Graphite Nanosheets Research Articles

Stable and reversible zinc metal anode with fluorinated graphite nanosheets surface coating

Stable and reversible zinc metal anode with fluorinated graphite nanosheets surface coating

Enhanced synergistic antiviral effects of thermally expanded graphite and copper oxide nanosheets in the form of a novel nanocomposite against herpes simplex virus type 1

Herpes simplex virus type 1 (HSV-1) is responsible for a wide range of human infections, including skin and mucosal ulcers, encephalitis, and keratitis. The gold standard for treating HSV-1 infections is acyclovir. However, the use of this drug is associated with several limitations such as toxic reactions and the development of drug-resistant strains. So, there is an urgent need to discover and develop novel and effective agents against this virus. For the first time, this study aimed to investigate the antiviral effects of the Thermally Expanded Graphite (TEG)-copper oxide (CuO) nanocomposite against HSV-1 and compare results with its constituent components. After microwave (MW)-assisted synthesis of TEG and CuO nanosheets as well as MW-CuO/TEG nanocomposite and characterization of all these nanomaterials, an MTT assay was used to determine their cytotoxicity. The quantitative real-time PCR was then used to investigate the effects of these nanomaterials on viral load. Three-hour incubation of HSV-1 with TEG nanosheets (500 μg/mL), MW-CuO nanosheets (15 μg/mL), and MW-CuO/TEG nanocomposite (35 μg/mL) resulted in a decrease in viral load with an inhibition rate of 31.4 %, 49.2 %, and 74.4 %, respectively. The results from the post-treatment assay also showed that TEG nanosheets (600 μg/mL), MW-CuO nanosheets (15 μg/mL), and MW-CuO/TEG nanocomposite (10 μg/mL) led to a remarkable decrease in viral load with an inhibition rate of 56.9 %, 63 %, and 99.9 %, respectively. The combination of TEG and MW-CuO nanosheets together and the formation of a nanocomposite structure display strong synergy in their ability to inhibit HSV-1 infection. MW-CuO/TEG nanocomposites can be considered a suitable candidate for the treatment of HSV-1 infection.

Controllable size of graphite nanosheets and functionalized SiO2 microspheres with excellent anti-corrosive/wear function for superhydrophobic coating

The application of superhydrophobic coatings is limited by their complex fabrication process, expensive modification, and lack of durability. This study addresses these issues by proposing a simple and economical method for fabricating strong superhydrophobic coatings by scraping off the fluorinated suspension. This coating comprises epoxy resin (EP), graphene nanosheets, and modified silicon oxide on the Q235 steel substrate. The contact angle and sliding angle of we prepare the coating coating are 152.3° and <10° respectively, exhibiting excellent super-hydrophobicity. After being immersed in 3.5 % sodium chloride solution for 1440 minutes, the coating shows a resistance of 1.14×106 Ω cm2, which is two orders of magnitude higher than that of the coating immersed for 30 minutes (1.08×104 Ω cm2), indicating its excellent corrosion resistance. A 30-day salt spray corrosion test also confirms the good corrosion resistance of the coating. When the coating is polished 100 times under a load pressure of 500 g on 1000-mesh sandpaper, the contact angle is only reduced by 7 times, indicating its good abrasion resistance. In addition, the coating also has good weather resistance and self-repairing ability against ultraviolet radiation. This simple and environmentally friendly manufacturing method has great potential for large-scale practical applications in many fields.

Surface-Activated Graphite Oxide Nanosheets with Promoted U(VI) Adsorption Performance

Adsorption is widely regarded as the most promising method for uranium extraction. Among the various materials that have been studied, graphene oxide (GO) has attracted intensive interest because of its large specific surface area and abundant oxygen-containing functional groups. However, the layers tend to aggregate owing to pronounced Van der Waals forces, which reduce the surface area and diminish the likelihood of contact between uranyl ions and adsorption sites. Graphite oxide is an intermediate product of GO, with a simple preparation process and low cost. In this study, graphite oxide nanosheets (GONs) were synthesized using graphite oxide powder as the raw material and the NaOH activation method. GONs possessed a larger specific surface area and more carboxyl groups, which resulted in an excellent uranium adsorption capacity. The maximum adsorption capacity was found to be 578.0 mg·g−1, and the adsorption rate was 90.8% within 30 min. The adsorption process closely resembled the pseudo-second-order model and the Langmuir model. The mechanism of uranium adsorption by GONs was the synergistic coordination of -COOH and -OH with U(VI). This research suggests that the novel uranium adsorbent GONs can be applied to efficiently capture U(VI) from radioactive wastewater.

