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The filtration performance and light transmittance of nanofiber air filters are restricted by their thick fiber diameter, large pore size, and substrate dependence, which can be solved by constructing substrate‐free fibrous membranes with true nanoscale diameters and ultrathin thicknesses, however, it has proven to be extremely challenging. Herein, a roust approach is presented to create free‐standing polyurethane (PU) nanofiber/nets air filters composed of bonded nanofibers and 2D nanonets for particular matter (PM) capture via combining electrospinning/netting technique and facile peel off process from designed substrates. This strategy causes widely distributed Steiner‐tree structured nanonets with diameters of ≈20 nm and bonded scaffold nanofibers to assemble into ultrathin membranes with small pore size, high porosity, and robust mechanical strength on a large scale based on ionic liquid inspiration and surface structure optimization of receiver substrates. As a consequence, the resulting free‐standing PU nanofiber/nets filters exhibit high PM1–0.5 removal efficiency of >99.00% and PM2.5–1 removal efficiency of >99.73%, maintaining high light transmittance of ≈70% and low pressure drop of 28 Pa; even achieve >99.97% removal efficiency with ≈40% transmittance for PM0.3 filtration, and robust purification capacity for real smoke PM2.5, making them promising high‐efficiency and transparent filtration materials for various filtration and separation applications.  相似文献   

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Li‐CO2 batteries are promising energy storage systems by utilizing CO2 at the same time, though there are still some critical barriers before its practical applications such as high charging overpotential and poor cycling stability. In this work, iridium/carbon nanofibers (Ir/CNFs) are prepared via electrospinning and subsequent heat treatment, and are used as cathode catalysts for rechargeable Li‐CO2 batteries. Benefitting from the unique porous network structure and the high activity of ultrasmall Ir nanoparticles, Ir/CNFs exhibit excellent CO2 reduction and evolution activities. The Li‐CO2 batteries present extremely large discharge capacity, high coulombic efficiency, and long cycling life. Moreover, free‐standing Ir/CNF films are used directly as air cathodes to assemble Li‐CO2 batteries, which show high energy density and ultralong operation time, demonstrating great potential for practical applications.  相似文献   

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Nitrogen‐doped carbon materials have attracted great interest in the energy storage due to the better electrochemical performances than the pristine carbon materials. In this work, a heterocyclic polyimide containing benzopyrrole and benzimidazole rings is carbonized to fabricate the free‐standing and flexible carbon membrane (CarbonPI) with a high packing density (0.89 cm?3), in which the location of nitrogen atoms in the doped configurations is easily controlled. XPS analysis indicates that quaternary nitrogen is the predominant nitrogen‐doped configurations. The high content of nitrogen effectively improves the wettability of the electrode materials. The CarbonPI membrane exhibits excellent volumetric capacitance (159.3 F cm?3 at 1 A g?1), high rate capability (127.5 F cm?3 at 7 A g?1), and long cycle life. TEM images reveal the very slight change of the microstructure of graphitic nanosheet of CarbonPI during the long charge/discharge cycles.  相似文献   

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Graphene/polyaniline multilayered nanostructures (GPMNs) are prepared using a straightforward process through which graphite is physically exfoliated with quaternary polyaniline (PANI)‐glue. This is only accomplished by sonication of the graphite flakes in an organic solvent to form continuous films with PANI. During the sonication, the conductive PANI‐glue is spontaneously intercalated between the graphene sheet layers without deterioration of the sp2 hybridized bonding structure. The resultant free‐standing, flexible films are composed of a network of overlapping graphene sheets and are shown to have a long‐range structure. The effects of different PANI content ratios and different interfacial energies (depending on the dispersion solvent) on the morphology and properties of the resulting GPMN are examined. It is found that GPMNs dispersed in water have a maximum specific capacitance of 390 F g−1 in a three‐electrode configuration. Importantly, the unique structural design of GPMNs enables their use as electrode materials for the fabrication of flexible, solid‐state electrochemical capacitors, which show an enhanced performance compared to graphene‐only devices. They exhibit a high specific capacitance of 200 F g−1, a cycling stability with capacitance retention of 82% after 5000 charge/discharge cycles, and, moreover, superior flexibility.  相似文献   

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