Inorganic Nanotubes Research Articles

Effect of the Chemical Composition and Geometry of Nanotubes on the Structure and Internal Rotation Barrier of Encapsulated Ammonia‐Boron Trifluoride: A Theoretical Investigation

AbstractThe study of the structure and conformational properties of ammonia–boron trifluoride in the cavity of 24 carbon and inorganic nanotubes using the PBE/3ζ DFT approximation showed that the conformational preference of the encapsulated molecule is determined by geometry and chemical composition of the host nanostructure. The combined effect of these factors leads to the predominance of eclipsed conformation of guest molecule for four endoclusters. In other cases, the main minimum on the potential energy surface corresponds to the staggered or pseudo‐staggered forms of BF3←NH3. The guest molecule carries the electric charge and has a shortened B←N bond. These conclusions are confirmed by the results of the virtual reaction of ammonia and boron trifluoride in the cavity of individual nanotubes.

Nanotubes and other nanostructures of VS2, WS2, and MoS2: Structural effects on the hydrogen evolution reaction

Vanadium sulfide (VS2) is a layered transition metal dichalcogenide (TMD), comparable in crystal structure to the well-known MoS2 and WS2. Theoretical predictions attribute much potential to VS2, since it is metallic-like and has an active basal plane, essential for catalytic performance. However, it is much less studied than other members of the TMD family due to the difficulties in synthesizing specific structures with controlled properties. Here we present unique structures of VS2 nanotubes and conduct a comparative study with other well-known inorganic nanotubes and nanostructures of MoS2 and WS2. We evaluate the effect of the curvature and strain, the abundance of surface defects, and the availability of surface sites in various structures by electrochemical methods. We show that MoS2 has the best intrinsic activity, which is enhanced by an extensive electrochemical surface area. The woven-like structure of the MoS2 nanotube walls provides a combined effect of strain, crystallinity, and defects. For WS2 structures, the strained surface of the nanotubes results in sites with higher intrinsic activity than the edge sites, but structures such as the nano-triangles, which provide a higher number of edge sites, exhibit competing activity. As for the VS2 structures, although theoretical calculations predict optimal active sites for the hydrogen evolution reaction (HER), they are extremely sensitive to stoichiometry variations that hamper their catalytic activity. Our findings contribute insights to the improvement and design of VS2–based nanocatalysts for the HER and shed light on the general factors that govern the activity in the unique TMD nanotubes family.

Electrospun nanofiber composite based on bimetallic metal–organic framework/halloysite nanotubes/deep eutectic solvents/molecularly imprinted polymers for thin film microextraction of sulfonamides in milk, eggs and chicken meat by HPLC analysis

Herein, electrospun nanofibers based on bimetallic metal–organic framework@ functionalized halloysite/deep eutectic solvents/molecularly imprinted polymers was synthesized as new solid phase extractant for thin film microextraction of sulfacetamide, sulfamethoxazole, sulfamethazine and silversulfadiazine by HPLC-UV analysis. After synthesizing new phase through electrospinning nanofibers and thin film fabrication, we effectively leverage the synergistic properties of these materials within the composite structure. The resultant thin film nanocomposite, which integrates molecularly imprinted nanofibers, highlights the presence of inorganic nanotubes called halloysite, functionalized with a deep eutectic solvent and bimetallic metal–organic frameworks. Characterization of synthesized thin films were successfully characterized for structural, morphological, and surface analysis using infrared spectroscopy (FTIR), X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDX) and scanning electron microscopy (SEM). In this study, a syringe design was employed for the microextraction of sulfonamides (SAs) using thin film microextraction, which is carried out in two stages: adsorption and desorption, both within the syringe. The effects of several experimental conditions on desorption stage, including desorption parameters including pH, desorption solvent type, and ultrasonication time were studied by the single factor at a time. A Box-Behnken design (BBD) was applied to optimize the significant variables to obtain the optimum extraction conditions. The detection limit of the method was 0.003 µg/L and also the limit of quantification method was in the range of 0.01 µg/L. These results demonstrate the presented thin film microextraction method can serve as a good candidate for the microextraction and determination of sulfonamides in food samples like milk, eggs and chicken meat.

On the Determination of Elastic Properties of Single-Walled Nitride Nanotubes Using Numerical Simulation.

