2D Carbon Nanomaterials Research Articles

Upcycling waste plastic into 2D-carbon nanomaterials for high-performance supercapacitors by incorporating NiCo2O4: a sustainable approach to renewable energy

A two-step catalytic pyrolysis method converts waste plastic into rGO and NiCo2O4 nanorods and NiCo2O4@WPrGO nanocomposites produced via hydrothermal method, yielding highly efficient electrode materials for supercapacitor technology.

MOC Composites for Construction: Improvement in Water Resistance by Addition of Nanodopants and Polyphenol.

The topic of modification of magnesium oxychloride cement (MOC) using specific functional additives is very much pronounced in the research of alternative building materials. This study deals with the co-doping of MOC by 1D and 2D carbon nanomaterials in order to improve its mechanical properties while using tannic acid (TA) as a surfactant. Furthermore, the effect of TA on MOC also improves its water resistance. As a filler, three size fractions of standard quartz sand are used. The proposed types of MOC-based composites show promising results considering their mechanical, macro- and microstructural, chemical, and hygric properties. The use of 1D and 2D nanoadditives and their mixture enables the improvement in the flexural strength and particularly the softening coefficient, which is the durability parameter characterizing the resistance of the prepared materials to water. After immersion in water for 24 h, the compressive strength of all tested specimens of modified composites was higher than that of the reference composite. Quantitatively, the developed co-doped composites show mechanical parameters comparable to or even better than those of commonly used Portland cement-based materials while maintaining high environmental efficiency. This indicates their potential use as an environmentally friendly alternative to Portland cement-based products.

Wearable Nano-Based Gas Sensors for Environmental Monitoring and Encountered Challenges in Optimization.

With a rising emphasis on public safety and quality of life, there is an urgent need to ensure optimal air quality, both indoors and outdoors. Detecting toxic gaseous compounds plays a pivotal role in shaping our sustainable future. This review aims to elucidate the advancements in smart wearable (nano)sensors for monitoring harmful gaseous pollutants, such as ammonia (NH3), nitric oxide (NO), nitrous oxide (N2O), nitrogen dioxide (NO2), carbon monoxide (CO), carbon dioxide (CO2), hydrogen sulfide (H2S), sulfur dioxide (SO2), ozone (O3), hydrocarbons (CxHy), and hydrogen fluoride (HF). Differentiating this review from its predecessors, we shed light on the challenges faced in enhancing sensor performance and offer a deep dive into the evolution of sensing materials, wearable substrates, electrodes, and types of sensors. Noteworthy materials for robust detection systems encompass 2D nanostructures, carbon nanomaterials, conducting polymers, nanohybrids, and metal oxide semiconductors. A dedicated section dissects the significance of circuit integration, miniaturization, real-time sensing, repeatability, reusability, power efficiency, gas-sensitive material deposition, selectivity, sensitivity, stability, and response/recovery time, pinpointing gaps in the current knowledge and offering avenues for further research. To conclude, we provide insights and suggestions for the prospective trajectory of smart wearable nanosensors in addressing the extant challenges.

Sustainable and Scalable Synthesis of 2D Ultrathin Hierarchical Porous Carbon Nanosheets for High-Performance Supercapacitor.

2D carbon nanomaterials such as graphene, carbon nanosheets, and their derivatives, representing the emerging class of advanced multifunctional materials, have gained great research interest because of their extensive applications ranging from electrochemistry to catalysis. However, sustainable and scalable synthesis of 2D carbon nanosheets (CNs) with hierarchical architecture and irregular structure via a green and low-cost strategy remains a great challenge. Herein, prehydrolysis liquor (PHL), an industrial byproduct of the pulping industry, is first employed to synthesize CNs via a simple hydrothermal carbonization technique. After mild activation with NH4 Cl and FeCl3 , the as-prepared activated CNs (A-CN@NFe) display an ultrathin structure (≈3 nm) and a desirable specific surface area (1021 m2 g-1 ) with hierarchical porous structure, which enables it to be both electroactive materials and structural support materials in nanofibrillated cellulose/A-CN@NFe/polypyrrole (NCP) nanocomposite, and thus endowing nanocomposite with impressive capacitance properties of 2546.3 mF cm-2 at 1 mA cm-2 . Furthermore, the resultant all-solid-state symmetric supercapacitor delivers a satisfactory energy storage ability of 90.1 µWh cm-2 at 250.0 µW cm-2 . Thus, this work not only opens a new window for sustainable and scalable synthesis of CNs, but also offers a double profits strategy for energy storage and biorefinery industry.

