Synthesis and Characterization of Ultra-Fine Tin Oxide Fibers Using Electrospinning

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.