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The surface chemistry of iron oxide nanocrystals: surface reduction of γ-Fe 2 O 3 to Fe 3 O 4 by redox-active catechol surface ligands
The effect of surface functionalization on the structural and magnetic properties of catechol-functionalized iron oxide magnetic (γ-Fe 2 O 3 ) nanocrystals was investigated. γ-Fe 2 O 3 nanocrystals (NCs) were synthesized from iron acetyl acetonate in phenyl ether with 1,2-tetradecanediol, oleic acid...
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Published in: | Journal of materials chemistry. C, Materials for optical and electronic devices Materials for optical and electronic devices, 2018, Vol.6 (2), p.326-333 |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The effect of surface functionalization on the structural and magnetic properties of catechol-functionalized iron oxide magnetic (γ-Fe
2
O
3
) nanocrystals was investigated. γ-Fe
2
O
3
nanocrystals (NCs) were synthesized from iron acetyl acetonate in phenyl ether with 1,2-tetradecanediol, oleic acid, and oleylamine. X-ray powder diffraction in combination with Mössbauer spectroscopy revealed the presence of γ-Fe
2
O
3
(maghemite) particles only. Replacement of oleic acid (OA) with catechol-type 3,4-dihydroxyhydrocinnamic acid (DHCA) or polydentate polydopamine acrylate (PDAm) surface ligands leads to a pronounced change of the magnetic behavior of the γ-Fe
2
O
3
nanocrystals and separated them into two distinctive magnetic entities. XPS and Mössbauer spectroscopy revealed the shell to be reduced with a magnetite (Fe
3
O
4
) contribution of up to 33% of the total mass while the core remained maghemite (γ-Fe
2
O
3
). The magnetic interaction between the maghemite core and the magnetite shell strongly reduced the anisotropy constant of the nanocrystals and the effective magnetization. Our experiments show that the surface chemistry strongly affects the phase distribution and the macroscopic magnetic properties of iron oxide nanopowders. |
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ISSN: | 2050-7526 2050-7534 |
DOI: | 10.1039/C7TC04795A |