Search Results (52)

Carbon nanotubes (CNTs) functionalized with metal oxides exhibit synergistic properties that enhance their performance across various applications, particularly in electrochemistry. Recent advancements have highlighted the potential of CNT–metal oxide heterostructures, with a specific focus on their electrochemical properties, which are pivotal for applications in sensors, supercapacitors, batteries, and catalytic systems. Among these, nickel oxide (NiO)-modified CNTs have garnered significant attention due to their cost-effectiveness, facile synthesis, and promising gas-sensing capabilities. This study employs quantum-chemical calculations within the framework of density functional theory (DFT) to elucidate the interaction mechanisms between CNTs and NiO. The results demonstrate that the adsorption process leads to the formation of stable CNT-NiO complexes, with detailed analysis of adsorption energies, equilibrium distances, and electronic structure modifications. The single-electron spectra and density of states (DOS) of the optimized complexes reveal significant alterations in the electronic properties, particularly the modulation of the energy gap induced by surface and edge functionalization. Furthermore, the interaction of CNT-NiO composites with acetone (C₃H₆O) and carbon dioxide (CO₂) is modeled, revealing a physisorption-dominated mechanism. The adsorption of these gases induces notable changes in the electronic properties and charge distribution within the system, underscoring the potential of CNT-NiO composites for gas-sensing applications. This investigation provides a foundational understanding of the role of metal oxide modifications in tailoring the sensory activity of CNTs toward trace amounts of diverse substances, including metal atoms, inorganic molecules, and organic compounds. The findings suggest that CNT-NiO systems can serve as highly sensitive and selective sensing elements, with potential applications in medical diagnostics and environmental monitoring, thereby advancing the development of next-generation sensor technologies. Full article

Carbon nanotubes (CNTs) are widely used in electrochemical sensors due to their significant impact on the electroanalytical signal. However, there remain significant doubts regarding the origin of the improved electroanalytical response observed in CNT-based sensors, particularly concerning the precise role of CNTs in these systems. In particular, the origin of the electrochemical response is controversial, as it may be due to either electrocatalytic or non-electrocatalytic processes. The latter implies that the electroanalytical response is mainly governed by the mass transport phenomena within the porous CNT layer. This article briefly reviews the several comprehensive models based on the role of porosity (diffusion in a ‘thin-layer’) on the electrochemical behavior as well as on the electrocatalytic properties of CNTs to resolve conflicts arising from misinterpretations of the electroanalytical response of CNT-based sensors. However, even though there are some explanations and conclusions on this topic, they seem to be valuable for specific electroactive species, the type of CNTs and/or electrode architecture, the electrode surface, etc. Accordingly, general theories and conclusions are not yet defined, so different approaches to this topic are still needed, since the main phenomenological effects responsible for the nature of the electrochemical response of the electrodes modified with CNTs need to be determined in a rational way. Full article

Amperometric electrochemical sensing schemes, which are easily fabricated and can directly relate measured current with analyte concentrations, remain a promising strategy for the development of the portable, in situ detection of commonly employed adulterants. Xylazine (XYL) is a non-narcotic compound designed for veterinary use as a sedative known as Rompun^®. XYL is increasingly being abused as a recreational drug, as an opioid adulterant and, because of its chemical properties, has found unfortunate prominence as a date rape drug spiked into beverages. In this study, a systematic exploration and development of fouling-resistant, amperometric XYL sensors is presented. The sensing strategy features layer-by-layer (LBL) modification of glassy carbon electrodes (GCEs) with carbon nanotubes (CNTs) for sensitivity and the engagement of cyclodextrin host–guest chemistry in conjunction with polyurethane (PU) semi-permeable membranes for selectivity. The optimization of different materials and parameters during development created a greater fundamental understanding of the interfacial electrochemistry, allowing for a more informed subsequent design of effective sensors exhibiting XYL selectivity, effective sensitivity, rapid response times (<20 s), and low estimated limits of detection (~1 ppm). Most importantly, the demonstrated XYL sensors are versatile and robust, easily fabricated from common materials, and can effectively detect XYL at <10 ppm in both common alcoholic and non-alcoholic beverages, requiring only minimal volume (20 µL) of the spiked beverage for a standard addition analysis. Full article