Efficient eco-friendly synthesis of carbon nanotubes over graphite nanosheets from yellow corn: a one-step green approach

The present work reports the synthesis of multi-wall carbon nanotubes (MWCNTs) over graphite nanosheets by an easy and simple approach without using any external catalyst. Simply, yellow corn seeds were thermally annealed in a hydrogen atmosphere at 1050 °C for 3 h without any pretreatments. Notably, the growth of MWCNTs was observed to preferentially occur on the outer surface of the corn shell. This uncomplicated approach not only emphasizes the feasibility of synthesizing carbon nanomaterials using agricultural by-products but also underscores the potential applications of these synthesized materials in various fields. Samples were examined through a comprehensive analysis employing various techniques, including scanning electron microscopy (SEM), Raman spectroscopy, FTIR, X-ray diffraction (XRD), and high-resolution transmission electron microscopy (HRTEM). The findings unveiled the formation of rolled graphene accompanied by the presence of vertical multi-wall carbon nanotubes (MWCNTs) positioned over stacked graphene sheets. This detailed characterization provides insights into the structural features and arrangement of the synthesized materials, paving the way for a deeper understanding of their potential applications. The pyrolysis temperature is a crucial factor in the morphological characteristics of the synthesized carbon nanostructures. While graphene cage-like structures were obtained at 800 °C, small carbon nanotubes were grafted to larger ones and formed three-dimensional hierarchical morphologies when the annealing temperature increased to 900 °C. The growth mechanism of the carbon nanotubes was explained based on the jet self-extrusion of the generated gases through the inherent pores of the corn seeds. The current technique employed in manufacturing MWCNTs shows significant promise as a green synthesis method for producing catalyst-free MWCNTs suitable for industrial applications including sensors and energy storage materials.

Highly Stable, Bending-Tolerant, and Sustainable Flexible Heater through a Scalable Papermaking Procedure.

Flexible electrothermal heaters have attracted abundant attention in recent years due to their wide applications, but their preparation with high efficiency remains a challenge. Here in this work, a highly stable and bending-tolerant flexible heater was fabricated with graphite nanosheets and cellulose fibers through a scalable papermaking procedure. Its electrothermal property can be enhanced by a hot-pressing treatment and introduction of cationic polyacrylamide (CPAM) during the papermaking protocol. The flexible heater may quickly reach its maximum temperature of 239.8 °C in around 1 min at a voltage of 9 V. The power density was up to 375.3 °C cm2 w-1. It appeared to have a high tolerance for bending deformation with various curvatures, and the temperature remained stable even under 100 bending with frequency of around 0.17 Hz. Over 100 alternatively heating and cooling cycles, it worked stably as well. It was proved to be used as wearable heating equipment, soft heaters, and aircraft deicing devices, suggesting its great prospect in the field of heat management.

Acquisition of molecular rolling lubrication by self-curling of graphite nanosheet at cryogenic temperature

Friction as a fundamental physical phenomenon dominates nature and human civilization, among which the achievement of molecular rolling lubrication is desired to bring another breakthrough, like the macroscale design of wheel. Herein, an edge self-curling nanodeformation phenomenon of graphite nanosheets (GNSs) at cryogenic temperature is found, which is then used to promote the formation of graphite nanorollers in friction process towards molecular rolling lubrication. The observation of parallel nanorollers at the friction interface give the experimental evidence for the occurrence of molecular rolling lubrication, and the graphite exhibits abnormal lubrication performance in vacuum with ultra-low friction and wear at macroscale. The molecular rolling lubrication mechanism is elucidated from the electronic interaction perspective. Experiments and theoretical simulations indicate that the driving force of the self-curling is the uneven atomic shrinkage induced stress, and then the shear force promotes the intact nanoroller formation, while the constraint of atomic vibration decreases the dissipation of driving stress and favors the nanoroller formation therein. It will open up a new pathway for controlling friction at microscale and nanostructural manipulation.

