Waste cotton Fabric/MXene composite aerogel with heat generation and insulation for efficient electromagnetic interference shielding

Electromagnetic interference (EMI) shielding materials have become more and more indispensable due to serious electromagnetic-radiation pollution. Herein, waste cotton cellulose aerogels were prepared by dissolving waste cotton fabrics (WCF) in NaOH/urea aqueous solution, and MXene nanosheets were subsequently deposited on the cellulose aerogels by a facile dip coating method to obtain WCF/MXene composite aerogels. The WCF/MXene composite aerogels with highly porous network structure show remarkable electrical conductivity (8.2 Ω/sq of surface resistance), high EMI shielding effectiveness (EMI SE) in the range of 2–18 GHz (39.3–48.1 dB). The WCF/MXene aerogel possesses high SSE and SSE/t of 677.94–829.74 dB cm³ g^?1 and 3512.62–4299.17 dB cm² g^?1, respectively (2–18 GHz). In addition, the heating temperature of WCF/MXene composite aerogels reaches 199 °C when 3 V positive voltage is applied on them. The WCF/MXene composite aerogels possess excellent electromagnetic shielding effectiveness, heat generation property and insulation, which can be potentially used as multifunctional materials for EMI shielding, electrical-heating and high temperature protection.     

Super-insulating,ultralight and high-strength mullite-based nanofiber composite aerogels

Ceramic nanofiber aerogel is one of the most attractive insulation materials in recent years. However, its practical application ability is limited at high temperature due to high radiation heat transfer. Herein, we constructed a novel closed-cell/nanowire structured mullite-based nanofiber composite aerogel via electrospinning technology and solvothermal synthesis method. Hollow TiO₂ spheres were used as pore-making material and infrared opacifier to reduce fiber solid heat conduction and high temperature radiation heat transfer simultaneously. In addition, TiO₂ nanowires grown in-situ on the fiber surface further decrease the radiation heat transfer of aerogel and improve the mechanical properties. The unique structure endows the aerogel with high mechanical robustness (0.32–0.35 MPa, 10% strain), low density (39.2–47.5 mg/cm³) and ultralow thermal conductivity (~0.017 W m^?1 K^?1 at 25 ℃ and ~0.056 W m^?1 K^?1 at 1000 ℃). This work offers a novel strategy for the development of ceramic nanofiber aerogel at high temperature.     

Roll-to-roll processable MXene-rGO-PVA composite films with enhanced mechanical properties and environmental stability for electromagnetic interference shielding

MXene films promise potential electromagnetic interference (EMI) shielding materials, but poor scalable processability, environmental instability, and weak mechanical properties severely restrict their applications. Herein, we engineer the large-area, high-performance, and compact nacre-like MXene-based composite films through cooperative co-assembly of Ti₃C₂T_X MXene and reduced graphene oxide (rGO) in the presence of polyvinyl alcohol (PVA). The resulting MXene-rGO-PVA composite films benefit from enhanced bonding strength and extra chain bridging effect of linear PVA molecules enriched with hydroxyl groups. Therefore, the composite film achieves high tensile strength (～238 MPa) and toughness (～1.72 MJ m^?3) while having high conductivity of ～32 S cm^?1. A significant EMI shielding effectiveness (41.35 dB) is also demonstrated, with an excellent absolute shielding effectiveness of ～20,200 dB cm² g^?1 at only 12-μm thickness. Moreover, due to the synergistic effect of multiple components, the composite films maintain a stable EMI shielding performance in harsh environments (sonication, hot/cold annealing, and acid solution) with mechanical properties that fluctuate only within 10% compared to the original film. More importantly, commercial polyethylene terephthalate release liner can be applied for the film coating, facilitating continuous roll-to-roll production of large-area films and future applications.     

