Electrospinning amorphous SiO2-TiO2 and TiO2 nanofibers using sol-gel chemistry and its thermal conversion into anatase and rutile. Issue 5 (1st April 2018)

• Record Type: Journal Article
• Authors: Huang, Fei; Motealleh, Behrooz; Zheng, Wenjian; Janish, Matthew T.; Carter, C. Barry; Cornelius, Chris J.
• Is Part Of: Ceramics international. Volume 44:Issue 5(2018)
• Page Start: 4577
• Page End: 4585
• Publication Date: 2018-04-01
• Subjects: Sol-gel chemistry -- Inorganic sol electrospinning -- Nanocomposite fibers -- SiO2-TiO2 phase diagram; Ceramics -- Periodicals; Céramique industrielle -- Périodiques; Ceramics; Periodicals; Electronic journals; 666
• DOI: 10.1016/j.ceramint.2017.10.134
• Languages: English
• ISSNs: 0272-8842

Abstract

Abstract: SiO2 -TiO2 nanofibers were electrospun from partially hydrolyzed tetraethyl orthosilicate, and titanium isopropoxide using sol-gel chemistry. SiO2 -TiO2 sol phase diagrams were created summarizing the role of composition on solution homogeneity and electrospinnability. Inorganic nanofiber spinnability was studied without the addition of any organic polymer, oligomer, gelator, or binder. TiO2 concentration within SiO2 -TiO2 fibers ranged from 25 to 100 mol%. SiO2, SiO2 -TiO2, and TiO2 nanofiber structures were investigated using scanning electron microscopy and transmission electron microscopy. Inorganic fiber spinning was highly dependent on sol reaction temperature, time, and solution composition. At high TiO2 concentrations, twisted and ribbon-like nanofibers with dumbbell-shaped cross-sections were observed. This was attributed to jet branching and splitting during electrospinning. Electrospun fibers were amorphous at room temperature, but thermally converted into crystalline anatase, which underwent additional structural changes at higher temperatures into rutile. This anatase-rutile thermal phase transformation was highly dependent upon TiO2 concentration. Nanofiber composition, thermal stability, and crystalline structures were characterized by energy-dispersive X-ray spectroscopy; Fourier transform infrared spectroscopy, thermal gravimetric analysis, and wide-angle X-ray diffraction.