Graphene and its variants exhibit excellent electrical properties for the construction of enzymatic interfaces. In particular, the direct electron transfer of glucose oxidase on the electrode surface is a very important issue in the development of enzyme-based bioelectrodes. However, the number of studies conducted to assess how pristine graphene forms different interfaces with other carbon materials is insufficient. Enzyme-based electrodes (formed using carbon materials) have been extensively applied because of their low manufacturing costs and easy production techniques. In this study, the characteristics of a single-walled carbon nanotube/graphene-combined enzyme interface are analyzed at the atomic level using molecular dynamics simulations. The morphology of the enzyme was visualized using an elastic network model by performing normal-mode analysis based on electrochemical and microscopic experiments. Single-carbon electrodes exhibited poorer electrical characteristics than those prepared as composites with enzymes. Furthermore, the composite interface exhibited 4.61- and 2.45-fold higher direct electron efficiencies than GOx synthesized with single-carbon nanotubes and graphene, respectively. Based on this study, we propose that pristine graphene has the potential to develop glucose oxidase interfaces and carbon-nanotube–graphene composites for easy fabrication, low cost, and efficient electrode structures for enzyme-based biofuel cells. Full article

Flowable electrodes, a versatile alternative to traditional solid electrodes for electrochemical applications, exhibit challenges of high viscosity and carbon content, limiting flow and device performances. This study introduces colloidal suspensions of thin multiwall carbon nanotubes (MWCNTs) with diameters of 10–15 nm as electrode materials. These thin nanotubes, stabilized in water with a surfactant, form percolated networks, exhibiting high conductivity (50 ms/cm) and stability at a low carbon content (below 2 wt%). Colloidal clustering is enhanced by weak depletion attractive interactions. The resulting suspensions display yield stress and a shear thinning behavior with a low consistency index. They can easily flow at a nearly constant shear over a broad range of shear rates. They remain electrically conductive under shear, making them a promising option for flow electrochemical applications. This work suggests that the use of depletion-induced MWVNT aggregates addresses crucial issues in flow electrochemical applications, such as membrane fragility, operating energy, and pressure. These conductive colloidal suspensions thereby offer potential advancements in device performance and lifespan. Full article

In many electro-optical devices, the conductive layer is an important key functional element. Among others, unique indium tin oxide (ITO) contacts take priority. ITO structure is widely used as the optical transparent and electrically conductive material in general optoelectronics, biosensors and electrochemistry. ITO is one of the key elements in the liquid crystal (LC) displays, spatial light modulators (SLMs) and LC convertors. It should be mentioned that not only the morphology of this layer structure but also the surface features play an important role in the study of the physical parameters of the ITO. In order to switch the surface properties (roughness, average tilt angle and surface free energy) of the ITO via the laser-oriented deposition (LOD) method, carbon nanotubes (CNTs) were implanted. In the LOD technique, the CO₂ laser (λ = 10.6 μm, P = 30 W) with the control electric grid was used. The switching of the deposition conditions was provided via the varying electrical strength of the control grid in the range of 100–600 V/cm. The diagnostics of the surfaces were performed using AFM analysis and wetting angle measurements. The components of the surface free energy (SFE) were calculated using the OWRK method. The main experimental results are as follows: the roughness increases with a rise in the electric field strength during the deposition of the CNTs; the carbon nanotubes provide a higher level of the dispersive component of SFE (25.0–31.4 mJ/m² against 22.2 mJ/m² in the case of pure ITO); the CNTs allow an increase in the wetting angle of the 5CB liquid crystal drops from 38.35° to 58.95°. Due to the possibility of the switching properties of the ITO/CNT surfaces, these modifications have potential interest in microfluidics applications and are useful for the liquid crystal’s electro-optics. Full article

In this study, we present another approach to fabricating high-performance supercapacitor electrodes by combining activated carbon particles with carbon nanotubes (AC/CNT). We synthesized activated carbon from diverse biomass sources using a carbonization process and chemical activation with KOH. By incorporating carbon nanotubes, we significantly augmented the electrode’s surface area, resulting in exceptional ion transport and a substantial increase in specific capacitance. Our investigation reveals that the optimized composition, 85:10:5 of AC, CNT, and conductive additive, achieved outstanding specific capacitance values, notably 125.6 F g⁻¹ at 1 mV s⁻¹ and 118 F g⁻¹ at 1 A g⁻¹, along with a maximum energy density of 4 Wh kg⁻¹. Electrochemical impedance spectroscopy (EIS) further demonstrated the superior charge transfer capabilities of these electrodes, notably at a frequency range from 100 kHz to 10 mHz. Additionally, our research highlights the influence of different biomass precursors, such as apricot kernels, walnut shells, and rice husks, on the electrochemical behavior of these electrodes. Overall, this study provides valuable insights into the development of high-performance supercapacitors, emphasizing the potential of diverse biomass sources in optimizing electrode materials. Full article