Flexible Electrospun strawberry-like structure SiO2 aerogel nanofibers for thermal insulation

Herein, a novel flexible SiO₂ aerogel composite nanofiber membrane with strawberry-like structure and excellent thermal insulation properties, in which SiO₂ aerogel particles act as thermal insulation filler, was prepared by electrospinning technology. With the addition of nano-pore structure SiO₂ aerogel particles, the heat transfer path of the fibers inside the membrane became discontinuous, endowing the as-prepared membrane an ultra-low thermal conductivity of 30.3 mW/(m?K) and large surface area of 240 m²/g. Moreover, the nanofibers membrane also possesses the combined merits of excellent fire resistance, high-temperature stability, and temperature-invariant flexibility, rendering it a promising in the application of insulation and gas adsorption. The successful preparation of this flexible nanofiber membrane paves a new way to design materials with excellent thermal insulation and adsorption properties.     

Preparation of CuMn2O4/Ti3C2 MXene composite electrodes for supercapacitors with high energy density and study on their charge transfer kinetics

In this study, we present a novel electrode material that combines Ti₃C₂ MXene and high-capacity CuMn₂O₄ to increase the energy density of supercapacitors, which are a popular choice for energy storage due to their high-performance potential. The electrode material was synthesized using the hydrothermal method with varying deposition times (3 h, 6 h and 9 h), and the resulting composite materials were characterized using advanced analytical techniques. The CuMn₂O₄/MXene composite electrode synthesized at 3h exhibited exceptional performance, with a specific capacitance of 628 mF/cm² at 4 mA/cm², due to the enhanced electrical conductivity and charge storage properties of CuMn₂O₄ and MXene sheets. We also uncovered an intricate charge transfer mechanism and storage kinetics of CuMn₂O₄/MXene composite on a nickel foam electrode, revealing a diffusion-controlled energy storage mechanism with fast mass transportation. To demonstrate practicality, we constructed an asymmetric coin cell supercapacitor device using CuMn₂O₄/MXene composite synthesized at 3h and activated carbon as the positive and negative electrodes, respectively. The device showed a specific capacitance of 496 mF/cm² at 6 mA/cm² with cyclic stability of 80% for up to 10,000 cycles, and a power density of 1.5 mW/cm² at a higher energy density of 0.073 mWh/cm². Our results demonstrate the potential to significantly advance the development of high-performance supercapacitors by combining Ti₃C₂ MXene and high-capacity oxides, refining the synthesis process, and exploring innovative electrode architectures.     

The production of rGO/ RuO2 aerogel supercapacitor and analysis of its electrochemical performances

In this study, ruthenium was bonded to the reduced graphene oxide in an ultrasonic bath. The aerogel of the mixture was produced at −78 °C. Structural characterization of aerogels was done with XRD and FTIR, surface characterization was performed with STEM, and elemental analysis was conducted by EDX analysis. The produced aerogel composites were transformed into electrodes on conductive Nickel foam. IviumStat, a potentiostat/galvanostat device, was used for the electrochemical characterization of the symmetrical supercapacitors. According to CV voltammograms, rGO/RuO₂ aerogels' highest specific capacitance was calculated as 328.6 F g⁻¹ at a potential scan rate of 5 mV s⁻¹. The assembled rGO/RuO₂ aerogel-based supercapacitor cell offered a high energy density value of 31.1 W h kg⁻¹ even at the power density of 8.365 kW kg⁻¹; this is comparable to that of lead-acid and nickel-metal hybrid batteries.     

SiBCN ceramic aerogel/graphene composites prepared via sol-gel infiltration process and polymer-derived ceramics (PDCs) route

