C — Open Access Carbon Research Journal

Graphene is one of the new materials which has shown a large impact on the electronic industry due to its versatile properties, such as high specific surface area, high electrical conductivity, chemical stability, and large spectrum of electrochemical properties. The graphene material-based electronic industry has provided flexible devices which are inexpensive, simple and low power-consuming sensor tools, therefore opening an outstanding new door in the field of portable electronic devices. All these attractive advantages of graphene give a platform for the development of a new generation of devices in both food and environmental applications. Lipid-based sensors have proven to be a good route to the construction of novel devices with improved characteristics, such as fast response times, increased sensitivity and selectivity, and the possibility of miniaturization for the construction of portable biosensors. Therefore, the incorporation of a lipid substrate on graphene electrodes has provided a route to the construction of a highly sensitive and selective class of biosensors with fast response times and portability of field applications for the rapid detection of toxicants in the environment and food products. Full article

Carbon nanotubes have received enormous attention in the development of electrochemical sensors by promoting electron transfer reactions, decreasing the work overpotential within great surface areas. The growing concerns about environmental health emphasized the necessity of continuous monitoring of pollutants. Pesticides have been successfully used to control agricultural and public health pests; however, intense use can cause a number of damages for biodiversity and human health. In this sense, carbon nanotubes-based electrochemical sensors have been proposed for pesticide monitoring combining different electrode modification strategies and electroanalytical techniques. In this paper, we provide a review of the recent advances in the use of carbon nanotubes for the construction of electrochemical sensors dedicated to the environmental monitoring of pesticides. Future directions, perspectives, and challenges are also commented. Full article

Carbon dioxide (CO₂) emissions are one of the main reasons for the increase in greenhouse gasses in the earth’s atmosphere and carbon capture and sequestration (CCS) is known as an effective method to reduce CO₂ emissions on a larger scale, such as for fossil energy utilization systems. In this paper, the feasibility of capturing CO₂ using cryogenic liquefaction and improving the capture rate by expansion will be discussed. The main aim was to design an energy-saving scheme for an IGCC (integrated gasification combined cycle) power plant with CO₂ cryogenic liquefaction capture. The experimental results provided by the authors, using the feed gas specification of a 740 MW IGCC General Electric (GE) combustion power plant, demonstrated that using an orifice for further expanding the vent gas after cryogenic capture from 57 bar to 24 bar gave an experimentally observed capture rate up to 65%. The energy-saving scheme can improve the overall CO₂ capture rate, and hence save energy. The capture process has also been simulated using Aspen HYSYS simulation software to evaluate its energy penalty. The results show that a 92% overall capture rate can be achieved by using an orifice. Full article

Artificial hair flow sensors were fabricated using piezoresistive, radially grown carbon nanotube arrays on glass fibers and investigated for their dynamic aerodynamic response as measured within an instrumented plane-wave tube. The sensors were experimentally observed to provide both a large bandwidth of operation below first resonance and a strong resonance response at selected frequencies above first resonance. The frequency of first resonance was easily tunable by adjusting the length of the exposed hair and could be made to vary from a few hundred hertz to over 13 kHz. Higher frequency bands were accessible for a given hair length using higher-order resonance modes, up to five of which were observed. All of the responses were understood and modeled using a vibrating Euler-Bernoulli beam analysis. Full article

Dual-intercalation batteries implement graphite electrodes as both cathodes and anodes and offer high specific energy, inexpensive and environmentally sustainable materials, and high operating voltages. Our research investigated the influence of surface composition on capacities and cycling efficiencies of chemically functionalized all-graphite battery electrodes. We subjected coreshell spherical particles and synthetic graphite flakes to high-temperature air oxidation, and hydrogenation to introduce, respectively, –OH, and –H surface functional groups. We identified noticeable influences of electrode surface chemistry on first-cycle efficiencies and charge storage densities of anion and cation intercalation into graphite electrodes. We matched oxidized cathodes and hydrogenated anodes in dual-ion batteries and improved their overall performance. Our approach provides novel fundamental insight into the anion intercalation process and suggests inexpensive and environmentally sustainable methods to improve performance of these grid-scale energy storage systems Full article

