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A direct current (DC) arc discharge is a widely used method for large-scale production of metal nanoparticles, core–shell particles, and carbon nanotubes. Here, the growth of iron nanoparticles is explored in a modified DC arc discharge. Iron particles are produced by the evaporation of an anode, made from low-carbon steel. Methane admixture into argon gas serves as a carbon source. Electron microscopy and elemental analysis suggest that methane and/or products of its decomposition adhere to iron clusters forming a carbon shell, which inhibits iron particle growth until its full encapsulation, at which point the iron core growth is ceased. Experimental observations are explained using an aerosol growth model. The results demonstrate the path to manipulate metal particle size in a hydrocarbon arc environment. [ABSTRACT FROM AUTHOR]

[Display omitted] Electroactive coatings for smart wearable textiles based on a furan bio-epoxy monomer (BOMF) crosslinked with isophorone diamine (IPD) and additivated with carbon nanotubes (CNTs) are reported herein. The effect of BOMF/IPD molar ratio on the curing reaction, as well as on the properties of the crosslinked resins was first assessed, and it was found that 1.5:1 BOMF/IPD molar ratio provided higher heat of reaction, glass transition temperature, and mechanical performance. The resin was then modified with CNT to prepare electrically conductive nanocomposite films, which exhibited conductivity values increased by eight orders of magnitude upon addition of 5 phr of CNTs. The epoxy/CNT nanocomposites were finally applied as coatings onto a cotton fabric to develop electrically conductive, hydrophobic and breathable textiles. Notably, the integration of CNTs imparted efficient and reversible electrothermal behavior to the cotton fabric, showcasing its potential application in smart and comfortable wearable electronic devices. [ABSTRACT FROM AUTHOR]

[Display omitted] Owing to highly theoretical capacity of 3579 mAh/g for lithium-ion storage at ambient temperature, silicon (Si) becomes a promising anode material of high-performance lithium-ion batteries (LIBs). However, the large volume change (∼300 %) during lithiation/delithiation and low conductivity of Si are challenging the commercial developments of LIBs with Si anode. Herein, a sandwich structure anode that Si nanoparticles sandwiched between carbon nanotube (CNT) and silicon carbide (SiC) has been successfully constructed by acetylene chemical vapor deposition and magnesiothermic reduction reaction technology. The SiC acts as a stiff layer to inhibit the volumetric stress from Si and the inner graphited CNT plays as the matrix to cushion the volumetric stress and as the conductor to transfer electrons. Moreover, the combination of SiC and CNT can relax the surface stress of carbonaceous interface to synergistically prevent the integrated structure from the degradation to avoid the solid electrolyte interface (SEI) reorganization. In addition, the SiC (1 1 1) surface has a strong ability to adsorb fluoroethylene carbonate molecule to further stabilize the SEI. Consequently, the CNT/SiNPs/SiC anode can stably supply the capacity of 1127.2 mAh/g at 0.5 A/g with a 95.6 % capacity retention rate after 200 cycles and an excellent rate capability of 745.5 mAh/g at 4.0 A/g and 85.5 % capacity retention rate after 1000 cycles. The present study could give a guide to develop the functional Si anode through designing a multi-interface with heterostructures. [ABSTRACT FROM AUTHOR]

Tungsten carbides are important materials used in ceramic cements, machining tools, catalysts, sensors, and for hydrogen generation. Bulk W–C structures are highly complex; fundamental fully carburized WC and semi-carburized W 2 C are accompanied by structural transitions depending on the composition and temperature. The relationship between the structures, compositions, and temperatures is summarized in the W–C phase diagram. However, the high-temperature, stable, and single-crystalline nanoparticles related to the WC 1-x and W 2 C phases formed via energetic reactions accompanied by rapid cooling rates are not easy to determine considering the bulk phase diagram, and lead to fundamental questions regarding the origin of the nanophases. In this study, we propose a draft for the W–C nanophase diagram composed of the surface and gas-phase WC, WC 1-x , and W 2 C nanophases according to the composition and temperature. The model undergoes the process of a vapor–nanoliquid–nanophase starting from the gas-phase nucleation induced by an extremely high-temperature electrical explosion. In addition, the high-temperature reactivity and quenched nanophase, including its unique nanostructure, are related to the post-melt rheology, physical morphology, and steric hindrance of the solid matrix during an electrical explosion. [ABSTRACT FROM AUTHOR]

Recent interest in tissue engineering (TE) has focused on electrically conductive biomaterials. This has been inspired by the characteristics of the cells' microenvironment where signalling is supported by electrical stimulation. Numerous studies have demonstrated the positive influence of electrical stimulation on cell excitation to proliferate, differentiate, and deposit extracellular matrix. Even without external electrical stimulation, research shows that electrically active scaffolds can improve tissue regeneration capacity. Tissues like bone, muscle, and neural contain electrically excitable cells that respond to electrical cues provided by implanted biomaterials. To introduce an electrical pathway, TE scaffolds can incorporate conductive polymers, metallic nanoparticles, and ceramic nanostructures. However, these materials often do not meet implantation criteria, such as maintaining mechanical durability and degradation characteristics, making them unsuitable as scaffold matrices. Instead, depositing conductive layers on TE scaffolds has shown promise as an efficient alternative to creating electrically conductive structures. A stratified scaffold with an electroactive surface synergistically excites the cells through active top-pathway, with/without electrical stimulation, providing an ideal matrix for cell growth, proliferation, and tissue deposition. Additionally, these conductive coatings can be enriched with bioactive or pharmaceutical components to enhance the scaffold's biomedical performance. This review covers recent developments in electrically active biomedical coatings for TE. The physicochemical and biological properties of conductive coating materials, including polymers (polypyrrole, polyaniline and PEDOT:PSS), metallic nanoparticles (gold, silver) and inorganic (ceramic) particles (carbon nanotubes, graphene-based materials and Mxenes) are examined. Each section explores the conductive coatings' deposition techniques, deposition parameters, conductivity ranges, deposit morphology, cell responses, and toxicity levels in detail. Furthermore, the applications of these conductive layers, primarily in bone, muscle, and neural TE are considered, and findings from in vitro and in vivo investigations are presented. Tissue engineering (TE) scaffolds are crucial for human tissue replacement and acceleration of healing. Neural, muscle, bone, and skin tissues have electrically excitable cells, and their regeneration can be enhanced by electrically conductive scaffolds. However, standalone conductive materials often fall short for TE applications. An effective approach involves coating scaffolds with a conductive layer, finely tuning surface properties while leveraging the scaffold's innate biological and physical support. Further enhancement is achieved by modifying the conductive layer with pharmaceutical components. This review explores the under-reviewed topic of conductive coatings in tissue engineering, introducing conductive biomaterial coatings and analyzing their biological interactions. It provides insights into enhancing scaffold functionality for tissue regeneration, bridging a critical gap in current literature. [Display omitted] [ABSTRACT FROM AUTHOR]

Bioplastic is an emerging candidate for replacing traditional fossil‐based plastics due to its fewer carbon emissions, ease of recycling, and high degradability. Current research has shown that bioplastics benefit many applications, such as packaging, kitchenware, drug delivery, and sensors. However, high electrical resistance and poor stability of bioplastic are barriers to electronic components in robotic, bionic, and exoskeleton applications. Here, we introduce a novel bioplastic application as a strain sensor to estimate elbow angles for controlling exoskeletons. This study utilized extracted agar from red algae as the matrix, incorporating various concentrations of carbon nanotube (CNT) as a filler. The results were remarkable, with the increase in filler concentration not only improving strain from 0.8 to 1.1 but also stress from 35.2 to 45.8 kPa, surpassing commercial plastic by approximately two times. The optimized sensors have a response time of 0.16 s, a recovery time of 0.25 s, and stability over 10,000 cycles. Furthermore, the CNT‐bioplastic sensor is seamlessly integrated with the exoskeleton. Our work is a significant step toward using bioplastic in electronic applications. [ABSTRACT FROM AUTHOR]