In recent years, tubular nanostructures have been related to immense advances in various fields of science and technology. Considerable research efforts have been centred on the theoretical prediction and manufacturing of non-carbon nanotubes (NTs), which meet modern requirements for the development of novel devices and systems. In this context, diatomic inorganic nanotubes formed by atoms of elements from the 13th group of the periodic table (B, Al, Ga, In, Tl) and nitrogen (N) have received much research attention. In this study, the elastic properties of single-walled boron nitride, aluminium nitride, gallium nitride, indium nitride, and thallium nitride nanotubes were assessed numerically using the nanoscale continuum modelling approach (also called molecular structural mechanics). The elastic properties (rigidities, surface Young's and shear moduli, and Poisson's ratio) of nitride nanotubes are discussed with respect to the bond length of the corresponding diatomic hexagonal lattice. The results obtained contribute to a better understanding of the mechanical response of nitride compound-based nanotubes, covering a broad range, from the well-studied boron nitride NTs to the hypothetical thallium nitride NTs.

Amine-impregnated natural inorganic nanotubes via layer-by-layer electrostatically self-assembly approach for efficient CO2 adsorption

Developing cost-effective and high-performance solid amine adsorbents has considered as an important way to alleviate the greenhouse effect. How to precisely regulate its pore structure and surface interface characteristics, and how to cooperate to optimize the dynamic mass transfer and adsorption–desorption behavior of gas in the adsorbent are still challenging work. Herein, we demonstrated a facile and efficient approach to construct polyethyleneimine (PEI) impregnated halloysite nanotubes (HNTs) as an emerging nanocomposite for CO2 capture. Based on the natural electrostatic differences of inner and outer walls for HNTs, the hollow tubular structures of adsorbents were constructed by selective surface modification and layer-by-layer electrostatic self-assembly technology to improve the CO2 uptake capacity and cyclic stability, in which poly(sodium-p-styrene sulfonate) (PSS) and PEI were used as polyanionic and polycationic layer, respectively, to coat the inner walls of HNTs. The loading capacity of PSS-PEI composite ionic layers in HNTs and the influence of PSS polyanionic layer on PEI dispersion were specifically discussed according to the CO2 uptake capacity, adsorption heat, thermodynamics and kinetics of the adsorbents. The optimal PEI20-0.5PHNTs adsorbent exhibited a higher CO2 uptake of 0.87 mmol/g at 80 °C in the flow of 40 vol% N2/60 vol% CO2 than that of PEI20-HNTs, owing to the high amine efficiency due to the uniform dispersion of PEI in the electrostatic composite ionic layers. Furthermore, PEI20-0.5PHNTs reached 75 % of the maximum adsorption capacity at the 5th min of the adsorption process and released the most heat during adsorption at − 18.28 kJ/mol due to the presence of electrostatic composite ionic layers. PEI20-0.5PHNTs showed excellent cyclic stability with a slight loss of 7.4 %. The electrostatic self-assembled adsorbent obtained by layer-by-layer loading of PSS and PEI based on the unique surface charge characteristics of HNTs is an inspiration for the synthesis of cost-effective solid amine adsorbents for practical CO2 capture and separation.

Real-Time Monitoring of Adsorption-Induced Scrolling of Colloidal Inorganic Nanosheets.

Inorganic nanotubes have attracted much attention due to their unique physicochemical properties. Nanotubes can be prepared by scrolling exfoliated nanosheets under ambient conditions. However, how the nanosheet scrolled in its colloidal state has not been experimentally visualized. In this paper, we directly observed the scrolling process of nanosheets upon adsorption of organic cations. Exfoliated flat nanosheets of niobate and clay in aqueous colloids were found to scroll by adding organic cations, such as exfoliation reagents, to the colloids. Employment of cationic stilbazolium dye enabled in situ observation of the dye adsorption and scrolling by optical microscopy based on changes in color and morphology of the nanosheets. The scrolling was promoted for nanosheets adsorbed with a stilbazolium dye with a longer alkyl chain, suggesting that the interaction between the hydrophobic parts of the dye cations is the driving force of the scrolling. This finding should encourage research on the formation of nanotubes from nanosheets and also provides important guidelines for the selection of appropriate exfoliation reagents when exfoliating nanosheets from layered crystals.

New Cap-Holed AlP, GaP, and InP Nanotubes.

