metals with single-walled CNTs (SWCNTs) without any harsh or destructive methods due to the strong van der Waals forces. Herein, we demonstrate a one-step dispersion/hybridization of SWCNTs and a Cu-based complex and provide a mechanism derives from counterbalancing the electrostatic interactions via molecular-level charge transfer. The Cu-based complex-hybridized SWCNTs self-assemble and demonstrate suitable viscoelastic behaviors for various printing or coating processes. Finally, the nanostructured SWCNTs/Cu nanoparticle exhibits multifunctional electrothermal properties, electromagnetic interference shielding performances, and flexibilities. The proposed metal-complex-hybridized SWCNTs dispersions provide a wet process guideline for producing nanostructured electrodes.

Ultra-Mild Fabrication of Highly Concentrated SWCNT Dispersion Using Spontaneous Charging in Solvated Electron System.

The efficient dispersion of single-walled carbon nanotubes (SWCNTs) has been the subject of extensive research over the past decade. Despite these efforts, achieving individually dispersed SWCNTs at high concentrations remains challenging. In this study, we address the limitations associated with conventional methods, such as defect formation, excessive surfactant use, and the use of corrosive solvents. Our novel dispersion method utilizes the spontaneous charging of SWCNTs in a solvated electron system created by dissolving potassium in hexamethyl phosphoramide (HMPA). The resulting charged SWCNTs (c-SWCNTs) can be directly dispersed in the charging medium using only magnetic stirring, leading to defect-free c-SWCNT dispersions with high concentrations of up to 20 mg/mL. The successful dispersion of individual c-SWCNT strands is confirmed by their liquid-crystalline behavior. Importantly, the dispersion medium for c-SWCNTs exhibits no reactivity with metals, polymers, or other organic solvents. This versatility enables a wide range of applications, including electrically conductive free-standing films produced via conventional blade coating, wet-spun fibers, membrane electrodes, thermal composites, and core-shell hybrid microparticles.

Machine learning algorithms to optimize the properties of bio-based poly(butylene succinate-co- butylene adipate) nanocomposites with carbon nanotubes

Poly[(butylene succinate)-co-adipate] (PBSA)-based materials are gathering much attention in the packaging industry, agriculture, and other fields owed to their biocompatibility and biodegradability. Nonetheless, poor thermal and mechanical properties of biodegradable polymers, such as PBSA, have hampered their wide-spread use. Herein, a simple, cost-effective and scalable solution to improve the mechanical properties of PBSA is reported by using functionalized single-walled carbon nanotubes (SWCNTs). Different SWCNT loadings have been incorporated in the PBSA matrix via simple solution casting, and the ultrasonication conditions have been optimized to attain a homogenous SWCNT dispersion. The nanocomposites have been characterized in detail by scanning electron microscopy (SEM), Infrared spectroscopy, thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), tensile and impact strength tests. Unprecedented increments in stiffness were found at low nanotube loadings, ascribed to the outstanding reinforcing capability of the SWCNTs combined with their superior modulus and strong interfacial adhesion with the matrix via H-bonding, polar and CH-π interactions. Further, four machine learning (ML) algorithms, Polynomial Regression (PR), Support Vector Machines for Regression (SVR), Gradient Boosting (GB) and Artificial Neural Network (ANN), were applied to predict their mechanical properties. The algorithm´s performance was assessed using analytical parameters such as the coefficient of determination (R2), the mean square error (MSE) and the mean absolute error (MAE). The developed models exhibited strong performance, achieving R2 values ranging from 0.69 to 0.99 across the evaluated properties. The results corroborate that even when the same prediction model is used, its performance varies depending on the physical property to be predicted. Thus, SVR, GB, PR, and ANN were found to be the most effective for estimating the Young’s modulus, tensile strength, elongation at break and impact strength, respectively. This research holds great potential for advancing the field of modelling the mechanical properties of polymeric nanocomposites and their practical applications in various industries such as food, pharmaceutical and biomedicine. The development of accurate models for predicting nanocomposite properties would cheapen, simplify and systematize their design and production processes, resulting in improved final products and more efficient development procedures.