Carbon-based materials/metal hydroxide composite materials are one type of the most promising electrode materials for improving the performance of supercapacitors. They have the advantages of low cost, controllable morphology, high theoretical capacity, and excellent stability. In this study, nickel hydroxide nanosheets were grown vertically on the surface of carbon nanotubes (Ni(OH)2@CNTs) by a wet chemical method at low temperatures. The unique spatial configuration provides a larger specific surface area and exposes more electrochemically active sites, which is more conducive to improving electrochemical performance. The prominent conductivity of carbon nanotubes can quickly transfer electrons and improve the electrochemical cycling stability of the composite. The Ni(OH)2@CNTs composite exhibits excellent electrochemical performance with a specific capacitance of 1234 F g−1 at a current density of 1 A g−1 under a three-electrode system. In addition, an asymmetric supercapacitor (ASC) assembled using Ni(OH)2@CNTs as a cathode material shows an energy density of 65.63 W h kg−1 at a power density of 752.39 W kg−1 and a capacity retention rate of 85.9% after 10 000 cycles at a current density of 2 A g−1. The results indicate that Ni(OH)2@CNTs has prospects for application as a cathode material in high-performance supercapacitors. [ABSTRACT FROM AUTHOR]

3D carbon nanotube hybrid materials containing VO2 and V2O5 evenly distributed onto vertically aligned carbon nanotubes (VACNTs) is reported. Adjustable loading of particles in controllable sizes and shapes onto the VACNTs was developed via a stepwise chemical vapour deposition (CVD) approach. Solid VO(acac)2 is chosen as vanadium source. CO2 acts as reactive gas for the pre‐functionalisation of the VACNTs. The process temperature was identified as key parameter to control the deposited vanadium oxide phase. A temperature of 550 °C results in monoclinic VO2, while 600 °C results in the deposition of V2O5 onto the VACNT support. The morphology and the amount of deposited material was found to be dependent on the reactor dimensions and the degree of functionalisation of the carbon support. An increase of the D/G ratio of the VACNT from 0.75 to 1.08 caused by a CO2 treatment step within the process led to an increase of the particle coverage from a scarce coverage without prior CO2 treatment to a dense coverage of the VACNT support after 15 min of CO2 exposure time. Size and crystallinity of the as deposited particles can be further adjusted by a controlled heat treatment after VO(acac)2 precursor deposition. [ABSTRACT FROM AUTHOR]

Flexible electro‐optical dual‐mode sensor fibers with capability of the perceiving and converting mechanical stimuli into digital‐visual signals show good prospects in smart human‐machine interaction interfaces. However, heavy mass, low stretchability, and lack of non‐contact sensing function seriously impede their practical application in wearable electronics. To address these challenges, a stretchable and self‐powered mechanoluminescent triboelectric nanogenerator fiber (MLTENGF) based on lightweight carbon nanotube fiber is successfully constructed. Taking advantage of their mechanoluminescent‐triboelectric synergistic effect, the well‐designed MLTENGF delivers an excellent enhancement electrical signal of 200% and an evident optical signal whether on land or underwater. More encouragingly, the MLTENGF device possesses outstanding stability with almost unchanged sensitivity after stretching for 200%. Furthermore, an extraordinary non‐contact sensing capability with a detection distance of up to 35 cm is achieved for the MLTENGF. As application demonstrations, MLTENGFs can be used for home security monitoring, intelligent zither, traffic vehicle collision avoidance, and underwater communication. Thus, this work accelerates the development of wearable electro‐optical textile electronics for smart human‐machine interaction interfaces. [ABSTRACT FROM AUTHOR]

Tailored ribbing structures are obtained by large‐scale rolling in polymer PDMS thin‐films by adding carbon nanotubes (CNT) inclusions, which significantly improved the mechanical behavior of systems subjected to dynamic compressive strain rates. A nonlinear explicit dynamic three‐dimensional finite‐element (FE) scheme is used to understand and predict the thermomechanical response of the manufactured ribbed thin‐film structures subjected to dynamic in‐plane compressive loading. Representative volume element (RVE) FE models of the ribbed thin‐films are subjected to strain rates as high as 104 s−1 in both the transverse and parallel ribbing directions. Latin Hypercube Sampling of the microstructural parameters, as informed from experimental observations, provide the microstructurally based RVEs. An interior‐point optimization routine is also employed on a regression model trained from the FE predictions that can be used to design ribbed materials for multifunctional applications. The model verifies that damage can be mitigated in CNT‐PDMS systems subjected to dynamic compressive loading conditions by controlling the ribbing microstructural characteristics, such as the film thickness and the ribbing amplitude and wavelength. This approach provides a framework for designing materials that can be utilized for applications that require high strain rate damage tolerance, drag reduction, antifouling, and superhydrophobicity. [ABSTRACT FROM AUTHOR]

Optimizing both performance and stability under varying relative humidity (RH) conditions is crucial for proton exchange membrane fuel cells (PEMFCs). Therefore, effective management of mass transfer and water is an essential key factor. To further improve performance and stability, this paper reports a novel PEMFC design strategy that introduces carbon nanotube (CNT) sheets with titanium (Ti) deposited onto them as an additional functional layer using the sputtering method. The Ti‐CNT (as Ti‐deposited CNT is abbreviated to Ti‐CNT) sheets are inserted between the catalyst layer (CL) and the gas diffusion layer (GDL). This exhibit enhances performance across all testing conditions (25‐100% RH), which is attributed to their optimal pore structure and hydrophilic properties. It shows up to ≈94% higher power density and ≈60% improvement in charge transfer resistance compared to conventional. Moreover, stability tests conducted under a constant voltage demonstrated that this innovative design strategy significantly reduced degradation, thereby proving its superior stability. This novel design strategy of inserting Ti‐CNTs as a functional layer improves electrochemical performance and stability. [ABSTRACT FROM AUTHOR]

The development of wearable heat supply textiles in cold conditions utilizing the photothermal conversion effect is crucial for the advancement of wearable thermal management textiles that do not require any power supply connection or other external energy input. Here, a dual gelation strategy under gravity‐enhanced orientation is proposed to construct super‐strong bacterial cellulose (BC) aerogel fiber using BC as the matrix material and hydroxylated carbon nanotubes (HCNT) as the photothermal conversion material. Under the assistance of orientation property and dual network structure with soft–hard synergy, the silanized BC/HCNT (SBT) aerogel fiber has rich network, tensile strength up to 26.0 MPa, flexibilityand knittability. Thanks to the enhanced network backbone, after the introduction of the phase change material eicosane in SBT aerogel fiber (SBTE), the SBTE fiber achieves high enthalpy of 105 J g−1, low leakage, storage stabilityand super‐strong and tough mechanical properties of 23.9 MPa and 8.7 MJ m−3, while maintaining flexibility, knittabilityand hydrophobicity. The textile woven by SBTE fiber also exhibits a long‐lasting heat supply capacity at low temperatures and under real‐world conditions. Therefore, the finely designed SBTE fiber has the potential to be used in solar‐driven wearable heat supply textiles in cold weather. [ABSTRACT FROM AUTHOR]

ABSTRACT The electrophoretic deposition of multi‐walled carbon nanotubes (MWCNTs) has been well‐researched; however, preparatory steps lead to MWCNT coating contamination and deposits often have weak adhesion to the substrate. This work targets these two weaknesses. First, MWCNTs were functionalized by nonthermal, radiofrequency plasma, producing oxygenated MWCNTs (O‐MWCNTs), with which water‐based suspensions were prepared. Second, an ethane‐based plasma polymer was applied on the metallic substrate as an interlayer to improve coating adhesion. O‐MWCNT coatings were produced at 5–40 V for 1–60 min. Homogeneous coatings with thicknesses up to 10 µm were achieved, the composition was 90‐95 at% carbon with the balance element being oxygen, and coating adhesion without damage was confirmed for shear stresses up to 16 Pa. [ABSTRACT FROM AUTHOR]

