Carbon Nanotube Networks Research Articles

Synergistic effects of CNT-bridged dual-phase MoS2 on MXene as a ternary hybrid electrode for rapid sensing of chloramphenicol in aqueous media

The fabrication of a hybridized electrochemical sensor denoted CNT/MoS2/MXene for chloramphenicol (CAP) detection is described based on growing MoS2 nanoflakes on stacked Ti3C2Tx MXene and bridging the structure obtained with carbon nanotubes (CNTs). Herein, we introduce an acid-etched stacked Ti3C2Tx MXene as an interlayered structure to accommodate solvothermally grown layered MoS2 and a bridged CNT network for the efficient electrocatalytic sensing of CAP. The successful growth of MoS2 on the MXene surface prevented restacking of layered MXene and increased conductivity. Interconnected CNTs over the MoS2 nanoflake array served as an electron transport highway, accelerating the electron transport pathway and maintaining the structural stability of the MXene/MoS2 heterostructure. Morphologically, CNT/MoS2/MXene was found to have a functionalized multilayered structure and to have a greater electron transfer rate, and a larger electrochemically active surface area than the binary feature. Modifying the surface area of MXene with MoS2 and CNTs synergistically enhanced the transportation of kinetic barrier electrons and well-defined the redox cycle in the ferricyanide system. Further, the electrochemical detection of CAP using a CNT/MoS2/MXene electrode by cyclic voltammetry (CV) produced greater electrochemical responses than bare GCE, MXene, CNT-MoS2, and MoS2-MXene. In addition, scanning rates, the effects of different concentrations, and pH electrolyte tests showed that the GCE-CNT/MoS2/MXene electrode was suitable for the electrochemical sensing of CAP. Amperometric response, as determined by i-t profiles, showed the CNT/MoS2/MXene electrode had superior electrochemical sensing performance for CAP detection, a wide linear range (8 to 152 nM), a remarkably low detection limit (0.32 nM), a high sensitivity of 14.22 μA nM−1cm−2, and superior stability (96 % activity retention after four weeks). The synergistic effect of the ternary three-dimensional assembly with CNT bridging over hierarchical MoS2/MXene increased surface-active sites and electron transportation rates and enhanced CAP detection performance. Moreover, the proposed sensor demonstrated high selectivity and satisfactory recovery for milk, eye drops, and pork.

CO2 plasma inducing steel-slag with active sites for efficient growth of carbon nanotubes for the high-performance microwave absorption

As a solid waste generated in the metallurgical process, the highly efficient catalysis of steel-slag for carbon nanotube (CNT) growth remains a huge challenge. Herein, a CO2 plasma-inducing approach for modifying the steel-slag catalyst with rich active sites was developed for CNT growth in the chemical vapor deposition (CVD) process. Furthermore, the high-energy CO2 plasma refines the particles on the steel-slag surface, reducing the particle size on the surface of steel-slag effectively increasing the active sites of the catalyst. In addition, the thermal effect generated by the gas molecule ionization process under CO2 increases the background temperature of the steel-slag, and the interaction between the oxygen-active substances produced and the iron oxide on the surface of steel-slag undergoes an oxidation reaction upon full contact with high-energy particles, which greatly improves the catalytic efficiency of the steel-slag as a catalyst for CNT, and increases the catalytic efficiency by 50 % compared with the non-plasma modified steel-slag as a catalyst for catalyzing CNTs. In addition, catalytically grown CNTs encapsulate magnetic steel-slag catalysts to form a three-dimensional CNT network structure, with high-performance electromagnetic wave absorption. The composite absorbing material with a thickness of only 3.55 mm has a minimum absorption rate of −64.08 dB for electromagnetic waves at a frequency of 7.9 GHz. The dielectric and the magnetic loss of steel-slag lead to enhanced electromagnetic wave absorption. Therefore, this study provides an inexpensive and environmentally friendly idea for the design of high-efficiency CNT growth and solid waste catalyst modification synthesized with high-performance absorbers.

Flexible All-Carbon Nanoarchitecture Built from In Situ Formation of Nanoporous Graphene Within "Skeletal-Capillary" Carbon Nanotube Networks for Supercapacitors.

It is difficult for carbonaceous materials to combine a large specific surface area with flexibility. Here, a flexible all-carbon nanoarchitecture based on the in situ growth of nanoporous graphene within "skeletal-capillary" carbon nanotube (CNT) networks has been achieved by a chemical vapor deposition (CVD) process. Multi-path long-range conductivity is established, and the porous graphene provides a large specific surface area for charge storage. The flexibility of the films allows them to be directly used as binder-free electrodes for supercapacitors. Since the polymeric binders are saved, the supercapacitors exhibit a higher overall storage density.