The SiBCN ceramic aerogel/graphene composites were synthesized by combining a simple sol-gel infiltration process with CO₂ supercritical drying technology and polymer-derived ceramics route. In order to select the best preceramic sample for sintering, the micromorphology of PSNB aerogel/graphene composites fabricated with different graphene oxide solution concentrations were investigated. The microstructure evolution of the prepared SiBCN ceramic aerogel/graphene composites and phase composition were studied by SEM, TEM and XRD, the pore structure of the preceramic composites pyrolyzed at 1200 °C was tested by specific surface area and pore size analyzer. Furthermore, the compressive strain-stress curve and toughening mechanisms of composites were also investigated in detail. The results showed that all the preceramic composites and obtained ceramic aerogel composites possessed the mesoporous structure. The basic structure of SiBCN aerogel network changed from the initial spherical particles accumulation to the nanowires lapping with the sintering temperature increased from 800 °C to 1200 °C. After pyrolyzing at 1200 °C, the specific surface area and pore volume for the sample were 101.61 m² g⁻¹ and 1.43 cm³ g⁻¹, respectively, and a small amount of β-SiC crystalline phases were formed in amorphous ceramic matrix and had an relatively uniform distribution. Moreover, the paepared ceramic aerogel composites possessed a certain degree of toughness, the toughening mechanisms of composite samples mainly included the crack deflection, graphene pull-out, graphene bridging and graphene crumpling.     

Cage-like structured flexible hybrid fiber/SiO2 aerogel composite for noise reduction

The fiber/aerogel material prepared by the traditional method of sol-gel has a serious powder shedding phenomenon, and has serious environmental pollution and health hazards. In this study, an environmentally friendly porous sound absorption material with a cage-like structure, which used flexible ultrafine glass/quartz hybrid fibers (HFs) as the carrier and SiO₂ aerogel as the pore filler, was produced using the wet manufacturing process. The addition of aerogel enhanced the internal reflection of sound waves, reduced the propagation speed, increased the acoustic energy loss and improved the sound absorption coefficient (SAC). The noise reduction coefficient (NRC) reaches 0.49 in the range of 250–6300 Hz. The obtained composite presented a low density (73.5 mg/cm³) and heat resistance up to 500 °C.     

Mechanical and dielectric properties of reduced graphene oxide nanosheets/alumina composite ceramics

Reduced graphene oxide (rGO) nanosheets/alumina (Al₂O₃) composite ceramics were fabricated by hot-pressing sintering. The density, porosity, microhardness, flexural strength and complex permittivity were investigated to study their mechanical and dielectric properties. The results revealed that the rGO nanosheets were uniformly distributed in the Al₂O₃ matrix and that the composite ceramics were highly dense at 3.67–3.99 g/cm³. Due to low rGO hardness and elevated porosity, the microhardness exhibits a decreasing trend as the rGO content increases. The flexural strength first increased and then decreased with the escalation of rGO content, and the highest strength of 313.75 MPa was obtained at 3 wt%, increasing by 37.61% relative to that of the hot-pressing sintered Al₂O₃ ceramic. Owing to the enhanced interfacial polarization, dipole polarization, polarization relaxation loss and conductance loss, the real part and imaginary part of complex permittivity increase from 10.40 to 52.73 and from 0.08 to 28.86 as the rGO content rose from 0 wt% to 4 wt%, respectively.     

Electrochemical behavior of CuO/rGO nanopellets for flexible supercapacitor,non-enzymatic glucose,and H2O2 sensing application

In the present article, graphene oxide (GO) sheets and monoclinic copper oxide (CuO) nanocrystals are connected with each other and result in the formation of CuO/rGO nanopellets, and these nanopellets synthesized using coprecipitation method. The nanopellet structured CuO/rGO composite on carbon cloth, which act as current collector exhibits specific capacitance of 188 F g^?1 at a current density of 0.2 A g^?1 and up to 96.3% capacity retention after 2000 charge-discharge cycles. It shows a maximum energy density of 7.32 Wh kg^?1 and power density of 53 W kg^?1. The glucose sensing characteristics of CuO/rGO nanopellet is investigated on carbon cloth and ITO substrate. It shows glucose sensitivity of 0.805 mA mM^?1 cm^?2 and 0.2982 mA mM^?1 cm^?2 for a bundle like structured CuO/rGO composite on carbon cloth and ITO substrate, respectively. Further H₂O₂ sensing is studied on ITO substrate, which manifests H₂O₂ sensitivity of 84.39 μA mM^?1 cm^?2. The results indicate that nanopellet structured CuO/rGO composite could be a promising electrode material for supercapacitor, glucose, and H₂O₂ sensor.     