The structural, vibrational, and electronic properties of new inorganic X-phosphide nanotubes (ch-XPNT), with X = Al, Ga, or In and chirality of (5,5), are investigated. These new NTs display cap-hole ends, with the cap-hole features induced by the nonpassivated ends. Studies are based on density functional theory (DFT) using the M06-2X, PBE, and B3LYP functionals together with the LanL2DZ basis set. All nanostructures have been relaxed by minimizing the total energy, assuming a nonmagnetic nature and a total neutral charge. Note that the cap-hole NTs are terminated by a 10-atom ring, which in turn favors the geometrical ordering and yields stable structures. The (5,5) ch-XPNT are highly electrophilic and nonpolar, in addition to having high solvation energy values. Let us remark that solvation energies are produced by the intermolecular forces that involve the induced dipoles. Structural and vibrational results show that the X-P bonds are single bonds. Finally, results suggest that the inorganic nanotubes are structurally stable with semiconductor features, which means that their functionalization may yield interesting future applications.

Ultra-broadband bright light emission from a one-dimensional inorganic van der Waals material

One-dimensional (1D) van der Waals materials have emerged as an intriguing playground to explore novel electronic and optical effects. We report on inorganic one-dimensional SbPS4 nanotube bundles obtained via mechanical exfoliation from bulk crystals. The ability to mechanically exfoliate SbPS4 nanobundles offers the possibility of applying modern 2D material fabrication techniques to create mixed-dimensional van der Waals heterostructures. We find that SbPS4 can readily be exfoliated to yield long (>10 μm) nanobundles with thicknesses that range from 1.3 to 200 nm. We investigated the optical response of semiconducting SbPS4 nanobundles and discovered that upon excitation with blue light, they emit bright and ultra-broadband red light with a quantum yield similar to that of hBN-encapsulated MoSe2. We discovered that the ultra-broadband red light emission is a result of a large ∼1 eV exciton binding energy and a ∼200 meV exciton self-trapping energy, unprecedented in previous material studies. Due to the bright and ultra-broadband light emission, we believe that this class of inorganic 1D van der Waals semiconductors has numerous potential applications, including on-chip tunable nanolasers, and applications that require ultraviolet to visible light conversion, such as lighting and sensing. Overall, our findings open avenues for harnessing the unique characteristics of these nanomaterials, advancing both fundamental research and practical optoelectronic applications.

Modulations of the work function and morphology of a single MoS2 nanotube by charge injection.

Both the miniaturization of transistor components and the ongoing investigation of material systems with potential for quantum information processing have significantly increased current interest of researchers in semiconducting inorganic nanotubes. Here we report on an additional outstanding aspect of these nanostructures, namely the intrinsic coupling of electronic and mechanical properties. We observe electronic and morphology changes in a single MoS2 nanotube, exposed to charge injections by means of an atomic-force-microscopy tip. An elliptic deformation of the nanotube and helical twisting of the nanotube are visible, consistent with the reverse piezoelectric effect. Work-function changes are found to be dependent on the polarity of the injected carriers. An unexpected long-term persistence of the shape deformations is observed and explained with accumulation of structural defects and the resultant strain, which could cause a memory-like charge confinement and a long lasting modulation of the work function.

An anionic polyethersulfone membrane modified by poly(2-acrylamide-2-methylpropanesulfonic acid sodium salt) grafted carbon nanotubes

Polyethersulfone membrane is easy to be polluted, and the negative surface would help enhance improve the permeability and the anti-pollution performance; so how to anchor polymer brushes with negative groups to polyethersulfone membrane surface is a challenge. In this paper, polymer brushes of poly(2-acrylamide-2-methylpropanesulfonic acid sodium salt) is first grafted to carbon nanotubes to form an organic-inorganic hybrid additive, which is further anchored onto the membrane surface of polyethersulfone by blending method. The graft reaction is proceeded by surface initiated electrochemical atom transfer radical polymerization, where the introduction of electrochemical part is because it could help better control the growth of polymer brushes compared with the pristine atom transfer radical polymerization process. The carbon nanotubes grafted with poly(2-acrylamide-2-methylpropanesulfonic acid sodium salt) could anchor on the membrane surface because the there is a self-assemble process of organic-inorganic hybrid additive during phase inversion method, where the inorganic part carbon nanotubes firmly embedded into the membrane and the organic part can be fixed on membrane surface. The polyethersulfone membrane exhibits enhanced surface hydrophilicity, improved the permeability of the membrane, and good anti-fouling performance due to the negative charge and electrostatic repulsion brought by anionic surface of the modified membrane. When the mass of nanotubes grafted with poly(2-acrylamide-2-methylpropanesulfonic acid sodium salt) in the casting solution is 20 mg, the water flux can reach 365.5 L m−2 h−1, and the rejection ratios of both BSA and CR are close to 100% with good flux recovery and anti-fouling effect performance.