Dedoping of Carbon Nanotube Networks Containing Metallic Clusters and Chloride

Dedoping of Carbon Nanotube Networks Containing Metallic Clusters and Chloride

Damage sensing in multi-functional nanocomposite polymer bonded energetics with embedded multi-walled carbon nanotube sensing networks

Abstract This experimental investigation evaluates the strain and damage sensing abilities of multi-walled carbon nanotube (MWCNT) networks embedded in the binder phase of polymer-bonded energetics (PBEs). PBEs are a special class of particulate composite materials that consist of energetic crystals bound by a polymer matrix, wherein the polymer matrix serves to maintain the composite’s shape and form. The structural health monitoring (SHM) approach presented in this work exploits the piezoresistive properties of the distributed MWCNT networks. Major challenges faced during such implementation include the low binder concentrations of PBEs, the presence of conductive/non-conductive particulate phases, the high degree of heterogeneity in the PBE microstructure, and achieving the optimal MWCNT dispersion. In this study, ammonium perchlorate (AP) crystals as the oxidizer, Aluminum grains as the metallic fuel, and Polydimethylsiloxane (PDMS) as the binder are used as the constituents for fabricating PBEs. To study the effect of each constituent on the MWCNT network’s SHM abilities, various materials systems are comprehensively studied: MWCNT/PDMS materials are first evaluated to study the binder’s electromechanical response, followed by AP/MWCNT/PDMS to assess the impact of AP addition, and finally, AP/AL/MWCNT/PDMS to evaluate the impact of adding conductive aluminum grains. Compression samples (ASTM D695) were fabricated and subjected to monotonic compression. Electrical resistance is recorded in conjunction with the mechanical test via an LCR meter. Gauge factors relating to the change in normalized resistance to applied strain are calculated to quantify the electromechanical response. MWCNT dispersions and mechanical failure modes are analyzed via scanning electron microscopy imaging of the fracture surfaces. Correlations between the electrical behavior in response to the mechanical behavior are presented, and possible mechanisms that influence the electromechanical behavior are discussed. The results presented herein demonstrate the successful ability of MWCNT networks as SHM sensors capable of real-time strain and damage assessment of PBEs.

Cyclic loading effects on the heat-generation performance of carbon nanotube-embedded cement composites

Abstract This study investigates the heat-generation stability of carbon nanotube (CNT)/cement composites after exposing to cyclic loading conditions. The specimens were fabricated with varying CNT contents and levels of fly ash replacement. Results showed that increasing CNT content reduced electrical resistivity, while the impact on the electrical characteristics was found to be insubstantial, even though a considerable portion of fly ash was replaced. In addition, the electrical resistivity of the specimens after exposed to cyclic loading increased. Electrical heating tests revealed both negative and positive temperature coefficient effects depending on the applied voltages. Higher CNT contents improved the heat-generation capability, but the heating capability decreased after exposed to the cyclic loadings which is deduced from the damage of CNT networks during cyclic loadings. In this regard, the authors concluded that the heat-generation stability can be significantly affected by the applied loadings. Thus, the future research will be conducted to improve the heat-generation stability of the cement-based electrical heating systems as exposed to artificial deteriorations.

Collapse of G+/G- bands, modification of Breit–Wigner–Fano signals and structural amorphization in single wall carbon nanotube networks under great excess of sulfur

The identification of superconductivity and ferromagnetic to superconductive transitions in sulfur-modified carbons has recently attracted an important attention. Additional work is however needed to better understand the structural modification of the graphitic interfaces in presence of sulfur. Here we report on an advanced methodology which involves soaking of large amounts (in the order of 500 mg) of sulfur through several annealing cycles into bundles comprising of hollow single-wall/few-wall carbon nanotubes (SWCNTs). TEM, HRTEM, XRD and Raman spectroscopy characterization analyses reveal the presence of structural amorphization of the SWCNTs, with dramatic impact on the intensity of the G+ and a progressive vanishing of the G- signal-contribution. We demonstrate the presence of high sulfur content by employing both point and mapping energy dispersive X-rays (EDX maps) acquisitions, with high local quantities of sulfur in the order of 16 %. Interestingly, a complex variation in the contribution of the Breit-Wigner-Fano (BWF) band, with appearance of extra D, G+ and C-S band-contributions, is revealed by deconvolution-analyses. The appearance of these structural features is a clear indicator of structural amorphization of the CNTs, with consequential formation of C-S hybrid structures, which we analyze systematically with the aid of energy dispersive X-ray spectrum mapping and Raman point/mapping spectroscopy approaches.

