Please use this identifier to cite or link to this item:
http://idr.nitk.ac.in/jspui/handle/123456789/10294
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | George, G. | |
dc.contributor.author | Anandhan, S. | |
dc.date.accessioned | 2020-03-31T08:18:52Z | - |
dc.date.available | 2020-03-31T08:18:52Z | - |
dc.date.issued | 2015 | |
dc.identifier.citation | Materials Science in Semiconductor Processing, 2015, Vol.32, , pp.40-48 | en_US |
dc.identifier.uri | http://idr.nitk.ac.in/jspui/handle/123456789/10294 | - |
dc.description.abstract | NiO is a p-type semiconductor with wide band gap energy. In this study, nickel oxide nanofibers were fabricated by sol-gel electrospinning followed by high temperature calcination, using two sacrificial polymeric binders. Poly(2-ethyl-2-oxazoline) (PEtOx) in water and styrene-acrylonitrile random copolymer (SAN) in N,N- dimethylformamide (DMF) along with nickel (II) acetate tetrahydrate (NATH), as metal oxide precursor, were the two distinct polymeric systems used in this study. The morphological and structural properties of NiO fibers obtained from the aforementioned systems were compared with each other. The degradation behavior of the sacrificial polymeric binder imparted a significant effect on the properties of the obtained NiO fibers. The grain sizes and the activation energies for grain growth of NiO fibers from two systems were different. The non-stoichiometric NiO fibers obtained from the SAN/NATH system had a better ferromagnetic behavior as compared with that produced from the PEtOx/NATH system. This non-stoichiometry made a difference also in the optical band gap energies of the NiO nanofibers. 2015 Elsevier Ltd. | en_US |
dc.title | Comparison of structural, spectral and magnetic properties of NiO nanofibers obtained by sol-gel electrospinning from two different polymeric binders | en_US |
dc.type | Article | en_US |
Appears in Collections: | 1. Journal Articles |
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.