Preparation of monolith SiC aerogel with high surface area and large pore volume and the structural evolution during the preparation

Resorcinol–formaldehyde/silica composite (RF/SiO₂) aerogel was synthesized by sol–gel process followed by supercritical drying (SCD). Monolithic SiC aerogel was obtained from RF/SiO₂ aerogel after carbothermal reduction. The evolution of physical property, crystal structure, morphology and pore structure from RF/SiO₂ to SiC aerogel was investigated by different methods, such as X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM) and N₂ adsorption/desorption. The as-synthesized SiC aerogel presented typical mesoporous structure and possessed high porosity (91.8%), high surface area (328 m²/g) and large pore volume (2.28 cm³/g). Carbothermal reduction mechanism was also discussed based on the experiment and characterization results.     

Al-doping driven electronic structure of α-NiS hollow spheres modified by rGO as high-rate electrode for quasi-solid-state capacitor

Developing an optimized electronic structure of α-NiS electrode material is critical for its high-rate electrochemical performance of quasi-solid-state capacitor. Herein, Al³⁺ have been doped into α-NiS lattice and the reduced graphene oxide (rGO) is employed to modify Al-doping α-NiS, to alleviate the low-mobility charge of α-NiS. The electronic structure and electrochemical properties of α-NiS hollow spheres induced by Al-doping and rGO modification are investigated, both experimental characterization and theoretical results confirm Al-doping affect the electronic structure and electrochemical performance of α-NiS hollow spheres. In the composite of Al-doping α-NiS and rGO (named as Al_xNi_1-xS/rGO), the doped heteroatom improves the intrinsic electronic structure of α-NiS and the rGO provides a good electric conducting network, leading to an enhanced electrochemical performance of α-NiS as high-rate electrode material. After evaluation, the optimized Al_0.2Ni_0.8S/rGO composite shows a superior reversible capacity of 1096 C g^?1 at 2 A g^?1, and retains a capability of 471 C g^?1 at a high-rate of 30 A g^?1. Moreover, an asymmetric quasi-solid-state hybrid capacitors assembled by Al_0.2Ni_0.8S/rGO and activated carbon presents a high energy density of 30.6 Wh kg^?1. This work provides a foundational strategy for the modification of α-NiS through Al-doping and combining with rGO, which has a positive effect on α-NiS electrode material in quasi-solid-state hybrid capacitors.     

Ultra-broadband electromagnetic wave absorbent: In-situ generated silica modified conductive carbon fiber aerogels

The research and development of dielectric microwave absorbing materials with broad electromagnetic (EM) response is a significant project in EM wave absorption field. To achieve high-performance absorption and strong interfacial bonding at the same time, thermal-assisted in-situ bonding technology was applied to fabricating the dielectric composite absorbing materials. Thanks to the combination of vacuum filtration and in-situ hydrothermal reaction, the as-prepared binary composite aerogel shows both strong interface contacting and good mechanical stability. In addition, the carbon nanofibers/silica composite aerogel (CSA) exhibits ultra-broad effective bandwidth covering from S to Ku band, originated from the uniform dispersed silica aerogel in conductive carbon fiber network. In details, for CSA1 sample, the maximum reflection loss (RL) values and effective absorption bandwidth reach −46.2 dB (1.8 mm) and 5.2 GHz (1.5 mm). Meanwhile, the optimum RCS reduction values reaches 16.2 dB m² when the detection theta was set as 0°. For CSA2 sample, the effective absorption bandwidth reaches 8.64 GHz at 1.5 mm, and tends to possess lower frequency EM response covering the S-band. This work exhibits a kind of broad-bandwidth aerogel absorbers at low thickness, which shows huge potential in large-scale production of microwave absorbing devices.     