Graphdiyne oxide elicits a minor foreign-body response and generates quantum dots due to fast degradation

Graphdiyne (GDY) is a novel two-dimensional (2D) carbon allotrope that has attracted much attention in materials, physics, chemistry, and microelectronics for its excellent properties. Much effort has been devoted to exploring the biomedical applications of GDY in 2D carbon nanomaterials, especially for smart drugs and gene delivery. However, few studies have focused on the biocompatibility and potential environmental hazards of GDY and its derivatives. In this study, graphdiyne oxide (GDYO) and graphene oxide (GO) were obtained using different oxidation methods. Their cytotoxicity and hemolysis in vitro and biocompatibility in subcutaneous and peritoneal locations in vivo were compared. GDYO had very low biotoxicity in vitro and was moderately biocompatible in the muscle and abdominal cavity in vivo. Highly oxidized products and graphdiyne quantum dots (GDQDs) were observed in peritoneal cells. GDYO had better biocompatibility and its sheet size was easily diminished through oxidative degradation. Therefore, GDYO is a good candidate for use in 2D carbon nanomaterials in biomedicine.

Near-Infrared-II Activatable Symbiotic 2D Carbon-Clay Nanohybrids for Dual Imaging-Guided Combinational Cancer Therapy.

Two-dimensional (2D) nanomaterials hold great potential for cancer theranostic applications, yet their clinical translation faces great challenges of high toxicity and limited therapeutic/diagnostic modality. Here, we have created a kind of symbiotic 2D carbon-2D clay nanohybrids, which are composed of a novel 2D carbon nanomaterial (carbon nanochips, or CNC), prepared by carbonizing a conjugated polymer polydiiodobutadiyne, and a 2D layered aluminosilicate clay mineral montmorillonite (MMT). Intriguingly, with the formation of the nanohybrids, MMT can help the dispersion of CNC, while CNC can significantly reduce the hemolysis and toxicity of MMT. The symbiotic combination of CNC and MMT also leads to a synergistic anti-cancer theranostic effect. CNC has a strong absorption and high photothermal conversion efficiency in the second near-infrared region (NIR-II, 1000-1700 nm), while MMT contains Fe3+ that can facilitate the generation of reactive oxygen species from highly expressed H2O2 in tumor microenvironment. The nanohybrids not only enable a synergy of photothermal therapy and chemodynamic therapy to suppress the extremely rapid growth of RM1 tumors in mice but also allow for dual photoacoustic and magnetic imaging to guide the drug delivery and NIR-II irradiation execution, hence establishing a highly efficient and biosafe "all-in-one" theranostic platform for precision nanomedicine.

A sustainable and low-cost route to prepare magnetic particle-embedded ultra-thin carbon nanosheets with broadband microwave absorption from biowastes

Two-dimensional (2D) carbon nanomaterials have attracted extensive attention in the field of microwave absorption (MA) owing to their unique layered structure, tailorable atomic layer, tunable active surface, and high dielectric loss. Here, novel porous graphene-like heterostructures are facilely prepared through the carbonization of pomelo peel (PP)/prussian blue (PB) and PP/PB analogues (PBA). The magnetic particles derived from PB and PBA are uniformly distributed in the N-doped carbon (NC) ultra-thin nanosheets, which enhances the magnetic loss and improves the interfacial polarization. The optimized Fe/ZnO/NC-7 sample exhibits a maximum reflection loss (RLmax) of −58.12 dB at 2.05 mm, and an ultrabroad effective bandwidth (RL ≤ −10 dB) of 7.6 GHz is achieved at 1.9 mm, which covers nearly half of the measured frequency range. The superior MA performance of Fe/ZnO/NC-7 composite is ascribed to the unique magnetic particle-embedded carbon nanosheet, which not only optimizes the impedance matching but also enhances the electromagnetic wave (EMW) attenuation ability through 2D conductive networks and multiple polarization processes. Overall, this work offers an environmentally friendly method to prepare low-cost and high-performance microwave absorbers from biowastes, which exhibit superior application potential as compared to other 2D microwave absorbers including graphene and MXene.