Research on optimizing ultrasonic frequencies for efficient single-walled carbon nanotube dispersion in water using a focused ultrasonic system

Single-walled carbon nanotubes (SWCNTs) can be applied in a wide range of fields owing to their excellent mechanical rigidity, electrical conductivity, and thermal conductivity. However, their application is limited because of their strong van der Waals forces and poor dispersion owing to their hydrophobic properties. To address this problem, ultrasonic dispersion technology has been used in the industry. However, very few studies have investigated the surface damage or effectiveness of the surfactants of SWCNTs with a focus on the frequencies of specific ultrasonic equipment. In this study, the dispersibility of SWCNTs at frequencies of 270, 400, and 700 kHz was investigated using a new focused ultrasonic instrument. The dispersion stability of the samples was analyzed according to each frequency, and the SWCNT surface was studied in detail using field-emission transmission electron microscopy, Raman spectroscopy, and X-ray photoelectron spectroscopy. The adsorption of the polymeric surfactant to the SWCNT was most observed at 270 kHz, and the dispersion stability after processing at this frequency was better than that of the other samples. Therefore, the frequency of the ultrasonic intensity has a direct effect on the surface modification of SWCNTs.

Impact of surfactants on SWCNT dispersion in N-methylmorpholine N-Oxide for cellulose dissolution

A well dispersed slurry of single-walled carbon nanotube (SWCNT) and 60 % hydrated N-methylmorpholine N-oxide (NMMO) solution was prepared by probe sonicator. The proper dispersion of carbon nanotube (CNT) has been verified by optical microscope by varying the sonication time. Further, the slurry was concentrated to 76 % (for cellulose dissolution) and during this process some agglomeration of CNTs has been observed. The dispersion of CNT aggregation was checked by addition of surfactants like sodium dodecyl sulfate (SDS) and sodium dodecyl benzene sulfonate (SDBS) (with 2 % (w/w) with respect to CNT) to the surface of CNT. SDBS is giving better dispersion as compared to SDS when the slurry is heated to obtain 76 % NMMO as checked by optical microscope and UV–Vis spectrophotometer to get quantitative amount of dispersed CNT. 88 % dispersion has been obtained in case of SDBS-assisted CNT after heating followed by centrifugation of the concentrated solution. Similarly, 78 % dispersion has been observed in case of SDS-assisted CNT and 46 % dispersion in case of CNT without any surfactant. The stronger dispersion ability of SDBS could improve its use for SWCNT separation in NMMO solution which can be used further for cellulose dissolution to prepare lyocell fiber.

Enhancing thermoelectric performance of single-walled carbon nanotube films by poly(styrene sulfonate acid) dispersing and sequential base treatment

Despite single-walled carbon nanotubes (SWCNTs) have attracted great interest for thermoelectric (TE) conversion, the strong van der Waals forces between SWCNTs cause them to aggregate into bundles with poor dispersibility, which dramatically deteriorates the charge carrier transport, and thereby induces low electrical conductivity and TE power factor. Herein, we report a facile and efficient approach to enhance TE performance of SWCNTs via the addition of poly(styrene sulfonic acid) (PSSH) and sequential base treatment. PSSH is served as a dispersant and dopant to improve the dispersibility of SWCNTs and facilitate charge carrier conduction, contributing to high electrical conductivity of 3749 ± 122 S cm−1 and power factor of 117.7 ± 3.4 μW m−1 K−2 for 20 wt% PSSH/SWCNT composite film. Further base treatment induces partial removal of insulative PSSH and de-doping effect of SWCNTs, which decreases the barriers between adjacent nanotubes junctions and modulates charge carrier transport to synergistically optimize the electrical conductivity and Seebeck coefficient. With fine-tuning base treatment temperature, the PSSH/SWCNT composite film reaches highest power factor of 160.6 ± 7.9 μW m−1 K−2, higher than pristine SWCNTs of 70.2 ± 4.4 μW m−1 K−2. This work demonstrates the feasibility of this approach to boost the TE properties of SWCNTs, exhibiting potential application for high performance renewable energy harvesting.