Barocaloric cooling as an emerging cooling technology offers an eco‐friendly alternative to traditional vapor compression refrigeration. Research on barocaloric materials primarily concentrates on solid–solid phase change materials (PCMs), among which plastic crystals exhibit colossal barocaloric effect. Solid‐liquid PCMs such as paraffin also exhibit giant barocaloric effect, however, their potential is often overshadowed by leakage issues. In this work, a strategy is demonstrated by encapsulating solid‐liquid PCMs into porous carbon matrixes to generate a large family of colossal barocaloric materials. In practice, by orthogonally combining paraffins with encapsulation matrixes like graphene foam, carbon nanotube foam, and carbon foam, it can be obtained composites that work without leakage issues. The significant advantage is their colossal barocaloric effect with the highest entropy value up to 570 J K−1 kg−1 in paraffin‐20@graphene foam. Moreover, the composites possess thermal conductivity up to 89.9 W m−1 K−1 in paraffin‐20@carbon foam, and tunable working temperature in the range of 270—330 K. Most importantly, this strategy, demonstrated with 5 solid‐liquid PCMs and 3 encapsulation matrixes in this work, is just the beginning. Further exploration with more materials can develop a huge family of encapsulated solid‐liquid PCMs with colossal barocaloric performance for modern cooling technology. [ABSTRACT FROM AUTHOR]

Designing composites with rational structure and composition is a promising approach to obtain efficient electrocatalysts for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). In this study, zeolitic imidazolate frameworks-67 (ZIF-67) is employed as a self-sacrificing template to synthesize Co/carbon nanotubes (CNTs) precursor, which is subsequently in-situ nitrided and phosphorized to form cobalt phosphide/nitride/carbon nanotubes (Co 2 P/Co 4 N/CNTs) composite. The realized Co 2 P/Co 4 N composite exhibits heterogeneous nanoparticle microstucture with an average diameter of approximately 10 nm, encapsulated by carbon nanotubes with a porous dodecahedral array. Moreover, there is a well-defined interface between cobalt phosphide, cobalt nitride phases, and carbon nanotubes species. Benefiting from the synergistic effect of Co 4 N and Co 2 P, rich active sites, and high conductivity of CNTs, the composite catalyst demonstrates remarkable HER and OER activities, requiring overpotentials of 228 and 389 mV to support 100 mA cm−2 current density, respectively. This work presents a novel strategy for designing efficient bifunctional catalysts towards HER and OER. [Display omitted] • Co 2 P/Co 4 N/CNTs composite catalyst is prepared by in-situ converting ZIF-67 precursor. • The composite consist of CNTs encapsulated Co 2 P/Co 4 N heterogeneous nanoparticles. • The good interface of Co 2 P, Co 4 N and CNTs is in favor of improving conductivity and activity. • Co 2 P/Co 4 N/CNTs composite need 228 mV overpotential to support 100 mA cm−2 for HER. [ABSTRACT FROM AUTHOR]

Carbon nanotube (CNT)‐polyetherimide (PEI) hybrid nanofibrous veils were prepared through the electrospinning process to function as an interlayer in carbon fiber reinforced polymer composites (CFRP), and the effects of the addition of the hybrid fiber veils on the interlaminar fracture properties and flexural properties of CFRP were investigated. The results showed that interleaving CNT/PEI hybrid veils can effectively avoid long‐troubled trade‐off between mode‐I interlaminar fracture toughness and in‐plane properties when using thermoplastic toughening materials. Specifically, the GIc value and flexural strength of the laminates were increased by as much as 86.2% and 14.3%, respectively when CNT content was reached up to 0.7 wt% in CNT/PEI hybrid veil. This method adopts ultra‐low PEI and CNT additions, and the limited quantity of these additives demonstrates a notably high interlaminar toughening efficiency while concurrently enhancing the strength, rendering it a promising strategy for both toughening and strengthening. Highlights: PEI is used as a carrier to transport CNT to the CFRP interlaminar layers.PEI‐CNT hybrid fiber veils improve GIC and flexural strength of CFRP.PEI‐CNT hybrid fiber veils impede crack expansion through various mechanisms.This method adopts ultra‐low PEI and CNT additions. [ABSTRACT FROM AUTHOR]

We herein report the enhancement of thermal, electrical, electromagnetic interference (EMI) shielding, and mechanical performance of polyethylene (PE) nanocomposites by the introduction of non‐covalently modified multi‐walled carbon nanotube (MWCNT) and ethylene‐glycidyl methacrylate (EGMA) copolymer. For this purpose, benzylacetic acid‐functionalized MWCNT (BA‐M) is prepared by ball milling, and it is melt‐mixed with EGMA to prepare a masterbatch. The masterbatch is then melt‐compounded with neat PE to manufacture a series of PE/EGMA/BA‐M nanocomposites with 0.5–5 wt% MWCNTs. Electron microscopic and spectroscopic analyses confirm the successful fabrication of non‐covalently functionalized BA‐M, the uniform dispersity of MWCNTs in the PE matrix, and the chemical reactions between the carboxylic acid groups of BA‐M and the epoxy group of EGMA in the nanocomposites. Scanning calorimetric data reveals that BA‐M acts as an efficient nucleating agent for the crystallization of PE. The excellent dispersity and robust interfacial bonding of BA‐M in the PE matrix result in improved electrical and EMI shielding properties in PE/EGMA/BA‐M nanocomposites. Furthermore, the tensile strength, initial modulus, and impact strength of the nanocomposites gradually rise as the BA‐M content increases. Thus, the PE/EGMA/BA‐M nanocomposite containing 5 wt% MWCNT achieves excellent performance of EMI shielding effectiveness of ~14.7 dB/mm, tensile strength of ~34.5 MPa, initial modulus of ~295.7 MPa, and impact strength of ~539.9 J/m, which represent enhancements of ~265%, ~40%, ~82%, and ~452%, respectively, compared to pristine PE. Highlights: Non‐covalently modified MWCNT (BA‐M) was prepared by facile ball milling.PE nanocomposites with BA‐M and EGMA were prepared by masterbatch melt‐mixing.Excellent dispersity and interfacial bonding of MWCNT in the PE matrix were attained.Tensile strength and initial modulus of the nanocomposites were highly improved.EMI shielding effectiveness of the nanocomposite with 5 wt% MWCNT was ~14.7 dB/mm. [ABSTRACT FROM AUTHOR]

The development of innovative composite materials through the amalgamation of thermoplastic polyurethane (TPU) with bismuth sodium titanate (BNT) and carbon nanotube (CNT) fillers was investigated. Before the composite fabrication, the fillers' surfaces were treated to enhance their compatibility with the TPU matrix. Hybrid fillers of BNT and CNTs were fabricated by mixing the two types of filler particles through ball milling and subsequently annealing the mixture at 250°C. Melt‐blending and injection molding were utilized to synthesize the composites at 210°C processing temperature. The prepared composites showed significantly enhanced thermal conductivity, dielectric constant, thermal stability, and thermomechanical properties compared with the neat TPU matrix. For instance, the dielectric constant was enhanced by 340% upon the inclusion of 40 wt.% BNT and CNT fillers compared to the neat TPU matrix (40CBNT‐TPU has 13.2). In particular, the inclusion of BNT‐CNT particles in the TPU matrix improved the thermal conductivity of the TPU matrix by 1180% tremendously as compared to neat TPU (40CBNT‐TPU has 2.6 W/(m.K)). Highlights: Crystalline bismuth sodium titanate (BNT) is fabricated.Degradation of 8 wt.% of the IPDI‐treated BNT proves surface treatment.Dielectric constant (DC) improved by 340% compared to neat TPU.Thermal conductivity (TC) enhanced 11.4 times compared to neat TPU.Improvement in TC and DC will make it applicable in electronic materials. [ABSTRACT FROM AUTHOR]

