Morphology oriented surfactant dependent CoO and reaction time dependent Co3O4 nanocrystals from single synthesis method and their optical and magnetic properties
A simple solvothermal strategy has been developed to synthesize highly stable, pure phased CoO and Co 3 O 4 nanoparticles from Co(CH 3 COO) 2 ·4H 2 O precursor in ethanol solvent at 220 °C. The various phases of cobalt oxide (cubic CoO and Co 3 O 4 ) with controlled size and morphologies viz , nanoc...
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Veröffentlicht in: | CrystEngComm 2013-01, Vol.15 (42), p.8465-8474 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A simple solvothermal strategy has been developed to synthesize highly stable, pure phased CoO and Co
3
O
4
nanoparticles from Co(CH
3
COO)
2
·4H
2
O precursor in ethanol solvent at 220 °C. The various phases of cobalt oxide (cubic CoO and Co
3
O
4
) with controlled size and morphologies
viz
, nanocubes, hexagonal platelets and nanospheres could be obtained
via
varying only one parameter (either surfactant or reaction time) in this single synthesis method. XRD and HRTEM analyses revealed pure cubic phase CoO and Co
3
O
4
nanoparticles. The formation and shapes of CoO nanoparticles are surfactant dependent, whereas the formation and morphologies of Co
3
O
4
are time dependent. The optical absorbance studies showed two distinct broad absorption peaks and hence two optical band gaps for both CoO and Co
3
O
4
nanoparticles. CoO nanoparticles showed a wide band gap difference of 2.36 eV, while Co
3
O
4
nanoparticles were found to be semiconducting in nature with a 0.6 eV-1 eV band gap difference, which showed characteristic features of CoO and Co
3
O
4
nanoparticles, respectively. CoO nanoparticles showed interesting magnetic behaviour due to intrinsic antiferromagnetic structure and uncompensated surface spins, which was confirmed by VSM and EPR studies.
A single synthesis method is developed to synthesize cubic and rectangular shaped magnetic CoO and spherical and hexagonal platelet shaped Co
3
O
4
nanoparticles. |
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ISSN: | 1466-8033 1466-8033 |
DOI: | 10.1039/c3ce41502c |