Oligofluorene main-chain length-dependence on one-pot extraction of chirality-selective semiconducting single-walled carbon nanotubes

Abstract Polyfluorene and their derivatives are noted for being fascinating dispersants for single-walled carbon nanotubes (SWCNTs) because they selectively solubilize semiconducting (sem-) SWCNTs. However, the selective extraction mechanism of this unique behavior has not yet been fully clarified. In this paper, we describe a unique SWCNT solubilization behavior using 12 fluorene oligomers with different main-chain lengths (FOn, n = 2∼30), in which n is the number of fluorene-repeating unit. Sonication of SWCNTs using these oligofluorenes in toluene was found to solubilize SWCNTs when the main-chain length was longer than n = 12. Raman spectra revealed that selective sem-SWCNT extraction occurred when using the FOn with n ≥ 18, while, when using FOn (n = 12, 15), both sem- and metallic (met-) SWCNTs were solubilized. The (n,m)chiralites of the extracted SWCNTs using the fluorene oligomers differed from those using a homopolymer, poly(9,9′-di-n-octylfluorene) (PFO); that is, PFO extracted (9,7)SWCNTs well, while only FO30 slightly dissolved the (9,7)tubes, and when using other FOn (n = 12∼27), no (9,7)tubes were solubilized. The present study demonstrated the importance of the main-chain length of the oligofluorenes on selected chirality extraction of sem-SWCNTs, which is useful for designing fluorene-based compounds with selective extraction of sem-SWCNTs with a specific (n,m) chirality.

Improved Heat Dissipation of Dip-Coated Single-Walled Carbon Nanotube/Mesh Sheets with High Flexibility and Free-Standing Strength for Thermoelectric Generators

Single-walled carbon nanotubes (SWCNTs) are promising thermoelectric materials used in thermoelectric generators (TEGs) to power sensors. However, the limitation of SWCNTs is their high thermal conductivity, which makes it difficult to create a sufficient temperature difference. In this study, we fabricated dip-coated SWCNT/mesh sheets using an SWCNT dispersion. Several types of mesh materials were tested, and the most suitable material was polyphenylene sulfide (PPS). SWCNTs were uniformly deposited on the PPS mesh surface without filling the mesh openings. The SWCNT/PPS mesh sheets exhibited flexibility and free-standing strength. When the edge of the SWCNT/PPS mesh sheets were heated, a higher temperature gradient was produced compared with that of the conventional SWCNT film owing to the increase in heat dissipation. A flexible and free-standing TEG with an area of 1200 mm2, fabricated using SWCNT/PPS mesh sheets, exhibited an output voltage of 31.5 mV and maximum power of 631 nW at a temperature difference of 60 K (Tlow: 320 K). When the TEG was exposed to wind at 3 m/s, temperature difference further increased, and the performance of the TEG increased by a factor of 1.3 for output voltage and 1.6 for maximum power. Therefore, we demonstrated that the TEG’s performance could be improved using SWCNT/PPS mesh sheets.

Synthesis of a functionalized and photodegradable fluorene-based polymer for aqueous SWNT dispersion

Due to their tunability, conjugated polymers have received significant interest in the dispersion of single-walled carbon nanotubes (SWNTs). Indeed, interactions with conjugated polymers enable simultaneous solubility, extraction, and purification of...

Investigation of the surface mechanical properties of functionalized single-walled carbon nanotube (SWCNT) reinforced PDMS nanocomposites using nanoindentation analysis.

Functionalizing single-walled carbon nanotubes (SWCNT) with different chemical functional groups directly enhances their chemical adhesion and dispersion in viscous polymeric resins such as polydimethylsiloxane (PDMS). Nevertheless, the ideal surface polarity (hydrophilic or hydrophobic) for SWCNT to foster stronger chemical bonding with PDMS remains uncertain. This investigation delves into the impact of enhanced SWCNT dispersion within PDMS on the surface mechanical characteristics of this flexible composite system. We use carboxylic acid-functionalized SWCNT (COOH-SWCNT) and silane-functionalized SWCNT (sily-SWCNT), recognized for their hydrophilic and hydrophobic surface polarities, respectively, as reinforcing agents at ultra-low weight percentage loadings: 0.05 wt%, 0.5 wt%, and 1 wt%. We perform quasi-static nanoindentation analysis employing a Berkovich tip to probe the localized mechanical behavior of PDMS-SWCNT films at an indentation depth of 1 μm. Plastic deformation within the samples, denoted as plastic work (Wp), as well as the elastic modulus (E), hardness (H), and contact stiffness (Sc) of the composites are examined from the force-displacement curves to elucidate the enhancement in the surface mechanical attributes of the composite films.