In this study, the vibrational properties of single- and double-layer graphene sheets (GSs) with attached nanoparticles are analyzed based on the nonlocal elasticity theory. The potential applications of atomic-scale mass sensing are presented using GSs with simply supported boundary condition. The frequency equation for GSs with an attached nanoparticle is derived to investigate the vibration frequency of the GSs under thermal environment. Using the proposed model, the relationship between the frequency shifts of graphene-based mass sensor and the attached nanoparticles is obtained. The nonlocal effect and the temperature dependence on the variation of frequency shifts with the attached nanomass and the positions on the GS are investigated and discussed in detail. The obtained results show that the nanomass can be easily detected by using GS resonator which provides a highly sensitive nanomechanical element in sensor systems. The vibrational frequency shift of GS increases with increasing the temperature dependence. The double-layer GSs (DLGSs) have higher sensitivity than the single-layer GSs (SLGSs) due to high frequency shifts. Full article

Growing demand for developing ultrasensitive electrochemical bioassays has led to the design of numerous signal amplification strategies. In this context, carbon-based nanomaterials have been demonstrated to be excellent tags for greatly amplifying the transduction of recognition events and simplifying the protocols used in electrochemical biosensing. This relevant role is due to the carbon-nanomaterials’ large surface area, excellent biological compatibility and ease functionalization and, in some cases, intrinsic electrochemistry. These carbon-based nanomaterials involve well-known carbon nanotubes (CNTs) and graphene as well as the more recent use of other carbon nanoforms. This paper briefly discusses the advantages of using carbon nanostructures and their hybrid nanocomposites for amplification through tagging in electrochemical biosensing platforms and provides an updated overview of some selected examples making use of labels involving carbon nanomaterials, acting both as carriers for signal elements and as electrochemical tracers, applied to the electrochemical biosensing of relevant (bio)markers. Full article

The expansion product from the sulfuric acid dehydration of para-nitroaniline has been characterized and studied for CO₂ adsorption. The X-ray photoelectron spectroscopy (XPS) characterization of the foam indicates that both N and S contents (15 and 9 wt%, respectively) are comparable to those separately reported for nitrogen- or sulfur-containing porous carbon materials. The analysis of the XPS signals of C1s, O1s, N1s, and S2p reveals the presence of a large number of functional groups and chemical species. The CO₂ adsorption capacity of the foam is 7.9 wt% (1.79 mmol/g) at 24.5 °C and 1 atm in 30 min, while the integral molar heat of adsorption is 113.6 kJ/mol, indicative of the fact that chemical reactions characteristic of amine sorbents are observed for this type of carbon foam. The kinetics of adsorption is of pseudo-first-order with an extrapolated activation energy of 18.3 kJ/mol comparable to that of amine-modified nanocarbons. The richness in functionalities of H₂SO₄-expanded foams represents a valuable and further pursuable approach to porous carbons alternative to KOH-derived activated carbons. Full article

Sodium ion batteries (SIBs) have attracted lots of attention over last few years due to the abundance and wide availability of sodium resources, making SIBs the most cost-effective alternative to the currently used lithium ion batteries (LIBs). Many efforts are underway to find effective anodes for SIBs since the commercial anode for LIBs, graphite, has shown very limited capacity for SIBs. Among many different types of carbons, hard carbons—especially these derived from biomass—hold a great deal of promise for SIB technology thanks to their constantly improving performance and low cost. The main scope of this mini-review is to present current progress in preparation of negative electrodes from biomass including aspects related to precursor types used and their impact on the final carbon characteristics (structure, texture and composition). Another aspect discussed is how certain macro- and microstructure characteristics of the materials translate to their performance as anode for Na-ion batteries. In the last part, current understanding of factors governing sodium insertion into hard carbons is summarized, specifically those that could help solve existing performance bottlenecks such as irreversible capacity, initial low Coulombic efficiency and poor rate performance. Full article