This study evaluated the effect of multi‐walled carbon nanotubes (MWCNT) addition on the thermomechanical, and electrical responses of unidirectional flax fibers/Elium acrylic modified carbon nanotubes‐based composite. The manufacturing process of these laminated composites involved infusing the nanofillers onto the fibers, ensuring good dispersion of MWCNT within the matrix. Regardless of the rate of incorporated nanotubes, this study revealed a significant deterioration of the mechanical properties in tension and viscoelastic properties of the Elium acrylic resin‐based nanocomposite. The electrical conductivity significantly increased for all nanocomposites and laminated composites. In contrast to the nanocomposite, the unidirectional flax fibers/MWCNT/Elium acrylic composite exhibited a considerable improvement in mechanical properties. An increase in Young's modulus and stress at break of about 27% and 23% respectively, was achieved for the material loaded with 2 wt% of MWCNT. The presence of MWCNT reduces the saturation weight by 5% for the unidirectional composite filled with an amount of 1.5 wt% in MWCNT. Highlights: Improving the electrical properties of nanocomposites and unidirectional fibers (UD) composites.Improving the mechanical properties of Elium/flax/multi‐walled carbon nanotubes (MWCNT) composites.Influence of MWCNTs on the water absorption of UD composites.Influence of MWCNT on the glass transition temperature of nanocomposites.Inhibiting polymerization of MWCNT with Elium. [ABSTRACT FROM AUTHOR]

This study addresses the applications of non-uniform heat source/sink and viscous dissipation in the magnetohydrodynamic (MHD) flow of Casson nanoparticles toward a porous stretchable sheet. The free convective flow for the inclusion of thermal buoyancy along with dissipative heat encourages the flow phenomena. The governing equations of the flow model are presented in terms of partial differential equations and then transformed into a system of ordinary differential equations using similarity transformations. These systems of equations are solved numerically by using the Runge–Kutta fourth-order method with a very efficient shooting technique. The effects of various parameters such as the Casson parameter, elastic parameter, porosity parameter, Prandtl number, non-uniform heat source/sink constant, Eckert number, skin fraction and Nusselt number on the flow area are computed and represented graphically. The present results reflect that the velocity of nanoparticles declined effectively with the porosity parameter and nanoparticle volume fraction. The temperature profile is increased with the elastic parameter and heat source parameter while decreasing with the Eckert number and Casson fluid parameter. Moreover, it is observed that when the Hartmann number is maximum, a retardation in wall shear force against nanoparticles volume fraction is marked. [ABSTRACT FROM AUTHOR]

Ultrafine ruthenium nanoparticles are encapsulated by single-atom Ni-bonded graphitic carbon nitride (g-C3N4) layers anchored on carbon nanotubes (Ru/Ni-CNCT). The enhanced electronic interaction between Ru nanoparticles and Ni–N(O)–C sites anchored in g-C3N4 layers promotes water adsorption/dissociation and hydrogen evolution. [ABSTRACT FROM AUTHOR]

Anti-Stokes Raman thermometry, a rapidly evolving field in Raman spectroscopy, was investigated for in situ cellular temperature measurementsa critical aspect in photothermal cancer therapy. In this study, multiwalled carbon nanotubes decorated with gold nanorods (MWCNTs-GNRs) were employed as nanothermometer probes. Characterization involved the analysis of individual Raman spectra acquired at various powers and initial temperatures. The changes observed in the Raman spectra of MWCNTs-GNRs, particularly in response to variations in temperature and excitation power, provide the necessary information to develop a reliable Raman thermometry. This methodology facilitated the extraction of the intrinsic photothermal heating coefficient of MWCNTs-GNRs, offering essential insights into their thermometric properties. An evaluation was extended to incubating MWCNTs-GNRs with prostate cancer PC3 cell lines, where anti-Stokes and Stokes signals were measured at different laser powers to assess in situ cellular temperatures. Temperature maps for a selected area were generated for MWCNTs-GNRs and a single PC3 cell incubated with MWCNTs-GNRs with data standard error analysis performed to indicate a certain level of reliability in temperature measurement accuracy. Cell viability was determined through trypan blue assays, and the obtained temperatures were correlated with viability outcomes at different laser powers. Our investigation encompassed a temperature range spanning 60–100 °C, transcending the critical temperature threshold of 50 °C, which is associated with inducing cell demise. The study highlights the potential of MWCNTs-GNRs as nanothermometer probes for targeted photothermal therapies. [ABSTRACT FROM AUTHOR]

Fully embedded and spatially diffuse sensors are central to the advancement of civil and construction engineering. Indeed, they serve as an enabling technology necessary for addressing the current challenges associated with through‐life management and structural health monitoring of existing structures and infrastructures. The need to identify structural issues early on has driven the integration of such embedded sensing capabilities into construction materials, turning passive structures into proactive, self‐aware “entities,” commonly referred to as Smart Structures. The economic rationale behind this endeavor is underscored by the vital significance of continuous monitoring, which enables prompt anomaly assessment and thus mitigates the risks of potential structural failures. This is particularly relevant for road and rail infrastructures, as they represent a substantial and enduring investment for any nation. Given that a large majority of these large infrastructures are composed of concrete and reinforced concrete, both academics and construction companies are continuously researching micro‐ and nano‐engineered self‐sensing solutions specifically tailored for this building material. This comprehensive review paper reports the latest advances in the field of self‐sensing concrete as of 2024, with an emphasis on intrinsic self‐sensing concrete, that is, electrically conductive functional fillers. A critical analysis and a discussion of the findings are provided. Based on the perceived existing gaps and demands from the industry, the field's future perspectives are also briefly outlined. [ABSTRACT FROM AUTHOR]

In this study, a breathable and strain‐insensitive multi‐layered electronic skin (e‐skin) capable of real‐time detection and distinction of electrocardiogram (ECG) signals, temperature, and skin hydration is developed. Leveraging a scalable benchtop method, sensing elements are transferred onto porous and hydrophobic substrates, followed by multi‐layer stacking to enable multimodal sensing. The sensing elements, a combination of carbon nanotube and nanoporous carbon (CNT@NPC) ink, are applied using strain‐insensitive patterned masks, then spray‐coated with styrene–ethylene–butylene–styrene (SEBS) to create a hierarchical porous network through phase separation. The CNT@NPC networks exhibit an improvement in strain insensitivity with active sensing capabilities due to their adaptable molecular tuning capacity and exceptional electrical conductivity. The porous SEBS substrate offers strong bonding with CNT@NPC attributed to the π–π interactions and high kinetic energy dispersion from spray coating allowing effective transfer. This unique design facilitates breathability, and miniaturization that minimizes the interference between different sensing modalities, ensuring accurate and reliable data acquisition. The breathability (3.49 mg cm−2 h−1) and the non‐smearing nature of the multi‐layered e‐skin enables simultaneous monitoring of temperature (0.198% °C−1), skin hydration (relative humidity = 0.77% %−1), and ECG (26 ± 1 dB) with continuous data transmission to a remote smartphone interface. [ABSTRACT FROM AUTHOR]

The recent observations of superconductive ordering in low-dimensional systems comprising twisted and rhombohedral ABC-stacked multilayer graphene have attracted significant attention. One-dimensional moiré superlattices and flat-bands have been interestingly reported to occur also in collapsed chiral carbon nanotubes. In this work we report the unusual stabilization of hexagonal moiré-like superlattices in partially-collapsed carbon nano-onions (CNOs). Such a structural transition was identified by employing indium-isopropoxide as a growth-promoter, during the pyrolysis of fixed quantities of ferrocene, dichlorobenzene and sulfur. Raman point and mapping spectroscopy analyses highlight a significant enhancement in the D-band intensity with the increase of the indium-isopropoxide concentration, up to a maximum for a precursor quantity of 10 mg. A uniform growth product consisting of stacking-faults-rich partially collapsed CNOs is demonstrated. Larger amounts of indium-isopropoxide were instead found to yield a transition from CNO to carbon nanotubes (CNTs) and consequential depletion of the D-band intensity-parameter. [ABSTRACT FROM AUTHOR]

