Designing Fe‐Based Amorphous Alloys With both Ultra‐High Magnetization and Ultra‐Low Coercivity Through Artificial Intelligence
Source abstract
Abstract
Abstract Designing soft magnetic alloys with high magnetization and low coercivity is of special interest for application in high‐frequency and high‐power electric and electronic components. In this work, high‐precision machine‐learning models based on 536 different Fe‐based amorphous alloys are developed. It reveals that the electronegativity difference (δχ) and mixing enthalpy (ΔHmix) of the alloying elements play critical roles in determining the saturated magnetization (Bs) of amorphous alloys. Specifically, smaller δχ can strengthen the biased distribution of spin‐up and spin‐down electrons as is revealed by ab initio simulations. Based on these findings, a series of advanced amorphous/nanocrystalline alloys with Bs higher than 1.90 T and coercivity (Hc) as low as 1.2 A m−1 are designed, which also have good amorphous forming ability owing to the suitable mixing enthalpy. The designed alloys with high Bs and low Hc hold promising application potentials in electronic components of high power density and low energy loss.
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Research context
OpenAlex topics: Metallic Glasses and Amorphous Alloys · Magnetic properties of thin films · Magnetic Properties and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Laboratory of Magnetic Materials and Devices and Zhejiang Province Key Laboratory of Magnetic Materials and Application Technology Ningbo Institute of Materials Technology and Engineering Chinese Academy of Sciences Ningbo 315201 China
Center of Materials Science and Optoelectronics Engineering University of Chinese Academy of Sciences Beijing 100049 China
Funding
National Key Research and Development Program of China · National Natural Science Foundation of China
References (51)
Show source-provided references
1. 10.1126/science.aao019510.1126/science.aao0195 ↗
2. 10.1109/MIE.2010.93586010.1109/MIE.2010.935860 ↗
3. 10.1016/j.actamat.2012.10.04010.1016/j.actamat.2012.10.040 ↗
4. 10.7498/aps.67.2017147310.7498/aps.67.20171473 ↗
5. 10.1007/s11837-012-0350-010.1007/s11837-012-0350-0 ↗
6. 10.1016/j.jmrt.2022.07.05110.1016/j.jmrt.2022.07.051 ↗
7. 10.1016/j.scriptamat.2023.11566610.1016/j.scriptamat.2023.115666 ↗
8. 10.1016/j.jallcom.2022.16573510.1016/j.jallcom.2022.165735 ↗
9. Huo Z. X. · Processes · 2022 · 10
10. 10.1063/1.494689410.1063/1.4946894 ↗
11. Mueller T. · Rev. Comp. Ch. · 2016 · 29 · 186
12. 10.1038/s41586-023-06735-910.1038/s41586-023-06735-9 ↗
13. 10.1016/j.actamat.2019.03.01210.1016/j.actamat.2019.03.012 ↗
14. 10.1016/j.matdes.2019.10837810.1016/j.matdes.2019.108378 ↗
15. 10.1016/j.actamat.2020.05.00610.1016/j.actamat.2020.05.006 ↗
16. 10.1126/sciadv.aaq156610.1126/sciadv.aaq1566 ↗
17. 10.1126/science.abo494010.1126/science.abo4940 ↗
18. 10.1038/s42256-019-0138-910.1038/s42256-019-0138-9 ↗
19. 10.1016/j.commatsci.2018.05.01810.1016/j.commatsci.2018.05.018 ↗
20. 10.1016/j.jfds.2017.05.00110.1016/j.jfds.2017.05.001 ↗
21. 10.1016/j.neucom.2017.11.07710.1016/j.neucom.2017.11.077 ↗
22. Chen T. Q. · 2016
23. 10.1023/A:101093340432410.1023/A:1010933404324 ↗
24. 10.1007/s00521-015-2113-710.1007/s00521-015-2113-7 ↗
25. 10.1186/1471-2105-8-2510.1186/1471-2105-8-25 ↗
26. 10.1093/bioinformatics/btq13410.1093/bioinformatics/btq134 ↗
27. Lundberg S. M. · 2017 · 4768
28. 10.1016/S1359-6454(99)00300-610.1016/S1359-6454(99)00300-6 ↗
29. Srivastava A. P. · 2024 · 293
30. 10.1002/adma.20220586310.1002/adma.202205863 ↗
31. 10.1016/j.jallcom.2020.15707110.1016/j.jallcom.2020.157071 ↗
32. 10.1016/j.jallcom.2019.15254910.1016/j.jallcom.2019.152549 ↗
33. 10.1016/j.jmst.2021.11.03810.1016/j.jmst.2021.11.038 ↗
34. 10.2320/matertrans1989.32.9310.2320/matertrans1989.32.93 ↗
35. 10.1063/1.34214910.1063/1.342149 ↗
36. 10.1063/5.009266210.1063/5.0092662 ↗
37. 10.1016/S1359-6462(01)00700-X10.1016/S1359-6462(01)00700-X ↗
38. 10.1016/S0304-8853(00)00136-010.1016/S0304-8853(00)00136-0 ↗
39. 10.1063/1.36909910.1063/1.369099 ↗
40. Yoshizawa Y. · Advances in Nanocrystallization · 1999 · 307 · 51
41. 10.1016/S0921-5093(96)10693-610.1016/S0921-5093(96)10693-6 ↗
42. 10.4028/www.scientific.net/MSF.179-181.49710.4028/www.scientific.net/MSF.179-181.497 ↗
43. 10.1063/1.35455510.1063/1.354555 ↗
44. 10.1063/1.36900710.1063/1.369007 ↗
45. 10.4028/www.scientific.net/MSF.307.5110.4028/www.scientific.net/MSF.307.51 ↗
46. Pedregosa F. · J. Mach. Learn Res. · 2011 · 12 · 2825
47. 10.1063/1.36053710.1063/1.360537 ↗
48. 10.1016/0927-0256(96)00008-010.1016/0927-0256(96)00008-0 ↗
49. 10.1063/1.481232310.1063/1.4812323 ↗
50. 10.1103/PhysRevLett.78.139610.1103/PhysRevLett.78.1396 ↗
51. 10.1080/0026897840010120110.1080/00268978400101201 ↗