کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1488753 | 992295 | 2013 | 4 صفحه PDF | دانلود رایگان |

In this paper, nickel nanofibers were prepared by electrospinning polyvinyl alcohol/nickel nitrate precursor solution followed by high temperature calcination in air and deoxidation in hydrogen atmosphere. The thermal stability of the as-electrospun PVA/Ni(NO3)2 composite nanofibers were characterized by TG–DSC. The morphologies and structures of the as-prepared samples were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), field-emission scanning electronmicroscope (FE-SEM) and field-emission transmission electron microscopy (FE-TEM). The hysteresis loops (M–H loops) were measured by Physical Property Measurement System (PPMS). The results indicate that: the PVA and the nickel nitrate were almost completely decomposed at 460 °C and the products were pure nickel nanofibers with face-centered cubic (fcc) structure. Furthermore, the as-prepared nickel nanofibers had a continuous structure with rough surface and high degree of crystallization. The average diameter of nickel nanofibers was about 135 nm. The nanofibers showed a stronger coercivity of 185 Oe than value of bulk nickel.
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► The nickel nanofibers have been obtained by electrospinning method.
► The nickel nanofibers had rough surface which was consisted of mass nanoparticles.
► The average diameter of nickel nanofibers is about 135 nm and high degree of crystallization.
► The Hc, Ms, and Mr were estimated to be 185 Oe, 51.9 and 16.9 emu/g respectively.
Journal: Materials Research Bulletin - Volume 48, Issue 7, July 2013, Pages 2426–2429