Creation of nanoscale magnetic fields using nano-magnet arrays
Source abstract
Abstract
We present the fabrication of nano-magnet arrays, comprised of two sets of interleaving SmCo5 and Co nano-magnets, and the subsequent development and implementation of a protocol to program the array to create a one-dimensional rotating magnetic field. We designed the array based on the microstructural and magnetic properties of SmCo5 films annealed under different conditions, also presented here. Leveraging the extremely high contrast in coercivity between SmCo5 and Co, we applied a sequence of external magnetic fields to program the nano-magnet arrays into a configuration with alternating polarization, which based on simulations creates a rotating magnetic field in the vicinity of nano-magnets. Our proof-of-concept demonstration shows that complex, nanoscale magnetic fields can be synthesized through coercivity contrast of constituent magnetic materials and carefully designed sequences of programming magnetic fields.
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Research context
OpenAlex topics: Magnetic properties of thin films · Magnetic and transport properties of perovskites and related materials · Topological Materials and Phenomena
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Sandia National Laboratories 1 , Albuquerque, New Mexico 87185, USA
Los Alamos National Laboratory 2 , Los Alamos, New Mexico 87545, USA
Colorado School of Mines, Department of Physics 3 , Golden, Colorado 80401, USA
Center for Integrated Nanotechnologies, Sandia National Laboratories 4 , Albuquerque, New Mexico 87123, USA
Funding
Sandia National Laboratories · Basic Energy Sciences
References (23)
Show source-provided references
1. J. Am. Chem. Soc. · 2006 · 128 · 738310.1021/ja061529k ↗
2. J. Mater. Chem. B · 2015 · 3 · 224110.1039/c4tb02023e ↗
3. Proc. Natl. Acad. Sci. U.S.A. · 2005 · 102 · 886010.1073/pnas.0500409102 ↗
4. Appl. Phys. Lett. · 2001 · 79 · 330810.1063/1.1419049 ↗
5. Phys. Rev. B · 2012 · 85 · 02050310.1103/physrevb.85.020503 ↗
6. Phys. Rev. Lett. · 2012 · 109 · 23680110.1103/physrevlett.109.236801 ↗
7. Phys. Rev. B · 2013 · 88 · 22050210.1103/physrevb.88.220502 ↗
8. Solid State Commun. · 2017 · 262 · 110.1016/j.ssc.2017.06.003 ↗
9. Phys. Rev. B · 2017 · 95 · 14050410.1103/physrevb.95.140504 ↗
10. Phys. Rev. Applied · 2018 · 10 · 05407110.1103/physrevapplied.10.054071 ↗
11. Phys. Rev. Lett. · 2010 · 105 · 07700110.1103/physrevlett.105.077001 ↗
12. Phys. Rev. Lett. · 2010 · 105 · 17700210.1103/physrevlett.105.177002 ↗
13. J. Appl. Phys. · 1965 · 36 · 97210.1063/1.1714283 ↗
14. J. Appl. Phys. · 1999 · 85 · 614810.1063/1.370025 ↗
15. 2006
16. Sci. China Phys. Mech. · 2012 · 55 · 179810.1007/s11433-012-4838-y ↗
17. J. Mater. Chem. · 2011 · 21 · 1687310.1039/c1jm11753j ↗
18. J. Appl. Phys. · 2010 · 107 · 09A70410.1063/1.3334493 ↗
19. J. Phys. Condens. Matter · 2013 · 25 · 41600410.1088/0953-8984/25/41/416004 ↗
20. Appl. Phys. Lett. · 2013 · 102 · 16240210.1063/1.4802908 ↗
21. Appl. Phys. Lett. · 2005 · 87 · 07250510.1063/1.2011787 ↗
22. J. Appl. Phys. · 2000 · 87 · 696510.1063/1.372901 ↗
23. Phys. Rev. Lett. · 2008 · 101 · 03720510.1103/physrevlett.101.037205 ↗