Capacitive deionization and electrochemical performance of a hierarchical porous electrodes enabled by nitrogen and phosphorus doped CNTs and removable NaCl template

Capacitive Deionization (CDI) is an electrochemical desalination technique based on the electrical double layer, which accumulate salts from the water stream; however, achieving higher salt adsorption for low-concentration salt is hindered due to several obstacles, such as low adsorption capacity and slow kinetics on the electrode surface. In this study, we reported a novel electrode fabrication method designed to enhance the hydrophilicity of the electrode material and activate hierarchical porosity, making a more accessible adsorption surface area. This modification enables more than 210 % improvement in salt adsorption capacity, achieving 17.5 mg g-1 in a single pass process with good stability in an 850 mg/L NaCl solution at 1.2 V, surpassing most reported carbon-based electrodes under similar operating conditions. Electrode formulation consists of Nitrogen (N) and Phosphorus (P) doped hierarchical carbon nanotubes (CNTs) network blended with additional NaCl as a green and removable template to reach higher levels of porosity. The electrochemical sorption behavior of the sample was characterized over a voltage range of –0.5 to 0.7 V. Furthermore, the electrode materials were characterized utilizing various characterization methods, including Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), X-ray Diffraction (XRD), Raman Spectroscopy, Fourier Transformed Infrared (FTIR), X-ray Photoelectron Spectroscopy (XPS), and Brunauer-Emmett-Teller (BET) to explore the correlation between microstructure, morphology, and properties. Our finding reveals that not only N and P can affect adsorption, but also the novel cathode preparation method, which employs a removable NaCl templated hierarchical porous electrode, has a profound effect on the electrochemical and CDI results. This finding will open a new perspective in designing electrodes for all electrochemical systems.

Machine learning for nano-level defect detection in aligned random carbon nanotubes-reinforced electrically conductive nanocomposite

Machine learning allows fast nano-scale defect detection in polymer-impregnated aligned carbon nanotube (CNT) nanocomposites. Digital twins were populated by TEM-validated geometry; considered defects were flat cracks and close-to-spherical voids. Finite-element analysis of piezoresistive response was conducted by embedment of CNT network into matrix. Identification of a defect by change in CNT network piezoresistivity was challenged by: (1) randomness of CNTs’ shapes and placement, ML training happened on random realisations; (2) high strength of CNTs leading to the preservation of conductive paths along CNTs and changes only in conductivities of tunnelling contacts. “Artificial approximation“ was introduced to economise computer time multi-fold: ML was trained on cases with artificially degraded tunnelling conductivities within the defect. Three ML models: XGBoost, fully connected, and convolution neural networks were employed. All models managed the task for near-spherical voids, but performed poorly for flat cracks, due to the limited number of tunnelling contacts in crack volume. When trained on the mixed set of voids and cracks, both neural networks demonstrated the ability to learn the difference and detected even cracks, while XGBoost was not up to the challenge. By metrics, the convolutional neural network demonstrated the highest accuracy of predictions.

Wet-Spinning Carbon Nanotube/Shape Memory Polymer Composite Fibers with High Actuation Stress and Predesigned Shape Change.

Actuators based on shape memory polymers and composites incorporating nanomaterial additives have been extensively studied; achieving both high output stress and precise shape change by low-cost, scalable methods is a long-term-desired yet challenging task. Here, conventional polymers (polyurea) and carbon nanotube (CNT) fillers are combined to fabricate reinforced composite fibers with exceptional actuation performance, by a wet-spinning method amenable for continuous production. It is found that a thermal-induced shrinkage step could obtain densified strong fibers, and the presence of CNTs effectively promotes the tensile orientation of polymer molecular chains, leading to much improved mechanical properties. Consequently, the CNT/ polyurea composite fibers exhibit stresses as high as 33MPa within 0.36 s during thermal actuation, and stresses up to 22MPa upon electrical stimulation enabled by the built-in conductive CNT networks. Utilizing the flexible thin fibers, various shape change behavior are also demonstrated including the conversion between different structures/curvatures, and recovery of predefined simple patterns. This high-performance composite fibers, capable of both thermal and electrical actuation and produced by low-cost materials and fabrication process, may find many potential applications in wearable devices, robotics, and biomedical areas.

