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Synthesis and characterization of PB(ZR0.52, TI0.48)O3 nanofibers by electrospinning, and dielectric properties of PZT-Resin composite
Lead zirconate titanate (PZT) / Poly vinil pyrolidone (PVP) nanofibers were spun from spinnable solution by electrospinning method. Zirconium n-propoxide, Titanium isopropoxide and Lead acetate trihydrate were solved in 2-Metoxy ethanol to obtain a precursor solution with a suitable viscosity. The o...
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Published in: | Materials letters 2012-05, Vol.75, p.61-64 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Lead zirconate titanate (PZT) / Poly vinil pyrolidone (PVP) nanofibers were spun from spinnable solution by electrospinning method. Zirconium n-propoxide, Titanium isopropoxide and Lead acetate trihydrate were solved in 2-Metoxy ethanol to obtain a precursor solution with a suitable viscosity. The obtained mats were calcined at 550, 600, 650, 700 and 800°C for 2h. The morphology and crystalline phase of PZT nanofibers were characterized using X-ray diffraction (XRD) and Scanning electron microscopy (SEM). XRD spectra indicated the formation of perovskite Pb(Zr0.52, Ti0.48)O3 phase at 600°C. Fibers had diameters between 50 to 500nm by controlling of the process parameters. Aging time and PVP percentage were found to have a significant influence on the nanofibers morphology. Increasing PVP and aging lead to increased viscosity and a correlated increase in green fiber diameter. The dielectric constant of PZT nanofibers were measured at 1kHz.
► We synthesized perovskite lead zirconate titanate fibres between 50 to 500nm. ► The PVP percentage has a significant influence on the nanofibers morphology. ► The Aging time have a significant influence on the nanofibers morphology. ► Increasing PVP and aging lead to increased viscosity. ► The dominant phase of tetragonal perovskite PZT was detected. |
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ISSN: | 0167-577X 1873-4979 |
DOI: | 10.1016/j.matlet.2012.01.082 |