Journal article
Optically and microwave-induced magnetization precession in [Co/Pt]/NiFe exchange springs
- Abstract:
- Microwave and heat assisted magnetic recording are two competing technologies that have greatly increased the capacity of hard disk drives. The efficiency of the magnetic recording process can be further improved by employing non-collinear spin structures that combine perpendicular and in-plane magnetic anisotropy. Here, we investigate both microwave and optically excited magnetization dynamics in [Co/Pt]/NiFe exchange spring samples. The resulting canted magnetization within the nanoscale [Co/Pt]/NiFe interfacial region allows for optically stimulated magnetization precession to be observed for an extended magnetic field and frequency range. The results can be explained by formation of an imprinted domain structure, which locks the magnetization orientation and makes the structures more robust against external perturbations. Tuning the canted interfacial domain structure may provide greater control of optically excited magnetization reversal and optically generated spin currents, which are of paramount importance for future ultrafast magnetic recording and spintronic applications.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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- Files:
-
-
(Preview, Accepted manuscript, 690.4KB, Terms of use)
-
- Publisher copy:
- 10.1021/acsami.0c14058
Authors
- Publisher:
- American Chemical Society
- Journal:
- ACS Applied Materials and Interfaces More from this journal
- Volume:
- 12
- Issue:
- 46
- Pages:
- 52116-52124
- Publication date:
- 2020-11-06
- Acceptance date:
- 2020-10-23
- DOI:
- EISSN:
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1944-8252
- ISSN:
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1944-8244
- Language:
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English
- Keywords:
- Pubs id:
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1139398
- Local pid:
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pubs:1139398
- Deposit date:
-
2020-10-23
Terms of use
- Copyright holder:
- American Chemical Society
- Copyright date:
- 2020
- Rights statement:
- © 2020 American Chemical Society
- Notes:
- This is the accepted manuscript version of the article. The final version is available from the American Chemical Society at https://pubs.acs.org/
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