Due to their internal gain mechanism, emerging nanomaterial‐based infrared phototransistors show significant promise for highly sensitive detection; however, they usually suffer from high dark current (Idark) and thus high noise, which restricts the actual detection capability of the detector. Here, a semiconducting carbon nanotube (CNT) film‐based phototransistor is proposed with an ultralow Idark and a high response through the adoption of stacked ZnO/PbS colloidal quantum dot heterojunctions as the photogate to absorb the infrared photons and generate a photovoltage. Solution‐derived semiconducting CNTs with diameters ranging from 0.8 to 1.1 nm are utilized to create a network film that serves as the active channel of the transistor and provides an off‐state current as low as ≈50 fA; this enables an ultralow dark current (pA level) in the infrared phototransistor. By tuning the back‐gate bias, the synergistic modulation is demonstrated of the sensor response and electronic noise and achieve a high detectivity of 5.7 × 1013 Jones under an incident power density of 0.81 nW cm−2 and 1300 nm infrared radiation. These findings provide a promising approach for attaining weak light infrared detection based on nanomaterial‐based photodetectors. [ABSTRACT FROM AUTHOR]

Our research attempted to investigate the impact of calcination on the synthesis procedure, thickness dependency, and catalytic phases of carbon nanotubes (CNTs) exhibiting a foam-like design. The sol-gel technique of combustion was used to generate three different stoichiometric molar proportions of extremely active Fe:Mo:MgO catalyst significantly powder (namely 1:0.5:13, 1:1:13, and 1:1:50). The crystalline phases of the catalysts were modified by calcination under Air, inert (Ar) and reduced (H 2) atmospheres. XRD, scanning electron microscopy (SEM), in addition to Energy Dispersive X-ray (EDX) analysis were utilized to examine the development of the catalytic compounds' morphological phases, size of particles, shape, and composition of elements.The crystalline shapes, sizes and other morphological characteristics of the highly active catalysts were studied by TEM. Additionally, the BET surface area as well as the average particle diameter, volume of pore, and radius of pore were ascertained using the N 2 sorption isotherm evaluation. Then, the combination of uncalcined and calcined catalysts were employed to generate CNT foams through CVD approach. The CNT foam development findings were examined using a variety of physicochemical strategies. From these studies, we established the relation between the catalytic phases and the growth of MWCNTs with foam-like morphology. Finally, the change of the growth mechanism and diameter of the MWCNT foams over the active catalysts based on the stoichiometric molar ratios between the catalyst and support was analyzed through TEM studies. [ABSTRACT FROM AUTHOR]

Antibiotic resistance is a crisis that is escalating nowadays. Thus, therapeutic drug monitoring (TDM) is crucial to personalize the dose. Point‐of‐care (POC) devices are very effective in TDM where drug concentration can be easily and continuously monitored. This work describes for the first time the use of inexpensive, transportable, efficacious, and eco‐friendly POC solid‐state potentiometric sensor for the TDM of Flucloxacillin (FLU) in spiked plasma samples. This was achieved by using an innovative glassy carbon electrode modified with ion sensing membrane doped with carbon nanotubes. Optimization of the sensing membrane composition was performed using different plasticizers and by adding an ionophore. This was followed by doping the ion sensing membrane with carbon nanotubes which resulted in enhancing the sensor's sensitivity towards FLU. Over a concentration range from 1.0×10−5–1.0×10−2 M FLU, a linear response was obtained with a slope of 56.6 mV/decade. Our proposed sensor has been validated according to IUPAC recommendations with acceptable results.It was effectively employed for a selective determination of FLU in the presence of a co‐formulated antibiotic (Amoxicillin), along with other excipients in the dosage form, and in spiked plasma samples, without any interference. The whiteness of the method was assessed, which proves the high greenness and superb functionality of our proposed method. [ABSTRACT FROM AUTHOR]

In this work, a facile synthesis procedure was developed to deposit Pt−Pd dendrites using the chronopotentiometry (CP) method on polyaniline/carbon nanotube composites. The morphology of the bimetallic Pt−Pd dendrites exhibited a petal‐like shape. The results indicated that multi‐walled carbon nanotubes with larger diameters (approximately 60 nm) demonstrated enhanced support capabilities for achieving uniform dispersion of Pt−Pd dendrites. The electrochemical mass activity for methanol oxidation reaction (MOR) of Pt72Pd28/PANI/CNTs composites reached 670 mA mg−1Pt+Pd, representing a 1.2‐fold increase compared to that of Pt/C. Moreover, the If/Ib value of Pt72Pd28/PANI/CNTs catalyst was 1.9 times higher than that of Pt/C catalyst. Notably, the Pt72Pd28 dendrites displayed superior catalytic performance and COad tolerance in comparison to commercial Pt/C catalysts, as evidenced by their high mass activity and If/Ib value. These research findings present a novel approach for preparing highly active Pt−Pd binary catalysts. [ABSTRACT FROM AUTHOR]

Flexible zinc‐air batteries are leading power sources for next‐generation smart wearable electronics. However, flexible zinc‐air batteries suffer from the highly‐corrosive safety risk and limited lifespan due to the absence of reliable solid‐state electrolytes (SSEs). Herein, a single‐anion conductive SSE with high‐safety is constructed by incorporating a highly amorphous dual‐cation ionomer into a robust hybrid matrix of functional carbon nanotubes and polyacrylamide polymer. The as‐fabricated SSE obtains dual‐penetrating ionomer‐polymer networks and hierarchical ionic highways, which contribute to mechanical robustness with 1200 % stretchability, decent water uptake and retention, and superhigh ion conductivity of 245 mS ⋅ cm−1 and good Zn anode reversibility. Remarkably, the flexible solid‐state zinc‐air batteries delivers a high specific capacity of 764 mAh ⋅ g−1 and peak power density of 152 mW ⋅ cm−2 as well as sustains excellent cycling stability for 1050 cycles (350 hours). This work offers a new paradigm of OH− conductors and broadens the definition and scope of OH− conductors. [ABSTRACT FROM AUTHOR]

Tin-sulphide (SnS 2) nanosheets coupled with carbon nanotube (CNT) have been synthesized with different proportions of CNT (5 wt %, 10 wt %, and 20 wt %) to investigate their properties for photoelectrochemical (PEC) water-splitting applications. Microscopic studies revealed that the nanosheets of SnS 2 are uniformly dispersed on CNT. SnS 2 and SnS 2 /CNT nanocomposite photoanodes were fabricated using the spray coating method for photoelectrochemical studies. Under similar light illumination, the current density of SnS 2 /CNT-10 nanocomposite photoanode is ∼8.5 times higher compared to SnS 2 photoanode at 1.0 V vs Ag/AgCl. The enhancement in PEC performance is attributed to the conducting nature of CNT and the larger band bending induced by CNT. The CNT conducting network facilitates the effective transfer of charge carriers. Also, the electron-accepting nature of CNT helps to improve the overall PEC performance by lowering the rate of recombination of charge carriers. Further, the presence of sulphur vacancies in SnS 2 /CNT nanocomposite prolongs the life of photogenerated charge carriers, improves its separation efficiency, and provides more surface-active sites for electrochemical reactions. A potential explanation for observed enhancement is provided and supported by electrochemical impedance spectroscopy (EIS) and Mott-Schottky results. These results highlight the substantial potential of SnS 2 /CNT nanocomposites for photoelectrochemical water-splitting applications. • SnS 2 /CNT nanocomposite is synthesized using In-situ hydrothermal technique. • Higher surface area provides more electrochemical active sites for redox reactions. • CNT facilitates the efficient transfer of photogenerated charge carriers. • A ∼8.5 times higher current density is observed in SnS 2 /CNT than SnS 2 photoanode. [ABSTRACT FROM AUTHOR]