Size Effect of Graphite Nanosheet-Induced Anti-Corrosion of Hydrophobic Epoxy Coatings

In order to broaden the selectivity of graphite nanosheet additives on epoxy resin-based coatings and verify the size effect, this work aims to dope graphite nanosheets of different sizes into the three-dimensional structure produced by cross-linking and curing epoxy resin and polyamide resin. In addition, a micro-nano level secondary structure and a surface with special roughness are constructed to obtain the composite epoxy hydrophobic coating. The influence of the size effect of graphite nanosheets on the hydrophobic performance and corrosion resistance of the coating is summarized as well. Among them, the optimized doping size (2.2 μm) of graphite nanosheets in the epoxy coating showed the largest impedance arc of 2.58 × 108 Ω cm2, which could form an excellent nano-network covering the micropores to impede the diffusion of corrosive medium. Through simulation calculation analysis, we also found that the edge site of graphene is more effective in capturing H2O and O2; therefore, a smaller size of graphene with a large edge can be more favorable. This work will be used as a reference for the industrial application of graphite anti-corrosive coating.

Core-shell engineering of graphite nanosheets reinforced PVDF toward synchronously enhanced dielectric properties and thermal conductivity

Polymer composites integrating high dielectric permittivity (ε′) but low loss, large breakdown strength (Eb) and thermal conductivity (TC), have attracted widespread attention in electronic devices and power systems. To simultaneously achieve these properties in graphite nanosheet (GNS)/poly(vinylidene fluoride, PVDF), the GNS were first encapsulated by a layer of aluminum oxide (Al2O3), and then incorporated into PVDF, and the resulting PVDF nanocomposites’ dielectric properties and TC were explored in terms of the Al2O3 shell thickness and filler loading. The insulating Al2O3 shell serves as a barrier layer for the formation of leakage current and long-distance electron migration thus resulting in much lower dielectric loss and conductivity of the GNS@Al2O3/PVDF. It effectively mitigates the dielectric mismatch between the filler and host matrix, further introduces more traps that can capture charge carriers, and increases the barrier height for electron detrapping subsequently preventing the growth of electric trees and elevating the Eb. Moreover, the Al2O3 interlayer alleviates both the phonon density state and phonon impedance mismatches between the filler and matrix and facilitates the interfacial phonon transport thus leading to improved TC. The dielectric parameters and TC of the GNS@Al2O3/PVDF can be simultaneously modulated by optimizing the Al2O3′s thickness. This work offers an effective approach for designing and fabricating the polymeric nanodielectrics concurrently integrating high ε′ but low loss, enhanced Eb, and TC for prospective applications in power equipment and microelectronic devices.

Ultra-sensitive electrochemical sensor based on in situ grown ultrafine HKUST-1 nanoparticles @ graphite nanosheets and core-shell structured MoO3-polypyrrole nanowires for the detection of rutin in orange juice.

Rutin extracted from natural plants has important medical value, so developing accurate and sensitive quantitative detection methods is one of the most important tasks. In this work, HKUST-1@GN/MoO3-Ppy NWs were utilized to develop a high-performance rutin electrochemical sensor in virtue of its high conductivity and electrocatalytic activity. The morphology, crystal structure, and chemical element composition of the fabricated sensor composites were characterized by SEM, TEM, XPS, and XRD. Electrochemical techniques including EIS, CV, and DPV were used to investigatethe electrocatalytic properties of the prepared materials. The electrochemical test conditions were optimized to achieve efficient detection of rutin. The 2-electron 2-proton mechanism, consisting of several rapid and sequential phases, is postulated to occur during rutin oxidation. The results show that HKUST-1@GN/MoO3-Ppy NWs have the characteristics of large specific surface area, excellent conductivity, and outstanding electrocatalytic ability. There is a significant linear relationship between rutin concentration and the oxidation peak current of DPV. The linear range is 0.50-2000 nM, and the limit of detection is 0.27 nM (S/N = 3). In addition, the prepared electrode has been confirmed to be useful for rutin analysis in orange juice.

Electromagnetic Cellularized Patch with Wirelessly Electrical Stimulation for Promoting Neuronal Differentiation and Spinal Cord Injury Repair.

Although stem cell therapy holds promise for the treatment of spinal cord injury (SCI), its practical applications are limited by the low degree of neural differentiation. Electrical stimulation is one of the most effective ways to promote the differentiation of stem cells into neurons, but conventional wired electrical stimulation may cause secondary injuries, inflammation, pain, and infection. Here, based on the high conductivity of graphite and the electromagnetic induction effect, graphite nanosheets with neural stem cells (NSCs) are proposed as an electromagnetic cellularized patch to generate in situ wirelessly pulsed electric signals under a rotating magnetic field for regulating neuronal differentiation of NSCs to treat SCI. The strength and frequency of the induced voltage can be controlled by adjusting the rotation speed of the magnetic field. The generated pulsed electrical signals promote the differentiation of NSCs into functional mature neurons and increase the proportion of neurons from 12.5% to 33.7%. When implanted in the subarachnoid region of the injured spinal cord, the electromagnetic cellularized patch improves the behavioral performance of the hind limbs and the repair of spinal cord tissue in SCI mice. This work opens a new avenue for remote treatment of SCI and other nervous system diseases.