The influence of laser-induced alignment on Z-scan properties of 2D carbon nanomaterials suspension dependent on polarization

The Z-scan technique uses a single beam that can be used for observing the nonlinear or optical limiting properties of materials. For the first time, the Z-scan properties dependent on the polarization of 2D carbon nanomaterial suspension were experimentally investigated using optical Z-scan technology. The Z-scan curves of graphene and graphene oxide (GO) in N-methyl-2-pyrrolidinone suspensions exhibited strong polarization-dependent characteristics. In paper, a reverse saturated absorption (RSA) dip surrounded the lens focus when the horizontal polarized beam was focused in the suspension, and two saturated absorption (SA) peaks appeared adjacent to the dip. However, for the vertical polarized beam, only one RSA dip surrounded the lens focus, and the threshold was higher than the SA for a horizontally polarized beam. The transmission of RSA for the GO suspension was evidently lower than that of the graphene suspension. The polarization-dependent characteristic can be ascribed to the laser-induced alignment in case the suspension is moved in or out of the beam focal point. Furthermore, the polarization-dependent 2D carbon nanomaterial suspension can be applied in several practical purposes such as 2D material-based optical and opto-fludic devices.

A Quantitative Chemical Method for Determining the Surface Concentration of Stone-Wales Defects for 1D and 2D Carbon Nanomaterials.

A quantitative method is proposed to determine Stone–Wales defects for 1D and 2D carbon nanostructures. The technique is based on the diene synthesis reaction (Diels–Alder reaction). The proposed method was used to determine Stone–Wales defects in the few-layer graphene (FLG) nanostructures synthesized by the self-propagating high-temperature synthesis (SHS) process in reduced graphene oxide (rGO) synthesized based on the method of Hammers and in the single-walled carbon nanotubes (SWCNT) TUBAL trademark, Russia. Our research has shown that the structure of FLG is free of Stone–Wales defects, while the surface concentration of Stone–Wales defects in TUBAL carbon nanotubes is 1.1 × 10−5 mol/m2 and 3.6 × 10−5 mol/m2 for rGO.

New analytical strategies Amplified with 2D carbon nanomaterials for electrochemical sensing of food pollutants in water and soils sources

Pharmaceutical and food pollutants have threatened global health. Pharmacotherapy has left a positive impression in the field of health and life of people and animals. However, the many unresolved problems brought along with residues of pharmaceuticals in the environmental and food. Consumption of the world's freshwater resources, toxic chemicals, air pollution, plastic waste directly affects water and soil resources. Pesticides have a wide role in pollutants. Therefore, the determination of pesticides is significant to eliminate their negative effects on living things. Nowadays, there are many analytical methods available. However, new analysis methods are still being researched due to certain limitations of traditional methods. Electrochemical sensors have drawn attention because of their superior properties, such as short analysis time, affordability, high sensitivity, and selectivity. The development of new analytical strategies for assessing risks from pharmaceutical to food pollutants in water and soil sources is important for the measurement of different pollutants.Moreover, the 2D-carbon nanomaterials used in the development of electrochemical sensors are widely utilized to enlarge the surface area, increase porosity, and make easy immobilization. Graphene (graphene derivations) and carbon nanotubes integrated nanosensors are widely used for the determination of pesticides. 2D-carbon nanomaterials can be tailored according to the purpose of the study. The characterization and synthesis methods of 2D-carbon nanomaterials are widely explained. Furthermore, enzyme nanobiosensors, especially Acetylcholinesterase (AChE), are widely used to determine pesticides. The three main topics are focused on in this review: 2D-carbon nanomaterials, pesticides that threaten life, and the application of 2D-carbon nanomaterials-based electrochemical sensors. The various developed 2D-carbon nanomaterials-based electrochemical sensors were applied in pharmaceutical forms, fruits, tap/lake water, beverages, and soils sources. This work aims to indicate the recently published paper related to pesticide analysis and highlight the importance of 2D-nanomaterials on sensors.