The co-pyrolysis of torrefied oiltea camellia shells (OCS) and reused polypropylene (PP) was investigated for pyrolysis oil, pyrolysis gas and carbon nanotubes (CNTs) distribution characters in a two-stage pyrolysis system. Compared with raw OCS/PP, the quality of pyrolysis oil from torrefied OCS and PP was upgraded while yield decreased gradually. In particular, torrefaction pretreatment was beneficial to the formation of aromatic hydrocarbons and the higher selectivity of phenols in pyrolysis oil. And serious N 2 torrefaction (260 N) and slight CO 2 torrefaction (200C) is more conducive to the synthesis of C6–C11 (gasoline component). In addition, torrefaction could contribute to lower volatiles, which resulted in a lower yield of CNTs. For comparison, higher graphitized CNTs was prepared from the co-pyrolysis of torrefied OCS and PP. Appropriate torrefaction temperature and atmosphere have a potential for high value conversion of pyrolysis oil, pyrolysis gas and CNTs from co-pyrolysis of biomass and plastics. [Display omitted] • Aromatic hydrocarbons and phenols were the main content obtained by torrefaction. • CO 2 torrefaction exhibited higher gas and lower bio-oil yield than N 2 torrefaction. • Production of liquid oil, CNTs and gas from torrefied biomass and plastics. • Strategies to facilitate biomass high value on products conversion were provided. [ABSTRACT FROM AUTHOR]

Prelithiation technology has emerged as an enabling approach towards the practical deployment of Silicon negative electrode‐based Li‐Ion batteries, leading to significant advancement in initial Coulombic efficiency (ICE), energy density and cycle life. In this study, an electrochemical prelithiation has been applied to Multi‐Walled Carbon Nanotubes (MWCNTs)‐containing Silicon‐rich Silicon/Graphite‐based negative electrode, eliminating almost ~51.03 % of its first irreversible capacity losses. In contrast, a benchmarking negative electrode utilizing Carbon black (Super P) as conductive additive is found to demonstrate a reduction of ~39.55 % after prelithiation, which is considerably lower compared to MWCNTs‐based electrode system. Post‐mortem analysis using Energy‐dispersive X‐ray (EDX) analysis with a Scanning Electron Microscope (SEM) and Attenuated Total Reflection Fourier Transform Infrared Spectroscopy (ATR‐FTIR) shows disparities between pristine‐cycled and prelithiated‐cycled negative electrodes. Overall, prelithiation enabled MWCNTs can be regarded as an essential additive component in Silicon‐based negative electrode systems for high‐energy density Li‐Ion batteries. [ABSTRACT FROM AUTHOR]

This review delves into the progress made in additive manufacturing through the incorporation of conductive fillers in nanocomposites. Emphasizing the critical role of percolation and conductivity, the study highlights advancements in material selection, particularly focusing on carbon nanotubes with low percolation thresholds. The practical applications of these nanocomposites in additive manufacturing polymer composites are explored, emphasizing the understanding of percolation thresholds. Furthermore, the present review paper investigates the potential of these materials as lightweight alternatives for electromagnetic interference shielding (EMI), particularly in key sectors such as automotive and aerospace industries. The integration of advanced materials, modeling techniques, and standardization is discussed as pivotal for successful implementation. Overall, the review underscores the significant strides in enhancing electrical properties and electromagnetic interference shielding capabilities through the strategic use of conductive filler nanocomposites in additive manufacturing. [ABSTRACT FROM AUTHOR]

Adrenaline (AD) is important in information transmission through the human central nervous system. Considering the significant biochemical functions of AD, the development of electrochemical sensors capable of detecting AD levels in living organisms has attracted considerable interest. In this study, AD was detected using electrochemical sensors developed based on Au nanoparticles/ionic liquids/N‐ and P‐co‐doped carbon nanotubes‐modified carbon cloth (AuNPs/ILs/N,P‐MWCNTs/CC) electrodes. AuNPs/ILs/N,P‐MWCNTs/CC composites were prepared on carbon cloth (CC) substrates using ionic liquids (ILs), N‐ and P‐co‐doped multi‐walled carbon nanotubes (N,P‐MWCNTs), and Au nanoparticles (AuNPs) as modified materials. The effects of pH and scanning speed were optimized and tested on the prepared composites. The results of cyclic voltammetry (CV) and differential pulse voltammetry (DPV) experiments showed that the modified ILs, N,P‐MWCNTs, and AuNPs effectively improved the oxidation performance of AD. In addition, the linear range obtained from the DPV scans of the AuNPs/ILs/N,P‐MWCNTs/CC composite material was 30–505 μmol/L, with a detection limit of 0.31 μmol/L. The fabricated sensors have good sensitivity (6.9 μA·mM−1·cm−2) for AD of 30–505 μM. Therefore, the electrochemical sensing method based on the AuNPs/ILs/N,P‐MWCNTs/CC composite material is a promising and reliable AD detection technology that also exhibits good selectivity in the presence of interfering substances such as folic acid and ibuprofen. In practical applications, this material can help realize real‐time AD detection to determine whether athletes use doping and other illegal drugs before competitions and to perform synchronous detection. [ABSTRACT FROM AUTHOR]

Molybdenum disulfide (MoS2) is a promising alternative to graphite anodes in battery materials. Therefore, it is critical to scrutinize their structural stability and charge storage capacity during battery operation. Herein, freestanding electrodes consisting of MoS2‐incorporated carbon nanotube aerogels are fabricated using a simple yet scalable hydrothermal method, as used in lithium‐ion batteries. The outer nitrogen‐doped graphitic carbon (NGr) layers support efficient charge transport, even under a substantial compressive environment, and improve the structural integrity, showing significant improvements in battery performance, such as a high rate capacity of 820 mAh g−1 at the current density of 5 A g−1 and 94% capacity retention after 170 cycles (1170 mAh g−1 at 1 A g−1 after 170 cycles), even in the absence of polymer binders and conductive additives. The resulting NGr/MoS2/single‐walled carbon nanotubes freestanding electrodes have great potential to increase the volumetric and gravimetric energy density of batteries. [ABSTRACT FROM AUTHOR]

Herein, a new energy cycle called the "hydrogen iodide (HI) cycle" is proposed that involves the repeated generation of solar hydrogen and battery power. Solar hydrogen generation using an HI solution allows for the use of a narrow‐bandgap photocatalyst. It is demonstrated that the addition of single‐walled carbon nanotubes (SWCNTs) effectively enhances solar hydrogen generation from HI solution with methylammonium lead iodide. Electron microscopy observations and spectroscopic experiments reveal that SWCNTs improve hydrogen generation by adsorbing byproduct iodine molecules. Additionally, a zinc‐iodine battery, utilizing paper I@SWCNTs recovered from the photocatalyst test cell and zinc metal, operates efficiently with an initial cell voltage of approximately 1.2 V. The battery's capacity, corresponding to the amount of encapsulated iodine molecules, indicates that SWCNTs can effectively adsorb the byproduct iodine molecules within the photocatalyst test cell. It is also discussed that the electrolyte solution after the discharge experiment should include iodide ions, indicating that the solution after battery discharge returns to the starting point of the "HI cycle." Raman measurements reveal that I@SWCNTs are transformed back into empty tubes during the discharge experiment. Therefore, SWCNTs can be repeatedly used in the new cyclic energy scheme referred to as the "HI cycle." [ABSTRACT FROM AUTHOR]

The electrochemical reduction of CO2 (eCO2RR) that exclusively produces one product at industrial current density is crucial for the substantial storage of renewable energy. Modulating the electronic structure of atomically dispersed catalysts can effectively regulate the adsorption of rate‐determining‐step intermediates to achieve the desired products. Here, the study constructs a hybrid catalyst consisting of single Ag atoms and Ag atomic clusters supported on nitrogen‐doped multi‐walled carbon nanotubes that can effectively regulate the important intermediate structure of *COOH. The X‐ray photoelectron and X‐ray absorption near‐edge spectroscopies demonstrate that turning Ag single atoms into Ag clusters can weaken the electron transfer between Ag–N and present a relatively rich electron state. Thus, the rate‐determining step of *COOH massive formation is significantly accelerated, as proven by in situ synchrotron infrared spectroscopy and density functional theory calculations. Using this strategy, a CO Faradaic efficiency outperforming 99% from −0.3 to −0.8 V (vs reversible hydrogen electrode) with current densities above 200 mA cm−2 and a half‐cell energetic efficiency of 86% is achieved. This work highlights a promising approach to advancing synergistic catalysts for achieving more controllable and efficient eCO2RR. [ABSTRACT FROM AUTHOR]