In this study, we present an innovative ion-beam doping technique for the controlled modification of the near-surface region of multi-walled carbon nanotubes (MWCNTs) aimed at creating pyridinic and pyrrolic nitrogen defects in their walls. This method involves the irradiation of MWCNTs with nitrogen ions using a high-dose ion implanter, resulting in the incorporation of nitrogen atoms into the nanotube structure. The structural and chemical changes induced by the ion-beam treatment were thoroughly characterized. Scanning electron microscopy (SEM) analysis revealed subtle changes in nanotube morphology, while X-ray diffraction (XRD) measurements exhibited altered peak intensities and a shift in the (002) reflection peak, indicating structural modifications, which correlates with transmission electron microscopy (TEM) data. X-ray photoelectron spectroscopy (XPS) analysis confirmed the successful embedding of nitrogen, mainly in pyridinic and pyrrolic configurations, as evidenced by the presence of corresponding lines in the N1s spectrum. Our findings demonstrate the feasibility of precisely engineering nitrogen defects in MWCNTs using the ion-beam doping technique. This approach is expected to be promising for the use of carbon nanotubes surface-functionalized with nitrogen atoms in the development of new devices for electronics, electrochemistry, catalysis, etc. Full article

High mass loading (ca. 30 mg/cm²) electrodes were prepared with carbon recovered from catalytic methane cracking (MC). As-fabricated supercapacitors displayed 74% of capacitance retention from 6 mA/cm² to 60 mA/cm² and a Ragone plot’s slope of −7 Wh/kW (compared to 42% and −31 Wh/kW, respectively, for high mass loading devices fabricated with commercial carbon). The high-rate capability of the MC-recovered carbon is attributed to the presence of carbon black and carbon nanotubes produced during the reaction, which likely increased the electronic and ionic conductivity within the electrode. These results suggest that the by-product of this hydrogen generation route might be a suitable active material for supercapacitors. Full article

3D-RISM-KH molecular solvation theory based on statistical mechanics has been an engine of the multiscale methods framework, which also includes molecular simulation techniques. Its applications range from the solvation energy of small molecules to the phase behavior of polymers and biomolecules. Molecular solvation theory predicts and explains the molecular mechanisms and functioning of a variety of chemical and biomolecular systems. This includes the self-assembly and conformational stability of synthetic organic rosette nanotubes (RNTs), the aggregation of peptides and proteins related to neurodegeneration, the binding of ligands to proteins, and the solvation properties of biomolecules related to their functions. The replica RISM-KH-VM molecular solvation theory predicts and explains the structure, thermodynamics, and electrochemistry of electrolyte solutions sorbed in nanoporous carbon supercapacitor electrodes, and is part of recent research and development efforts. A new quasidynamics protocol couples multiple time step molecular dynamics (MTS-MD) stabilized with an optimized isokinetic Nosé–Hoover (OIN) thermostat driven by 3D-RISM-KH mean solvation forces at gigantic outer time steps of picoseconds, which are extrapolated forward at short inner time steps of femtoseconds with generalized solvation force extrapolation (GSFE). The OIN/3D-RISM-KH/GSFE quasidynamics is implemented in the Amber Molecular Dynamics package. It is validated on miniprotein 1L2Y and protein G in ambient aqueous solution, and shows the rate of sampling 150 times faster than in standard MD simulations on these biomolecules in explicit water. The self-consistent field version of Kohn–Sham DFT in 3D-RISM-KH mean solvation forces is implemented in the Amsterdam Density Functional (ADF) package. Its applications range from solvation thermochemistry, conformational equilibria, and photochemistry to activation barriers of different nanosystems in solutions and ionic liquids. Full article