Ultra-high strength multicomponent composites based on reactive magnesia: Tailoring of material properties by addition of 1D and 2D carbon nanoadditives

In this study a novel high-performance construction composites based on MOC (magnesium oxychloride cement) co-doped by graphene and multi-walled carbon nanotubes were developed. These materials were studied in order to create a possible alternative to the commonly used Portland cement (PC) with sufficient water resistance and very good mechanical properties. The influence of the content of the carbon-based nanoadditives on the mechanical, macro- and micro-structural, chemical and physical properties was analyzed. Among the analytical methods, X-ray diffraction, scanning electron microscopy, energy dispersive spectroscopy, high-resolution transmission electron microscopy, Fourier-transform infrared spectroscopy and others were used. Overall, three groups of samples were prepared, one reference and two containing the combined dopants. The combined effect of the 1D and 2D carbon nanomaterials resulted in highly increased flexural strength (up to 42.1%), compressive strength (up to 18.2%) and decrease in the water absorption coefficient (up to 48.2%), which is crucial for this type of binder. As the composite adopted the properties of the single dopants, the thermal conductivity also increased. The overall enhancement of the MOC matrix is connected to the significant drop in porosity when the carbon-based nanoadditives are used. The obtained results might show a potential route in the development of high-performance environmentally sustainable alternatives to PC.

Comparative investigation of bioflavonoid electrocatalysis in 1D, 2D, and 3D carbon nanomaterials for simultaneous detection of naringin and hesperidin in fruits.

Electrocatalysis of bioflavonoids in carbon nanomaterials plays an important role in electrochemical sensors for the detection of their content in fruits. In this study, three types of carbon nanomaterials with 1D, 2D, and 3D structures, namely carbon nanotubes (CNTs), graphene oxide (GO), and Ketjen black (KB), were modified onto glassy carbon electrodes for the electrocatalysis of hesperidin and naringin, which are two important bioflavonoids in fruits. As a result, the CNT-modified electrodes showed the highest electrocatalytic activity for both hesperidin and naringin compared to GO and KB. The morphology and surface chemistry of the carbon nanomaterials were characterized. The structural defects and carbon status of carbon nanomaterials are proposed to be the most important factors affecting the electrocatalysis of hesperidin and naringin. Finally, a CNT-based electrochemical sensor was fabricated to simultaneously detect hesperidin and naringin. Real sample tests on the fruit extract of Citrus grandis “Tomentosa” show that the proposed electrochemical sensors with high recovery thus could be employed in practical applications.

Electrochemical Growth of High-Strength Carbon Nanocoils in Molten Carbonates.

The reported mechanical strength of carbon nanocoils (CNCs) obtained from traditional preparation of catalytic acetylene pyrolysis is far below its theoretical value. Herein, we report a molten salt electrolysis method that employs CO32- as feedstock to grow CNCs without using metal catalyst. We meticulously mediate the alkalinity of molten carbonate to tune the electrochemical reduction of CO32- on graphite electrode to selectively grow CNCs in Li2CO3-Na2CO3-K2CO3-0.001 wt %Li2O. Graphite substrate, current density, and alkalinity of molten salt dictate the growth of CNCs. In addition, the electrolytic CNCs shows a spring constant of 1.92-39.41 N/m and a shear modulus of 21-547 GPa, which are 10-200 times that of CNCs obtained from catalyst-assisted gas-to-solid conversions. Overall, this paper opens up an electrochemical way to prepare CNCs through liquid-to-solid conversion without using catalysts and acetylene, providing new perspectives on green synthesis of 1D carbon nanomaterials with high mechanical strength.

Electrochemical impedimetric analysis of different dimensional (0D–2D) carbon nanomaterials for effective biosensing of L-tyrosine

Electrochemical biosensors employing nano-transduction surfaces are considered highly sensitive to the morphology of nanomaterials. Various interfacial parameters namely charge transfer resistance, double layer capacitance, heterogeneous electron transfer rate and diffusion limited processes, depend strongly on the nanostructure geometry which eventually affects the biosensor performance. The present work deals with a comparative study of electrochemical impedance-based detection of L-tyrosine (or simply tyrosine) by employing carbon nanostructures (graphene quantum dots, single walled carbon nanotubes (CNTs) and graphene) along with tyrosinase as the bio-receptor. Specifically, the role of carbon nanostructures (i.e. 0D, 1D and 2D) on charge transfer resistance is investigated by applying time-varying electric field at the nano-bioelectrode followed by calculating the heterogeneous electron transfer rate, double layer capacitor current and their effects on limits of detection and sensitivities towards tyrosine recognition. A theoretical model based on Randel’s equivalent circuit is proposed to account for the redox kinetics at various carbon nanostructure/enzyme hybrid surfaces. It was observed that, the 1D morphology (single walled CNTs) exhibited lowest charge transfer resistance ∼2.62 kΩ (lowest detection limit of 0.61 nM) and highest electron transfer rate ∼0.35 μm s−1 (highest sensitivity 0.37 kΩ nM−1 mm−2). Our results suggest that a suitable morphology of carbon nanostructure would be essential for efficient and sensitive detection of tyrosine.