In this paper, we have developed a theoretical formalism to investigate the nonlinear absorption of high-power Hermite cosh-Gaussian laser beam in arrays of cylindrical carbon nanotubes in the presence of an external static magnetic field. As the incident Hermite cosh-Gaussian laser beam interacts with the carbon nanotubes, the atoms associated with this medium get excited and became ionized resulting to form the preformed plasma. The field of laser beam radiation causes to displace the electrons cylinder with respect to ion cylinder. Due to the displacement of electron cylinder, an electrostatic restoration force will be taken in to consideration and this causes the nonlinearity. An analytic expression of effective nonlinear absorption coefficient of Hermite cosh-Gaussian laser beam is calculated. The maximum nonlinear effective absorption is achieved as the laser beam frequency approaches near the 1 / 2 times the electron plasmon frequency. The absorption process of laser beam on the surface of carbon nanotube enhanced in the presence of static magnetic field. The absorption of laser beam is strongly dependent on various parameters such as electron cyclotron frequency, decentered parameter, electron–ion collisional frequency, transverse propagation distance, laser mode index, and beam width parameter. This tunable and enhanced laser beam absorption on the surface of carbon nanotube might be applicable in electron heating and high harmonic generation. [ABSTRACT FROM AUTHOR]

This article simply aims to compare two case studies concerning the purification, using carbon nanotubes, of water contaminated by the following two different common pollutants: benzoic acid and diesel. In particular, the aim is to highlight how the different natures of both of the polluting molecules and the carbon nanotubes play a fundamental role in water treatment. These two pollutants were taken into consideration because of their different chemical natures: benzoic acid is a polar pollutant, while the molecules present in diesel are substantially nonpolar. The carbon nanotubes used were both functionalized and nonfunctionalized. Functionalization is a process that allows for the introduction of functional groups onto the surface of carbon nanotubes. In this research, carboxylic functionalization was performed, which allowed for the insertion of carboxylic groups through attacks with sulfuric and nitric acids. Thanks to the results obtained, it was possible to quantify the optimization of the purification process depending on the types of carbon nanotubes and polluting molecules considered. The functionalized nanotubes exhibited greater performances in the treatment of water contaminated by benzoic acid compared to the nonfunctionalized ones. Instead, in the treatment of water contaminated by diesel, a greater purification capacity was shown by the nonfunctionalized carbon nanotubes compared to the functionalized ones. [ABSTRACT FROM AUTHOR]

Due to a rise in industrial pollutants in modern life, the climate and energy crisis have grown more widespread. One of the best ways to deal with dye degradation, hydrogen production, and carbon dioxide reduction issues is the photocatalytic technique. Among various methods, catalytic technology has demonstrated tremendous promise in recent years as a cheap, sustainable, and environmentally benign technology. The expeditious establishment of carbon-based metal nanoparticles as catalysts in the disciplines of materials and chemical engineering for catalytic applications triggered by visible light is largely attributed to their advancement. There have been many wonderful catalysts created, but there are still many obstacles to overcome, which include the cost of catalysts being reduced and their effectiveness being increased. Carbon-based materials exhibit a unique combination of characteristics that make them ideal catalysts for various reaction types. These characteristics include an exceptional electrical conductivity, well-defined structures at the nanoscale, inherent water repellency, and the ability to tailor surface properties for specific applications. This versatility allows them to be effective in diverse catalytic processes, encompassing organic transformations and photocatalysis. The emergence of carbon-based nanostructured materials, including fullerenes, carbon dots, carbon nanotubes, graphitic carbon nitride, and graphene, presents a promising alternative to conventional catalysts. This review focuses on the diverse functionalities of these materials within the realm of catalysis materials for degradation, hydrogen production, and carbon dioxide reduction. Additionally, it explores the potential for their commercialization, delving into the underlying mechanisms and key factors that influence their performance. It is anticipated that this review will spur more research to develop high-performance carbon-based materials for environmental applications. [ABSTRACT FROM AUTHOR]

Toxic intermediates in food caused by chloramphenicol (CP) and furazolidone (FZ) have gained interest in research toward their detection. Hence, fast, reliable, and accurate detection of CP and FZ in food products is of utmost importance. Here, a novel molybdenum disulfide-connected carbon nanotube aerogel/poly (3,4-ethylenedioxythiophene) [MoS2/CNTs aerogel/PEDOT] nanocomposite materials are constructed and deposited on the pretreated carbon paste electrode (PCPE) by a facile eletropolymerization method. The characterization of MoS2/CNTs aerogel/PEDOT nanocomposite was analyzed by scanning electron microscopy (SEM), cyclic voltammetry, and differential pulse voltammetry. The modified MoS2/CNTs aerogel/PEDOT nanocomposite has improved sensing characteristics for detecting CP and FZ in PBS solution. For this work, we have studied various parameters like electrocatalytic activity, the effect of scan rates, pH variation studies, and concentration variation studies. Under optimum conditions, the modified electrode exhibited superior sensing ability compared to the bare and pretreated CPE. This improvement in electrocatalytic activity can be the higher conductivity, larger surface area, increased heterogeneous rate constant, and presence of more active sites in the MoS2/CNTs aerogel/PEDOT nanocomposite. The modified electrode demonstrated distinct electrochemical sensing toward the individual and simultaneous analysis of CP and FZ with a high sensitivity of 0.701 µA. µM−1.cm−2 for CP and 0.787 µA. µM−1.cm−2 for FZ and a low detection limit of 3.74 nM for CP and 3.83 nM for FZ with good reproducibility, repeatability, and interferences. Additionally, the prepared sensor effectively detects CP and FZ in food samples (honey and milk) with an acceptable recovery range and a relative standard deviation below 4%. [ABSTRACT FROM AUTHOR]

The present work intended to explore the synergistic effects of incorporating carbon nanotubes infused with magnesium oxide nanofluid and dragon fruit extract as a natural additive in photovoltaic–thermal collector systems on its performance in terms of both electrical and thermal energy yield. The proposed methodology was meticulously developed and implemented to assess the efficiency of a hybrid system integrating nano-phase change material and nanofluid in a photovoltaic–thermal configuration. This novel setup was subjected to a comprehensive comparative analysis against a traditional liquid-cooled photovoltaic–thermal system and a standalone photovoltaic module. The study also encompassed variations in cooling techniques, including water with different flow rates for the photovoltaic–thermal system, and the incorporation of nano-phase change material and nanofluid with varying concentrations and flow rates within the hybrid collector. The outcomes demonstrated that at these respective flow rates, the maximum thermal efficiency of the photovoltaic–thermal collector stood at 66.28% and 74.02%. Likewise, the peak electrical efficiency at the same flow rates was recorded as 20.79% and 21.96%. The outcomes of the investigation highlight the higher thermal conductivity of the nanofluid compared to the base fluid, leading to a slight augmentation in fluid density and viscosity. The results obtained from this investigation were found to be consistent with those documented in existing scientific literature. [ABSTRACT FROM AUTHOR]

For the first time the sensitive determination of carbendatim (CRB) is reported utilizing a well-designed sensing architecture based on vanadium diselenide-multiwalled carbon nanotube (VSMC). FTIR, XRD, FESEM, EDS, and EIS were employed to evaluate the sensor's structural integrity, and the results demonstrated the successful integration of nanomaterials, resulting in a robust and sensitive electrochemical sensor. Cyclic voltammetry (CV) and chronoamperometric (CA) investigations showed that the sensor best performed at pH 8.0 (BRB) with an excellent detection limit of 9.80 nM with a wide linear range of 0.1 to 10.0 µM. A more thermodynamically viable oxidation of CRB was observed at the VSMC/GCE, with a shift of 200 mV in peak potential towards the less positive side compared with the unmodified GCE. In addition, the sensor demonstrated facile heterogeneous electron transfer, favorable anti-fouling traits in the presence of a wide range of interferents, good stability, and reproducible analytical performance. Finally, the developed sensor was validated for real-time quantification of CRB from spiked water, food, and bio-samples, which depicted acceptable recoveries (98.6 to 101.5%) with RSD values between 0.35 and 2.23%. Further, to derive the possible sensing mechanism, the valence orbitals projected density of states (PDOS) for C, H, and N atoms of an isolated CRB molecule, VSe2 + CNT and VSe2 + CNT + CRB were calculated using density functional theory (DFT) calculations. The dominant charge transfer from the valence 2p-orbitals of the C and N atoms of CRB to CNT is responsible for the electrochemical sensing of CRB molecules. [ABSTRACT FROM AUTHOR]