Dimerization Effects and Negative Strain Energy in Silicon Monosulfide Nanotubes.

We report on the construction and characterization of silicon monosulfide nanotubes that were obtained by rolling up two-dimensional materials isoelectronic to phosphorene in the recently discovered layered Pmma and β phases. We relaxed and studied the nanotube structures using computational methods within density functional theory (DFT). We found that the nanotubes with a thick Pmma layer remain stable at room temperature, and their electronic properties depend on their diameters. Small-diameter nanotubes display metallic character, while nanotubes with increasing diameter show semiconducting ground states due to the dimerization in the silicon-silicon distances that opens a gap, leading to interesting optical properties in the near-infrared region. Furthermore, we discovered β SiS monolayer nanotubes having negative strain energies, similar to the well-known imogolite inorganic nanotubes. The combined thermal stability, compelling optical properties, and diverse applications of these silicon monosulfide nanotubes underscore the demand for novel synthesis methods to fully explore their potential in various fields.

Novel 3D-Printed Biocarriers from Aluminosilicate Materials

The addition of biocarriers can improve biological processes in bioreactors, since their surface allows for the immobilization, attachment, protection, and growth of microorganisms. In addition, the development of a biofilm layer allows for the colonization of microorganisms in the biocarriers. The structure, composition, and roughness of the biocarriers’ surface are crucial factors that affect the development of the biofilm. In the current work, the aluminosilicate zeolites 13X and ZSM-5 were examined as the main building components of the biocarrier scaffolds, using bentonite, montmorillonite, and halloysite nanotubes as inorganic binders in various combinations. We utilized 3D printing to form pastes into monoliths that underwent heat treatment. The 3D-printed biocarriers were subjected to a mechanical analysis, including density, compression, and nanoindentation tests. Furthermore, the 3D-printed biocarriers were morphologically and structurally characterized using nitrogen adsorption at 77 K (LN2), scanning electron microscopy (SEM), and X-ray diffraction (XRD). The stress–strain response of the materials was obtained through nanoindentation tests combined with the finite element analysis (FEA). These tests were also utilized to simulate the lattice geometries under compression loading conditions to investigate their deformation and stress distribution in relation to experimental compression testing. The results indicated that the 3D-printed biocarrier of 13X/halloysite nanotubes was endowed with a high specific surface area of 711 m2/g and extended mesoporous structure. Due to these assets, its bulk density of 1.67 g/cm3 was one of the lowest observed amongst the biocarriers derived from the various combinations of materials. The biocarriers based on the 13X zeolite exhibited the highest mechanical stability and appropriate morphological features. The 13X/halloysite nanotubes scaffold exhibited a hardness value of 45.64 MPa, which is moderate compared to the rest, while it presented the highest value of modulus of elasticity. In conclusion, aluminosilicate zeolites and their combinations with clays and inorganic nanotubes provide 3D-printed biocarriers with various textural and structural properties, which can be utilized to improve biological processes, while the most favorable characteristics are observed when utilizing the combination of 13X/halloysite nanotubes.

Chiral Nanoparticle Chains on Inorganic Nanotube Templates.

Fabrication of chiral assemblies of plasmonic nanoparticles is a highly attractive and challenging task, with promising applications in light emission, detection, and sensing. So far, primarily organic chiral templates have been used for chirality inscription. Despite recent progress in using chiral ionic liquids in synthesis, the use of organic templates significantly limits the variety of nanoparticle preparation techniques. Here, we demonstrate the utilization of seemingly achiral inorganic nanotubes as templates for the chiral assembly of nanoparticles. We show that both metallic and dielectric nanoparticles can be attached to scroll-like chiral edges propagating on the surfaces of WS2 nanotubes. Such assembly can be performed at temperatures as high as 550 °C. This large temperature range significantly widens the portfolio of nanoparticle fabrication techniques, allowing us to demonstrate a variety of chiral nanoparticle assemblies, ranging from metals (Au, Ga), semiconductors (Ge), and compound semiconductors (GaAs) to oxides (WO3).

