Using structural phase transitions to enhance the coercivity of ferromagnetic films
Source abstract
Abstract
Storing information in magnetic recording technologies requires careful optimization of the recording media’s magnetic properties. For example, heat-assisted magnetic recording (HAMR) relies on a prerecording heating step that momentarily lowers the coercivity of the ferromagnetic recording media, and thereby decreases the energy expenditure for each writing operation. However, this process currently requires local temperature increases of several hundred Kelvins, which in turn can cause heat spreading, damage the write head, and limit recording rates. Here, we describe a general mechanism for dramatically tuning the coercivity of ferromagnetic films over small temperature ranges, by coupling them to an adjacent layer that undergoes a structural phase transition with large volume changes. The method is demonstrated in Ni/FeRh bilayers where the Ni layer was deposited at 300 K and 523 K, above and below the FeRh metamagnetic transition at 370 K. When the Ni layer is grown at high temperatures, the 1% FeRh lattice expansion relative to room temperature alters the Ni’s crystallographic texture during growth and leads to a 500% increase in coercivity upon cooling through the FeRh’s metamagnetic transition. Our analysis suggests this effect is related to domain wall pinning across grain boundaries with different orientations and strain states. This work highlights the promise of thermally tuning the coercivity of ferromagnetic materials through structural coupling to underlying films that could enable simplified heatsink designs and expand the selection of materials compatible with HAMR.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Magnetic properties of thin films · Theoretical and Computational Physics · Magnetic Properties and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
NIST Center for Neutron Research, National Institute of Standards and Technology 1 , Gaithersburg, Maryland 20899, USA
Department of Materials Science and Engineering, University of Florida 2 , Gainesville, Florida 32611, USA
Department of Physics, Colorado State University 3 , Fort Collins, Colorado 80523, USA
References (40)
Show source-provided references
1. Nat. Commun. · 2012 · 3 · 103510.1038/ncomms2038 ↗
2. J. Appl. Phys. · 2014 · 115 · 17B70710.1063/1.4861213 ↗
3. J. Appl. Phys. · 2015 · 118 · 09390110.1063/1.4929760 ↗
4. Nat. Mater. · 2015 · 14 · 67910.1038/nmat4248 ↗
5. Proc. IEEE · 2008 · 96 · 181010.1109/jproc.2008.2004315 ↗
6. Nat. Photonics · 2009 · 3 · 18910.1038/nphoton.2009.40 ↗
7. IEEE Trans. Magn. · 2015 · 51 · 110.1109/tmag.2015.2439690 ↗
8. IEEE Trans. Magn. · 2016 · 53 · 110.1109/tmag.2016.2604261 ↗
9. J. Appl. Phys. · 2018 · 123 · 03430310.1063/1.5016873 ↗
10. Sci. Rep. · 2018 · 8 · 980710.1038/s41598-018-27688-4 ↗
11. Appl. Phys. Lett. · 2003 · 82 · 285910.1063/1.1571232 ↗
12. Nat. Commun. · 2013 · 4 · 172610.1038/ncomms2737 ↗
13. J. Appl. Phys. · 1962 · 33 · 134310.1063/1.1728721 ↗
14. J. Appl. Phys. · 1966 · 37 · 125710.1063/1.1708424 ↗
15. Phys. Rev. B · 2005 · 72 · 21443210.1103/physrevb.72.214432 ↗
16. IEEE Trans. Magn. · 2011 · 47 · 403310.1109/tmag.2011.2140363 ↗
17. J. Cryst. Growth · 2016 · 438 · 1910.1016/j.jcrysgro.2015.12.035 ↗
18. J. Phys. D: Appl. Phys. · 2016 · 49 · 32300210.1088/0022-3727/49/32/323002 ↗
19. Phys. Rev. · 1964 · 134 · A154710.1103/physrev.134.a1547 ↗
20. Phys. Rev. Lett. · 2012 · 109 · 11720110.1103/physrevlett.109.117201 ↗
21. Phys. Rev. B · 2008 · 77 · 18440110.1103/physrevb.77.184401 ↗
22. Sov. Phys. JETP · 1964 · 19 · 1348
23. Phys. Rev. B · 1994 · 50 · 419610.1103/physrevb.50.4196 ↗
24. New J. Phys. · 2013 · 15 · 01300810.1088/1367-2630/15/1/013008 ↗
25. J. Appl. Phys. · 1999 · 85 · 102610.1063/1.369224 ↗
26. J. Appl. Phys. · 2011 · 109 · 07C71710.1063/1.3556754 ↗
27. J. Appl. Phys. · 1996 · 79 · 168910.1063/1.360955 ↗
28. Curr. Opin. Colloid Interface Sci. · 2012 · 17 · 4410.1016/j.cocis.2011.11.001 ↗
29. J. Appl. Cryst. · 2018 · 51 · 150010.1107/s1600576718011974 ↗
30. B. B. Maranville , A.Green, and P. A.Kienzle, e-print arXiv:1801.04975 (2017).
31. IEEE Trans. Magn. · 2008 · 44 · 287510.1109/tmag.2008.2001846 ↗
32. Appl. Phys. Lett. · 2014 · 105 · 17240110.1063/1.4900619 ↗
33. Sci. Rep. · 2018 · 6 · 2270810.1038/srep22708 ↗
34. Phys. Rev. B · 2010 · 82 · 18441810.1103/physrevb.82.184418 ↗
35. J. Appl. Phys. · 2014 · 115 · 04391910.1063/1.4862961 ↗
36. APL Mater. · 2015 · 3 · 04180210.1063/1.4907282 ↗
37. Appl. Phys. Lett. · 2014 · 104 · 06241010.1063/1.4865587 ↗
38. J. Appl. Phys. · 1981 · 52 · 254410.1063/1.328996 ↗
39. J. Phys. Condens. Matter · 2003 · 15 · R84110.1088/0953-8984/15/20/202 ↗
40. 2000