Graphite nanosheets exfoliated by supercritical carbon dioxide for aluminium-ion battery

Aluminium-ion batteries (AIBs), using commercial graphite as cathodes, stand out as promising secondary energy-storage devices for industrial application. While exfoliating graphite to graphite nanosheets holds substantial theoretical potential for significantly enhancing AIB performance, traditional redox strategies have the drawback of introducing defects and functional groups. In this work, graphite nanosheets exfoliated by supercritical carbon dioxide (GNS-20) were explored for high-performance AIB cathodes. Electrochemical tests showed that the specific capacity of GNS-20 for an AIB cathode was 152 mAh/g at a current density of 4 A/g during 1000 cycles, which was 1.9 times higher than that of natural graphite and 1.47 times higher than that of defect-rich reduced graphene oxide. Further, the regulation of the interlayer pore structure of GNS-20 proved instrumental in enhancing its AIB performance. Modulating the porosity of graphite nanosheets by adjusting the exfoliation pressure had a significant impact. The porosity of graphite nanosheets at an exfoliation pressure of 20 MPa was 86.7%, while the porosity at 15 MPa was 71.5% and that at 10 MPa was 69.7%, the latter two corresponding to capacities of 117 and 99 mAh/g (4 A/g), respectively. This approach simplifies the process and aligns with environmental principles, offering significant potential for various graphite nanosheet applications.

Novel multiphase nano Ni3Bi2S2/NiS anchored on graphite nanosheet for high-capacity sodium-ion battery anodes

In the context of scalable electrode production via ball-milling, achieving high cycling stability and electrochemical performance in bifunctional anodes for sodium ion batteries (SIBs) is crucial yet remains a significant challenge. To address these objectives, we have developed a unique hybrid anode nanocomposite characterized by its local multiphase nature. This composite involves the incorporation of novel ternary-Ni-Bi-S/binary-Ni-S nanomaterials onto exfoliated graphite nanosheets (Ni3Bi2S2/NiS-G) through a facile ball-milling process. Our combined experimental and theoretical investigations suggest that the interactions between graphite nanosheets and the layered structure of Ni3Bi2S2/NiS, along with the discharge products of Na2S, play pivotal roles in enhancing the Na+ diffusion rate and stability of the hierarchical configuration anode. Upon testing, the novel Ni3Bi2S2/NiS-G shows overwhelmingly higher electrochemical performance compared to the Ni3Bi2S2/NiS counterpart, the Ni3Bi2S2/NiS-G delivered a reversible capacity of 489.9 mAh/g at 0.2 A/g after 400 cycles, and displayed a high capacity of 387.3 and 339.6 mAh/g after 500 cycles at 1 A/g and 2 A/g, respectively, yielding a high capacity retention ratio of 84.8 % and 82.8 % of the 1st cycle. This work provided a novel approach for developing new bifunctional anode electrodes with high capacity and rate performance as well as superior cycling stability.

A study on novel dual-functional photothermal material for high-efficient solar energy harvesting and storage

The solar-heat storage efficiency of devices based on phase change materials (PCMs) is limited due to the light absorption and internal heat transfer within the PCMs, unclear thermal conductivity-enhancement mechanism within nanocomposite PCMs, and uncontrollable photothermal-interface modulation. Therefore, a novel controllable strategy was proposed in this study to fabricate dual-functional photothermal storage three-dimensional (3D) phase change blocks (PCBs) with higher thermal conductivity (27.98 W/m·K) and spectral absorption (98.03 %) compared to those of most previously reported PCM-based devices. The as-synthesized PCBs contained millimeter-sized graphite plates with horizontal Van der Waals bonds and oriented micro/nanoscale graphite nanosheets. The structural properties of thin PCM layers between the PCB sheets have synergistically reduced the internal interfacial thermal resistance of the PCBs. Laser-controllable induction was used to fabricate integrated biomimetic-forest 3D optical absorbers on the high thermal conductivity interface of the PCBs, which significantly reduced the thermal resistance of the optical-thermal interface. The resulting 3D-PCBs, integrated with thermoelectric generators, powered portable electronic devices, expanding the applications of traditional PCM heat-storage devices. Therefore, this study will guide the future design of high-performance solar-thermal storage PCMs with a wide range of practical applications.

