RESUMEN
Vehicles operating in space need to withstand extreme thermal and electromagnetic environments in light of the burgeoning of space science and technology. It is imperatively desired to high insulation materials with lightweight and extensive mechanical properties. Herein, a boron-silica-tantalum ternary hybrid phenolic aerogel (BSiTa-PA) with exceptional thermal stability, extensive mechanical strength, low thermal conductivity (49.6 mW m-1 K-1), and heightened ablative resistance is prepared by an expeditious method. After extremely thermal erosion, the obtained carbon aerogel demonstrates noteworthy electromagnetic interference (EMI) shielding performance with an efficiency of 31.6 dB, accompanied by notable loading property with specific modulus of 272.8 kN·m kg-1. This novel design concept has laid the foundation for the development of insulation materials in more complex extreme environments.
RESUMEN
Owing to their excellent physical and chemical properties, the carbon fibre reinforced poly(ether-ether-ketone) composites (CF/PEEK) are widely used in aerospace applications such as rockets, missiles, and high-speed vehicles. However, both carbon fibre (CF) and poly(ether-ether-ketone) (PEEK) have inert molecular chain structures, which seriously affect the interfacial properties of CF/PEEK composites. In this study, to improve the properties of CF/PEEK composites, carboxylated PEEK (PEEK-COOH) with different carboxylation degrees is synthesized as the sizing agent by a "two-step" method. Then, the activated CF surface is coated by PEEK-COOH sizing layers with different functionalization degrees to prepare the CF/PEEK composites. The results show that the interfacial properties of CF/PEEK composites are improved after applying the sizing agent. When the carboxylation degree of PEEK-COOH is 19.61%, the flexural strength, flexural modulus, and interlaminar shear strength (ILSS) of CF/PEEK composites reach 489.34 MPa, 25.387 GPa, and 81.3 MPa, respectively. In addition, the use of PEEK-COOH sizing agents can form an excellent transition layer between CF and PEEK, creating an efficient stress transfer system and facilitating an even stress distribution between CF and PEEK. Furthermore, the main mechanism of material fracture changes from CF debonding to CF and resin fracture.
Asunto(s)
Cetonas , Polímeros , Fibra de Carbono/química , Ensayo de Materiales , Polímeros/química , Cetonas/químicaRESUMEN
Nanomaterials with tunnel structures are extremely attractive to be used for electrode materials in electrochemical energy storage devices. Tunnel-structured Ti-doped Na4Mn9O18 nanoparticles (TNMO-NPs) were synthesized by a facile and high-production method of the solid-state reaction with a high-energy ball-milling process. As electrode materials in the supercapacitor cell, the as-synthesized TNMO-NPs exhibit a high specific capacity of 284.93 mA h g-1 (0.57 mA h cm-2/1025.75 F g-1). A superior rate capability with a decay of 36% is achieved by increasing the scan rates from 2 to 25 mV s-1. To further explore the storage mechanism of Ti-doped Na4Mn9O18 materials, density functional theory (DFT) calculations were used to calculate the activation energy for the ion immigration in the electrode, and the results show that the minimum ion diffusion barrier energy is 0.272 eV, indicating that the sodium ions could insert into the system easily. Through the scan-rate-dependent cyclic voltammetry analysis, the capacity value indicates a mixed charge storage of capacitive behavior and Na+ intercalation progress. A maximum energy density of 77.81 W h kg-1 at a power density of 125 W kg-1 is achieved, and a high energy density of 54.79 W h kg-1 is maintained even at an ultrahigh power density of 3750 W kg-1. The TNMO-NP supercapacitors show excellent flexibility at various bent (0-180°) states. The capacitive performance of the TNMO-NPs makes them promising cathode materials for flexible supercapacitors with high specific capacities and high energy densities.
RESUMEN
One-dimensional tunnel and layer frame crystal structure materials are extremely attractive for energy storage in electrode materials. The energy storage properties of the electrode materials depend on their conductivity. Furthermore, the conductivity of electrode materials can be tailored through combination or doping with other materials, which transforms their properties from semiconductor to semimetallic or metallic and allow them to show unequaled performance for storage devices. In this work, heterostructures of manganese oxide (MnO) and modified sodium titanate (Na2Ti6O13) (MnO@Na2Ti6O13) nanowires are attained by the in situ thermal decomposition method. The heterojunction between MnO and Na2Ti6O13 allows the semiconductor properties of pure Na2Ti6O13 to show remarkable metallic behavior for improving the electrochemical performance. The capacitance of MnO@Na2Ti6O13 heterojunction nanowires can reach 272.3 F g-1, a power intensity of 250 W kg-1 at the energy density of 37.83 Wh kg-1 and retain 5000 W kg-1 at 6.67 Wh kg-1 as well. The energy storage mechanism of the MnO@Na2Ti6O13 heterostructure is studied by density functional theory. All of the results show that the MnO@Na2Ti6O13 heterostructure material has the potential to be an excellent supercapacitor material in the future.
RESUMEN
LiCoO2 (LCO) usually can deliver high energy density but low power density in Li-ion batteries (LIBs). Whether LCO could be used as electrode material for high-performance supercapacitors is dependent on promoting its power density. Owing to Faradaic redox reactions taking place on its surfaces or inside crystals through ion intercalation/deintercalation from the surfaces, increasing the specific area of LCO is a key factor to promote its rate capability. Herein, we report a facile strategy to prepare LCO nano-flakes with high specific area exceeding that of currently used micro-scale particles in LIBs. LCO as a nano-flake structure is expected to have a high fraction of Li atom exposure, which benefits fast redox reactions taking place on the surfaces. An LCO-based electrode exhibits an excellent specific capacitance of 581.3 F g-1 at 0.5 A g-1, high power density of 2262 W kg-1 at an energy density of 41.0 Wh kg-1, and good cycling stability (83.9% capacitance retention at 6 A g-1 after 2000 cycles) in LiCl aqueous electrolyte. Faradaic redox behaviors have been analyzed, indicating an ideal diffusion-controlled process. Moreover, a full solid-state symmetric supercapacitor is assembled using LCO nano-flake-based electrodes, which presents good performance with light weight and flexibility. Impressively, three charged supercapacitors in series can light 100 green light emitting diodes for 14 min. LCO in nano-flake structure form with high power density could be an excellent material for superior supercapacitors.