No abstract

Carbon nanofibers were produced from polyacrylonitrile/N, N-Dimethyl Formamide (PAN/DMF) precursor solution using electrospinning and vacuum pyrolysis at temperatures from 773-1273 K for 0.5, 2, and 5 h, respectively. Their conductance was determined from I -V curves. The length and cross-section area of the nanofibers were evaluated using optical microscope and scanning probe microscopes, respectively, and were used for their electrical conductivity calculation. It was found that the conductivity increases sharply with the pyrolysis temperature, and increases considerably with pyrolysis time at the lower pyrolysis temperatures of 873, 973, and 1073 K, but varies, less obviously, with pyrolysis time at the higher pyrolysis temperatures of 1173 and 1273 K. This dependence was attributed to the thermally activated transformation of disordered to graphitic carbons. KeywordsCarbon, conductivity measurement, electrostatic processes, nanotechnology This material is posted here with permission of the IEEE. Such permission of the IEEE does not in any way imply IEEE endorsement of any of the University of Pennsylvania's products or services. Internal or personal use of this material is permitted. However, permission to reprint/republish this material for advertising or promotional purposes or for creating new collective works for resale or redistribution must be obtained from the IEEE by writing to pubs-permissions@ieee.org. By choosing to view this document, you agree to all provisions of the copyright laws protecting it. Abstract-Carbon nanofibers were produced from polyacrylonitrile/N, N-Dimethyl Formamide (PAN/DMF) precursor solution using electrospinning and vacuum pyrolysis at temperatures from 773-1273 K for 0.5, 2, and 5 h, respectively. Their conductance was determined from -curves. The length and cross-section area of the nanofibers were evaluated using optical microscope and scanning probe microscopes, respectively, and were used for their electrical conductivity calculation. It was found that the conductivity increases sharply with the pyrolysis temperature, and increases considerably with pyrolysis time at the lower pyrolysis temperatures of 873, 973, and 1073 K, but varies, less obviously, with pyrolysis time at the higher pyrolysis temperatures of 1173 and 1273 K. This dependence was attributed to the thermally activated transformation of disordered to graphitic carbons.

Tin oxide (SnO 2 ) microfibres in the rutile structure were synthesized using electrospinning and metallorganic decomposition techniques. Fibres were electrospun from a precursor solution containing 20 mg poly(ethylene oxide) (molecular weight 900 000), 2 ml chloroform and 1 ml dimethyldineodecanoate tin, and sintered in the air for 2 h at 400, 600 and 800 • C, respectively. Scanning electron microscopy, x-ray diffraction and Raman microspectrometry were used to characterize the sintered fibres. The results showed that the synthesized fibres are composed of SnO 2 .

Abstract:We performed an extensive characterization of an electrospinning process to evaluate how the process parameters and precursor solution characteristics affect the fibers morphology. The work was conducted using precursor solutions with different concentrations of polyacrylonitrile (PAN) diluted in a fixed amount of N,N dimethylformamide (DMF). Fibers obtained with this process can find important applications in the field of nanosensors. The characteristics of the electrospun fibers were analyzed as a function of the solution viscosity, applied voltage and distance between the needle tip (positive electrode) and the collector plate (grounded electrode). The electrical current was monitored during the deposition process and its behavior was correlated with the characteristics of the fibers obtained. Our results demonstrate that the diameter of the fibers increases with increasing viscosity and applied voltage. The number of deposited fibers also increases with the applied voltage. Also, viscosity and applied voltage strongly affect the shape, length and morphology of the fibers. Of particular interest, we demonstrated that by monitoring the electrical current it is possible to control the fibers morphology and bead concentration. The distance between tip and collector plate determines the way the fibers arrive on the collector plate. A main contribution of this study was the definition of conditions to controllably obtain fibers that are smooth and that present diameters in the range between 140 and 300 nm.

Ultrafine tin oxide (SnO2) fibers having a rutile structure, with diameter ranging from 100 nm to several micrometers, were synthesized using electrospinning and metallorganic decomposition techniques. In this work, we propose a precursor solution that is a mixture of pure SnO2 sol made from SnCl4:H2O:C3H7OH:2‐C3H7OH at a molar ratio of 1:9:9:6, and a viscous solution made from poly(ethylene oxide) (PEO) (molecular weight 900 000) and chloroform (CHCl3) at a ratio of 200 mg PEO/10 mL CHCl3. This solution allows to obtain an appropriate viscosity for the electrospinning process. The as‐deposited fibers were sintered at 400°, 500°, 600°, 700°, and 800°C in air for 2 h. Scanning electron microscopy, scanning probe microscopy, X‐ray diffraction, Raman microspectrometry, and X‐ray photoelectron spectroscopy (XPS) were used to characterize the sintered fibers and elucidate the chemical reaction during sintering. The results showed that up to the sintering temperature of 700°C, the synthesized fibers are composed of SnO2. XPS was found to reflect the complicate chemical changes caused by the sintering process.