Combining machine learning and molecular dynamics to predict strength-toughness and energy dissipation mechanisms of hybrid double-crosslinked CNT networks

Cross-linking has a significant strengthening effect on the mechanical properties of carbon nanoparticles, but there are still great challenges in how to control their mechanical properties through precise cross-linking ratios. Therefore, we use coarse-grained molecular dynamics (CGMD) to simulate its mechanical properties as data samples and combine it with machine learning methods to predict the optimal strength and toughness of carbon nanotubes (CNTs) corresponding to optimal cross-linking conditions. We found that the cross-linking density range is 2.60 ∼ 2.75 × 10-4/nm3, and the strong and weak cross-linking ratio range is 91 % S+9% W∼95 % S+5% W, which is the optimal range to achieve the mechanical properties of CNTs. Excessively high cross-link density and strong bond ratios can reduce the total number of cross-link bond breaks, thus decreasing their toughness. Meanwhile, high cross-linking density has a greater impact on the shear and slip between CNTs, tending to make CNTs brittle. Our proposed new approach for extracting data from coarse-grained models can obtain substantial optimization results without requiring much simulation computation. Furthermore, these cross-linking strategies and machine learning algorithms proposed in this work can provide a theoretical basis for controlling the mechanical properties of CNT materials, and also open up a new way for functional network materials other than CNTs.

Dual carbon confining SnO2 nanocrystals as high-performance anode for sodium-ion batteries

The increasing global demand for sustainable energy sources has driven research into sodium-ion batteries (SIBs) for large-scale energy storage. However, their electrochemical performance is hindered by poor reaction kinetics and significant volume expansion in electrode materials. In this work, we developed a dual-carbon-confined SnO2 nanocrystal anode (CNTs@SnO2@NC) designed for high-performance SIBs. This innovative structure uses carbon nanotubes (CNTs) and a nitrogen-doped carbon (NC) coating to stabilize SnO2, ensuring structural integrity during charge/discharge cycles. The CNTs network in CNTs@SnO2@NC can alleviate the agglomeration of SnO2 nanocrystals to a certain extent; With its superior electronic conductivity, CNTs can enhance the anode's conductivity and function as an electronic highway; The sodiophilic properties and good electrical conductivity of CNTs enable sodium ions to migrate rapidly on the surface of the nanotubes. Moreover, numerous external defects and active sites generated by nitrogen doping enhance the sodium ion absorption capabilities; The existence of nitrogen-doped carbon coating can effectively accommodate the volume changes of SnO2 and enhance the structural stability of CNTs@SnO2@NC composites during the repeated charge and discharge cycles. As a result, the CNTs@SnO2@NC composite demonstrates excellent electrochemical performance, achieving capacity of 235 mAh g−1 at 0.1 A g−1 over 100 cycles and 102 mAh g−1 at 1.0 A g−1 over 300 cycles. In a full-cell configuration with a Na3V2(PO4)3 cathode, it delivers 38 mAh g−1 at 100th cycle at 0.1 A g−1. This study underscores the substantial improvements achieved by dual-carbon confinement for high-performance SIB anodes, offering a promising direction for future anode material design.

Investigation on Junction Contacts of Semiconducting Carbon Nanotube Networks Using Conductive Atomic Force Microscopy.

Semiconductor single-walled carbon nanotube (s-SWNT) networks have gained prominence in electronic devices due to their cost-effectiveness, relatively production-naturality, and satisfactory performance. Configuration, density, and resistance of SWNT-SWNT junctions are considered crucial factors influencing the overall conductivity of s-SWNT networks. In this study, we present a method for inferring the lower bounds of the SWNT-SWNT junction resistance in s-SWNT networks based on conductive atomic force microscopy TUNA images. This method further enables the proposal of a classification for SWNT-SWNT junctions based on the current behavior relative to their surroundings. The three types of SWNT-SWNT junctions are denoted as (i) true contact (T), (ii) poor contact (P), and (iii) false contact (F). Of them, the true and poor contacts, respectively, represent good and poor electrical contact for the subject SWNT-SWNT junctions whose electrical conductivity hardly improves under external tip pressure, while that of the false contact can be further improved by external pressure. Statistical analysis demonstrates that while T-type junctions make a significant contribution to network conductivity, their proportion accounts for only approximately 40%. The P-type and F-type junctions, which constitute over 60% of the total, may be a contributing factor that constrains the overall conductivity of the s-SWNT networks. The height ratio of the junction to the sum of two SWNTs was also observed to exhibit variations among the three types. Finally, we propose a three-dimensional model to elucidate the formation mechanism underlying each type of junction. The present study provides insights into the performance of spontaneous contacts between s-SWNTs in the networks, and the systematic image acquisition and junction classification processes may provide support for future advancements in these networks.