Carbon nanostructural materials have gained the spotlight as promising anode materials for energy storage; they exhibit unique physico-chemical properties such as large surface area, short Li⁺ ion diffusion length, and high electrical conductivity, in addition to their long-term stability. However, carbon-nanostructured materials have issues with low areal and volumetric densities for the practical applications in electric vehicles, portable electronics, and power grid systems, which demand higher energy and power densities. One approach to overcoming these issues is to design and apply a three-dimensional (3D) electrode accommodating a larger loading amount of active anode materials while facilitating Li⁺ ion diffusion. Furthermore, 3D nanocarbon frameworks can impart a conducting pathway and structural buffer to high-capacity non-carbon nanomaterials, which results in enhanced Li⁺ ion storage capacity. In this paper, we review our recent progress on the design and fabrication of 3D carbon nanostructures, their performance in Li-ion batteries (LIBs), and their implementation into large-scale, lightweight, and flexible LIBs. Full article

Carbon aerogels are highly porous materials with a large inner surface area. Due to their high electrical conductivity they are excellent electrode materials in supercapacitors. Their brittleness, however, imposes certain limitations in terms of applicability. In that context, novel carbon aerogels with varying degree of flexibility have been developed. These highly porous, light aerogels are characterized by a high surface area and possess pore structures in the micrometer range, allowing for a reversible deformation of the aerogel network. A high ratio of pore size to particle size was found to be crucial for high flexibility. For dynamic microstructural analysis, compression tests were performed in-situ within a scanning electron microscope allowing us to directly visualize the microstructural flexibility of an aerogel. The flexible carbon aerogels were found to withstand between 15% and 30% of uniaxial compression in a reversible fashion. These findings might stimulate further research and new application fields directed towards flexible supercapacitors and batteries. Full article

The performance of synergetic hybrid aerogel materials of vanadia and graphene as electrode materials in supercapacitors was evaluated. The hybrid materials were synthesized by two methods. In Method I, premade graphene oxide (GO) hydrogel was first chemically reduced by L-ascorbic acid and then soaked in vanadium triisopropoxide solution to obtain V₂O₅ gel in the pores of the reduced graphene oxide (rGO) hydrogel. The gel was supercritically dried to obtain the hybrid aerogel. In Method II, vanadium triisopropoxide was hydrolyzed from a solution in water with GO particles uniformly dispersed to obtain the hybrid gel. The hybrid aerogel was obtained by supercritical drying of the gel followed by thermal reduction of GO. The electrode materials were prepared by mixing 80 wt % hybrid aerogel with 10 wt % carbon black and 10 wt % polyvinylidene fluoride. The hybrid materials in Method II showed higher capacitance due to better interactions between vanadia and graphene oxide particles and more uniform vanadia particle distribution. Full article

In this work, we investigated a simple one-step process for the formation of chemical bonds between multi-walled carbon nanotubes (MWCNTs) and benzyl-type side chain radicals generated by UV photolysis of polystyrene derivatives containing the chloromethyl (–CH₂Cl) group. Poly(4-chloromethyl)styrene, or styrene/4-(chloromethyl)styrene random copolymer, was mixed with MWCNTs in 1-methyl-2-pyrrolidone and irradiated with ultraviolet (UV) light. Films of polymer/MWCNT mixtures before and after UV irradiation were fabricated, and then examined by X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy. According to the XPS analysis, the amount of Cl atoms in the mixture was found to decrease upon UV irradiation, indicating that the Cl atoms generated by photolysis of chloromethyl groups escaped from the reaction system in the form of gaseous Cl₂. The structural change of CNTs after UV irradiation was also observed by comparing the G/D ratios (the intensity ratio of the G to D bands) of the Raman spectra obtained before and after UV irradiation. Similar phenomena were also confirmed in the case of the polymer/MWCNT mixture containing hydroxylammonium chloride as a dispersant of MWCNTs. These results confirmed the UV-induced covalent bond formation between polymer side chains and MWCNTs. Full article