2D Carbon Nanomaterials as Promising Adsorbents of Uranium

2D Carbon Nanomaterials as Promising Adsorbents of Uranium

Acrylonitrile‐based polymer/graphene nanocomposites: A review

AbstractPolymer composite materials fabricated from acrylonitrile‐derived polymers (such as polyacrylonitrile, nitrile butadiene rubber, styrene‐acrylonitrile, acrylonitrile butadiene styrene) with suitable fillers have found tremendous applications due to their highly desirable properties. Graphene, a versatile 2D carbon nanomaterial, with extraordinary properties has been adopted as an effective filler component of a wide range of acrylonitrile‐based polymer composites. The modified and functionalized graphene‐based nanomaterials were incorporated into the acrylonitrile‐based polymer matrix to enhance their various properties. In contrast to conventional 1D carbon nanoparticles, the incorporation of this graphene into the polymer matrix resulted excellent improvement in mechanical, electrical, rheological, and thermal, as well as frictional properties. This has offered advances in diverse applications such as sensors, flexible electronics, Li–S battery, damping, structural, microwave shielding, aircraft, spacecraft, automobile, and so forth. Particularly, the excellent EMI (Electromagnetic interference) shielding ability of these acrylonitrile‐based polymer/graphene composites has been explored widely in microelectronics. This review focuses on the recent progress and new strategies in the development of different acrylonitrile‐based polymer/graphene nanocomposites.

Functionalized Reduced Graphene Oxide as a Versatile Tool for Cancer Therapy.

Cancer is one of the deadliest diseases in human history with extremely poor prognosis. Although many traditional therapeutic modalities—such as surgery, chemotherapy, and radiation therapy—have proved to be successful in inhibiting the growth of tumor cells, their side effects may vastly limited the actual benefits and patient acceptance. In this context, a nanomedicine approach for cancer therapy using functionalized nanomaterial has been gaining ground recently. Considering the ability to carry various anticancer drugs and to act as a photothermal agent, the use of carbon-based nanomaterials for cancer therapy has advanced rapidly. Within those nanomaterials, reduced graphene oxide (rGO), a graphene family 2D carbon nanomaterial, emerged as a good candidate for cancer photothermal therapy due to its excellent photothermal conversion in the near infrared range, large specific surface area for drug loading, as well as functional groups for functionalization with molecules such as photosensitizers, siRNA, ligands, etc. By unique design, multifunctional nanosystems could be designed based on rGO, which are endowed with promising temperature/pH-dependent drug/gene delivery abilities for multimodal cancer therapy. This could be further augmented by additional advantages offered by functionalized rGO, such as high biocompatibility, targeted delivery, and enhanced photothermal effects. Herewith, we first provide an overview of the most effective reducing agents for rGO synthesis via chemical reduction. This was followed by in-depth review of application of functionalized rGO in different cancer treatment modalities such as chemotherapy, photothermal therapy and/or photodynamic therapy, gene therapy, chemotherapy/phototherapy, and photothermal/immunotherapy.

Fabrication of High Performance PET/TLCP Fibers through the Synergistic Interfacial Enhancement and Compatibilization of Functional 1D and 2D Carbon Nanomaterials