Highly homogeneous and stable single-walled carbon nanotubes dispersion modified by polyvinylpyrrolidone and alkanolamine in water.

A novel noncovalent surface modification of commercial single-walled carbon nanotubes (SWCNTs) was successfully carried out by using ball grinding technology between SWCNTs and mixed dispersants (polyvinylpyrrolidone (PVP) and alkanolamine), affording a highly homogeneous and stable PA-SWCNTs dispersion in water. The homogeneous dispersibility and long storage stability were systematically investigated by transmittance spectroscopy, absorption spectroscopy, zeta potential analyzer, sedimentation photo and transmittance electron microscopy. Under the optimized conditions, the PA-SWCNTs dispersion modified with 0.7 wt% PVP and 0.25 wt% alkanolamine under the condition of total 6 h ball grinding time using paint shaker can be easily well-dispersed in water and has good storage stability, and no sedimentation is observed more than one month. From an industrial perspective, this method is green and easy to operate in industry.

Advanced hydrophobic cotton threads enhanced with graphene/SWCNT nanocomposites for exceptionally high electrical conductivity

This study investigates the fabrication and characterization of conductive threads using graphene and single-walled carbon nanotubes (SWCNTs), focusing on their application in wearable electronics and smart textiles. We employed the drop casting method to coat cotton threads with a polar solvent-based dispersion of graphene and SWCNTs, aiming to enhance their electrical conductivity and hydrophobic properties. Our results demonstrate that the electrical conductivity of these conductive threads significantly increases with the concentration of graphene and SWCNTs, reaching a peak conductivity of 68.75 S. cm−1 in threads coated with a SWCNT layer followed by a graphene layer. These threads exhibit metallic behavior across a broad temperature range (room temperature to 130 °C) and maintain electrical stability over an extended period. Additionally, varying degrees of hydrophobicity were observed among the different thread compositions. A washability study revealed that threads with a bilayer of SWCNT and graphene maintained higher electrical conductivity after multiple wash cycles compared to those fabricated with a mixed layer of these materials. This research not only highlights the potential of graphene and SWCNTs in developing advanced conductive threads but also addresses the challenges in scalability and reproducibility, paving the way for future innovations in smart textile applications.

Tunable Thermoelectric Performance of the Nanocomposites Formed by Diketopyrrolopyrrole/Isoindigo-Based Donor-Acceptor Random Conjugated Copolymers and Carbon Nanotubes.

This paper presents the development of thermoelectric properties in nanocomposites comprising donor-acceptor random conjugated copolymers and single-walled carbon nanotubes (SWCNTs). The composition of the conjugated polymers, specifically the ratio of diketopyrrolopyrrole (DPP) to isoindigo (IID), is manipulated to design a series of random conjugated copolymers (DPP0, DPP5, DPP10, DPP30, DPP50, DPP90, DPP95, and DPP100). The objective is to improve the dispersion of SWCNTs into smaller bundles, leading to enhanced thermoelectric properties of the polymer/SWCNT nanocomposite. This dispersion strategy promotes an interconnected conducting network, which plays a critical role in optimizing the thermoelectric performance. Accordingly, the effects of morphologies on the thermoelectric properties of the nanocomposites are systematically investigated. The DPP95/SWCNT nanocomposite exhibits the strongest interaction, resulting in the highest power factor (PF) of 711.1 μW m-1 K-2, derived from the high electrical conductivity of 1690 S cm-1 and Seebeck coefficient of 64.8 μV K-1. The prototype flexible thermoelectric generators assembled with a DPP95/SWCNT film achieve a maximum power output of 20.4 μW m-2 at a temperature difference of 29.3 K. These findings highlight the potential of manipulating the composition of random conjugated copolymers and incorporating SWCNTs to efficiently harvest low-grade waste heat in wearable thermoelectric devices.