Multifunctional MXene–Fe3O4–Carbon Nanotube Composite Electrodes for High Active Mass Asymmetric Supercapacitors

Ti3C2Tx–Fe3O4–carbon nanotube composites were prepared for electrochemical energy storage in the negative electrodes of supercapacitors. The electrodes show a remarkably high areal capacitance of 6.59 F cm−2 in a neutral Na2SO4 electrolyte, which was obtained by the development of advanced nanofabrication strategies and due to the synergistic effect of the individual components. Enhanced capacitance was achieved using the in-situ synthesis method for the Fe3O4 nanoparticles. The superparamagnetic behavior of the Fe3O4 nanoparticles facilitated the fabrication of electrodes with a reduced binder content. Good mixing of the components was achieved using a celestine blue co-dispersant, which adsorbed on the inorganic components and carbon nanotubes and facilitated their co-dispersion and mixing. The capacitive behavior was optimized by the variation of the electrode composition and mass loading in a range of 30–45 mg cm−2. An asymmetric device was proposed and fabricated, which contained a Ti3C2Tx–Fe3O4–carbon nanotube negative electrode and a polypyrrole–carbon nanotube positive electrode for operation in an Na2SO4 electrolyte. The asymmetric supercapacitor device demonstrated high areal capacitance and excellent power-density characteristics in an enlarged voltage window of 1.6 V. This investigation opens a new avenue for the synthesis and design of MXene-based asymmetric supercapacitors for future energy storage devices.

Excellent and effective interfacial transition layer with an organic/inorganic hybrid carbon nanotube network structure for basalt fiber reinforced high-performance thermoplastic composites

Basalt fiber reinforced high-performance thermoplastic (BFRHTP) composites are promising materials for application in military, aerospace, chemical, automobile, and other high-tech industries. However, their mechanical properties are still largely limited by poor interfacial properties because of the smooth, inert, and low-energy surface of BF. In this study, an organic/inorganic hybrid sizing agent was used for BF surface modification to construct an appropriate modulus transition layer for the interface with a combination of soft and rigid phases. Organic poly(ether nitrile) (PEN) and inorganic carboxylic multi-walled carbon nanotubes (MWCNT-COOH) in hybrid sizing agents (PEN/CNT) were respectively used as soft and rigid phases to design the interfacial structure. The tensile strength, flexural strength, interlaminar and interfacial shear strength of the basalt fiber reinforced poly(phthalazinone ether nitrile ketone) composites were increased by 60, 33, 62, and 144%, respectively. This approach provides a simple, green, and promising strategy for enhancing the interfacial properties of BFRHTP composites.

Application of Surface-Modified Nanoclay in a Hybrid Adsorption-Ultrafiltration Process for Enhanced Nitrite Ions Removal: Chemometric Approach vs. Machine Learning

Herein, we report the results of a study on combining adsorption and ultrafiltration in a single-stage process to remove nitrite ions from contaminated water. As adsorbent, a surface-modified nanoclay was employed (i.e., Nanomer® I.28E, containing 25-30 wt. % trimethyl stearyl ammonium). Ultrafiltration experiments were conducted using porous polymeric membranes (Ultracel® 10 kDa). The hybrid process of adsorption-ultrafiltration was modeled and optimized using three computational tools: (1) response surface methodology (RSM), (2) artificial neural network (ANN), and (3) support vector machine (SVM). The optimal conditions provided by machine learning (SVM) were found to be the best, revealing a rejection efficiency of 86.3% and an initial flux of permeate of 185 LMH for a moderate dose of the nanoclay (0.674% w/v). Likewise, a new and more retentive membrane (based on PVDF-HFP copolymer and halloysite (HS) inorganic nanotubes) was produced by the phase-inversion method, characterized by SEM, EDX, AFM, and FTIR techniques, and then tested under optimal conditions. This new composite membrane (PVDF-HFP/HS) with a thickness of 112 μm and a porosity of 75.32% unveiled an enhanced rejection efficiency (95.0%) and a lower initial flux of permeate (28 LMH). Moreover, molecular docking simulations disclosed the intermolecular interactions between nitrite ions and the functional moiety of the organonanoclay.