AbstractThe maleic anhydride functionalized graphene oxide (GO‐MA) is fabricated by an efficient and solvent‐free Diels–Alder reaction. Polyethylene terephthalate (PET)/thermotropic liquid crystal polyester (TLCP), PET/TLCP/GO‐MA, PET/TLCP/aminated multi‐walled carbon nanotubes (MWCNTs‐NH2), and PET/TLCP/GO‐MA/MWCNTs‐NH2 composite fibers are systematically melt‐spun. The structure and compatibilizing effects of GO‐MA and MWCNTs‐NH2 on the mechanical, thermal, and crystallization properties of the composite fibers are indicated. The non‐isothermal crystallization kinetics and X‐ray diffraction (XRD) data show that TLCP and nanofillers can change the crystalline morphology of PET. The mechanical properties of the fibers rise with increasing TLCP content. The tensile strength 929 MPa and modulus 17.5 GPa of the fibers with 7 wt% TLCP and 0.25 wt% nanofillers (0.1 wt% GO‐MA and 0.15 wt% MWCNTs‐NH2) are significantly higher than those with 7 wt% TLCP (tensile strength 622 MPa and modulus 16.1 GPa) and even higher than those with 15% TLCP (tensile strength 836 MPa, and modulus 18.0 GPa). When the GO‐MA and MWCNTs‐NH2 co‐exist, the anti‐dripping phenomenon is improved. Therefore, the TLCP, GO, and MWCNTs synergistically strengthens the mechanical properties. This is promising for the industrial fabrication of high‐strength fibers.

Addition of Carbon Nanodots for Improving Charge/Discharge Characteristics of Lithium Metal Anode

Lithium metal is considered as the most promising anode material for high-energy-batteries due to its high theoretical capacity and low electrochemical potential. However, dendrite formation due to uncontrollable Li growth during cycling is a major challenge. Lithium dendrite growth leads to low coulombic efficiency, short cycle life, and safety issues. To solve the problem, addition of 2D carbon nano material that lead uniform Li deposition has been reported[1]. Here, we report carbon nanodots (CND) as an electrolyte additive which can suppress dendrite growth and keep stable Li metal deposition/dissolution process. CND has defect sites and functional groups that attract Li ions and serve as a Lithiophilic nucleation site for uniform nucleation.Electrochemical properties were evaluated with the charge / discharge cycles of Li symmetric cell in Li(G3)TFSI/HFE electrolyte in Fig. 1 Voltage drop that seems to be short circuit was confirmed in 88 cycles without CND. On the other hand, no short circuit was confirmed for 100 cycles with CND, confirming an improvement of cycle life. In addition, with CND, it showed lower overpotential than that of without CND which was suggested low film resistance. Fig. 2 shows the coulombic efficiency of Cu/Li half cell. Without CND, unstable CE was confirmed after 50 cycle. It is considered that the irreversible capacity due to side reaction and dead lithium caused a CE reduce. With CND, it showed stable and high CE (> 95 %) for 100 cycles. It was suggested that excessive side reactions and dead lithium were suppressed by the CND addition. It is obviously indicated that addition of CND contributes to improvement of cycle ability and coulombic efficiencies for lithium metal anode. Reference [1] X. Cheng, et al. Nature communications, 8, 336 (2017). Figure 1

Processing Methods Used in the Fabrication of Macrostructures Containing 1D Carbon Nanomaterials for Catalysis

A large number of methodologies for fabrication of 1D carbon nanomaterials have been developed in the past few years and are extensively described in the literature. However, for many applications, and in particular in catalysis, a translation of the materials to a macro-structured form is often required towards their use in practical operation conditions. This review intends to describe the available methods currently used for fabrication of such macro-structures, either already applied or with potential for application in the fabrication of macro-structured catalysts containing 1D carbon nanomaterials. A review of the processing methods used in the fabrication of macrostructures containing 1D sp2 hybridized carbon nanomaterials is presented. The carbon nanomaterials here discussed include single- and multi-walled carbon nanotubes, and several types of carbon nanofibers (fishbone, platelet, stacked cup, etc.). As the processing methods used in the fabrication of the macrostructures are generally very similar for any of the carbon nanotubes or nanofibers due to their similar chemical nature (constituted by stacked ordered graphene planes), the review aggregates all under the carbon nanofiber (CNF) moniker. The review is divided into methods where the CNFs are synthesized already in the form of a macrostructure (in situ methods) or where the CNFs are previously synthesized and then further processed into the desired macrostructures (ex situ methods). We highlight in particular the advantages of each approach, including a (non-exhaustive) description of methods commonly described for in situ and ex situ preparation of the catalytic macro-structures. The review proposes methods useful in the preparation of catalytic structures, and thus a number of techniques are left out which are used in the fabrication of CNF-containing structures with no exposure of the carbon materials to reactants due to, for example, complete coverage of the CNF. During the description of the methodologies, several different macrostructures are described. A brief overview of the potential applications of such structures in catalysis is also offered herein, together with a short description of the catalytic potential of CNFs in general.