Nanopore structure of highly enriched double-walled carbon nanotube network assemblies

An efficient catalytic chemical vapor deposition method utilizing an Fe-Mo/MgO-supported catalyst was developed, allowing the highly selective synthesis of double-walled carbon nanotubes (DWCNTs) in high yield, exceeding 89 %. The carbon yield, tube diameter, and crystallinity of the synthesized DWCNTs were characterized using high-resolution transmission electron microscopy, field-emission scanning electron microscopy, thermogravimetric analysis, and Raman spectroscopy. The nanopore structure and adsorption characteristics of the DWCNTs purified by removing the support and catalyst (i.e., Fe-Mo/MgO) were analyzed via N2 adsorption–desorption measurements at 77 K. A remarkable advantage of the highly enriched DWCNTs with small bundle network structures is that guest molecules can easily access the outer (i.e., external) surface of the DWCNTs, resulting in a large specific surface area (SSA) of >691 m2 g−1 and pore volume of 2.70 mL g−1 in the double-walled structures. Thus, highly enriched DWCNTs with large pore volumes and SSAs prepared via facile solution-based processes can yield CNT-based structures for applications in high-performance energy storage.

Polymer Coating Enabled Carrier Modulation for Single-Walled Carbon Nanotube Network Inverters and Antiambipolar Transistors.

The control of the performance of single-walled carbon nanotube (SWCNT) random network-based transistors is of critical importance for their applications in electronic devices, such as complementary metal oxide semiconducting (CMOS)-based logics. In ambient conditions, SWCNTs are heavily p-doped by the H2O/O2 redox couple, and most doping processes have to counteract this effect, which usually leads to broadened hysteresis and poor stability. In this work, we coated an SWCNT network with various common polymers and compared their thin-film transistors' (TFTs') performance in a nitrogen-filled glove box. It was found that all polymer coatings will decrease the hysteresis of these transistors due to the partial removal of charge trapping sites and also provide the stable control of the doping level of the SWCNT network. Counter-intuitively, polymers with electron-withdrawing functional groups lead to a dramatically enhanced n-branch in their transfer curve. Specifically, SWCNT TFTs with poly (vinylidene fluoride) coating show an n-type mobility up to 61 cm2/Vs, with a decent on/off ratio and small hysteresis. The inverters constructed by connecting two ambipolar TFTs demonstrate high gain but with certain voltage loss. P-type or n-type doping from polymer coating layers could suppress unnecessary n- or p-branches, shift the threshold voltage and optimize the performance of these inverters to realize rail-to-rail switching. Similar devices also demonstrate interesting antiambipolar performance with tunable on and off voltage when tested in a different configuration.

The Stability of UV-Defluorination-Driven Crosslinked Carbon Nanotubes: A Raman Study.

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

Physical properties of industrially produced carbon nanotube yarns for use in structural nanocomposites

Industrially-produced carbon nanotube (CNT) networks are a promising base for high-performance, continuous CNT nanocomposites, motivating widespread use in research and application development. Floating catalyst chemical vapor deposition (FCCVD) is a scalable, widely-adopted approach for synthesis of CNT networks; however, FCCVD can yield networks with organic impurities which complicate their characterization and processing. Herein, we analyze two varieties of FCCVD-synthesized commercial CNT yarn to explore the effects of densification and purification as they relate to forming infiltrated polymer composites. First, the fluid permeabilities and porosities of neat roving and chemically-stretched CNT yarns (CSYs) are estimated and compared to gas adsorption studies, which suggest high-tenacity CSYs are largely impermeable, leading to dry-core composites when polymer infiltration is attempted. Next, the presence and effects of oxygen-rich amorphous carbon impurities in the CSYs are identified and found to exist at the scale of CNT bundles, wherein the amorphous carbon behaves like a hygroscopic polymer matrix in a composite. Removal of the amorphous carbon phase in a 130%-increase in specific surface area, as quantified by BET analysis, and a statistically significant reduction in tensile properties. We discuss challenges in estimating yarn alignment and crystallinity resulting from these factors, and place our results in context of past studies analyzing intrinsic organic coatings in FCCVD-synthesized CNT networks.