A nanocomposite of cobalt nanoparticle (CoNP) functionalized carbon nanotube (Co@CNT) was prepared and used to modify a glassy carbon electrode (Co@CNT/GCE). Characterization indicates the morphology of Co@CNT is CoNPs adhering on CNTs. With the nano-interface, Co@CNT provides large surface area, high catalytic activity, and efficient electron transfer, which makes Co@CNT/GCE exhibiting satisfactory electrochemical response toward quercetin (QC) and folic acid (FA). The optimum pH values for the detection of FA and QC are 7.0 and 3.0, respectively. The saturated absorption capacity (Γ*) and catalytic rate constant (kcat) of Co@CNT/GCE for QC and FA are calculated as 1.76 × 10−9, 3.94 × 10−10 mol∙cm−2 and 3.04 × 102, 0.569 × 102 M−1∙s−1. The linear range for both FA and QC is estimated to be 5.0 nM–10 μM, and the LODs (3σ/s) were 2.30 nM and 2.50 nM, respectively. The contents of FA and QC in real samples determined by Co@CNT/GCE are comparable with the results determined by HPLC. The recoveries were in the range 90.5 ~ 114% and the total RSD was lower than 8.67%, which further confirms the reliability of the proposed electrode for practical use. [ABSTRACT FROM AUTHOR]

Structural health monitoring (SHM) of composite materials is of great significance in various practical applications. However, it is a challenge to accurately monitor the damage of composites without affecting their mechanical properties. In this paper, an embedded sensing layer based on carbon nanotube-coated glass fiber is designed, combined with electrical resistance tomography (ERT) for in situ damage monitoring. Multi-wall carbon nanotube-coated glass fiber (MWCNT-GF) is prepared and embedded into laminates as an in situ sensing layer. Low-velocity impact experiments demonstrate that the embedded sensing layer has high compatibility with the composite laminates and has no adverse effect on its impact response; although, the energy absorption behavior of glass fiber-reinforced polymer (GFRP) laminates containing MWCNT-GF occurs about 10% earlier than that of GFRP laminates overall. ERT technology is used to analyze the laminates after a low-velocity impact test. The results show that the in situ monitoring method with the embedded MWCNT-GF sensing layer can achieve high precision in imaging localization of impact damage, and the error of the detected damage area is only 4.5%. [ABSTRACT FROM AUTHOR]

Carbon nanotubes (CNTs) are often regarded as semi-rigid, all-carbon polymers. However, unlike conventional polymers that can form 3D networks such as hydrogels or elastomers through crosslinking in solution, CNTs have long been considered non-crosslinkable under mild conditions. This perception changed with our recent discovery of UV-defluorination-driven direct crosslinking of CNTs in solution. In this study, we further investigate the thermal stability of UV-defluorination-driven crosslinked CNTs, revealing that they are metastable and decompose more readily than either pristine or fluorinated CNTs under Raman laser irradiation. Using Raman spectroscopy under controlled laser power, we examined both single-walled and multi-walled fluorinated CNTs. The results demonstrate that UV-defluorinated CNTs exhibit reduced thermal stability compared to their pristine or untreated fluorinated counterparts. This instability is attributed to the strain on the intertube crosslinking bonds resulting from the curved carbon lattice of the linked CNTs. The metallic CNTs in the crosslinked CNT networks decompose and revert to their pristine state more readily than the semiconducting ones. The inherent instability of crosslinked CNTs leads to combustion at temperatures approximately 100 °C lower than those required for non-crosslinked fluorinated CNTs. This property positions crosslinked CNTs as promising candidates for applications where mechanically robust, lightweight materials are needed, along with feasible post-use removal options. [ABSTRACT FROM AUTHOR]

The hybridization of single-walled carbon nanotubes (SWCNTs) and Cu nanoparticles offers a promising strategy for creating highly conductive and mechanically stable fillers for flexible printed electronics. In this study, we report the ultrafast synthesis of SWCNT/Cu hybrid nanostructures and the fabrication of flexible electrodes under ambient conditions through a laser-induced photo-thermal reaction. Thermal energy generated from the nonradiative relaxation of the π-plasmon resonance of SWCNTs was utilized to reduce the Cu-complex (known as a metal–organic decomposition ink) into Cu nanoparticles. We systematically investigated the effects of SWCNT concentration and output laser power on the structural and electrical properties of the SWCNT/Cu hybrid electrodes. The SWCNT/Cu electrodes achieved a minimum electrical resistivity of 46 μohm·cm, comparable to that of the metal-based printed electrodes. Mechanical bending tests demonstrated that the SWCNT/Cu electrodes were highly stable and durable, with no significant deformation observed even after 1000 bending cycles. Additionally, the electrodes showed rapid temperature increases and stable Joule heating performance, reaching temperatures of nearly 80 °C at an applied voltage of less than 3.5 V. [ABSTRACT FROM AUTHOR]

Defect-containing carbon nanotube materials were prepared by subjecting two commercial multiwalled carbon nanotubes (MWCNTs) of different purities to purification (HCl) and oxidative conditions (HNO3) and further heat treatment to remove surface oxygen groups. The as-prepared carbon materials were physicochemically characterized to observe changes in their properties after the different treatments. TEM microscopy shows morphological modifications in the MWCNTs after the treatments such as broken walls and carbon defects including topological defects. This leads to both higher surface areas and active sites. The carbon defects were analysed by Raman spectroscopy, but the active surface area (ASA) and the electrochemical active surface area (EASA) values showed that not all the defects are equally active for oxygen reduction reactions (ORRs). This suggests the importance of calculating either ASA or EASA in carbon materials with different structures to determine the activity of these defects. The as-prepared defect-containing multiwalled carbon nanotubes exhibit good catalytic performance due to the formation of carbon defects active for ORR such as edge sites and topological defects. Moreover, they exhibit good stability and methanol tolerances. The as-prepared MWCNTs sample with the highest purity is a promising defective carbon material for ORR because its activity is only related to high concentrations of active carbon defects including edge sites and topological defects. [ABSTRACT FROM AUTHOR]

The scaling of bulk Si-based transistors has reached its limits, while novel architectures such as FinFETs and GAAFETs face challenges in sub-10 nm nodes due to complex fabrication processes and severe drain-induced barrier lowering (DIBL) effects. An effective strategy to avoid short-channel effects (SCEs) is the integration of low-dimensional materials into novel device architectures, leveraging the coupling between multiple gates to achieve efficient electrostatic control of the channel. We employed TCAD simulations to model multi-gate FETs based on various dimensional systems and comprehensively investigated electric fields, potentials, current densities, and electron densities within the devices. Through continuous parameter scaling and extracting the sub-threshold swing (SS) and DIBL from the electrical outputs, we offered optimal MoS2 layer numbers and single-walled carbon nanotube (SWCNT) diameters, as well as designed structures for multi-gate FETs based on monolayer MoS2, identifying dual-gate transistors as suitable for high-speed switching applications. Comparing the switching performance of two device types at the same node revealed CNT's advantages as a channel material in mitigating SCEs at sub-3 nm nodes. We validated the performance enhancement of 2D materials in the novel device architecture and reduced the complexity of the related experimental processes. Consequently, our research provides crucial insights for designing next-generation high-performance transistors based on low-dimensional materials at the scaling limit. [ABSTRACT FROM AUTHOR]