Eco-friendly poly(vinyl alcohol)/delaminated V2C MXene high-k nanocomposites with low dielectric loss enabled by moderate polarization and charge density at the interface

High-dielectric-constant (high-k) polymer/conductor composites with low dielectric loss are desirable for energy storage. However, high leakage currents from interfacial regions with high charge density are difficult to handle. In this work, high permittivity and low dielectric loss were achieved in poly(vinyl alcohol) (PVA)/V₂C MXene nanocomposite films fabricated by solution casting by taking advantage of the interfacial compatibility and moderate interfacial charge density of the nanocomposites. Water-soluble PVA was utilized as the polymer matrix. Delaminated V₂C MXene nanosheets with appropriate conductivity were prepared and used as the filler. The mild interface polarization of the nanocomposites was responsible for achieving favourable permittivity values. The small gap between the work functions of PVA and V₂C contributed to moderate interfacial charge density values and thus low dielectric loss values. A proportional correlation between the interfacial charge density and the conductivity of composites was also verified. The depth of charge injection from the MXene to PVA was found to be half of the interlamellar spacing of the delaminated MXene. The dependence of the electrical properties of the nanocomposites on the frequency and MXene content was also studied. The composite with 4 wt% MXene exhibited a permittivity of ~24 (16 times that of PVA) and a dielectric loss of ~0.14 (1.5 times that of PVA) at 1 kHz, as well as breakdown strength of ~31 MV m⁻¹ (63% of PVA). This work might enable environmentally friendly fabrication of promising composite dielectrics.     

A novel efficient RhB absorbent of Mo2N/MoO2 composite nanofibers for wastewater treatment

Mo₂N/MoO₂ composite nanofibers have been prepared via an electrospinning and controlled nitridation process. The composite nanofibers exhibit a highly efficient Rhodamine B (RhB) absorption behavior with a rate constant of 0.153 g min⁻¹ mg⁻¹, which is about 20 times of the commercial-activated carbon material. Furthermore, the nanofibers show stable absorption activity after recycled by an environmental friendly procedure for four times. The excellent absorption performance of Mo₂N/MoO₂ composite nanofibers demonstrates a promising application of Mo₂N-related materials as an absorbent for wastewater treatment.     

A new As3Mo8V4/PANi/rGO composite for high performance supercapacitor electrode

Herein, [As₂^IIIAs^VMo₈^VIV₄^IVO₄₀]₂[Cu^ICu₂^II(pz)₄]₂·9H₂O/polyaniline/reduced graphene oxide (pz = pyrazine, abbreviated to As₃Mo₈V₄/PANi/rGO) composite is first assembled, characterized and systematically explored for its supercapacitor performance. As₃Mo₈V₄/PANi/rGO composite shows a exceptional specific capacitance (2351 F g^?1 at 1 A g^?1) and outstanding cyclic stability (96.9% after 5000 cycles). The symmetric supercapacitor exhibits high specific capacitance of 1295 F g^?1 at 1 A g^?1 and excellent energy density of 88.1 Wh kg^-1 at power density of 349.6 W kg^-1, while maintaining a notable capacitance retention of 85.7% after 5000 cycles at 2 A g^-1. The above results confirm the potential application of As₃Mo₈V₄/PANi/rGO composite in energy storage devices.     

Rapid preparation of Palygorskite/Al2O3 composite aerogels with superhydrophobicity,high-temperature thermal insulation and improved mechanical properties

Al₂O₃ aerogels are widely employed in heat insulation and flame retardancy because of their unique combination of low thermal conductivity and exceptional high-temperature stability. However, the mechanical properties of Al₂O₃ aerogel are poor, and the preparation time is considerably long. In this study, we present a simple and scalable approach to construct monolithic Pal/Al₂O₃ composite aerogels using solvothermal treatment instead of traditional solvent replacement, which remarkably shortened the preparation time. Subsequently, to obtain stable superhydrophobicity (θ > 152°), the Pal/Al₂O₃ aerogel was modified by gas-phase modification method. The obtained Pal/Al₂O₃ composite aerogels demonstrate the integrated properties of low density (0.078–0.106 g/cm³), low thermal conductivity (1000 °C, 0.143 W/(m·K)), good mechanical properties (Young's modulus, 1.6 MPa), and good heat resistance. The monolithic Pal/Al₂O₃ composite aerogels with improved mechanical performance and improved thermal stability can show great potential in the field of thermal insulation.     