S, N, and O tri-doped graphite nanosheets-based gas diffusion electrode boosts highly selective electrosynthesis of H2O2

Electrochemical synthesis of hydrogen peroxide (H2O2) via oxygen reduction reaction (ORR) is a promising environmentally friendly approach for on-site production of H2O2. The development of economically feasible cathodes with high activity and selectivity is of utmost importance to enable the large-scale application of the process of H2O2 electrosynthesis. Herein, a novel electrocatalyst of sulfur, nitrogen, and oxygen tri-doped graphite nanosheets (SNOGNSs) was developed, which exhibited the selectivity of up to 97.4 % for the electrosynthesis of H2O2, significantly higher than that of flake graphite (FG, 51.4 %), OGNSs (72.8 %) and NOGNSs (90.9 %). The gas diffusion electrode (GDE) was fabricated using SNOGNSs as catalysts, and the accumulation of H2O2 reached 732.8–1044.4 mg/Lh−1 at 0.3–0.5 A electrolytic current. The mechanism of the synergistic enhancement of two-electron ORR by S, N, and O tri-doping was revealed utilizing density functional theory (DFT) calculations. This work offers a suitable alternative for on-site clean production of H2O2 that can be applied in electrochemical advanced oxidation processes.

High-Rate Performance of a Designed Si Nanoparticle–Graphite Nanosheet Composite as the Anode for Lithium-Ion Batteries

A silicon nanoparticle–graphite nanosheet composite was prepared via a facile ball milling process for use as the anode for high-rate lithium-ion batteries. The size effect of Si nanoparticles on the structure and on the lithium-ion battery performance of the composite is evaluated. SEM and TEM analyses show a structural alteration of the composites from Si nanoparticle-surrounded graphite nanosheets to Si nanoparticle-embedded graphite nanosheets by decreasing the size of Si nanoparticles from 250 nm to 40 nm. The composites with finer Si nanoparticles provide an effective nanostructure containing encapsulated Si and free space. This structure facilitates the indirect exposure of Si to electrolyte and Si expansion during cycling, which leads to a stable solid–electrolyte interphase and elevated conductivity. An enhanced rate capability was obtained for the 40 nm Si nanoparticle–graphite nanosheet composite, delivering a specific capacity of 276 mAh g−1 at a current density of 1 C after 1000 cycles and a rate capacity of 205 mAh g−1 at 8 C.

Unravelling the role of poly(methyl methacrylate) (PMMA) molecular weight in poly(vinylidene fluoride) (PVDF)/PMMA/expanded graphite (ExGr) blend nanocomposites: Insights into morphology, thermal behavior, electrical conductivity, and wetting property

Poly(vinylidene fluoride) (PVDF) based conducting polymer composites with carbon nanomaterials can be used for mechanical energy harvesting through piezoelectric or triboelectric effect. This study aims to investigate the influence of PMMA molecular weight on the electrical, thermal, and wetting properties of PVDF/40 wt.% PMMA blend nanocomposites reinforced with expanded graphite (ExGr). The blend nanocomposites with 40 wt.% PMMA have been prepared by solution blending method by using two different molecular weights of PMMA whose melt flow indices are 2 g/10 min and 2.3 g/10 min. The coexistence of the electroactive gamma and non-polar alpha phases of PVDF in the blend nanocomposites has been confirmed by X-ray diffraction, Fourier transform infrared spectroscopy and differential scanning calorimetry analyses. While overall crystallinity (%) of low molecular weight PMMA employed blend nanocomposites is lower than that of high molecular weight PMMA blended nanocomposites, the electroactive gamma phase has been found to increase in the former blend nanocomposites. The dispersion of graphite nanosheets has been observed to be better in high molecular weight PMMA employed blend nanocomposites which results in higher electrical conductivity. Impedance analysis of PVDF-40 wt.% PMMA-2 wt.% ExGr blend nanocomposite with high molecular weight PMMA results in enhanced interjunction capacitance (74.5 pF) in comparison to low molecular weight PMMA mixed blend nanocomposites (68 pF). Water contact angle (WCA) increases with molecular weight of PMMA and ExGr loading level. Thermogravimetric analysis has shown that the char content (above 500°C) is slightly higher for the blend with low molecular weight PMMA than with high molecular weight PMMA.

