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Formation and magnetization reversal mechanisms of nano-size Fe arrays prepared on anodic aluminum oxide templates
Vertically aligned Fe arrays have been self-assembled on anodic aluminum oxide templates by evaporation. The rims of the pores, which act as obstacles to the stacking of atoms, prevent them from forming continuous films. By controlling the Fe nominal thicknesses ( τ n ) from 400 to 5 nm, the morphol...
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Published in: | Thin solid films 2010-07, Vol.518 (18), p.5300-5303 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Vertically aligned Fe arrays have been self-assembled on anodic aluminum oxide templates by evaporation. The rims of the pores, which act as obstacles to the stacking of atoms, prevent them from forming continuous films. By controlling the Fe nominal thicknesses (
τ
n
) from 400 to 5
nm, the morphology is changed from continuous film to isolated arrays, leading to the change of the predominant magnetization reversal from domain wall motion to spin rotation. For samples with
τ
n
<
59
nm, isolated, rather than interconnected, morphology is formed. In this range, the coercivity shows a spectacular change for
τ
n
=
47
nm, with an array diameter of about 52
nm, achieving a maximum of about 38
kA/m. The critical dimension of single-domain array is therefore determined. The magnetostatic and exchange interactions are reduced due to the thermal fluctuation, and the magnetization leaves from the in-plane direction to be randomly distributed in 3-D, for
τ
n
<
27
nm. |
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ISSN: | 0040-6090 1879-2731 |
DOI: | 10.1016/j.tsf.2010.04.020 |