Significant performance enhancement of Zn-ion hybrid supercapacitors based on microwave-assisted pyrolyzed active carbon via synergistic effect of NaHCO3 activation and CNT networks

Zinc-ion hybrid supercapacitors (ZIHSCs) represents a promising technological approach for large-scale energy storage with the combined advantages of supercapacitors and zinc-ion batteries. Unfortunately, it is still challengeable to quickly fabricate low-cost, high-performance carbonaceous cathode materials at relatively low temperature. To address such issues, herein, taking waste Eucommia ulmoides Oliver (EUO) wood as an example, we present a novel microwave-assisted carbonization (MWC) approach at relatively low temperature to quickly prepare active carbon, and we present a synergistic strategy to significantly enhance the electrochemical performance by introducing sodium bicarbonate activation (SA) and constructing conductive carbon nanotubes (CNT) networks. The MWC-SA@CNT hybrid exhibits outstanding specific capacitance of 344.2 F/g at 0.2 A/g within three-electrode system, much better than conventional high-temperature pyrolyzed AC, MWC carbon, and MWC-SA carbon. The superior performance of MWC-SA@CNT can be attributed to the synergistic effect of its large specific surface area of 1102.7 m2/g, high mesoporous percentage of 53.5%, and rich –OH and CO groups due to microwave-assisted carbonization and sodium bicarbonate activation, and rich electron transport paths due to the presence of CNT networks. Furthermore, ZIHSCs assembled by MWC-SA@CNT cathode could delivers impressive performance with excellent capacity (194.37 mA h/g at current density of 1 A/g), energy density (142.30 Wh/kg), and durability (capacitance retention rate of 97.65% after 5000 cycles). This work offers a rapid and low-temperature method for preparing wood-based active carbon with rich nanopores and strong conductivity to improve performance of Zinc ion storage.

Carbon Nanotubes Connecting and Encapsulating MoS2-Doped SnO2 Nanoparticles as an Excellent Lithium Storage Performance Anode Material.

Doping and carbon encapsulation modifications have been proven to be effective methods for enhancing the lithium storage performance of batteries. The hydrothermal method and ball milling are commonly used methods for material synthesis. In this study, a composite anode material rich in carbon nanotubes (CNTs) conductive tubular network connection and encapsulation of SnO2-MoS2@CNTs (SMC) was synthesized by combining these two methods. In this highly conductive network, nano-SnO2 particles are uniformly dispersed and embedded in MoS2 with a layered structure, and the obtained SnO2-MoS2 composite material is tightly connected and encapsulated by the tubular network of CNTs. It is worth noting that the incorporation of layered MoS2 not only effectively anchors the SnO2 nanoparticles, but also provides a broader space for lithium-ion movement due to the larger interlayer spacing. The conductive network of CNTs shortens the diffusion path of electrons and Li+ and provides more diffusion channels. The reversible capacity of the SnO2-MoS2@CNTs nanocomposite material remains at 1069.3 mA h g-1 after 320 cycles at 0.2 A g-1, and it exhibits excellent long-term cycling stability, maintaining 904.5 mA h g-1 after 1000 cycles at 1.0 A g-1. The composite material demonstrates excellent pseudocapacitive contribution rate performance, with a contribution rate of 87% at 2.0 mV s-1. The results indicate that SnO2-MoS2@CNTs has excellent electrochemical lithium storage performance and is a promising anode material for lithium-ion batteries.

FeNi-LDH nanoflakes on Co-encapsulated CNT networks for stable and efficient ampere-level current density oxygen evolution

Developing low-cost but efficient electrocatalysts for continuous oxygen evolution reaction (OER) at ampere-level current densities can promote the hydrogen economy. LDHs are promising electrocatalysts to replace noble-metal-based catalysts for efficient OER, and rationally constructing LDH-based heterostructures can further boost their OER activities. Herein, we report the anchoring of FeNi-LDH nanoflakes onto MOF-derived carbon nanotube (CNT) networks on carbon cloth to obtain the self-supported LDH/CNT/CC. Benefiting from the advantages of its CNT network and the highly-active sites of its three-layer heterostructure, the optimized LDH/CNT/CC only requires a low overpotential of 200 mV at 10 mA cm−2 and exhibits robust stability under continuous electrolysis for 160 h at an ampere-level current density of 1 A cm−2. Theoretical calculations show three-layer FeNi-LDH(001)/graphene(002)/Co(111) slab has the lowest OER energy barrier, and its graphene layer can gain electrons from the FeNi-LDH and Co to show the most suitable binding strength for intermediates to facilitate OER.