The morphology and chemical composition of carbon nanofibers in situ grown on a large carbon-fiber woven fabric are studied using SEM measurements, X-ray Diffraction, X-ray Flourescence, and X-ray Photoelectron Spectroscopy. Results show that nanofibers can have a density and a morphology potentially advantageous for application in polymer-matrix composites. The fiber surface functional groups significantly change after the growth and this also potentially provides a better interfacial adhesion. These advantages can be controlled, e.g., by the catalyst loading and the type of solvent used for its deposition. Full article

In theoretical studies of chemical reactions the reaction thermochemistry is usually reported for the stoichiometric reaction at standard conditions (ΔG°, ΔH°, ΔS°). We describe the computation of the equilibrium concentrations of the CO₂-adducts for the general capture reaction CO₂ + Capture System ⇆ CO₂-adduct (GCR) and the rubisco-type capture reaction CO₂ + Capture System ⇆ CO₂-adduct + H₂O (RCR) with consideration of the reaction CO₂(g) ⇆ CO₂(aq) via Henry’s law. The resulting equations are evaluated and graphically illustrated as a function of atmospheric CO₂ concentration and as a function of temperature. The equations were applied to the thermochemistry of small molecule rubisco-model reactions and series of additional model reactions to illustrate the range of the Gibbs free enthalpy for the effective reversible capture and of the reaction entropy for economic CO₂ release at elevated temperature. A favorable capture of free enthalpy is of course a design necessity, but not all exergonic reactions are suitable CO₂ capture systems. Successful CO₂ capture systems must allow for effective release as well, and this feature is controlled by the reaction entropy. The principle of using a two-pronged capture system to ensure a large negative capture entropy is explained and highlighted in the graphical abstract. It is hoped that the presentation of the numerical examples provides useful guidelines for the design of more efficient capture systems. Full article

The application of carbon nanotubes (CNTs) as metal-free catalysts is a novel approach for heterogeneous liquid phase catalytic systems. Textural and chemical modifications by liquid/gas phase or mechanical treatments, as well as solid state reactions, were successfully applied to obtain carbon nanotubes with different surface functionalities. Oxygen, nitrogen, and sulfur are the most common heteroatoms introduced on the carbon surface. This short-review highlights different routes used to develop metal-free carbon nanotube catalysts with enhanced properties for Advanced Oxidation Processes. Full article

Within this short communication article, we consider the value that closer and earlier collaboration between engineers and social scientists could offer the research, development, demonstration and deployment (RDD & D) of industrial technologies. We consider perspectives taken from both the social sciences and engineering in order to highlight the prejudices and misunderstandings that currently limit the extent and quality of such collaboration. It is reasoned that the complex engineering challenges of the future demand a move towards greater interdisciplinarity. Current successful approaches towards fostering interdisciplinarity within the Carbon Dioxide Utilisation (CDU) research community are then used to illustrate the benefits of employing a more holistic approach to the design and introduction of new industrial technologies. It is our hope that this article will catalyse similar collaborative research efforts within other sectors. Full article

Graphene oxide (GO) has been shown to be reduced by several microorganisms. Recent studies of the growth of Geobacter species in the presence of GO and electricity production by recovery of electrons on the reduced form of GO (rGO) have indicated substantial benefits of GO and GO-respiring bacteria (GORB) in microbial electrochemical systems. In this study, we enriched GORB from a coastal sample to investigate the distribution and phylogenetic variety of GORB in seawater environments. X-ray photoelectron spectroscopy (XPS) and four-terminal probing revealed that the enriched microbial community (designated as CS culture) reduced GO and self-aggregated into a conductive hydrogel complex with rGO (the CS-rGO complex). In the process of GO reduction, certain bacterial populations grew in a manner that was dependent on GO respiration coupled with acetate oxidization. High-throughput sequencing of 16S rRNA as a biomarker revealed the predominance of Desulfomonas species at 92% of the total bacterial population in the CS culture. The CS-rGO complex produced electricity with acetate oxidization, exhibiting less than 1 Ω/cm³ of charge transfer resistance. Thus, these results suggested that Desulfomonas species could grow on rGO and produce electricity via the reduced form of GO. Full article