Loading…
Electrospun NiO nanofibers as high performance anode material for Li-ion batteries
We report the synthesis and electrochemical performance of one dimensional NiO nanofibers by simple electrospinning technique and subsequently heat treated at 800 °C to yield single phase material. After the heat treatment, thickness and crystal size electrospun NiO is found ∼1 μm and 100 nm, respec...
Saved in:
Published in: | Journal of power sources 2013-04, Vol.227, p.284-290 |
---|---|
Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | We report the synthesis and electrochemical performance of one dimensional NiO nanofibers by simple electrospinning technique and subsequently heat treated at 800 °C to yield single phase material. After the heat treatment, thickness and crystal size electrospun NiO is found ∼1 μm and 100 nm, respectively. The electrospun nanofibers are subjected to various characterizations such as X-ray diffraction with Rietveld refinement, scanning electron microscopy and transmission electron microscopy (TEM). Half-cell assembly is used to evaluate the Li-uptake properties and found maximum reversible capacity of ∼784 mA h g−1 at current density of 80 mA g−1 with operating potential of ∼1.27 V vs. Li. The test cell rendered good cycleability and exhibits capacity retention of over 75% of reversible capacity after 100 cycles. The conversion mechanism of metallic nanoparticles (Ni0) are validated though ex-situ TEM measurements. Rate performance studies are also conducted and delivered good cycling properties under such high current studies.
[Display omitted]
► Electrospinning technique is used to synthesize high performance NiO nanofibers. ► NiO nanofibers rendered good cycleability and retained ∼75% initial capacity after 100 cycles. ► Ex-situ TEM analysis confirmed the formation of Ni0 particles during conversion reaction. |
---|---|
ISSN: | 0378-7753 1873-2755 |
DOI: | 10.1016/j.jpowsour.2012.11.050 |