Electrospun PAN membranes toughened and strengthened by TPU/SHNT for high-performance lithium-ion batteries

Membrane separators should have robust characteristics to ensure that batteries have a high discharge capacity and could shun the probability of thermal runaway. In this study, thermoplastic polyurethane (TPU) and inorganic surface-modified halloysite nanotube (SHNT) are considered to improve the toughness and strength of electrospun polyacrylonitrile (PAN) fibers. This is because TPU is elastic, while SHNT has a high aspect ratio and a special hollow structure. The obtained PAN/TPU/SHNT membrane exhibits improvement in its overall performance. It exhibits excellent thermal stability, increased flexibility, and high ionic conductivity. More importanly, the tensile strength of membranes increases to 28.5 MPa and observed a significant vibration amplitude, which is signifying better flexibility and elasticity. With PAN/TPU/SHNT-3 as a battery separator, the lithium-ion battery delivers a capacity of 108.41 mAh/g and a retention of 98.30 % at 2C for 100 cycles. These data on capacity and retention are higher than those of Celgard 2400. Incorporating SHNT to improve the fiber strength and TPU for its elasticity into electrospun PAN membrane separators should prove effective in enhancing not only the electrochemical performance but also the safety of batteries.

UV-Visible photo-reactivity of permanently polarized inorganic nanotubes coupled to gold nanoparticles.

Hybrid aluminosilicate nanotubes (Imo-CH3) have the ability to trap small organic molecules inside their hydrophobic internal cavity while being dispersed in water owing to their hydrophilic external surface. They also display a curvature-induced polarization of their wall, which favors reduction outside the nanotubes and oxidation inside. Here, we coupled bare plasmonic gold nanoparticles (GNPs) with Imo-CH3 and analyzed for the first time the redox reactivity of these hybrid nano-reactors upon UV illumination. We show that the coupling between GNPs and Imo-CH3 significantly enhances the nanotube photocatalytic activity, with a large part of water reduction occurring directly on the gold surface. The coupling mechanism strongly influences the initial H2 production rate, which can go from ×10 to more than ×90 as compared to bare Imo-CH3 depending on the synthesis route of the GNPs. The present results show that this hybrid photocatalytic nano-reactor benefits from a synergy of polarization and confinement effects that facilitate efficient H2 production.

Polyacrylonitrile‐based electrospun nanofibers – A critical review

AbstractThis review is based on the fundamental aspects and applications of polyacrylonitrile (PAN)‐based electrospun composite nanofibers. Various electrospinning techniques have been discussed here. polyacrylonitrile is an acrylic polymer of commercial significance that has superior thermal, mechanical, electrical, and chemical properties. The integration of polyacrylonitrile nanofibers with nanoparticles including carbon nanotubes, graphene nanosheets, graphene oxide, metal oxides, and their combinations has greatly improved the physicochemical properties of the polyacrylonitrile electrospun nanofibers. The enhanced features of polyacrylonitrile nanofibers have resulted from interfacial bonding of nitrile groups with the nanofiller used, chemical compositions, hydrophobicity, porosity, and wettability of these nanofibers. This article fundamentally features a few key possibilities of polyacrylonitrile‐based electrospun composite nanofibers and their applications. A special focus has been made on polyacrylonitrile‐based inorganic nanoparticles, graphene nanosheets, graphene oxide, and carbon nanotubes embedded electrospun nanofibers, for their potential applications in supercapacitors, high power batteries, filtration membranes, electromagnetic interference shielding, and strain sensors. Achieving low cost, high selectivity, excellent recyclability, and high absorption capability are the major challenges for electrospun nanofiber fabrications. These electrospun nanofibers require extensive research in the future to advance the technologies to bring them to the commercial market.

Layer-by-layer macroassembly of inorganic CNTs and MXenes with organic PVA for enhancing the interfacial properties of carbon fiber/epoxy composites

In this study, two inorganic nanomaterials, MXenes and carbon nanotubes (CNTs), with different dimensions were directly used to modify carbon fiber (CF) fabrics using polyvinyl alcohol (PVA) as an organic binder through the layer-by-layer vacuum filtration method to improve the weak interface between the CF fabrics and epoxy (EP) resin matrix. These two-dimensional nanomaterials are observed to bond tightly to CF fabrics, and the wettability of CF fabrics is significantly improved owing to the organic–inorganic multistage interface structure. The surface energy of MXenes–CNTs–CF fabrics was 86% higher than that of pure CF fabrics. Correspondingly, the interlaminar shear strength (ILSS) of MXenes–CNTs–CF/EP composites was 30% higher than that of the pure CF/EP composites. Our study demonstrates a novel, simple, and effective method for modifying the interfacial properties between CFs and polymers using nanomaterials.