436 resultados para heterostructured nanofibers


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Au-doped polyacrylonitrile–polyaniline core–shell nanofibers are fabricated via electrospinning and subsequent gas-phase polymerization, providing a very high field-effect mobility of up to 11.6 cm2 V−1 s−1. This method is also suitable for other conducting polymers and may eventually lead to a new and simplified fabrication of high-performance polymer organic field-effect transistors.

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A new enzymeless glucose sensor has been fabricated via electrospinning technology and subsequent calcination. The morphology and structure of the as-prepared nanofibers have been characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray diffraction (XRD). The electrocatalytic oxidation of glucose in alkaline medium at nickel oxide modified glassy carbon electrodes has been investigated. The modified electrodes offer excellent electrocatalytic activity toward the glucose oxidation at low positive potential (0.3 V). Glucose has been determined chronoamperometrically at the surface of NiO nanofibers modified electrode in 0.5 mM NaOH. Under the optimized condition, the calibration curve is linear in the concentration range of 2 × 10−3 mM∼1 mM, and 1 mM∼9.5 mM. The detection limit (signal-to-noise 3) and response time are 3.394 × 10−6 M and 2 s, respectively. The NiO electrospun nanofibers is easy to prepare and feasible in economy. The modified electrode is steady and can be used repeatedly, so it is reasonable to expect its broad use in non-enzymatic glucose sensor.

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In the present work, carbon nanofibers were prepared by pyrolysis of freeze-dried cellulose nanofiber and the effect of pyrolysis conditions on the properties of carbon nanofiber was studied. SEM analysis revealed that slow heating rates below 400oC are critical to maintain the fibrous morphology after carbonization. The present study demonstrated the possibility of producing carbon nanofibers of ≤ 30 nm in diameter by a simple and scalable method.

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In this study, two power supplies having positive/ground and negative/ground electrode output ends were used separately for electrospinning of polyacrylonitrile nanofibers. Depending on type of power supply and electrode connection, electrospinning led to different fiber diameters and deposition areas. The nozzle was connected to a high voltage end while the collector was grounded. Regardless of power supply used, finer fibers with a larger deposition area were obtained, compared to that using the same setup but with a reverse electrode connection. With an increase in the applied voltage, fiber deposition area, and productivity increased for all electrode connections. Grounded nozzles provide much better control over fiber deposition than the reverse electrode connections. Finite element modeling was used to analyze the electric field profile in the electrospinning zone. It was revealed that high electric intensity was mainly located in the part that was charged with a high voltage electrode, which could explain the differences in fiber diameter and deposition area.

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In this study, we have improved carbon nanofiber interconnection by using two electrospinning methods: conventional electrospinning and side-by-side bicomponent electrospinning to produce polyvinylpyrrolidone (PVP)/polyacrylonitrile (PAN) blend nanofibers and PVP/PAN side-by-side bicomponent nanofibers respectively. Upon carbonization, the nanofibers showed inter-bonded morphologies. PVP here functioned to bind nanofibers during carbonization. The inter-boned fibrous morphology was highly affected by the PVP/PAN ratio and the electrospinning method. Carbon nanofibers prepared by the bicomponent electrospinning were found to have larger capacitances compared to those prepared by the conventional electrospinning. The influence of electrospinning method, PAN/PVP ratio on the crystallinity of carbon nanofibers, their surface morphology and capacitor performance were examined. The influence mechanism was elucidated as well.