We developed and optimized an electrocatalytic filtration system to catalytically hydrodechlorinate chlorophenolic compounds. A key part of the system was the cathode, which consisted of a filter constructed with electroactive carbon nanotubes (CNTs) functionalized with atomically precise gold nanoclusters (AuNCs). In the functional membrane electrode, the AuNCs attached to the CNTs functioned as a highly effective hydrodechlorination catalyst. Additionally, the ligands of the AuNCs facilitated the binding of the AuNCs with the CNT and protected the Au core from agglomeration. Atomic H* was the primary reactive species in the system, but direct reduction by cathode electrons also contributed to the elimination of 2,4-dichlorophenol (2,4-DCP) by hydrodechlorination. The generated atomic H* was able to break the C–Cl bond to achieve the rapid hydrodechlorination of 2,4-DCP into phenol, with 91.5% 2,4-DCP removal within 120 min. The AuNC catalysts attached to the CNT exceeded the best catalytic activity of larger nanoparticles (e.g., AuNPs), while the flow-through construction performed better than a standard batch reactor due to the convection-enhanced mass transport. The study provides an environmentally friendly strategy for the elimination of pervasive halogenated organic contaminants using a highly efficient, stable and recyclable system for hydrodechlorination that integrates nanofiltration and electrochemistry. Full article

The engineering of carbon nanotubes in the last decades resulted in a variety of applications in electronics, electrochemistry, and biomedicine. A number of reports also evidenced their valuable application in agriculture as plant growth regulators and nanocarriers. In this work, we explored the effect of seed priming with single-walled carbon nanotubes grafted with Pluronic P85 polymer (denoted P85-SWCNT) on Pisum sativum (var. RAN-1) seed germination, early stages of plant development, leaf anatomy, and photosynthetic efficiency. We evaluated the observed effects in relation to hydro- (control) and P85-primed seeds. Our data clearly revealed that seed priming with P85-SWCNT is safe for the plant since it does not impair the seed germination, plant development, leaf anatomy, biomass, and photosynthetic activity, and even increases the amount of photochemically active photosystem II centers in a concentration-dependent manner. Only 300 mg/L concentration exerts an adverse effect on those parameters. The P85 polymer, however, was found to exhibit a number of negative effects on plant growth (i.e., root length, leaf anatomy, biomass accumulation and photoprotection capability), most probably related to the unfavorable interaction of P85 unimers with plant membranes. Our findings substantiate the future exploration and exploitation of P85-SWCNT as nanocarriers of specific substances promoting not only plant growth at optimal conditions but also better plant performance under a variety of environmental stresses. Full article

Electrochemical sensors consisting of screen-printed electrodes (SPEs) are recurrent devices in the recent literature for applications in different fields of interest and contribute to the expanding electroanalytical chemistry field. This is due to inherent characteristics that can be better (or only) achieved with the use of SPEs, including miniaturization, cost reduction, lower sample consumption, compatibility with portable equipment, and disposability. SPEs are also quite versatile; they can be manufactured using different formulations of conductive inks and substrates, and are of varied designs. Naturally, the analytical performance of SPEs is directly affected by the quality of the material used for printing and modifying the electrodes. In this sense, the most varied carbon nanomaterials have been explored for the preparation and modification of SPEs, providing devices with an enhanced electrochemical response and greater sensitivity, in addition to functionalized surfaces that can immobilize biological agents for the manufacture of biosensors. Considering the relevance and timeliness of the topic, this review aimed to provide an overview of the current scenario of the use of carbonaceous nanomaterials in the context of making electrochemical SPE sensors, from which different approaches will be presented, exploring materials traditionally investigated in electrochemistry, such as graphene, carbon nanotubes, carbon black, and those more recently investigated for this (carbon quantum dots, graphitic carbon nitride, and biochar). Perspectives on the use and expansion of these devices are also considered. Full article

To meet the requirements of novel therapies, effective treatments should be supported by diagnostic tools characterized by appropriate analytical and working parameters. These are, in particular, fast and reliable responses that are proportional to analyte concentration, with low detection limits, high selectivity, cost-efficient construction, and portability, allowing for the development of point-of-care devices. Biosensors using nucleic acids as receptors has turned out to be an effective approach for meeting the abovementioned requirements. Careful design of the receptor layers will allow them to obtain DNA biosensors that are dedicated to almost any analyte, including ions, low and high molecular weight compounds, nucleic acids, proteins, and even whole cells. The impulse for the application of carbon nanomaterials in electrochemical DNA biosensors is rooted in the possibility to further influence their analytical parameters and adjust them to the chosen analysis. Such nanomaterials enable the lowering of the detection limit, the extension of the biosensor linear response, or the increase in selectivity. This is possible thanks to their high conductivity, large surface-to-area ratio, ease of chemical modification, and introduction of other nanomaterials, such as nanoparticles, into the carbon structures. This review discusses the recent advances on the design and application of carbon nanomaterials in electrochemical DNA biosensors that are dedicated especially to modern medical diagnostics. Full article