A graphene nanoflake-based flexible composite phase change material for enhanced heat dissipation in chip cooling

Efficient heat dissipation is a key requirement for stable performance retention and failure prevention of microelectronic components. In practical applications, the interface thermal resistance between the component and the heat dissipation unit affects the heat dissipation effect. Thermal interface materials (TIM) are used to fill the voids at the solid interface between the device and the heat sink to create a thermally conductive path for heat dissipation. Phase change materials (PCMs) are candidates as TIM for next-generation electronic devices due to their excellent latent heat storage. However, some inherent problems of PCMs, such as low thermal conductivity, high solid-state rigidity, and easy leakage, also limit their application in the thermal management of electronic equipment. This study prepared a biomass cotton cloth substrate with a woven structure attached to graphite nanosheets and further constructed a thermally conductive matrix through drying or high-temperature carbonization. Through the composite of thermally conductive matrix and paraffin wax (PW), a flexible phase change thermal interface composite material was obtained. The phase change enthalpy of composite materials is as high as 157.7 J/g. The thermal conductivity of the composite material is 293.7 % higher than that of pure PW. On its excellent flexibility and structural strength, the composite material can better adapt to the thermal interface, reduce contact thermal resistance, and thus achieve good leakage resistance. The flexible phase-change TIM developed in this study have broad application prospects in the fields of chip heat dissipation and thermal management of wearable electronic devices.

Enhanced levofloxacin degradation through efficient activation of peroxymonosulfate using N-doped bulged multilayer Graphene: Harnessing interface structure to regulate carrier concentration and transport speed

Nitrogen (N)-doped carbon materials are regarded as potential catalysts for advanced oxidation procedures due to their efficiency and environmentally friendly nature. Nevertheless, the low carrier concentration, slow charge transfer, and limited mass transfer efficiency hinder satisfactory catalytic performance. Herein, we present the novel use of graphite nanosheets as precursors to synthesize nanoporous N-doped mesoporous expanded and bulged multilayer graphene (EG@N-x) with varying proportions for peroxydisulfate (PMS) activation. The EG@N-2.5 catalyst demonstrates a degradation rate of 0.140 min−1, and over 90 % of LEVO (24 mg/L) was decomposed in 10 min. Additionally, the EG@N-2.5/PMS system possessed a broad pH range of efficiency (1.0–7.0), exceptional anti-interference performance against anions and humic acid (HA), and marvelous reusability, which can be attributed to the superior PMS activation performance of EG@N-x by lowering the EHOMO − ELUMO (EPD = 0.014433) gap, and reducing the adsorption binding energy (Eads = -2.33 eV), enhancing the amount of charge transfer (Q = 0.6190 e) in the EG@N-x/PMS system. The removal of LEVO is primarily attributed to the mechanism of singlet oxygen (1O2) mechanism and the metastable reactive complexes in electron transfer. Decarboxylation, defluorination, and depiperazinylation are three dominant reaction pathways. Moreover, the EG@N-x/PMS system demonstrates adequate mineralization of LEVO under various organic and environmental conditions, reducing effluent biotoxicity.

Self-supporting oxygen vacancy-rich α-MnO2 nanowire/few-layer graphite/SWNT bundle composite film for high-performance flexible aqueous zinc-ion battery cathode

The increasing demand for flexible and wearable electronic devices has led to widespread interest in flexible electrochemical energy storage devices. However, the transformation of the battery structure from conventional to flexible presents a great challenge to the battery design. Herein, we developed a facile method for the preparation of a self-supporting composite film consisting of oxygen-vacancy rich MnO2 nanowires (NWs), few-layer graphite nanosheets (FLGs), and single-walled carbon nanotube (SWNT) bundles as the cathode of flexible zinc-ion batteries. This ternary interwoven interconnection 3D structure enhances the electrochemical performance of the battery and realizes fast charge transfer; oxygen vacancies in the MnO2 NWs caused by heat treatment (300 °C in Ar) allow for rapid intercalation and diffusion of Zn2+. The interwoven FLGs and SWNT bundles improve the electrical conductivity, and the robust interactions between the two carbon nanomaterials and the MnO2 NWs effectively make the composite film with excellent mechanical properties. This self-supporting flexible electrode exhibits a high specific capacity of 374 mAh/g at 0.4 A/g, maintains a Coulombic efficiency of ∼ 100 % after 1600 cycles at 2 A/g, and has a high energy density of 651.5 Wh kg−1 at 65.2 W kg−1. Moreover, the flexible zinc ion batteries assembled with the electrode demonstrate good mechanical properties and a high reversible specific capacity of 343 mAh/g after 75 bending cycles. Based on these findings, we believe that this composite film holds great promise as a cathode material in flexible energy storage applications.