Flash sintering of alumina/reduced graphene oxide composites

The flash sintering behavior of Al₂O₃/reduced graphene oxide (rGO) composites was investigated. rGO was used as a composite component and a conductive additive. Under the electric fields of 250–400 V cm⁻¹, the flash event occurred at extremely low temperatures of 236–249 °C. The current density limit played a significant role in the degree of densification. A larger current density resulted in a higher density of the sample. However, current densities larger than 33.33 A cm⁻² resulted in broken samples because of the localization of high current density coupled with the formation of hot spots. Flash sintering at a furnace temperature of 800 °C, electric field of 300 V cm⁻¹ and current density limit of 33.33 A cm⁻² produced nearly completely dense Al₂O₃/rGO composites. In addition to the current limit, the furnace temperature is also a key parameter that controls the degree of densification to achieve “safe” flash sintering.     

Polar bear hair inspired ternary composite ceramic aerogel with excellent interfacial bonding and efficient infrared transmittance for thermal insulation

Highly porous, heat resisting ceramic aerogels are considered as promising materials for high-temperature insulation. However, the general structural characteristics of ceramic aerogel, such as poor mechanical strength and transparency to infrared radiation, pose a major obstacle to their practical application. In this paper, we report a general strategy to prepare hollow mullite fiber (HMF) structures by coaxial electrostatic spinning and grow TiO₂ nanorods (TiO₂/NAs) in situ on HMF. The ternary composite ceramic aerogel material was prepared by filling the pores of HMF-TiO₂/NAs with SiCN aerogel. The TiO₂/NAs increased the fiber/aerogel interfacial bonding of the composite (0.392 MPa, 30% strain) and improved the IR transmittance (∼0%, 1200 ℃) without sacrificing their low density and thermal conductivity. In addition, low thermal conductivity (0.041 W/(m·K), 1200 °C) and excellent high-temperature insulation properties allow the composite aerogel to meet the urgent need for lightweight, high-strength, high-temperature insulation systems for spacecraft.     

NiFe-NiFe2O4/rGO composites: Controlled preparation and superior lithium storage properties

Binary transition-metal oxides with spinel structure have great potential as advanced anode materials for lithium-ion batteries (LIBs). Herein, NiFe-NiFe₂O₄/ reduced graphene oxide (rGO) composites are obtained via a facile cyanometallic framework precursor strategy to improve the lithium storage performance of NiFe₂O₄. In the composites, NiFe-NiFe₂O₄ nanoparticles with adjustable mass ratios of NiFe₂O₄ to NiFe alloy are homogeneously deposited on rGO sheets. As anode material for LIBs, the optimized NiFe-NiFe₂O₄/rGO composite displays remarkably enhanced lithium storage performance with an initial specific capacity as high as 1362 mAh g⁻¹ at 0.1 A g⁻¹ and a decent capacity retention of ca. 80% after 130 cycles. Besides, the composite delivers a reversible capacity of 550 mAh g⁻¹ at 1 A g⁻¹ after 300 cycles. During the charge–discharge cycles, the aggregation of the NiFe-NiFe₂O₄ nanoparticles and the structural collapse of the electrode can be well alleviated by rGO sheets. Moreover, the conductivity of the electrode can be significantly improved by the well-conductive NiFe alloy and rGO sheets. All these contribute to the improved lithium storage performance of NiFe-NiFe₂O₄/rGO composites.